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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">ppan</journal-id><journal-title-group><journal-title xml:lang="en">Personalized Psychiatry and Neurology</journal-title><trans-title-group xml:lang="ru"><trans-title>Personalized Psychiatry and Neurology</trans-title></trans-title-group></journal-title-group><issn pub-type="epub">2712-9179</issn><publisher><publisher-name>V. M. Bekhterev National Medical Research Centre for Psychiatry and Neurology of the Ministry of Health of the Russian Federation (Bekhterev NMRC PN)</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.52667/2712-9179-2025-5-4-26-68</article-id><article-id custom-type="elpub" pub-id-type="custom">ppan-147</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>A Personalized Approach to Phytotherapy for Pain and Inflammation in Patients with Intervertebral Disc Degeneration: Prospects and Limitations</article-title><trans-title-group xml:lang="ru"><trans-title></trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Ashkhotov</surname><given-names>Azamat V.</given-names></name></name-alternatives><bio xml:lang="en"><p>192019 Saint Petersburg</p></bio><email xlink:type="simple">ashkhotov.v@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Trefilova</surname><given-names>Vera V.</given-names></name></name-alternatives><bio xml:lang="en"><p>192019 Saint Petersburg</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Shirukova</surname><given-names>Asiyat M.</given-names></name></name-alternatives><bio xml:lang="en"><p>192019 Saint Petersburg</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Shnayder</surname><given-names>Natalia A.</given-names></name></name-alternatives><bio xml:lang="en"><p>192019 Saint Petersburg; 660022 Krasnoyarsk</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Petrova</surname><given-names>Marina M.</given-names></name></name-alternatives><bio xml:lang="en"><p>660022 Krasnoyarsk</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Chavyr</surname><given-names>Vera S.</given-names></name></name-alternatives><bio xml:lang="en"><p>660022 Krasnoyarsk</p></bio><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff xml:lang="en" id="aff-1"><institution>V.M. Bekhterev National Medical Research Centre for Psychiatry and Neurology</institution><country>Russian Federation</country></aff><aff xml:lang="en" id="aff-2"><institution>V.M. Bekhterev National Medical Research Centre for Psychiatry and Neurology; V.F. Voino-Yasenetsky Krasnoyarsk State Medical University</institution><country>Russian Federation</country></aff><aff xml:lang="en" id="aff-3"><institution>V.F. Voino-Yasenetsky Krasnoyarsk State Medical University</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>24</day><month>12</month><year>2025</year></pub-date><volume>5</volume><issue>4</issue><fpage>26</fpage><lpage>68</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Ashkhotov A.V., Trefilova V.V., Shirukova A.M., Shnayder N.A., Petrova M.M., Chavyr V.S., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Ashkhotov A.V., Trefilova V.V., Shirukova A.M., Shnayder N.A., Petrova M.M., Chavyr V.S.</copyright-holder><copyright-holder xml:lang="en">Ashkhotov A.V., Trefilova V.V., Shirukova A.M., Shnayder N.A., Petrova M.M., Chavyr V.S.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.jppn.ru/jour/article/view/147">https://www.jppn.ru/jour/article/view/147</self-uri><abstract><p>Phytotherapy, as a traditional medicine method, has diverse therapeutic properties that can be used for disease-modifying therapy of intervertebral disc degeneration (IDD) in humans. Of particular interest are herbal remedies for the correction of chronic inflammation (primarily cytokine imbalance). The aim of this descriptive review is to update knowledge about herbal methods that are promising or traditionally used for the correction of cytokine imbalance in IDD. The results of preclinical and clinical studies and publications of historical interest on the traditional use of herbal remedies in Eastern and Western medicine were analyzed. Most herbal remedies for the correction of cytokine imbalance in IDD have evidence classes C and D, while the number of herbal remedies with evidence classes A and B is still small, despite many years and even centuries of experience in traditional medicine. In recent decades, there has been a trend toward increased research interest in this topic, with a growing number of preclinical studies of herbal remedies in animal models of IDD and arthritis (including arthritis of the facet joints of the spine). This review has demonstrated that traditional herbal medicine has not lost its clinical significance and can be used as a component of disease-modifying therapy for IDD in humans. Planning and conducting new preclinical and clinical studies of herbal remedies for this disease are necessary to increase the level of evidence for their use in clinical practice in accordance with modern requirements.</p></abstract><kwd-group xml:lang="en"><kwd>phytotherapy</kwd><kwd>cytokines</kwd><kwd>cytokine status</kwd><kwd>disk degeneration</kwd><kwd>biomarker</kwd><kwd>chronic inflammation</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Organization WH. WHO traditional medicine strategy: 2014–2023. 2013. https://www.who.int/publications/i/item/9789241506096.</mixed-citation><mixed-citation xml:lang="en">Organization WH. WHO traditional medicine strategy: 2014–2023. 2013. https://www.who.int/publications/i/item/9789241506096.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Efremova, T. F. Herbal medicine. Modern explanatory dictionary of the Russian language: In 3 volumes - M.: AST, Astrel, Harvest, 2006; 3: R - Ya., 544.</mixed-citation><mixed-citation xml:lang="en">Efremova, T. F. Herbal medicine. Modern explanatory dictionary of the Russian language: In 3 volumes - M.: AST, Astrel, Harvest, 2006; 3: R - Ya., 544.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Walker, A.F. Herbal medicine: the science of the art. Proc. Nutr. Soc. 2006; 65:145–152. https://doi.org/10.1079/pns2006487.</mixed-citation><mixed-citation xml:lang="en">Walker, A.F. Herbal medicine: the science of the art. Proc. Nutr. Soc. 2006; 65:145–152. https://doi.org/10.1079/pns2006487.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Spelman, K.; Duke, J.A.; Bogenschutz-Godwin, M.J. The synergy principle in plants, pathogens, insects, herbivores and humans. In: Kaufman, P.B. (Ed.), Natural Products from Plants. 2006b; 2e. CRC Press, Boca Raton, FL, 475–501.</mixed-citation><mixed-citation xml:lang="en">Spelman, K.; Duke, J.A.; Bogenschutz-Godwin, M.J. The synergy principle in plants, pathogens, insects, herbivores and humans. In: Kaufman, P.B. (Ed.), Natural Products from Plants. 2006b; 2e. CRC Press, Boca Raton, FL, 475–501.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Agoston, V.; Csermely, P.; Pongor, S. Multiple weak hits confuse complex systems: a transcriptional regulatory network as an example. Phys Rev E Stat Nonlin Soft Matter Phys. 2005; 71:051909. https://doi.org/10.1103/PhysRevE.71.051909.</mixed-citation><mixed-citation xml:lang="en">Agoston, V.; Csermely, P.; Pongor, S. Multiple weak hits confuse complex systems: a transcriptional regulatory network as an example. Phys Rev E Stat Nonlin Soft Matter Phys. 2005; 71:051909. https://doi.org/10.1103/PhysRevE.71.051909.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Williamson, E.M. Synergy and other interactions in phytomedicines. Phytomedicine. 2001; 8:401-409. https://doi.org/10.1078/0944-7113-00060.</mixed-citation><mixed-citation xml:lang="en">Williamson, E.M. Synergy and other interactions in phytomedicines. Phytomedicine. 2001; 8:401-409. https://doi.org/10.1078/0944-7113-00060.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Ernst, E. Herbal medicines put into context. BMJ. 2003, 327, 881-882. https://doi.org/10.1136/bmj.327.7420.881.</mixed-citation><mixed-citation xml:lang="en">Ernst, E. Herbal medicines put into context. BMJ. 2003, 327, 881-882. https://doi.org/10.1136/bmj.327.7420.881.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Wagner, H. Phytomedicine research in Germany. Environ. Health Perspect. 1999; 107:779–781. doi: 10.1289/ehp.99107779.</mixed-citation><mixed-citation xml:lang="en">Wagner, H. Phytomedicine research in Germany. Environ. Health Perspect. 1999; 107:779–781. doi: 10.1289/ehp.99107779.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Shnayder, N.A.; Ashkhotov, A.V.; Trefilova, V.V.; Nurgaliev, Z.A.; Novitsky, M.A.; Petrova, M.M.; Narodova, E.A.; Al-Zamil, M.; Chumakova, G.A.; Garganeeva, N.P.; Nasyrova, R.F. Molecular basic of pharmacotherapy of cytokine imbalance as a component of intervertebral disc degeneration treatment. Int. J. Mol. Sci. 2023; 24:7692.</mixed-citation><mixed-citation xml:lang="en">Shnayder, N.A.; Ashkhotov, A.V.; Trefilova, V.V.; Nurgaliev, Z.A.; Novitsky, M.A.; Petrova, M.M.; Narodova, E.A.; Al-Zamil, M.; Chumakova, G.A.; Garganeeva, N.P.; Nasyrova, R.F. Molecular basic of pharmacotherapy of cytokine imbalance as a component of intervertebral disc degeneration treatment. Int. J. Mol. Sci. 2023; 24:7692.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Sommer, C. Animal studies on neuropathic pain: the role of cytokines and cytokine receptors in pathogenesis and therapy. Schmerz. 1999; 13:315- 323. https://doi.org/10.1007/s004829900038.</mixed-citation><mixed-citation xml:lang="en">Sommer, C. Animal studies on neuropathic pain: the role of cytokines and cytokine receptors in pathogenesis and therapy. Schmerz. 1999; 13:315- 323. https://doi.org/10.1007/s004829900038.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Engel, A.; Kern, W.V.; Murdter, G.; Kern, P. Kinetics and correlation with body temperature of circulating interleukin-6, interleukin-8, tumor necrosis factor alpha and interleukin-1 beta in patients with fever and neutropenia. Infection. 1994; 22:160-164. https://doi.org/10.1007/BF01716695.</mixed-citation><mixed-citation xml:lang="en">Engel, A.; Kern, W.V.; Murdter, G.; Kern, P. Kinetics and correlation with body temperature of circulating interleukin-6, interleukin-8, tumor necrosis factor alpha and interleukin-1 beta in patients with fever and neutropenia. Infection. 1994; 22:160-164. https://doi.org/10.1007/BF01716695.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Wichers, M.; Maes, M. The psychoneuroimmunopathophysiology of cytokine-induced depression in humans. Int J Neuropsychopharmacol. 2002; 5:375- 388. https://doi.org/10.1017/S1461145702003103.</mixed-citation><mixed-citation xml:lang="en">Wichers, M.; Maes, M. The psychoneuroimmunopathophysiology of cytokine-induced depression in humans. Int J Neuropsychopharmacol. 2002; 5:375- 388. https://doi.org/10.1017/S1461145702003103.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Belardelli, F.; Ferrantini, M. Cytokines as a link between innate and adaptive antitumor immunity. Trends Immunol. 2002; 23:201-208. doi: 10.1016/s1471-4906(02)02195-6.</mixed-citation><mixed-citation xml:lang="en">Belardelli, F.; Ferrantini, M. Cytokines as a link between innate and adaptive antitumor immunity. Trends Immunol. 2002; 23:201-208. doi: 10.1016/s1471-4906(02)02195-6.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Burns, J.J.; Zhao, L.; Will Taylor, E.; Spelman, K. The influence of traditional herbal formulas on cytokine activity. Toxicology. 2010; 278(1):40-159, https://doi.org/10.1016/j.tox.2009.09.020.</mixed-citation><mixed-citation xml:lang="en">Burns, J.J.; Zhao, L.; Will Taylor, E.; Spelman, K. The influence of traditional herbal formulas on cytokine activity. Toxicology. 2010; 278(1):40-159, https://doi.org/10.1016/j.tox.2009.09.020.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang, Y.W.; Wu, C.Y.; Cheng, J.T. Merit of Astragalus polysaccharide in the improvement of early diabetic nephropathy with an effect on mRNA expressions of NF-kappaB and IkappaB in renal cortex of streptozotoxin-induced diabetic rats. J Ethnopharmacol. 2007; 114(3):387-92. https://doi.org/10.1016/j.jep.2007.08.024.</mixed-citation><mixed-citation xml:lang="en">Zhang, Y.W.; Wu, C.Y.; Cheng, J.T. Merit of Astragalus polysaccharide in the improvement of early diabetic nephropathy with an effect on mRNA expressions of NF-kappaB and IkappaB in renal cortex of streptozotoxin-induced diabetic rats. J Ethnopharmacol. 2007; 114(3):387-92. https://doi.org/10.1016/j.jep.2007.08.024.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Rader, D.J. Inflammatory markers of coronary risk. N Engl J Med. 2000; 343:1179-1182. doi: 10.1056/NEJM200010193431609.</mixed-citation><mixed-citation xml:lang="en">Rader, D.J. Inflammatory markers of coronary risk. N Engl J Med. 2000; 343:1179-1182. doi: 10.1056/NEJM200010193431609.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Hodge, G.; Hodge, S.; Han, P. Allium sativum (garlic) suppresses leukocyte inflammatory cytokine production in vitro: potential therapeutic use in the treatment of inflammatory bowel disease. Cytometry. 2002; 48:209-215. https://doi.org/10.1002/cyto.10133.</mixed-citation><mixed-citation xml:lang="en">Hodge, G.; Hodge, S.; Han, P. Allium sativum (garlic) suppresses leukocyte inflammatory cytokine production in vitro: potential therapeutic use in the treatment of inflammatory bowel disease. Cytometry. 2002; 48:209-215. https://doi.org/10.1002/cyto.10133.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Ebadi, M.S. Pharmacodynamic basis of herbal medicine. Boca Raton, FL, CRC Press. 2002.</mixed-citation><mixed-citation xml:lang="en">Ebadi, M.S. Pharmacodynamic basis of herbal medicine. Boca Raton, FL, CRC Press. 2002.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Huang, K.C.; Williams, W.M. The pharmacology of chinese herbs. 2nd ed. Boca Raton, CRC Press. 1999.</mixed-citation><mixed-citation xml:lang="en">Huang, K.C.; Williams, W.M. The pharmacology of chinese herbs. 2nd ed. Boca Raton, CRC Press. 1999.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Khyade, M.S.; Vaikos, N.P. Phytochemical and antibacterial properties of leaves of Alstonia scholaris. R. Br. Afr J Biotechnol. 2009, 8, 6434–6436.</mixed-citation><mixed-citation xml:lang="en">Khyade, M.S.; Vaikos, N.P. Phytochemical and antibacterial properties of leaves of Alstonia scholaris. R. Br. Afr J Biotechnol. 2009, 8, 6434–6436.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Tiwari, O.P.; Sharma, M. Anti-arthritic evaluation of some traditionally used medicinal plants in FCA induced arthritis in rats. J Drug Deliv Ther. 2017; 7:74–79. https://doi.org/10.22270/jddt.v7i4.1475.</mixed-citation><mixed-citation xml:lang="en">Tiwari, O.P.; Sharma, M. Anti-arthritic evaluation of some traditionally used medicinal plants in FCA induced arthritis in rats. J Drug Deliv Ther. 2017; 7:74–79. https://doi.org/10.22270/jddt.v7i4.1475.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Gupta, S.; Mishra, K.P.; Singh, S.B.; Ganju, L. Inhibitory effects of andrographolide on activated macrophages and adjuvant-induced arthritis. Inflammopharmacology. 2018; 26:447–456. https://doi.org/10.1007/s10787-017-0375-7.</mixed-citation><mixed-citation xml:lang="en">Gupta, S.; Mishra, K.P.; Singh, S.B.; Ganju, L. Inhibitory effects of andrographolide on activated macrophages and adjuvant-induced arthritis. Inflammopharmacology. 2018; 26:447–456. https://doi.org/10.1007/s10787-017-0375-7.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Li, Y.; He, S.; Tang, J.; Ding, N.; Chu, X.; Cheng, L.; Ding, X.; Liang, T.; Feng, S.; Rahman, S.U.; Wang, X. Andrographolide inhibits inflammatory cytokines secretion in LPS-stimulated RAW264. 7 cells through suppression of NF-jB/ MAPK signaling pathway. Evid Based Complement Alternat Med. 2017; 2017:8248142. https://doi.org/10.1155/2017/8248142.</mixed-citation><mixed-citation xml:lang="en">Li, Y.; He, S.; Tang, J.; Ding, N.; Chu, X.; Cheng, L.; Ding, X.; Liang, T.; Feng, S.; Rahman, S.U.; Wang, X. Andrographolide inhibits inflammatory cytokines secretion in LPS-stimulated RAW264. 7 cells through suppression of NF-jB/ MAPK signaling pathway. Evid Based Complement Alternat Med. 2017; 2017:8248142. https://doi.org/10.1155/2017/8248142.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Kast, R.E. Borage oil reduction of rheumatoid arthritis activity may be mediated by increased cAMP that suppresses tumor necrosis factor-alpha. Int Immunopharmacol. 2001; 1:2197–2199. https://doi.org/10.1016/s1567-5769(01)00146-1.</mixed-citation><mixed-citation xml:lang="en">Kast, R.E. Borage oil reduction of rheumatoid arthritis activity may be mediated by increased cAMP that suppresses tumor necrosis factor-alpha. Int Immunopharmacol. 2001; 1:2197–2199. https://doi.org/10.1016/s1567-5769(01)00146-1.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Venkatesh, H.N.; Sudharshana, T.; Umesh, A.; Thippeswamy, S.; Kiragandur, M.; Devihalli, M. Antifungal and antimycotoxigenic properties of chemically characterised essential oil of Boswellia serrata Roxb. ex Colebr. Int J Food Prop. 2017; 20:1856–1868. https://doi.org/10.1080/10942912.2017.1354882</mixed-citation><mixed-citation xml:lang="en">Venkatesh, H.N.; Sudharshana, T.; Umesh, A.; Thippeswamy, S.; Kiragandur, M.; Devihalli, M. Antifungal and antimycotoxigenic properties of chemically characterised essential oil of Boswellia serrata Roxb. ex Colebr. Int J Food Prop. 2017; 20:1856–1868. https://doi.org/10.1080/10942912.2017.1354882</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Gonen, T.; Amital, H. Cannabis and Cannabinoids in the treatment of rheumatic diseases. Rambam Maimonides Med J. 2020; 11:e0007. https://doi.org/10.5041/RMMJ.10389.</mixed-citation><mixed-citation xml:lang="en">Gonen, T.; Amital, H. Cannabis and Cannabinoids in the treatment of rheumatic diseases. Rambam Maimonides Med J. 2020; 11:e0007. https://doi.org/10.5041/RMMJ.10389.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Nagarkatti, P.; Pandey, R.; Rieder, S.A.; Hegde, V.L.; Nagarkatti, M. Cannabinoids as novel anti-inflammatory drugs. Future Med Chem. 2009; 1:1333–1349. https://doi.org/10.4155/fmc.09.93.</mixed-citation><mixed-citation xml:lang="en">Nagarkatti, P.; Pandey, R.; Rieder, S.A.; Hegde, V.L.; Nagarkatti, M. Cannabinoids as novel anti-inflammatory drugs. Future Med Chem. 2009; 1:1333–1349. https://doi.org/10.4155/fmc.09.93.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Shimizu, T.; Takahata, M.; Kameda, Y.; Endo, T.; Hamano, H.; Hiratsuka, S.; Ota, M.; Iwasaki, N. Sialic acid-binding immunoglobulin-like lectin 15 (Siglec-15) mediates periarticular bone loss, but not joint destruction, in murine antigen-induced arthritis. Bone. 2015; 79:65–70. https://doi.org/10.1016/j.bone.2015.05.029.</mixed-citation><mixed-citation xml:lang="en">Shimizu, T.; Takahata, M.; Kameda, Y.; Endo, T.; Hamano, H.; Hiratsuka, S.; Ota, M.; Iwasaki, N. Sialic acid-binding immunoglobulin-like lectin 15 (Siglec-15) mediates periarticular bone loss, but not joint destruction, in murine antigen-induced arthritis. Bone. 2015; 79:65–70. https://doi.org/10.1016/j.bone.2015.05.029.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Kulkarni, Y.A.; Agarwal, S.; Garud, M.S. Effect of Jyotishmati (Celastrus paniculatus) seeds in animal models of pain and inflammation. J Ayurveda Int Med. 2015; 6(2):82-88. https://doi.org/10.4103/0975-9476.146540.</mixed-citation><mixed-citation xml:lang="en">Kulkarni, Y.A.; Agarwal, S.; Garud, M.S. Effect of Jyotishmati (Celastrus paniculatus) seeds in animal models of pain and inflammation. J Ayurveda Int Med. 2015; 6(2):82-88. https://doi.org/10.4103/0975-9476.146540.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Kothavade, P.S.; Bulani, V.; Deshpande, P.; Chowdhury, A.; Juvekar, A. The petroleum ether fraction of Celastrus paniculatus Willd. seeds demonstrates antiarthritic effect in adjuvant-induced arthritis in rats. J Tradit Chin Med Sci. 2015; 2:183–193. https://doi.org/10.1016/j.jtcms.2016.02.004.</mixed-citation><mixed-citation xml:lang="en">Kothavade, P.S.; Bulani, V.; Deshpande, P.; Chowdhury, A.; Juvekar, A. The petroleum ether fraction of Celastrus paniculatus Willd. seeds demonstrates antiarthritic effect in adjuvant-induced arthritis in rats. J Tradit Chin Med Sci. 2015; 2:183–193. https://doi.org/10.1016/j.jtcms.2016.02.004.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Vetal, S.; Bodhankar, S.; Mohan, V.; Thakurdesai, P. Anti-inflammatory and anti-arthritic activity of type-A procyanidine polyphenols from bark of Cinnamomum zeylanicum in rats. Food Sci Human Wellness. 2013; 2: 59–67. https://doi.org/10.1016/j.fshw.2013.03.003.</mixed-citation><mixed-citation xml:lang="en">Vetal, S.; Bodhankar, S.; Mohan, V.; Thakurdesai, P. Anti-inflammatory and anti-arthritic activity of type-A procyanidine polyphenols from bark of Cinnamomum zeylanicum in rats. Food Sci Human Wellness. 2013; 2: 59–67. https://doi.org/10.1016/j.fshw.2013.03.003.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Qadir, M.M.; Bhatti, A.; Ashraf, M.U.; Sandhu, M.A.; Anjum, S.; John, P. Immunomodulatory and therapeutic role of Cinnamomum verum extracts in collagen-induced arthritic BALB/c mice. Inflammopharmacology. 2018; 26:157–170. https://doi.org/10.1007/s10787-017-0349-9.</mixed-citation><mixed-citation xml:lang="en">Qadir, M.M.; Bhatti, A.; Ashraf, M.U.; Sandhu, M.A.; Anjum, S.; John, P. Immunomodulatory and therapeutic role of Cinnamomum verum extracts in collagen-induced arthritic BALB/c mice. Inflammopharmacology. 2018; 26:157–170. https://doi.org/10.1007/s10787-017-0349-9.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Mahmoud, N.; Ahmed, O.M. Citrus limon and paradisi fruit peel hydroethanolic extracts prevent the progress of complete Freund’s adjuvant-induced arthritis in male Wistar rats. Adv Anim Vet Sci. 2018; 6:443–455. https://doi.org/10.17582/journal.aavs/2018/6.10.443.455.</mixed-citation><mixed-citation xml:lang="en">Mahmoud, N.; Ahmed, O.M. Citrus limon and paradisi fruit peel hydroethanolic extracts prevent the progress of complete Freund’s adjuvant-induced arthritis in male Wistar rats. Adv Anim Vet Sci. 2018; 6:443–455. https://doi.org/10.17582/journal.aavs/2018/6.10.443.455.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Zou, G.S.; Li, S.-J.; Zheng, S.-l.; Pan, X.; Huang, Z.-p. Lemon-Peel extract ameliorates rheumatoid arthritis by reducing xanthine oxidase and inflammatory cytokine levels. J Taiwan Inst Chem Eng. 2018; 93:54–62. https://doi.org/10.1016/j.jtice.2018.07.036</mixed-citation><mixed-citation xml:lang="en">Zou, G.S.; Li, S.-J.; Zheng, S.-l.; Pan, X.; Huang, Z.-p. Lemon-Peel extract ameliorates rheumatoid arthritis by reducing xanthine oxidase and inflammatory cytokine levels. J Taiwan Inst Chem Eng. 2018; 93:54–62. https://doi.org/10.1016/j.jtice.2018.07.036</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Kim, B.H.; Yoon, J.H.; Yang, J.I.; Myung, S.J.; Lee, J.H.; Jung, E.U.; Yu, S.J.; Kim, Y.J.; Lee, H.S.; Kim, C.Y. Guggulsterone attenuates activation and survival of hepatic stellate cell by inhibiting nuclear factor kappa B activation and inducing apoptosis. J Gastroenterol Hepatol. 2013; 28:1859–1868. https://doi.org/10.1111/jgh.12314.</mixed-citation><mixed-citation xml:lang="en">Kim, B.H.; Yoon, J.H.; Yang, J.I.; Myung, S.J.; Lee, J.H.; Jung, E.U.; Yu, S.J.; Kim, Y.J.; Lee, H.S.; Kim, C.Y. Guggulsterone attenuates activation and survival of hepatic stellate cell by inhibiting nuclear factor kappa B activation and inducing apoptosis. J Gastroenterol Hepatol. 2013; 28:1859–1868. https://doi.org/10.1111/jgh.12314.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Kamarudin, T.A.; Othman, F.; Mohd Ramli, E.S.; Md Isa, N.; Das, S. Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count. EXCLI J. 2012; 11:226-236.</mixed-citation><mixed-citation xml:lang="en">Kamarudin, T.A.; Othman, F.; Mohd Ramli, E.S.; Md Isa, N.; Das, S. Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count. EXCLI J. 2012; 11:226-236.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Alvarez, L.; Rios, M.Y.; Esquivel, C.; Chávez, M.I.; Delgado, G.; Aguilar, M.I.; Villarreal, M.L.; Navarro, V. Cytotoxic isoflavans from eysenhardtia p olystachya. J Nat Prod. 1998, 61, 767–770. https://doi.org/10.1021/np970586b.</mixed-citation><mixed-citation xml:lang="en">Alvarez, L.; Rios, M.Y.; Esquivel, C.; Chávez, M.I.; Delgado, G.; Aguilar, M.I.; Villarreal, M.L.; Navarro, V. Cytotoxic isoflavans from eysenhardtia p olystachya. J Nat Prod. 1998, 61, 767–770. https://doi.org/10.1021/np970586b.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Maurya, S.K.; Raj, K.; Srivastava, A.K. Antidyslipidaemic activity of Glycyrrhiza glabra in high fructose diet induced dyslipidaemic Syrian golden hamsters. Indian J Clin Biochem. 2009, 24, 404-9. https://doi.org/10.1007/s12291-009-0072-4.</mixed-citation><mixed-citation xml:lang="en">Maurya, S.K.; Raj, K.; Srivastava, A.K. Antidyslipidaemic activity of Glycyrrhiza glabra in high fructose diet induced dyslipidaemic Syrian golden hamsters. Indian J Clin Biochem. 2009, 24, 404-9. https://doi.org/10.1007/s12291-009-0072-4.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Fard, M.T.; Arulselvan, P.; Karthivashan, G.; Adam, S.K.; Fakurazi, S. Bioactive extract from Moringa oleifera inhibits the pro-inflammatory mediators in lipopolysaccharide stimulated macrophages. Pharmacogn Mag. 2015, 11(4), S556-63. https://doi.org/10.4103/0973-1296.172961.</mixed-citation><mixed-citation xml:lang="en">Fard, M.T.; Arulselvan, P.; Karthivashan, G.; Adam, S.K.; Fakurazi, S. Bioactive extract from Moringa oleifera inhibits the pro-inflammatory mediators in lipopolysaccharide stimulated macrophages. Pharmacogn Mag. 2015, 11(4), S556-63. https://doi.org/10.4103/0973-1296.172961.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Mahdi, H.J.; Khan, N.A.K.; Asmawi, M.Z.B.; Mahmud, R.; A/L Murugaiyah, V. In vivo anti-arthritic and anti-nociceptive effects of ethanol extract of Moringa oleifera leaves on complete Freund’s adjuvant (CFA)-induced arthritis in rats. Integr Med Res. 2018, 7, 85–94. https://doi.org/10.1016/j.imr.2017.11.002.</mixed-citation><mixed-citation xml:lang="en">Mahdi, H.J.; Khan, N.A.K.; Asmawi, M.Z.B.; Mahmud, R.; A/L Murugaiyah, V. In vivo anti-arthritic and anti-nociceptive effects of ethanol extract of Moringa oleifera leaves on complete Freund’s adjuvant (CFA)-induced arthritis in rats. Integr Med Res. 2018, 7, 85–94. https://doi.org/10.1016/j.imr.2017.11.002.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Rout, G.R.; Mahato, A.; Senapati, S. In vitro clonal propagation of Nyctanthes arbor tristis Linn.-a medicinal tree. Hort Sci (Prague). 2007, 34, 84–89. https://doi.org/10.1007/s10535-008-0101-9</mixed-citation><mixed-citation xml:lang="en">Rout, G.R.; Mahato, A.; Senapati, S. In vitro clonal propagation of Nyctanthes arbor tristis Linn.-a medicinal tree. Hort Sci (Prague). 2007, 34, 84–89. https://doi.org/10.1007/s10535-008-0101-9</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Held, S.; Schieberle, P.; Somoza, V. Characterization of aterpineol as an anti-inflammatory component of orange juice by in vitro studies using oral buccal cells. J Agric Food Chem. 2007, 55, 8040–8046. https://doi.org/10.1021/jf071691m.</mixed-citation><mixed-citation xml:lang="en">Held, S.; Schieberle, P.; Somoza, V. Characterization of aterpineol as an anti-inflammatory component of orange juice by in vitro studies using oral buccal cells. J Agric Food Chem. 2007, 55, 8040–8046. https://doi.org/10.1021/jf071691m.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Uroos, M.; Abbas, Z.; Sattar, S.; Umer, N.; Shabbir, A.; Shafiq-Ur-Rehman; Sharif, A. Nyctanthes arbor-tristis ameliorated FCA-induced experimental arthritis: a comparative study among different extracts. Evid Based Complement Altern Med. 2017, 15, 93. https://doi.org/10.1155/2017/4634853.</mixed-citation><mixed-citation xml:lang="en">Uroos, M.; Abbas, Z.; Sattar, S.; Umer, N.; Shabbir, A.; Shafiq-Ur-Rehman; Sharif, A. Nyctanthes arbor-tristis ameliorated FCA-induced experimental arthritis: a comparative study among different extracts. Evid Based Complement Altern Med. 2017, 15, 93. https://doi.org/10.1155/2017/4634853.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Yarnell, E. Herbs for rheumatoid arthritis. Altern Complement Ther. 2017, 23, 149–156. https://doi.org/10.1089/act.2017.29123.eya.</mixed-citation><mixed-citation xml:lang="en">Yarnell, E. Herbs for rheumatoid arthritis. Altern Complement Ther. 2017, 23, 149–156. https://doi.org/10.1089/act.2017.29123.eya.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Bang, J.S.; Oh, D.H.; Choi, H.M.; Sur, B.J.; Lim, S.J.; Kim, J.Y.; Yang, H.I.; Yoo, M.C.; Hahm, D.H.; Kim, K.S. Anti-inflammatory and antiarthritic effects of piperine in human interleukin 1b-stimulated fibroblast-like synoviocytes and in rat arthritis models. Arthritis Res Ther. 2009, 11, R49. https://doi.org/10.1186/ar2662.</mixed-citation><mixed-citation xml:lang="en">Bang, J.S.; Oh, D.H.; Choi, H.M.; Sur, B.J.; Lim, S.J.; Kim, J.Y.; Yang, H.I.; Yoo, M.C.; Hahm, D.H.; Kim, K.S. Anti-inflammatory and antiarthritic effects of piperine in human interleukin 1b-stimulated fibroblast-like synoviocytes and in rat arthritis models. Arthritis Res Ther. 2009, 11, R49. https://doi.org/10.1186/ar2662.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Balbir-Gurman, A.; Fuhrman, B.; Braun-Moscovici, Y.; Markovits, D.; Aviram, M. Consumption of pomegranate decreases serum oxidative stress and reduces disease activity in patients with active rheumatoid arthritis: a pilot study. Israel Med Assoc J. 2011, 13, 474–479.</mixed-citation><mixed-citation xml:lang="en">Balbir-Gurman, A.; Fuhrman, B.; Braun-Moscovici, Y.; Markovits, D.; Aviram, M. Consumption of pomegranate decreases serum oxidative stress and reduces disease activity in patients with active rheumatoid arthritis: a pilot study. Israel Med Assoc J. 2011, 13, 474–479.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Sun, K.; Zhu, L.G.; Wei, X.; Yin, H.; Zhan, J.W.; Yin, X.L.; Han, T. Research progress in mechanism of Chinese herbal compounds and monomers in delaying lumbar intervertebral disc degeneration. Zhongguo Zhong Yao Za Zhi. 2022, 47, 2400–8. https://doi.org/10.19540/j.cnki.cjcmm.20211020.401.</mixed-citation><mixed-citation xml:lang="en">Sun, K.; Zhu, L.G.; Wei, X.; Yin, H.; Zhan, J.W.; Yin, X.L.; Han, T. Research progress in mechanism of Chinese herbal compounds and monomers in delaying lumbar intervertebral disc degeneration. Zhongguo Zhong Yao Za Zhi. 2022, 47, 2400–8. https://doi.org/10.19540/j.cnki.cjcmm.20211020.401.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Cui, X.; Trinh, K.; Wang, Y.J. Chinese herbal medicine for chronic neck pain due to cervical degenerative disc disease. Cochrane Database Syst Rev. 2010, 2010, Cd006556. https://doi.org/10.1002/14651858.CD006556.pub2.</mixed-citation><mixed-citation xml:lang="en">Cui, X.; Trinh, K.; Wang, Y.J. Chinese herbal medicine for chronic neck pain due to cervical degenerative disc disease. Cochrane Database Syst Rev. 2010, 2010, Cd006556. https://doi.org/10.1002/14651858.CD006556.pub2.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Yin, W.; Wang, T.S.; Yin, F.Z.; Cai, B.C. Analgesic and anti-inflammatory properties of brucine and brucine N-oxide extracted from seeds of Strychnos nux-vomica. J Ethnopharmacol. 2003, 88, 205–214. https://doi.org/10.1016/s0378-8741(03)00224-1.</mixed-citation><mixed-citation xml:lang="en">Yin, W.; Wang, T.S.; Yin, F.Z.; Cai, B.C. Analgesic and anti-inflammatory properties of brucine and brucine N-oxide extracted from seeds of Strychnos nux-vomica. J Ethnopharmacol. 2003, 88, 205–214. https://doi.org/10.1016/s0378-8741(03)00224-1.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Ekambaram, S.; Perumal, S.S.; Subramanian, V. Evaluation of antiarthritic activity of Strychnos potatorum Linn seeds in Freund’s adjuvant induced arthritic rat model. BMC Complement Altern Med. 2010, 10, 56. https://doi.org/10.1186/1472-6882-10-56.</mixed-citation><mixed-citation xml:lang="en">Ekambaram, S.; Perumal, S.S.; Subramanian, V. Evaluation of antiarthritic activity of Strychnos potatorum Linn seeds in Freund’s adjuvant induced arthritic rat model. BMC Complement Altern Med. 2010, 10, 56. https://doi.org/10.1186/1472-6882-10-56.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Lad, H.; Bhatnagar, D. Amelioration of oxidative and inflammatory changes by Swertia chirayita leaves in experimental arthritis. Inflammopharmacology. 2016, 24, 363–375. https://doi.org/10.1007/s10787-016-0290-3.</mixed-citation><mixed-citation xml:lang="en">Lad, H.; Bhatnagar, D. Amelioration of oxidative and inflammatory changes by Swertia chirayita leaves in experimental arthritis. Inflammopharmacology. 2016, 24, 363–375. https://doi.org/10.1007/s10787-016-0290-3.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Mandeville, A.; Cock, I.E. Terminalia chebula Retz. fruit extracts inhibit bacterial triggers of some autoimmune diseases and potentiate the activity of tetracycline. Indian J Microbiol. 2018, 58, 496–506. https://doi.org/10.1007/s12088-018-0754-9.</mixed-citation><mixed-citation xml:lang="en">Mandeville, A.; Cock, I.E. Terminalia chebula Retz. fruit extracts inhibit bacterial triggers of some autoimmune diseases and potentiate the activity of tetracycline. Indian J Microbiol. 2018, 58, 496–506. https://doi.org/10.1007/s12088-018-0754-9.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Ahmad, V.U.; Yasmeen, S.; Ali, Z.; Khan, M.A.; Choudhary, M.I.; Akhtar, F.; Miana, G.A.; Zahid, M. Taraxacin, a new guaianolide from Taraxacum wallichii. J. Nat. Prod. 2000, 63(7), 1010–1011. doi: 10.1021/np990495+.</mixed-citation><mixed-citation xml:lang="en">Ahmad, V.U.; Yasmeen, S.; Ali, Z.; Khan, M.A.; Choudhary, M.I.; Akhtar, F.; Miana, G.A.; Zahid, M. Taraxacin, a new guaianolide from Taraxacum wallichii. J. Nat. Prod. 2000, 63(7), 1010–1011. doi: 10.1021/np990495+.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Schutz, K.; Carle, R.; Schieber, A. Taraxacum - a review on its phytochemical and pharmacological profile. J. Ethnopharmacol. 2006, 107(3), 313–323. https://doi.org/10.1016/j.jep.2006.07.021.</mixed-citation><mixed-citation xml:lang="en">Schutz, K.; Carle, R.; Schieber, A. Taraxacum - a review on its phytochemical and pharmacological profile. J. Ethnopharmacol. 2006, 107(3), 313–323. https://doi.org/10.1016/j.jep.2006.07.021.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">San, Z.; Fu, Y.; Li, W.; Zhou, E.; Li, Y.; Song, X.; Wang, T.; Tian, Y.; Wei, Z.; Yao, M.; Cao, Y.; Zhang, N. Protective effect of taraxasterol on acute lung injury induced by lipopolysaccharide in mice. Int. Immunopharmacol. 2014, 19(2), 342–350. https://doi.org/10.1016/j.intimp.2014.01.031.</mixed-citation><mixed-citation xml:lang="en">San, Z.; Fu, Y.; Li, W.; Zhou, E.; Li, Y.; Song, X.; Wang, T.; Tian, Y.; Wei, Z.; Yao, M.; Cao, Y.; Zhang, N. Protective effect of taraxasterol on acute lung injury induced by lipopolysaccharide in mice. Int. Immunopharmacol. 2014, 19(2), 342–350. https://doi.org/10.1016/j.intimp.2014.01.031.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang, X.M.; Xiong, H.Z.; Li, H.Y.; Cheng, Y. Protective effect of taraxasterol against LPS-induced endotoxic shock by modulating inflammatory responses in mice. Immunopharmacol. Immunotoxicol. 2014, 36(1), 11–16. https://doi.org/10.3109/08923973.2013.861482.</mixed-citation><mixed-citation xml:lang="en">Zhang, X.M.; Xiong, H.Z.; Li, H.Y.; Cheng, Y. Protective effect of taraxasterol against LPS-induced endotoxic shock by modulating inflammatory responses in mice. Immunopharmacol. Immunotoxicol. 2014, 36(1), 11–16. https://doi.org/10.3109/08923973.2013.861482.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Liu, J.T.; Xiong, H.Z.; Cheng, Y.; Cui, C.D.; Zhang, X.; Xu, L.; Zhang, X.M. Effects of taraxasterol on ovalbumin-induced allergic asthma in mice. J. Ethnopharmacol. 2013, 148(3), 787–793. https://doi.org/10.1016/j.jep.2013.05.006.</mixed-citation><mixed-citation xml:lang="en">Liu, J.T.; Xiong, H.Z.; Cheng, Y.; Cui, C.D.; Zhang, X.; Xu, L.; Zhang, X.M. Effects of taraxasterol on ovalbumin-induced allergic asthma in mice. J. Ethnopharmacol. 2013, 148(3), 787–793. https://doi.org/10.1016/j.jep.2013.05.006.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Chen, J.; Wu, W.; Zhang, M.; Chen, C. Taraxasterol suppresses inflammation in IL-1β-induced rheumatoid arthritis fibroblast-like synoviocytes and rheumatoid arthritis progression in mice. Int Immunopharmacol. 2019, 70, 274-283. https://doi.org/10.1016/j.intimp.2019.02.029.</mixed-citation><mixed-citation xml:lang="en">Chen, J.; Wu, W.; Zhang, M.; Chen, C. Taraxasterol suppresses inflammation in IL-1β-induced rheumatoid arthritis fibroblast-like synoviocytes and rheumatoid arthritis progression in mice. Int Immunopharmacol. 2019, 70, 274-283. https://doi.org/10.1016/j.intimp.2019.02.029.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Jin, X.N.; Yan, E.Z.; Wang, H.M.; Sui, H.J.; Liu, Z.; Gao, W.; Jin, Y. Hyperoside exerts anti-inflammatory and anti-arthritic effects in LPS-stimulated human fibroblast-like synoviocytes in vitro and in mice with collagen-induced arthritis. Acta Pharmacol. Sin. 2016, 37(5), 674–686. https://doi.org/10.1038/aps.2016.7.</mixed-citation><mixed-citation xml:lang="en">Jin, X.N.; Yan, E.Z.; Wang, H.M.; Sui, H.J.; Liu, Z.; Gao, W.; Jin, Y. Hyperoside exerts anti-inflammatory and anti-arthritic effects in LPS-stimulated human fibroblast-like synoviocytes in vitro and in mice with collagen-induced arthritis. Acta Pharmacol. Sin. 2016, 37(5), 674–686. https://doi.org/10.1038/aps.2016.7.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Shnayder, N.A.; Ashhotov, A.V.; Trefilova, V.V.; Nurgaliev, Z.A.; Novitsky, M.A.; Vaiman, E.E.; Petrova, M.M.; Nasyrova, R.F. Cytokine imbalance as a biomarker of intervertebral disk degeneration. Int J Mol Sci. 2023, 24(3), 2360. https://doi.org/10.3390/ijms24032360.</mixed-citation><mixed-citation xml:lang="en">Shnayder, N.A.; Ashhotov, A.V.; Trefilova, V.V.; Nurgaliev, Z.A.; Novitsky, M.A.; Vaiman, E.E.; Petrova, M.M.; Nasyrova, R.F. Cytokine imbalance as a biomarker of intervertebral disk degeneration. Int J Mol Sci. 2023, 24(3), 2360. https://doi.org/10.3390/ijms24032360.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Nair, V.; Singh, S.; Gupta, Y.K. Anti-arthritic and disease modifying activity of Terminalia chebula Retz. in experimental models. J Pharm Pharmacol. 2010, 62, 1801–1806. https://doi.org/10.1111/j.2042-7158.2010.01193.x.</mixed-citation><mixed-citation xml:lang="en">Nair, V.; Singh, S.; Gupta, Y.K. Anti-arthritic and disease modifying activity of Terminalia chebula Retz. in experimental models. J Pharm Pharmacol. 2010, 62, 1801–1806. https://doi.org/10.1111/j.2042-7158.2010.01193.x.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Prasad, L.; Husain Khan, T.; Jahangir, T.; Sultana, S. Chemomodulatory effects of Terminalia chebula against nickel chloride induced oxidative stress and tumor promotion response in male Wistar rats. J Trace Elem Med Biol. 2006, 20, 233–239. https://doi.org/10.1016/j.jtemb.2006.07.003.</mixed-citation><mixed-citation xml:lang="en">Prasad, L.; Husain Khan, T.; Jahangir, T.; Sultana, S. Chemomodulatory effects of Terminalia chebula against nickel chloride induced oxidative stress and tumor promotion response in male Wistar rats. J Trace Elem Med Biol. 2006, 20, 233–239. https://doi.org/10.1016/j.jtemb.2006.07.003.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Khan, M.A.; Subramaneyaan, M.; Arora, V.K.; Banerjee, B.D.; Ahmed, R.S. Effect of Withania somnifera (Ashwagandha) root extract on amelioration of oxidative stress and autoantibodies production in collagen-induced arthritic rats. J Complement Integr Med. 2015, 12(2), 117-25. https://doi.org/10.1515/jcim-2014-0075.</mixed-citation><mixed-citation xml:lang="en">Khan, M.A.; Subramaneyaan, M.; Arora, V.K.; Banerjee, B.D.; Ahmed, R.S. Effect of Withania somnifera (Ashwagandha) root extract on amelioration of oxidative stress and autoantibodies production in collagen-induced arthritic rats. J Complement Integr Med. 2015, 12(2), 117-25. https://doi.org/10.1515/jcim-2014-0075.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Singh, D.; Aggarwal, A.; Maurya, R.; Naik, S. Withania somnifera inhibits NF-jB and AP-1 transcription factors in human peripheral blood and synovial fluid mononuclear cells. Phytother Res. 2007, 21, 905–913. https://doi.org/10.1002/ptr.2180.</mixed-citation><mixed-citation xml:lang="en">Singh, D.; Aggarwal, A.; Maurya, R.; Naik, S. Withania somnifera inhibits NF-jB and AP-1 transcription factors in human peripheral blood and synovial fluid mononuclear cells. Phytother Res. 2007, 21, 905–913. https://doi.org/10.1002/ptr.2180.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Khan, M.A.; Ahmed, R.S.; Chandra, N.; Arora, V.K.; Ali, A. In vivo, extract from Withania somnifera root ameliorates arthritis via regulation of key immune mediators of inflammation in experimental model of arthritis. Antiinflamm Antiallergy Agents Med Chem. 2019, 18, 55–70. https://doi.org/10.2174/1871523017666181116092934.</mixed-citation><mixed-citation xml:lang="en">Khan, M.A.; Ahmed, R.S.; Chandra, N.; Arora, V.K.; Ali, A. In vivo, extract from Withania somnifera root ameliorates arthritis via regulation of key immune mediators of inflammation in experimental model of arthritis. Antiinflamm Antiallergy Agents Med Chem. 2019, 18, 55–70. https://doi.org/10.2174/1871523017666181116092934.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Song, C.; Chen, R.; Cheng, K.; Zhou, D.; Mei, Y.; Yan, J.; Liu, Z. Exploring the pharmacological mechanism of Duhuo Jisheng Decoction in treating intervertebral disc degeneration based on network pharmacology. Medicine (Baltimore). 2023, 102(22), e33917. https://doi.org/10.1097/MD.0000000000033917.</mixed-citation><mixed-citation xml:lang="en">Song, C.; Chen, R.; Cheng, K.; Zhou, D.; Mei, Y.; Yan, J.; Liu, Z. Exploring the pharmacological mechanism of Duhuo Jisheng Decoction in treating intervertebral disc degeneration based on network pharmacology. Medicine (Baltimore). 2023, 102(22), e33917. https://doi.org/10.1097/MD.0000000000033917.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Liu, Z.C.; Wang, Z.L.; Huang, C.Y.; Fu, Z.J.; Liu, Y.; Wei, Z.C.; Liu, S.G.; Ma, C.; Shen, J.L.; Duan, D.D. Duhuo Jisheng decoction inhibits SDF-1-induced inflammation and matrix degradation in human degenerative nucleus pulposus cells in vitro through the CXCR4/NF-κB pathway. Acta Pharmacol Sin. 2018, 39, 912–22. https://doi.org/10.1038/aps.2018.36.</mixed-citation><mixed-citation xml:lang="en">Liu, Z.C.; Wang, Z.L.; Huang, C.Y.; Fu, Z.J.; Liu, Y.; Wei, Z.C.; Liu, S.G.; Ma, C.; Shen, J.L.; Duan, D.D. Duhuo Jisheng decoction inhibits SDF-1-induced inflammation and matrix degradation in human degenerative nucleus pulposus cells in vitro through the CXCR4/NF-κB pathway. Acta Pharmacol Sin. 2018, 39, 912–22. https://doi.org/10.1038/aps.2018.36.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Amitani, M.; Amitani, H.; Sloan, R. A.; Suzuki, H.; Sameshima, N.; Asakawa, A.; Nerome, Y.; Owaki, T.; Inui, A.; Hoshino, E. The translational aspect of complementary and alternative medicine for cancer with particular emphasis on Kampo. Frontiers in Pharmacology. 2015, 6, 150. https://doi.org/10.3389/fphar.2015.00150.</mixed-citation><mixed-citation xml:lang="en">Amitani, M.; Amitani, H.; Sloan, R. A.; Suzuki, H.; Sameshima, N.; Asakawa, A.; Nerome, Y.; Owaki, T.; Inui, A.; Hoshino, E. The translational aspect of complementary and alternative medicine for cancer with particular emphasis on Kampo. Frontiers in Pharmacology. 2015, 6, 150. https://doi.org/10.3389/fphar.2015.00150.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Shimato, Y.; Ota, M.; Asai, K.; Atsumi, T.; Tabuchi, Y.; Makino, T. Comparison of byakujutsu (Atractylodes rhizome) and sojutsu (Atractylodes lancea rhizome) on anti-inflammatory and immunostimulative effects in vitro. Journal of Natural Medicines. 2018, 72(1), 192–201. https://doi.org/10.1007/s11418-017-1131-4</mixed-citation><mixed-citation xml:lang="en">Shimato, Y.; Ota, M.; Asai, K.; Atsumi, T.; Tabuchi, Y.; Makino, T. Comparison of byakujutsu (Atractylodes rhizome) and sojutsu (Atractylodes lancea rhizome) on anti-inflammatory and immunostimulative effects in vitro. Journal of Natural Medicines. 2018, 72(1), 192–201. https://doi.org/10.1007/s11418-017-1131-4</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Nakada, Y.; Takano, N.; Arai, M. Clinical reasoning in Kampo education for teaching Kampo beginners. Tokai Journal of Experimental &amp; Clinical Medicine. 2018, 43(2), 68–73.</mixed-citation><mixed-citation xml:lang="en">Nakada, Y.; Takano, N.; Arai, M. Clinical reasoning in Kampo education for teaching Kampo beginners. Tokai Journal of Experimental &amp; Clinical Medicine. 2018, 43(2), 68–73.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Cui, J.; Shin, T.; Kawano, T.; Sato, H.; Kondo, E.; Toura, I.; Kaneko, Y.; Koseki, H.; Kanno, M.; Taniguchi, M. Requirement for Vα14 T cells in IL-12-mediated rejection of tumors. Science. 1997, 278, 1623–1626. https://doi.org/10.1126/science.278.5343.</mixed-citation><mixed-citation xml:lang="en">Cui, J.; Shin, T.; Kawano, T.; Sato, H.; Kondo, E.; Toura, I.; Kaneko, Y.; Koseki, H.; Kanno, M.; Taniguchi, M. Requirement for Vα14 T cells in IL-12-mediated rejection of tumors. Science. 1997, 278, 1623–1626. https://doi.org/10.1126/science.278.5343.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Matsumoto, T.; Sakurai, H.M.; Kiyohara, H.; Yamada, H. Orally administered decoction of Kampo (Japanese herbal) medicine “Juzen -Taiho –To” modulates cytokine secretion and induces NKT cells in mouse liver. Immunopharmacology. 2000, 46, 149–161. https://doi.org/10.1016/s0162-3109(99)00166-6.</mixed-citation><mixed-citation xml:lang="en">Matsumoto, T.; Sakurai, H.M.; Kiyohara, H.; Yamada, H. Orally administered decoction of Kampo (Japanese herbal) medicine “Juzen -Taiho –To” modulates cytokine secretion and induces NKT cells in mouse liver. Immunopharmacology. 2000, 46, 149–161. https://doi.org/10.1016/s0162-3109(99)00166-6.</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Fujiki, K.; Nakamura, M.; Matsuda, T.; Isogai, M.; Ikeda, M.; Yamamoto, Y.; Kitamura, M.; Sazaki, N.; Yakushiji, F.; Suzuki, S.; Tomiyama, J.; Uchida, T.; Taniguchi, K. IL-12 and IL-18 induction and subsequent NKT activation effects of the Japanese botanical medicine Juzentaihoto. Int J Mol Sci. 2008, 9(7), 1142-1155. doi: 10.3390/ijms9071142.</mixed-citation><mixed-citation xml:lang="en">Fujiki, K.; Nakamura, M.; Matsuda, T.; Isogai, M.; Ikeda, M.; Yamamoto, Y.; Kitamura, M.; Sazaki, N.; Yakushiji, F.; Suzuki, S.; Tomiyama, J.; Uchida, T.; Taniguchi, K. IL-12 and IL-18 induction and subsequent NKT activation effects of the Japanese botanical medicine Juzentaihoto. Int J Mol Sci. 2008, 9(7), 1142-1155. doi: 10.3390/ijms9071142.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Nishikawa, H.; Sakaguchi, S. Regulatory T cells in cancer immunotherapy. Current Opinion in Immunology. 2014, 27, 1–7. https://doi.org/10.1016/j.coi.2013.12.005.</mixed-citation><mixed-citation xml:lang="en">Nishikawa, H.; Sakaguchi, S. Regulatory T cells in cancer immunotherapy. Current Opinion in Immunology. 2014, 27, 1–7. https://doi.org/10.1016/j.coi.2013.12.005.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Matsumoto, T.; Moriya, M.; Kiyohara, H.; Tabuchi, Y.; Yamada, H. H. a Kampo (traditional Japanese herbal) medicine, and its polysaccharide portion stimulate G-CSF secretion from intestinal epithelial cells. Evidence-based Complementary and Alternative Medicine. 2010, 7(3), 331–340. https://doi.org/10.1093/ecam/nen007.</mixed-citation><mixed-citation xml:lang="en">Matsumoto, T.; Moriya, M.; Kiyohara, H.; Tabuchi, Y.; Yamada, H. H. a Kampo (traditional Japanese herbal) medicine, and its polysaccharide portion stimulate G-CSF secretion from intestinal epithelial cells. Evidence-based Complementary and Alternative Medicine. 2010, 7(3), 331–340. https://doi.org/10.1093/ecam/nen007.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Takaku, S.; Shimizu, M.; Takahashi, H. Japanese Kampo medicine Ninjin’yoeito synergistically enhances tumor vaccine effects mediated by CD8+ T cells. Oncology Letters. 2017, 13(5), 3471–3478. https://doi.org/10.3892/ol.2017.5937.</mixed-citation><mixed-citation xml:lang="en">Takaku, S.; Shimizu, M.; Takahashi, H. Japanese Kampo medicine Ninjin’yoeito synergistically enhances tumor vaccine effects mediated by CD8+ T cells. Oncology Letters. 2017, 13(5), 3471–3478. https://doi.org/10.3892/ol.2017.5937.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Kiyomi, A.; Matsuda, A.; Nara, M.; Yamazaki, K.; Imai, S.; Sugiura, M. Immunological differences in human peripheral blood mononuclear cells treated with traditional japanese herbal medicines Hochuekkito, Juzentaihoto, and Ninjin'yoeito from different pharmaceutical companies. Evid Based Complement Alternat Med. 2021, 2021, 7605057. https://doi.org/10.1155/2021/7605057.</mixed-citation><mixed-citation xml:lang="en">Kiyomi, A.; Matsuda, A.; Nara, M.; Yamazaki, K.; Imai, S.; Sugiura, M. Immunological differences in human peripheral blood mononuclear cells treated with traditional japanese herbal medicines Hochuekkito, Juzentaihoto, and Ninjin'yoeito from different pharmaceutical companies. Evid Based Complement Alternat Med. 2021, 2021, 7605057. https://doi.org/10.1155/2021/7605057.</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu, L.; Yu, C.; Zhang, X.; Yu, Z.; Zhan, F.; Yu, X.; Wang, S.; He, F.; Han, Y.; Zhao, H. The treatment of intervertebral disc degeneration using Traditional Chinese Medicine. Journal of Ethnopharmacology. 2020, 263, 113117. https://doi.org/10.1016/j.jep.2020.113117.</mixed-citation><mixed-citation xml:lang="en">Zhu, L.; Yu, C.; Zhang, X.; Yu, Z.; Zhan, F.; Yu, X.; Wang, S.; He, F.; Han, Y.; Zhao, H. The treatment of intervertebral disc degeneration using Traditional Chinese Medicine. Journal of Ethnopharmacology. 2020, 263, 113117. https://doi.org/10.1016/j.jep.2020.113117.</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Sun, J.; Li, X.; Zhou, H.; Liu, X.; Jia, J.; Xie, Q.; Peng, S.; Sun, X.; Wang, Q.; Yi, L. Anti-GAPDH Autoantibody is associated with increased disease activity and intracranial pressure in systemic Lupus Erythematosus. J Immunol Res. 2019, 2019, 7430780. https://doi.org/10.1155/2019/7430780.</mixed-citation><mixed-citation xml:lang="en">Sun, J.; Li, X.; Zhou, H.; Liu, X.; Jia, J.; Xie, Q.; Peng, S.; Sun, X.; Wang, Q.; Yi, L. Anti-GAPDH Autoantibody is associated with increased disease activity and intracranial pressure in systemic Lupus Erythematosus. J Immunol Res. 2019, 2019, 7430780. https://doi.org/10.1155/2019/7430780.</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang, Y.; Zhang, Q.; Wang, H.; Tang, D.; Zhang, Y.; Yimo, Z.; Yu, L. Expressions of IFN-γ and IL-4 before and after Treatment of Lupus Nephritis with Traditional Chinese Medicine Combined with Cyclophosphamide and Their Values for Efficacy Prediction and Evaluation. Iran J Public Health. 2020, 49(5), 886-895.</mixed-citation><mixed-citation xml:lang="en">Jiang, Y.; Zhang, Q.; Wang, H.; Tang, D.; Zhang, Y.; Yimo, Z.; Yu, L. Expressions of IFN-γ and IL-4 before and after Treatment of Lupus Nephritis with Traditional Chinese Medicine Combined with Cyclophosphamide and Their Values for Efficacy Prediction and Evaluation. Iran J Public Health. 2020, 49(5), 886-895.</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Xing, Q.; Fu, L.; Yu, Z.; Zhou, X. Efficacy and safety of integrated Traditional Chinese medicine and western medicine on the treatment of rheumatoid arthritis: a meta-analysis. Evidence Based Complementary and Alternative Medicine: eCAM. 2020, 2020, 15. https://doi.org/10.1155/2020/4348709.4348709.</mixed-citation><mixed-citation xml:lang="en">Xing, Q.; Fu, L.; Yu, Z.; Zhou, X. Efficacy and safety of integrated Traditional Chinese medicine and western medicine on the treatment of rheumatoid arthritis: a meta-analysis. Evidence Based Complementary and Alternative Medicine: eCAM. 2020, 2020, 15. https://doi.org/10.1155/2020/4348709.4348709.</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Abe, H.; Sakaguchi, M.; Arichi, S. Pharmacological studies on a prescription containing Bupleuri Radix (IV). Effects of saikosaponin on the anti-inflammatory action of glucocorticoid. Nihon Yakurigaku Zasshi. 1982, 80(2), 155–161.</mixed-citation><mixed-citation xml:lang="en">Abe, H.; Sakaguchi, M.; Arichi, S. Pharmacological studies on a prescription containing Bupleuri Radix (IV). Effects of saikosaponin on the anti-inflammatory action of glucocorticoid. Nihon Yakurigaku Zasshi. 1982, 80(2), 155–161.</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Yamazaki, K.; Kiyomi, A.; Imai, S.; Sugiura, M. Saireito (114) Increases IC50 and changes T-cell phenotype when used in combination with prednisolone therapy in human peripheral blood mononuclear cells. Evid Based Complement Alternat Med. 2022, 2022, 9738989. https://doi.org/10.1155/2022/9738989.</mixed-citation><mixed-citation xml:lang="en">Yamazaki, K.; Kiyomi, A.; Imai, S.; Sugiura, M. Saireito (114) Increases IC50 and changes T-cell phenotype when used in combination with prednisolone therapy in human peripheral blood mononuclear cells. Evid Based Complement Alternat Med. 2022, 2022, 9738989. https://doi.org/10.1155/2022/9738989.</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Fujii, O.; Kanai, T.; Kouzuma, S.; Baba, K.; Miki, A.; Hyodo, H.; Yamashita, T.; Unno, N.; Taketani, Y. Herbal medicines, Sairei-to and Tokishakuyaku-san, differently modulate the release of cytokines from decidual versus peripheral blood mononuclear cells. American Journal of Reproductive Immunology. 2001, 46(5), 369–372. https://doi.org/10.1034/j.1600-0897.2001.d01-26.x.</mixed-citation><mixed-citation xml:lang="en">Fujii, O.; Kanai, T.; Kouzuma, S.; Baba, K.; Miki, A.; Hyodo, H.; Yamashita, T.; Unno, N.; Taketani, Y. Herbal medicines, Sairei-to and Tokishakuyaku-san, differently modulate the release of cytokines from decidual versus peripheral blood mononuclear cells. American Journal of Reproductive Immunology. 2001, 46(5), 369–372. https://doi.org/10.1034/j.1600-0897.2001.d01-26.x.</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Korean Pharmacopuncture Institute. Pharmacopuncturology, Elsevier Korea, Seoul. 2011.</mixed-citation><mixed-citation xml:lang="en">Korean Pharmacopuncture Institute. Pharmacopuncturology, Elsevier Korea, Seoul. 2011.</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Park, J.; Lee, H.; Shin, B.C.; Lee, M.S.; Kim, B.; Kim, J.I. Pharmacopuncture in Korea: a systematic review and meta-analysis of randomized controlled trials, evid. Based. Complement, Alternative Media. 2016, 2016, 4683121. https://doi.org/10.1155/2016/4683121.</mixed-citation><mixed-citation xml:lang="en">Park, J.; Lee, H.; Shin, B.C.; Lee, M.S.; Kim, B.; Kim, J.I. Pharmacopuncture in Korea: a systematic review and meta-analysis of randomized controlled trials, evid. Based. Complement, Alternative Media. 2016, 2016, 4683121. https://doi.org/10.1155/2016/4683121.</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Park, S.H.; Hong, J.Y.; Kim, W.K.; Shin, J.S.; Lee, J.; Ha, I.H.; Chung, H.J.; Lee, S.K. Effects of SHINBARO2 on rat models of lumbar spinal stenosis. Mediators Inflamm. 2019, 2019, 7651470. https://doi.org/10.1155/2019/7651470.</mixed-citation><mixed-citation xml:lang="en">Park, S.H.; Hong, J.Y.; Kim, W.K.; Shin, J.S.; Lee, J.; Ha, I.H.; Chung, H.J.; Lee, S.K. Effects of SHINBARO2 on rat models of lumbar spinal stenosis. Mediators Inflamm. 2019, 2019, 7651470. https://doi.org/10.1155/2019/7651470.</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Choi, H.S.; Lee, Y.J.; Kim, M.R.; Cho, J.H.; Kim, K.W.; Kim, E.J.; Ha, I.H. Survey of integrative treatment practices of Korean medicine doctors for cervical disc herniation: preliminary data for clinical practice guidelines. Evid Based Complement Alternat Med. 2019, 2019, 2345640. https://doi.org/10.1155/2019/2345640.</mixed-citation><mixed-citation xml:lang="en">Choi, H.S.; Lee, Y.J.; Kim, M.R.; Cho, J.H.; Kim, K.W.; Kim, E.J.; Ha, I.H. Survey of integrative treatment practices of Korean medicine doctors for cervical disc herniation: preliminary data for clinical practice guidelines. Evid Based Complement Alternat Med. 2019, 2019, 2345640. https://doi.org/10.1155/2019/2345640.</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Oliveira, C.B.; Maher, C.G.; Pinto, R.Z.; Traeger, A.C.; Lin, C.C.; Chenot, J.F.; van Tulder, M.; Koes, B.W. Clinical practice guidelines for the management of non-specific low back pain in primary care: an updated overview. Eur Spine J. 2018, 27, 2791–803. https://doi.org/10.1007/s00586-018-5673-2.</mixed-citation><mixed-citation xml:lang="en">Oliveira, C.B.; Maher, C.G.; Pinto, R.Z.; Traeger, A.C.; Lin, C.C.; Chenot, J.F.; van Tulder, M.; Koes, B.W. Clinical practice guidelines for the management of non-specific low back pain in primary care: an updated overview. Eur Spine J. 2018, 27, 2791–803. https://doi.org/10.1007/s00586-018-5673-2.</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Gao, W.; Feng, Z.; Zhang, S.; Wu, B.; Geng, X.; Fan, G.; Duan, Y.; Li, K.; Liu, K.; Peng, C. Anti-inflammatory and antioxidant effect of eucommia ulmoides polysaccharide in hepatic ischemia-reperfusion injury by regulating ROS and the TLR-4-NF-kappaB pathway. Biomed Res Int. 2020, 2020, 1860637. https://doi.org/10.1155/2020/1860637.</mixed-citation><mixed-citation xml:lang="en">Gao, W.; Feng, Z.; Zhang, S.; Wu, B.; Geng, X.; Fan, G.; Duan, Y.; Li, K.; Liu, K.; Peng, C. Anti-inflammatory and antioxidant effect of eucommia ulmoides polysaccharide in hepatic ischemia-reperfusion injury by regulating ROS and the TLR-4-NF-kappaB pathway. Biomed Res Int. 2020, 2020, 1860637. https://doi.org/10.1155/2020/1860637.</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">Kim, M.J.; Wang, H.S.; Lee, M.W. Anti-inflammatory effects of fermented bark of acanthopanax sessiliflorus and its isolated compounds on lipopolysaccharide-treated RAW 264. 7 macrophage cells. Evid Based Complement Alternat Med. 2020, 2020, 6749425. https://doi.org/10.1155/2020/6749425.</mixed-citation><mixed-citation xml:lang="en">Kim, M.J.; Wang, H.S.; Lee, M.W. Anti-inflammatory effects of fermented bark of acanthopanax sessiliflorus and its isolated compounds on lipopolysaccharide-treated RAW 264. 7 macrophage cells. Evid Based Complement Alternat Med. 2020, 2020, 6749425. https://doi.org/10.1155/2020/6749425.</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">Lee, S.G.; Lee, E.J.; Park, W.D.; Kim, J.B.; Kim, E.O.; Choi, S.W. Anti-inflammatory and anti-osteoarthritis effects of fermented Achyranthes japonica Nakai. J Ethnopharmacol. 2012, 142, 634–41. https://doi.org/10.1016/j.jep.2012.05.020.</mixed-citation><mixed-citation xml:lang="en">Lee, S.G.; Lee, E.J.; Park, W.D.; Kim, J.B.; Kim, E.O.; Choi, S.W. Anti-inflammatory and anti-osteoarthritis effects of fermented Achyranthes japonica Nakai. J Ethnopharmacol. 2012, 142, 634–41. https://doi.org/10.1016/j.jep.2012.05.020.</mixed-citation></citation-alternatives></ref><ref id="cit93"><label>93</label><citation-alternatives><mixed-citation xml:lang="ru">Hwang, L.; Ko, I.G.; Jin, J.J.; Kim, S.H.; Kim, C.J.; Jeon, J.W.; Han, J.H. Scolopendra subspinipes mutilans extract suppresses inflammatory and neuropathic pain in vitro and in vivo. Evid Based Complement Alternat Med. 2018, 2018, 5057372. https://doi.org/10.1155/2018/5057372.</mixed-citation><mixed-citation xml:lang="en">Hwang, L.; Ko, I.G.; Jin, J.J.; Kim, S.H.; Kim, C.J.; Jeon, J.W.; Han, J.H. Scolopendra subspinipes mutilans extract suppresses inflammatory and neuropathic pain in vitro and in vivo. Evid Based Complement Alternat Med. 2018, 2018, 5057372. https://doi.org/10.1155/2018/5057372.</mixed-citation></citation-alternatives></ref><ref id="cit94"><label>94</label><citation-alternatives><mixed-citation xml:lang="ru">He, J.; Li, X.; Wang, Z.; Bennett, S.; Chen, K.; Xiao, Z.; Zhan, J.; Chen, S.; Hou, Y.; Chen, J.; Wang, S.; Xu, J.; Lin, D. Therapeutic anabolic and anticatabolic benefits of natural chinese medicines for the treatment of osteoporosis. Front Pharmacol. 2019, 10, https://doi.org/1344. 10.3389/fphar.2019.01344.</mixed-citation><mixed-citation xml:lang="en">He, J.; Li, X.; Wang, Z.; Bennett, S.; Chen, K.; Xiao, Z.; Zhan, J.; Chen, S.; Hou, Y.; Chen, J.; Wang, S.; Xu, J.; Lin, D. Therapeutic anabolic and anticatabolic benefits of natural chinese medicines for the treatment of osteoporosis. Front Pharmacol. 2019, 10, https://doi.org/1344. 10.3389/fphar.2019.01344.</mixed-citation></citation-alternatives></ref><ref id="cit95"><label>95</label><citation-alternatives><mixed-citation xml:lang="ru">Jung, H.W.; Mahesh, R.; Park, J.H.; Boo, Y.C.; Park, K.M.; Park, Y.K. Bisabolangelone isolated from Ostericum koreanum inhibits the production of inflammatory mediators by down-regulation of NF-kappaB and ERK MAP kinase activity in LPS-stimulated RAW264. 7 cells .Int Immunopharmacol. 2010, 10, 155–62. https://doi.org/10.1016/j.intimp.2009.10.010.</mixed-citation><mixed-citation xml:lang="en">Jung, H.W.; Mahesh, R.; Park, J.H.; Boo, Y.C.; Park, K.M.; Park, Y.K. Bisabolangelone isolated from Ostericum koreanum inhibits the production of inflammatory mediators by down-regulation of NF-kappaB and ERK MAP kinase activity in LPS-stimulated RAW264. 7 cells .Int Immunopharmacol. 2010, 10, 155–62. https://doi.org/10.1016/j.intimp.2009.10.010.</mixed-citation></citation-alternatives></ref><ref id="cit96"><label>96</label><citation-alternatives><mixed-citation xml:lang="ru">Chao, W.W.; Lin, B.F. Bioactivities of major constituents isolated from Angelica sinensis (Danggui). Chin Med. 2011, 6, 29. https://doi.org/10.1186/1749-8546-6-29.</mixed-citation><mixed-citation xml:lang="en">Chao, W.W.; Lin, B.F. Bioactivities of major constituents isolated from Angelica sinensis (Danggui). Chin Med. 2011, 6, 29. https://doi.org/10.1186/1749-8546-6-29.</mixed-citation></citation-alternatives></ref><ref id="cit97"><label>97</label><citation-alternatives><mixed-citation xml:lang="ru">Cho, G.; Han, K.; Yoon, J. Stability test and quantitative and qualitative analyses of the amino acids in pharmacopuncture extracted from Scolopendra subspinipes mutilans. J Pharmacopuncture. 2015, 18, 44–55. https://doi.org/10.3831/KPI.2015.18.005.</mixed-citation><mixed-citation xml:lang="en">Cho, G.; Han, K.; Yoon, J. Stability test and quantitative and qualitative analyses of the amino acids in pharmacopuncture extracted from Scolopendra subspinipes mutilans. J Pharmacopuncture. 2015, 18, 44–55. https://doi.org/10.3831/KPI.2015.18.005.</mixed-citation></citation-alternatives></ref><ref id="cit98"><label>98</label><citation-alternatives><mixed-citation xml:lang="ru">Lee, H.; Hwang, J.S.; Lee, D.G. Scolopendin, an antimicrobial peptide from centipede, attenuates mitochondrial functions and triggers apoptosis in Candida albicans. Biochem J. 2017, 474, 635–45. https://doi.org/10.1042/BCJ20161039.</mixed-citation><mixed-citation xml:lang="en">Lee, H.; Hwang, J.S.; Lee, D.G. Scolopendin, an antimicrobial peptide from centipede, attenuates mitochondrial functions and triggers apoptosis in Candida albicans. Biochem J. 2017, 474, 635–45. https://doi.org/10.1042/BCJ20161039.</mixed-citation></citation-alternatives></ref><ref id="cit99"><label>99</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao, D.D.; Jiang, L.L.; Li, H.Y.; Yan, P.F.; Zhang, Y.L. Chemical components and pharmacological activities of terpene natural products from the genus paeonia. Molecules. 2016, 21, 10. https://doi.org/10.3390/molecules21101362.</mixed-citation><mixed-citation xml:lang="en">Zhao, D.D.; Jiang, L.L.; Li, H.Y.; Yan, P.F.; Zhang, Y.L. Chemical components and pharmacological activities of terpene natural products from the genus paeonia. Molecules. 2016, 21, 10. https://doi.org/10.3390/molecules21101362.</mixed-citation></citation-alternatives></ref><ref id="cit100"><label>100</label><citation-alternatives><mixed-citation xml:lang="ru">Cho, H.K.; Kim, S.Y.; Choi, M.J.; Baek, S.O.; Kwak, S.G.; Ahn, S.H. The effect of GCSB-5 a new herbal medicine on changes in pain behavior and neuroglial activation in a rat model of lumbar disc herniation. J Korean Neurosurg Soc. 2016, 59, 98–105. https://doi.org/10.3340/jkns.2016.59.2.98.</mixed-citation><mixed-citation xml:lang="en">Cho, H.K.; Kim, S.Y.; Choi, M.J.; Baek, S.O.; Kwak, S.G.; Ahn, S.H. The effect of GCSB-5 a new herbal medicine on changes in pain behavior and neuroglial activation in a rat model of lumbar disc herniation. J Korean Neurosurg Soc. 2016, 59, 98–105. https://doi.org/10.3340/jkns.2016.59.2.98.</mixed-citation></citation-alternatives></ref><ref id="cit101"><label>101</label><citation-alternatives><mixed-citation xml:lang="ru">Loffek, S.; Schilling, O.; Franzke, C.W. Series “matrix metalloproteinases in lung health and disease”: Biological role of matrix metalloproteinases: a critical balance. Eur Respir J. 2011, 38, 191–208. https://doi.org/10.1183/09031936.00146510.</mixed-citation><mixed-citation xml:lang="en">Loffek, S.; Schilling, O.; Franzke, C.W. Series “matrix metalloproteinases in lung health and disease”: Biological role of matrix metalloproteinases: a critical balance. Eur Respir J. 2011, 38, 191–208. https://doi.org/10.1183/09031936.00146510.</mixed-citation></citation-alternatives></ref><ref id="cit102"><label>102</label><citation-alternatives><mixed-citation xml:lang="ru">Kim, W.K.; Shin, J.S.; Lee, J.; Koh, W.; Ha, I.H.; Park, H.J.; Lee, S.K.; Hong, J.Y. Effects of the administration of Shinbaro 2 in a rat lumbar disk herniation model. Front. Neurol. 2023, 14, 1044724. https://doi.org/10.3389/fneur.2023.1044724.</mixed-citation><mixed-citation xml:lang="en">Kim, W.K.; Shin, J.S.; Lee, J.; Koh, W.; Ha, I.H.; Park, H.J.; Lee, S.K.; Hong, J.Y. Effects of the administration of Shinbaro 2 in a rat lumbar disk herniation model. Front. Neurol. 2023, 14, 1044724. https://doi.org/10.3389/fneur.2023.1044724.</mixed-citation></citation-alternatives></ref><ref id="cit103"><label>103</label><citation-alternatives><mixed-citation xml:lang="ru">Chung, H.J.; Lee, H.S.; Shin, J.S.; Lee, S.H.; Park, B.M.; Youn, Y.S.; Lee, S.K. Modulation of acute and chronic inflammatory processes by a traditional medicine preparation GCSB-5 both in vitro and in vivo animal models. J Ethnopharmacol. 2010, 130(3), 450-9. https://doi.org/10.1016/j.jep.2010.05.020.</mixed-citation><mixed-citation xml:lang="en">Chung, H.J.; Lee, H.S.; Shin, J.S.; Lee, S.H.; Park, B.M.; Youn, Y.S.; Lee, S.K. Modulation of acute and chronic inflammatory processes by a traditional medicine preparation GCSB-5 both in vitro and in vivo animal models. J Ethnopharmacol. 2010, 130(3), 450-9. https://doi.org/10.1016/j.jep.2010.05.020.</mixed-citation></citation-alternatives></ref><ref id="cit104"><label>104</label><citation-alternatives><mixed-citation xml:lang="ru">Spelman, K.; Burns, J.; Nichols, D.; Winters, N.; Ottersberg, S.; Tenborg, M. Modulation of cytokine expression by traditional medicines: a review of herbal immunomodulators. Alternative medicine review. 2006, 11(2), 128-50.</mixed-citation><mixed-citation xml:lang="en">Spelman, K.; Burns, J.; Nichols, D.; Winters, N.; Ottersberg, S.; Tenborg, M. Modulation of cytokine expression by traditional medicines: a review of herbal immunomodulators. Alternative medicine review. 2006, 11(2), 128-50.</mixed-citation></citation-alternatives></ref><ref id="cit105"><label>105</label><citation-alternatives><mixed-citation xml:lang="ru">Budai, M.M.; Varga, A.; Milesz, S.; Tőzsér, J.; Benkő, S. Aloe vera downregulates LPS-induced inflammatory cytokine production and expression of NLRP3 inflammasome in human macrophages. Mol Immunol. 2013, 56, 471–479. https://doi.org/10.1016/j.molimm.2013.05.005.</mixed-citation><mixed-citation xml:lang="en">Budai, M.M.; Varga, A.; Milesz, S.; Tőzsér, J.; Benkő, S. Aloe vera downregulates LPS-induced inflammatory cytokine production and expression of NLRP3 inflammasome in human macrophages. Mol Immunol. 2013, 56, 471–479. https://doi.org/10.1016/j.molimm.2013.05.005.</mixed-citation></citation-alternatives></ref><ref id="cit106"><label>106</label><citation-alternatives><mixed-citation xml:lang="ru">Kshirsagar, A.D.; Panchal, P.V.; Harle, U.N.; Nanda, R.K.; Shaikh, H.M. Anti-inflammatory and antiarthritic activity of anthraquinone derivatives in rodents. Int J Inflam. 2014, 2014, 690596. https://doi.org/10.1155/2014/690596.</mixed-citation><mixed-citation xml:lang="en">Kshirsagar, A.D.; Panchal, P.V.; Harle, U.N.; Nanda, R.K.; Shaikh, H.M. Anti-inflammatory and antiarthritic activity of anthraquinone derivatives in rodents. Int J Inflam. 2014, 2014, 690596. https://doi.org/10.1155/2014/690596.</mixed-citation></citation-alternatives></ref><ref id="cit107"><label>107</label><citation-alternatives><mixed-citation xml:lang="ru">Yagi, A.; Yu, B.P. Prophylactic aloe components on autoimmune diseases: barbaloin, aloe-emodin, emodin, and fermented butyrate. J Gastroenterol Hepatol Res. 2018, 7, 2535–2541. https://doi.org/10.17554/j.issn.2224-3992.2018.07.762.</mixed-citation><mixed-citation xml:lang="en">Yagi, A.; Yu, B.P. Prophylactic aloe components on autoimmune diseases: barbaloin, aloe-emodin, emodin, and fermented butyrate. J Gastroenterol Hepatol Res. 2018, 7, 2535–2541. https://doi.org/10.17554/j.issn.2224-3992.2018.07.762.</mixed-citation></citation-alternatives></ref><ref id="cit108"><label>108</label><citation-alternatives><mixed-citation xml:lang="ru">Yeşilada, E.; Küpeli, E. Berberis crataegina DC. Root exhibits potent anti-inflammatory, analgesic and febrifuge effects in mice and rats. J Ethnopharmacol. 2002, 79, 237–248. https://doi.org/10.1016/S0378-8741(01)00387-7.</mixed-citation><mixed-citation xml:lang="en">Yeşilada, E.; Küpeli, E. Berberis crataegina DC. Root exhibits potent anti-inflammatory, analgesic and febrifuge effects in mice and rats. J Ethnopharmacol. 2002, 79, 237–248. https://doi.org/10.1016/S0378-8741(01)00387-7.</mixed-citation></citation-alternatives></ref><ref id="cit109"><label>109</label><citation-alternatives><mixed-citation xml:lang="ru">Kumar, R.; Gupta, Y.K.; Singh, S. Anti-inflammatory and anti-granuloma activity of Berberis aristata DC. In experimental models of inflammation. Indian J Pharmacol. 2016, 48, 155–161. https://doi.org/10.4103/0253-7613.178831.</mixed-citation><mixed-citation xml:lang="en">Kumar, R.; Gupta, Y.K.; Singh, S. Anti-inflammatory and anti-granuloma activity of Berberis aristata DC. In experimental models of inflammation. Indian J Pharmacol. 2016, 48, 155–161. https://doi.org/10.4103/0253-7613.178831.</mixed-citation></citation-alternatives></ref><ref id="cit110"><label>110</label><citation-alternatives><mixed-citation xml:lang="ru">Alamgeer, Hasan, U.H.; Uttra, A.M.; Rasool, S. Evaluation of in vitro and in vivo anti-arthritic potential of Berberis calliobotrys. Bangladesh J Pharmacol. 2015, 10, 807–819. https://doi.org/10.3329/bjp.v10i4.23779.</mixed-citation><mixed-citation xml:lang="en">Alamgeer, Hasan, U.H.; Uttra, A.M.; Rasool, S. Evaluation of in vitro and in vivo anti-arthritic potential of Berberis calliobotrys. Bangladesh J Pharmacol. 2015, 10, 807–819. https://doi.org/10.3329/bjp.v10i4.23779.</mixed-citation></citation-alternatives></ref><ref id="cit111"><label>111</label><citation-alternatives><mixed-citation xml:lang="ru">Alamgeer, Uttra, A.M.; Hasan, U.H. Anti-arthritic activity of aqueous-methanolic extract and various fractions of Berberis orthobotrys Bien ex Aitch. BMC Complement Altern Med. 2017, 17(1), 371. https://doi.org/10.1186/s12906-017-1879-9.</mixed-citation><mixed-citation xml:lang="en">Alamgeer, Uttra, A.M.; Hasan, U.H. Anti-arthritic activity of aqueous-methanolic extract and various fractions of Berberis orthobotrys Bien ex Aitch. BMC Complement Altern Med. 2017, 17(1), 371. https://doi.org/10.1186/s12906-017-1879-9.</mixed-citation></citation-alternatives></ref><ref id="cit112"><label>112</label><citation-alternatives><mixed-citation xml:lang="ru">Ivanovska, N.; Philipov, S.; Hristov, M. Influence of berberine on T-cell mediated immunity. Immunopharmacol Immunotoxicol. 1999, 21, 771–786. https://doi.org/10.3109/08923979909007141.</mixed-citation><mixed-citation xml:lang="en">Ivanovska, N.; Philipov, S.; Hristov, M. Influence of berberine on T-cell mediated immunity. Immunopharmacol Immunotoxicol. 1999, 21, 771–786. https://doi.org/10.3109/08923979909007141.</mixed-citation></citation-alternatives></ref><ref id="cit113"><label>113</label><citation-alternatives><mixed-citation xml:lang="ru">Wang, Z.; Chen, Z.; Yang, S.; Wang, Y.; Huang, Z.; Gao, J.; Tu, S.; Rao, Z. Berberine ameliorates collagen induced arthritis in rats associated with anti-inflammatory and anti-angiogenic effects. Inflammation. 2014, 37, 1789. https://doi.org/10.1007/s10753-014-9909-y.</mixed-citation><mixed-citation xml:lang="en">Wang, Z.; Chen, Z.; Yang, S.; Wang, Y.; Huang, Z.; Gao, J.; Tu, S.; Rao, Z. Berberine ameliorates collagen induced arthritis in rats associated with anti-inflammatory and anti-angiogenic effects. Inflammation. 2014, 37, 1789. https://doi.org/10.1007/s10753-014-9909-y.</mixed-citation></citation-alternatives></ref><ref id="cit114"><label>114</label><citation-alternatives><mixed-citation xml:lang="ru">Yang, Y.; Qi, J.; Wang, Q.; Du, L.; Zhou, Y.; Yu, H.; Kijlstra, A.; Yang, P. Berberine suppresses Th17 and dendritic cell responses. Invest Ophthalmol Vis Sci. 2013, 54, 2516–2522. https://doi.org/10.1167/iovs.12-11217.</mixed-citation><mixed-citation xml:lang="en">Yang, Y.; Qi, J.; Wang, Q.; Du, L.; Zhou, Y.; Yu, H.; Kijlstra, A.; Yang, P. Berberine suppresses Th17 and dendritic cell responses. Invest Ophthalmol Vis Sci. 2013, 54, 2516–2522. https://doi.org/10.1167/iovs.12-11217.</mixed-citation></citation-alternatives></ref><ref id="cit115"><label>115</label><citation-alternatives><mixed-citation xml:lang="ru">Ivanovska, N.; Philipov, S. Study on the anti-inflammatory action of Berberis vulgaris root extract, alkaloid fractions and pure alkaloids. Int J lmmunopharmacol. 1996, 18, 553–561. https://doi.org/10.1016/S0192-0561(96)00047-1.</mixed-citation><mixed-citation xml:lang="en">Ivanovska, N.; Philipov, S. Study on the anti-inflammatory action of Berberis vulgaris root extract, alkaloid fractions and pure alkaloids. Int J lmmunopharmacol. 1996, 18, 553–561. https://doi.org/10.1016/S0192-0561(96)00047-1.</mixed-citation></citation-alternatives></ref><ref id="cit116"><label>116</label><citation-alternatives><mixed-citation xml:lang="ru">Mashwani, Z.; Khan, M.A.; Irum, S.; Ahmad, M. Antioxidant potential of root bark of Berberis lycium Royle. from Galliyat, Western Himalaya, Pakistan. Pak J Bot. 2013, 45, 231.</mixed-citation><mixed-citation xml:lang="en">Mashwani, Z.; Khan, M.A.; Irum, S.; Ahmad, M. Antioxidant potential of root bark of Berberis lycium Royle. from Galliyat, Western Himalaya, Pakistan. Pak J Bot. 2013, 45, 231.</mixed-citation></citation-alternatives></ref><ref id="cit117"><label>117</label><citation-alternatives><mixed-citation xml:lang="ru">Singh, J. K. Antihyperglycemic and anti-oxidant effect of Berberis aristata root extract and its role in regulating carbohydrate metabolism in diabetic rats. J Ethnopharmacol. 2009, 123, 22–26. https://doi.org/10.1016/j.jep.2009.02.038.</mixed-citation><mixed-citation xml:lang="en">Singh, J. K. Antihyperglycemic and anti-oxidant effect of Berberis aristata root extract and its role in regulating carbohydrate metabolism in diabetic rats. J Ethnopharmacol. 2009, 123, 22–26. https://doi.org/10.1016/j.jep.2009.02.038.</mixed-citation></citation-alternatives></ref><ref id="cit118"><label>118</label><citation-alternatives><mixed-citation xml:lang="ru">Koncic, M.Z.; Kremer, D.; Schuly, W.; Brantner, A.; Karlovic, K.; Kalodera, Z. Chemical differentiation of Berberis croatica vs B.vulgaris using HPLC fingerprinting. Croat Chem Acta. 2010, 83, 451–456.</mixed-citation><mixed-citation xml:lang="en">Koncic, M.Z.; Kremer, D.; Schuly, W.; Brantner, A.; Karlovic, K.; Kalodera, Z. Chemical differentiation of Berberis croatica vs B.vulgaris using HPLC fingerprinting. Croat Chem Acta. 2010, 83, 451–456.</mixed-citation></citation-alternatives></ref><ref id="cit119"><label>119</label><citation-alternatives><mixed-citation xml:lang="ru">Hanachi, P. Using HPLC to determination the composition and anti-oxidant activity of Berberis vulgaris. Eur J Sci Res. 2009, 29, 47–54.</mixed-citation><mixed-citation xml:lang="en">Hanachi, P. Using HPLC to determination the composition and anti-oxidant activity of Berberis vulgaris. Eur J Sci Res. 2009, 29, 47–54.</mixed-citation></citation-alternatives></ref><ref id="cit120"><label>120</label><citation-alternatives><mixed-citation xml:lang="ru">Ruiz, A.; Hermosí-Gutiérrez, I.; Mardones, C.; Vergara, C.; Herlitz, E.; Vega, M.; Dorau, C.; Winterhalter, P.; Von Baer, D. Polyphenols and anti-oxidant activity of Calafate (Berberis microphylla) fruits and other native berries from southern Chile. J Agric Food Chem. 2010, 58, 6081–6089. https://doi.org/10.1021/jf100173x.</mixed-citation><mixed-citation xml:lang="en">Ruiz, A.; Hermosí-Gutiérrez, I.; Mardones, C.; Vergara, C.; Herlitz, E.; Vega, M.; Dorau, C.; Winterhalter, P.; Von Baer, D. Polyphenols and anti-oxidant activity of Calafate (Berberis microphylla) fruits and other native berries from southern Chile. J Agric Food Chem. 2010, 58, 6081–6089. https://doi.org/10.1021/jf100173x.</mixed-citation></citation-alternatives></ref><ref id="cit121"><label>121</label><citation-alternatives><mixed-citation xml:lang="ru">Ghasemzadeh, A.; Ghasemzadeh, N. Flavonoids and phenolic acids: role and biochemical activity in plants and human. J Med Plant Res. 2011, 5, 6697–6703. https://doi.org/10.5897/JMPR11.1404.</mixed-citation><mixed-citation xml:lang="en">Ghasemzadeh, A.; Ghasemzadeh, N. Flavonoids and phenolic acids: role and biochemical activity in plants and human. J Med Plant Res. 2011, 5, 6697–6703. https://doi.org/10.5897/JMPR11.1404.</mixed-citation></citation-alternatives></ref><ref id="cit122"><label>122</label><citation-alternatives><mixed-citation xml:lang="ru">Alamgeer, Ambreen Malik, U.; Haseeb, A.; Umme Habiba, H.; Mueen Ahmad, C. Traditional medicines of plant origin used for the treatment of inflammatory disorders in Pakistan: A review. J Tradit Chin Med. 2018, 38(4), 636-656.</mixed-citation><mixed-citation xml:lang="en">Alamgeer, Ambreen Malik, U.; Haseeb, A.; Umme Habiba, H.; Mueen Ahmad, C. Traditional medicines of plant origin used for the treatment of inflammatory disorders in Pakistan: A review. J Tradit Chin Med. 2018, 38(4), 636-656.</mixed-citation></citation-alternatives></ref><ref id="cit123"><label>123</label><citation-alternatives><mixed-citation xml:lang="ru">Uttra, A.M.; Alamgeer, Shahzad, M.; Shabbir, A.; Jahan, S.; Bukhari, I.A.; Assiri, A.M. Ribes orientale: a novel therapeutic approach targeting rheumatoid arthritis with reference to pro-inflammatory cytokines, inflammatory enzymes and anti-inflammatory cytokines. J Ethnopharmacol. 2019, 237, 92–107. https://doi.org/10.1016/j.jep.2019.03.019.</mixed-citation><mixed-citation xml:lang="en">Uttra, A.M.; Alamgeer, Shahzad, M.; Shabbir, A.; Jahan, S.; Bukhari, I.A.; Assiri, A.M. Ribes orientale: a novel therapeutic approach targeting rheumatoid arthritis with reference to pro-inflammatory cytokines, inflammatory enzymes and anti-inflammatory cytokines. J Ethnopharmacol. 2019, 237, 92–107. https://doi.org/10.1016/j.jep.2019.03.019.</mixed-citation></citation-alternatives></ref><ref id="cit124"><label>124</label><citation-alternatives><mixed-citation xml:lang="ru">Valerio, M.; Awad, A.B. b-Sitosterol down-regulates some pro-inflammatory signal transduction pathways by increasing the activity of tyrosine phosphatase SHP-1 in J774A. 1 murine macrophages. Int Immunopharmacol. 2011, 11, 1012–1017. https://doi.org/10.1016/j.intimp.2011.02.018.</mixed-citation><mixed-citation xml:lang="en">Valerio, M.; Awad, A.B. b-Sitosterol down-regulates some pro-inflammatory signal transduction pathways by increasing the activity of tyrosine phosphatase SHP-1 in J774A. 1 murine macrophages. Int Immunopharmacol. 2011, 11, 1012–1017. https://doi.org/10.1016/j.intimp.2011.02.018.</mixed-citation></citation-alternatives></ref><ref id="cit125"><label>125</label><citation-alternatives><mixed-citation xml:lang="ru">Jain, H.; Dhingra, N.; Narsinghani, T.; Sharma, R. Insights into the mechanism of natural terpenoids as NF-jB inhibitors: an overview on their anticancer potential. Exp Oncol. 2016, 38, 158–168.</mixed-citation><mixed-citation xml:lang="en">Jain, H.; Dhingra, N.; Narsinghani, T.; Sharma, R. Insights into the mechanism of natural terpenoids as NF-jB inhibitors: an overview on their anticancer potential. Exp Oncol. 2016, 38, 158–168.</mixed-citation></citation-alternatives></ref><ref id="cit126"><label>126</label><citation-alternatives><mixed-citation xml:lang="ru">Reed, G.W.; Leung, K.; Rossetti, R.G.; Vanbuskirk, S.; Sharp, J.T.; Zurier, R.B. Treatment of rheumatoid arthritis with marine and botanical oils: an 18-month, randomized, and double-blind trial. Evid Based Complement Altern Med. 2014, 2014, 857456. https://doi.org/10.1155/2014/857456.</mixed-citation><mixed-citation xml:lang="en">Reed, G.W.; Leung, K.; Rossetti, R.G.; Vanbuskirk, S.; Sharp, J.T.; Zurier, R.B. Treatment of rheumatoid arthritis with marine and botanical oils: an 18-month, randomized, and double-blind trial. Evid Based Complement Altern Med. 2014, 2014, 857456. https://doi.org/10.1155/2014/857456.</mixed-citation></citation-alternatives></ref><ref id="cit127"><label>127</label><citation-alternatives><mixed-citation xml:lang="ru">Peng, W.; Wang, L.; Qiu, X.; Jiang, Y.; Han, T.; Pan, L.; Jia, X.; Qin, L.; Zheng, C. Therapeutic effects of Caragana pruinosa Kom. roots extract on type II collagen-induced arthritis in rats. J Ethnopharmacol. 2016, 191, 1–8. https://doi.org/10.1016/j.jep.2016.06.028.</mixed-citation><mixed-citation xml:lang="en">Peng, W.; Wang, L.; Qiu, X.; Jiang, Y.; Han, T.; Pan, L.; Jia, X.; Qin, L.; Zheng, C. Therapeutic effects of Caragana pruinosa Kom. roots extract on type II collagen-induced arthritis in rats. J Ethnopharmacol. 2016, 191, 1–8. https://doi.org/10.1016/j.jep.2016.06.028.</mixed-citation></citation-alternatives></ref><ref id="cit128"><label>128</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang, Q.; Peng, W.; Wei, S.; Wei, D.; Li, R.; Liu, J.; Peng, L.; Yang, S.; Gao, Y.; Wu, C.; Pu, X. Guizhi-ShaoyaoZhimu decoction possesses antiarthritic effects on type II collageninduced arthritis in rats via suppression of inflammatory reactions, inhibition of invasion &amp; migration and induction of apoptosis in synovial fibroblasts. Biomed Pharmacother. 2019, 118, 109367. https://doi.org/10.1016/j.biopha.2019.109367.</mixed-citation><mixed-citation xml:lang="en">Zhang, Q.; Peng, W.; Wei, S.; Wei, D.; Li, R.; Liu, J.; Peng, L.; Yang, S.; Gao, Y.; Wu, C.; Pu, X. Guizhi-ShaoyaoZhimu decoction possesses antiarthritic effects on type II collageninduced arthritis in rats via suppression of inflammatory reactions, inhibition of invasion &amp; migration and induction of apoptosis in synovial fibroblasts. Biomed Pharmacother. 2019, 118, 109367. https://doi.org/10.1016/j.biopha.2019.109367.</mixed-citation></citation-alternatives></ref><ref id="cit129"><label>129</label><citation-alternatives><mixed-citation xml:lang="ru">Adnan, M.; Jan, S.; Mussarat, S.; Tariq, A.; Begum, S.; Afroz, A.; Shinwari, Z. A review on ethnobotany, phytochemistry and pharmacology of plant genus CarallumaR. Br. J. Pharm. Pharmacol. 2014, 66, 1351–1368. https://doi.org/10.1111/ jphp.12265.</mixed-citation><mixed-citation xml:lang="en">Adnan, M.; Jan, S.; Mussarat, S.; Tariq, A.; Begum, S.; Afroz, A.; Shinwari, Z. A review on ethnobotany, phytochemistry and pharmacology of plant genus CarallumaR. Br. J. Pharm. Pharmacol. 2014, 66, 1351–1368. https://doi.org/10.1111/ jphp.12265.</mixed-citation></citation-alternatives></ref><ref id="cit130"><label>130</label><citation-alternatives><mixed-citation xml:lang="ru">Bin-Jumah, M.N. Antidiabetic effect of Monolluma quadrangula is mediated via modulation of glucose metabolizing enzymes, antioxidant defenses, and adiponectin in type 2 diabetic rats. Oxid. Med. Cell. Longev. 2019, 2019, 1–11. https://doi.org/ 10.1155/2019/6290143.</mixed-citation><mixed-citation xml:lang="en">Bin-Jumah, M.N. Antidiabetic effect of Monolluma quadrangula is mediated via modulation of glucose metabolizing enzymes, antioxidant defenses, and adiponectin in type 2 diabetic rats. Oxid. Med. Cell. Longev. 2019, 2019, 1–11. https://doi.org/ 10.1155/2019/6290143.</mixed-citation></citation-alternatives></ref><ref id="cit131"><label>131</label><citation-alternatives><mixed-citation xml:lang="ru">El-Shiekh, R.A.; El-Mekkawy, S.; Mouneir, S.M.; Hassan, A.; Abdel-Sattar, E. Therapeutic potential of russelioside B as anti-arthritic agent in Freund's adjuvant-induced arthritis in rats. J Ethnopharmacol. 2021, 270, 113779. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2021.113779.</mixed-citation><mixed-citation xml:lang="en">El-Shiekh, R.A.; El-Mekkawy, S.; Mouneir, S.M.; Hassan, A.; Abdel-Sattar, E. Therapeutic potential of russelioside B as anti-arthritic agent in Freund's adjuvant-induced arthritis in rats. J Ethnopharmacol. 2021, 270, 113779. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2021.113779.</mixed-citation></citation-alternatives></ref><ref id="cit132"><label>132</label><citation-alternatives><mixed-citation xml:lang="ru">Ray, S.; Nagaiah, K.; Khan, N.F. A study of anti-inflammatory activity of one novel C-21 steroidal glycoside known as carumbelloside-IV isolated from Caralluma umbellata. J. PharmaSciTech. 2012, 1, 12–14.</mixed-citation><mixed-citation xml:lang="en">Ray, S.; Nagaiah, K.; Khan, N.F. A study of anti-inflammatory activity of one novel C-21 steroidal glycoside known as carumbelloside-IV isolated from Caralluma umbellata. J. PharmaSciTech. 2012, 1, 12–14.</mixed-citation></citation-alternatives></ref><ref id="cit133"><label>133</label><citation-alternatives><mixed-citation xml:lang="ru">Seeka, C.; Prabpai, S.; Kongsaeree, P.; Tewtrakul, S.; Lhinhatrkool, T.; Sutthivaiyakit, S. Anti-inflammatory 12,20-epoxypregnane and 11,12-seco-Pregnane glycosides from the stems of Hoya kerrii. J. Nat. Prod. 2017, 80, 1714–1724. https://doi.org/ 10.1021/acs.jnatprod.6b00730.</mixed-citation><mixed-citation xml:lang="en">Seeka, C.; Prabpai, S.; Kongsaeree, P.; Tewtrakul, S.; Lhinhatrkool, T.; Sutthivaiyakit, S. Anti-inflammatory 12,20-epoxypregnane and 11,12-seco-Pregnane glycosides from the stems of Hoya kerrii. J. Nat. Prod. 2017, 80, 1714–1724. https://doi.org/ 10.1021/acs.jnatprod.6b00730.</mixed-citation></citation-alternatives></ref><ref id="cit134"><label>134</label><citation-alternatives><mixed-citation xml:lang="ru">Komarnytsky, S.; Ebora esposito, D.; Lexander Poulev, A.; Lya Raskin, I. Pregnane glycosides interfere with steroidogenic enzymes to down-regulate corticosteroid production in human adrenocortical H295R cells. J. Cell. Physiol. 2013, 228, 1120–1126. https://doi.org/10.1002/jcp.24262.</mixed-citation><mixed-citation xml:lang="en">Komarnytsky, S.; Ebora esposito, D.; Lexander Poulev, A.; Lya Raskin, I. Pregnane glycosides interfere with steroidogenic enzymes to down-regulate corticosteroid production in human adrenocortical H295R cells. J. Cell. Physiol. 2013, 228, 1120–1126. https://doi.org/10.1002/jcp.24262.</mixed-citation></citation-alternatives></ref><ref id="cit135"><label>135</label><citation-alternatives><mixed-citation xml:lang="ru">El-Hawary, S.S.; Mohammed, R.; Abouzid, S.; Ali, Y.; Elwekee, A. Anti-arthritic activity of 11-O-(40-O-methyl galloyl)-bergenin and Crassula capitella extract in rats. J. Pharm. Pharmacol. 2016, 68, 834–844. https://doi.org/10.1111/jphp.12566.</mixed-citation><mixed-citation xml:lang="en">El-Hawary, S.S.; Mohammed, R.; Abouzid, S.; Ali, Y.; Elwekee, A. Anti-arthritic activity of 11-O-(40-O-methyl galloyl)-bergenin and Crassula capitella extract in rats. J. Pharm. Pharmacol. 2016, 68, 834–844. https://doi.org/10.1111/jphp.12566.</mixed-citation></citation-alternatives></ref><ref id="cit136"><label>136</label><citation-alternatives><mixed-citation xml:lang="ru">Sun, X.; Liu, Y.; Yang, Y.; Liu, X.; Xiang, D. Anti-arthritic efect of total saponins from Clematis henryi Oliv. on collagen-induced arthritis rats. Eur J Infamm. 2016, 14(2), 71–77. https://doi.org/10.1007/s10787-019-00642-0.10.1177/1721727X16644448</mixed-citation><mixed-citation xml:lang="en">Sun, X.; Liu, Y.; Yang, Y.; Liu, X.; Xiang, D. Anti-arthritic efect of total saponins from Clematis henryi Oliv. on collagen-induced arthritis rats. Eur J Infamm. 2016, 14(2), 71–77. https://doi.org/10.1007/s10787-019-00642-0.10.1177/1721727X16644448</mixed-citation></citation-alternatives></ref><ref id="cit137"><label>137</label><citation-alternatives><mixed-citation xml:lang="ru">Pan, T.; Cheng, T.; Jia, Y.; Li, P.; Li, F. Anti-rheumatoid arthritis efects of traditional Chinese herb couple in adjuvant-induced arthritis in rats. J Ethnopharmacol. 2017, 205, 1–7. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2017.04.020.</mixed-citation><mixed-citation xml:lang="en">Pan, T.; Cheng, T.; Jia, Y.; Li, P.; Li, F. Anti-rheumatoid arthritis efects of traditional Chinese herb couple in adjuvant-induced arthritis in rats. J Ethnopharmacol. 2017, 205, 1–7. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2017.04.020.</mixed-citation></citation-alternatives></ref><ref id="cit138"><label>138</label><citation-alternatives><mixed-citation xml:lang="ru">Hasan, U.H.; Alamgeer, Shahzad, M.; Jahan, S.; Niazi, Z.R.; Bukhari, I.A.; Assiri, A.M.; Riaz, H. Inhibitory effects of Clematis orientalis aqueous ethanol extract and fractions on inflammatory markers in complete Freund's adjuvant-induced arthritis in Sprague-Dawley rats. Inflammopharmacology. 2019, 27(4), 781-797. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10787-018-0543-4.</mixed-citation><mixed-citation xml:lang="en">Hasan, U.H.; Alamgeer, Shahzad, M.; Jahan, S.; Niazi, Z.R.; Bukhari, I.A.; Assiri, A.M.; Riaz, H. Inhibitory effects of Clematis orientalis aqueous ethanol extract and fractions on inflammatory markers in complete Freund's adjuvant-induced arthritis in Sprague-Dawley rats. Inflammopharmacology. 2019, 27(4), 781-797. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10787-018-0543-4.</mixed-citation></citation-alternatives></ref><ref id="cit139"><label>139</label><citation-alternatives><mixed-citation xml:lang="ru">Scott, D.L.; Wolfe, F.; Huizinga, T.W. Rheumatoid arthritis. Lancet. 2010, 376, 1094–1108. https://doi.org/10.1007/s10787-019-00642-0.10.1016/S0140-6736(10)60826-4.</mixed-citation><mixed-citation xml:lang="en">Scott, D.L.; Wolfe, F.; Huizinga, T.W. Rheumatoid arthritis. Lancet. 2010, 376, 1094–1108. https://doi.org/10.1007/s10787-019-00642-0.10.1016/S0140-6736(10)60826-4.</mixed-citation></citation-alternatives></ref><ref id="cit140"><label>140</label><citation-alternatives><mixed-citation xml:lang="ru">Chaouche, T.M.; Haddouchi, F.; Ksouri, R.; Atik-Bekkara, F. Evaluation of antioxidant activity of hydromethanolic extracts of some medicinal species from South Algeria. J Chin Med Assoc. 2014, 77, 302–307. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jcma.2014.01.009.</mixed-citation><mixed-citation xml:lang="en">Chaouche, T.M.; Haddouchi, F.; Ksouri, R.; Atik-Bekkara, F. Evaluation of antioxidant activity of hydromethanolic extracts of some medicinal species from South Algeria. J Chin Med Assoc. 2014, 77, 302–307. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jcma.2014.01.009.</mixed-citation></citation-alternatives></ref><ref id="cit141"><label>141</label><citation-alternatives><mixed-citation xml:lang="ru">Jin, F. The pharmaceutical potential of compounds from Tasmanian Clematis species. 2012.</mixed-citation><mixed-citation xml:lang="en">Jin, F. The pharmaceutical potential of compounds from Tasmanian Clematis species. 2012.</mixed-citation></citation-alternatives></ref><ref id="cit142"><label>142</label><citation-alternatives><mixed-citation xml:lang="ru">Han, W.; Xiong, Y.; Li, Y.; Fang, W.; Ma, Y.; Liu, L.; Li, F.; Zhu, X. Anti-arthritic efects of clematichinenoside (AR-6) on PI3 K/Akt signaling pathway and TNF-α associated with collagen-induced arthritis. Pharm Biol. 2013, 51(1), 13–22. https://doi.org/10.1007/s10787-019-00642-0.10.3109/13880209.2012.698287.</mixed-citation><mixed-citation xml:lang="en">Han, W.; Xiong, Y.; Li, Y.; Fang, W.; Ma, Y.; Liu, L.; Li, F.; Zhu, X. Anti-arthritic efects of clematichinenoside (AR-6) on PI3 K/Akt signaling pathway and TNF-α associated with collagen-induced arthritis. Pharm Biol. 2013, 51(1), 13–22. https://doi.org/10.1007/s10787-019-00642-0.10.3109/13880209.2012.698287.</mixed-citation></citation-alternatives></ref><ref id="cit143"><label>143</label><citation-alternatives><mixed-citation xml:lang="ru">Bischof, S.C. Quercetin: potentials in the prevention and therapy of disease. Curr Opin Clin Nutr Metab Care. 2008, 11, 733–740. doi: 10.1097/MCO.0b013e32831394b8.</mixed-citation><mixed-citation xml:lang="en">Bischof, S.C. Quercetin: potentials in the prevention and therapy of disease. Curr Opin Clin Nutr Metab Care. 2008, 11, 733–740. doi: 10.1097/MCO.0b013e32831394b8.</mixed-citation></citation-alternatives></ref><ref id="cit144"><label>144</label><citation-alternatives><mixed-citation xml:lang="ru">Khan, S.; Dwivedi, C.; Parmar, V.; Srinivasan, K.K.; Shirwaikar, A. Methanol extract of dried exudate of Commiphora mukul prevents bone resorption in ovariectomized rats. Pharm Biol. 2012, 50, 1330–1336. https://doi.org/10.1007/s10787-019-00642-0.10.3109/13880209.2012.675339.</mixed-citation><mixed-citation xml:lang="en">Khan, S.; Dwivedi, C.; Parmar, V.; Srinivasan, K.K.; Shirwaikar, A. Methanol extract of dried exudate of Commiphora mukul prevents bone resorption in ovariectomized rats. Pharm Biol. 2012, 50, 1330–1336. https://doi.org/10.1007/s10787-019-00642-0.10.3109/13880209.2012.675339.</mixed-citation></citation-alternatives></ref><ref id="cit145"><label>145</label><citation-alternatives><mixed-citation xml:lang="ru">Chandrasekar, R.; Chandrasekar, S. Natural herbal treatment for rheumatoid arthritis-A review. Int J Pharm Sci Res. 2017, 8, 368.</mixed-citation><mixed-citation xml:lang="en">Chandrasekar, R.; Chandrasekar, S. Natural herbal treatment for rheumatoid arthritis-A review. Int J Pharm Sci Res. 2017, 8, 368.</mixed-citation></citation-alternatives></ref><ref id="cit146"><label>146</label><citation-alternatives><mixed-citation xml:lang="ru">Nair, V.; Singh, S.; Gupta, Y.K. Evaluation of disease modifying activity of Coriandrum sativum in experimental models. Indian J Med Res. 2012, 135(2), 240-5.</mixed-citation><mixed-citation xml:lang="en">Nair, V.; Singh, S.; Gupta, Y.K. Evaluation of disease modifying activity of Coriandrum sativum in experimental models. Indian J Med Res. 2012, 135(2), 240-5.</mixed-citation></citation-alternatives></ref><ref id="cit147"><label>147</label><citation-alternatives><mixed-citation xml:lang="ru">Qiao, C.F.; Li, Q.W.; Dong, H.; Xu, L.S.; Wang, Z.T. Studies on chemical constituents of two plants from Costus. Zhongguo Yao Xue Hui. 2002, 27, 123–125.</mixed-citation><mixed-citation xml:lang="en">Qiao, C.F.; Li, Q.W.; Dong, H.; Xu, L.S.; Wang, Z.T. Studies on chemical constituents of two plants from Costus. Zhongguo Yao Xue Hui. 2002, 27, 123–125.</mixed-citation></citation-alternatives></ref><ref id="cit148"><label>148</label><citation-alternatives><mixed-citation xml:lang="ru">Chandra, K.; Salman, A.S.; Mohd, A.; Sweety, R.; Ali, K.N. Protection against FCA induced oxidative stress induced DNA damage as a model of arthritis and In vitro anti-arthritic potential of costus speciosus rhizome extract. Inter J Pharma Phyto Res. 2015, 7, 383–389.</mixed-citation><mixed-citation xml:lang="en">Chandra, K.; Salman, A.S.; Mohd, A.; Sweety, R.; Ali, K.N. Protection against FCA induced oxidative stress induced DNA damage as a model of arthritis and In vitro anti-arthritic potential of costus speciosus rhizome extract. Inter J Pharma Phyto Res. 2015, 7, 383–389.</mixed-citation></citation-alternatives></ref><ref id="cit149"><label>149</label><citation-alternatives><mixed-citation xml:lang="ru">Henrotin, Y.; Malaise, M.; Wittoek, R.; de Vlam, K.; Brasseur, J.P.; Luyten, F.P.; Jiangang, Q.; Van den Berghe, M.; Uhoda, R.; Bentin, J.; De Vroey, T.; Erpicum, L.; Donneau, A.F.; Dierckxsens, Y. Bio-optimized Curcuma longa extract is efficient on knee osteoarthritis pain: a doubleblind multicenter randomized placebo controlled three-arm study. Arthritis Res Ther. 2019, 21(1), 179. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s13075-019-1960-5.</mixed-citation><mixed-citation xml:lang="en">Henrotin, Y.; Malaise, M.; Wittoek, R.; de Vlam, K.; Brasseur, J.P.; Luyten, F.P.; Jiangang, Q.; Van den Berghe, M.; Uhoda, R.; Bentin, J.; De Vroey, T.; Erpicum, L.; Donneau, A.F.; Dierckxsens, Y. Bio-optimized Curcuma longa extract is efficient on knee osteoarthritis pain: a doubleblind multicenter randomized placebo controlled three-arm study. Arthritis Res Ther. 2019, 21(1), 179. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s13075-019-1960-5.</mixed-citation></citation-alternatives></ref><ref id="cit150"><label>150</label><citation-alternatives><mixed-citation xml:lang="ru">Ratsch, C. The encyclopedia of psychoactive plants: Ethnopharmacology and its applications. Rochester, Park Street Press. 1998.</mixed-citation><mixed-citation xml:lang="en">Ratsch, C. The encyclopedia of psychoactive plants: Ethnopharmacology and its applications. Rochester, Park Street Press. 1998.</mixed-citation></citation-alternatives></ref><ref id="cit151"><label>151</label><citation-alternatives><mixed-citation xml:lang="ru">Gorsi, M.S.; Miraj, S. Ethnomedicinal survey of plants of Khanabad village and its allied areas, District Gilgit. Asian. J. Plant. Sci. 2002, 1, 604-615. https://doi.org/10.1007/s10787-019-00642-0.10.3923/ajps.2002.604.615</mixed-citation><mixed-citation xml:lang="en">Gorsi, M.S.; Miraj, S. Ethnomedicinal survey of plants of Khanabad village and its allied areas, District Gilgit. Asian. J. Plant. Sci. 2002, 1, 604-615. https://doi.org/10.1007/s10787-019-00642-0.10.3923/ajps.2002.604.615</mixed-citation></citation-alternatives></ref><ref id="cit152"><label>152</label><citation-alternatives><mixed-citation xml:lang="ru">Uttra, A.M.; Alamgeer, S.M.; Shabbir, A; Jahan, S. Ephedra gerardiana aqueous ethanolic extract and fractions attenuate Freund Complete Adjuvant induced arthritis in Sprague Dawley rats by downregulating PGE2, COX2, IL-1β, IL-6, TNF-α, NF-kB and upregulating IL-4 and IL-10. J Ethnopharmacol. 2018, 224, 482-496. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2018.06.018.</mixed-citation><mixed-citation xml:lang="en">Uttra, A.M.; Alamgeer, S.M.; Shabbir, A; Jahan, S. Ephedra gerardiana aqueous ethanolic extract and fractions attenuate Freund Complete Adjuvant induced arthritis in Sprague Dawley rats by downregulating PGE2, COX2, IL-1β, IL-6, TNF-α, NF-kB and upregulating IL-4 and IL-10. J Ethnopharmacol. 2018, 224, 482-496. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2018.06.018.</mixed-citation></citation-alternatives></ref><ref id="cit153"><label>153</label><citation-alternatives><mixed-citation xml:lang="ru">Babu, N.P.; Pandikumar, P.; Ignacimuthu, S. Lysosomal membrane stabilization and anti-inflammatory activity of Clerodendrum phlomidis L.f., a traditional medicinal plant. J. Ethnopharmacol. 2011, 135, 779-85. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2011.04.028.</mixed-citation><mixed-citation xml:lang="en">Babu, N.P.; Pandikumar, P.; Ignacimuthu, S. Lysosomal membrane stabilization and anti-inflammatory activity of Clerodendrum phlomidis L.f., a traditional medicinal plant. J. Ethnopharmacol. 2011, 135, 779-85. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2011.04.028.</mixed-citation></citation-alternatives></ref><ref id="cit154"><label>154</label><citation-alternatives><mixed-citation xml:lang="ru">Kyei, S.; Koffuor, G.A.; Boampong, J.N. Antiarthritic effect of aqueous and ethanolic leaf extracts of Pistia stratiotes in adjuvant-induced arthritis in Sprague-Dawley rats. J. Exp. Pharmacol. 2012, 4, 41-51. https://doi.org/10.1007/s10787-019-00642-0.10.2147/JEP.S29792.</mixed-citation><mixed-citation xml:lang="en">Kyei, S.; Koffuor, G.A.; Boampong, J.N. Antiarthritic effect of aqueous and ethanolic leaf extracts of Pistia stratiotes in adjuvant-induced arthritis in Sprague-Dawley rats. J. Exp. Pharmacol. 2012, 4, 41-51. https://doi.org/10.1007/s10787-019-00642-0.10.2147/JEP.S29792.</mixed-citation></citation-alternatives></ref><ref id="cit155"><label>155</label><citation-alternatives><mixed-citation xml:lang="ru">Kadam, P.; Bodhankar, S.L. Antiarthritic activity of ethanolic seed extracts of Diplocyclos palmatus (L) C. Jeffrey in experimental animals. Der. Pharm. Lett. 2013, 5, 233-242.</mixed-citation><mixed-citation xml:lang="en">Kadam, P.; Bodhankar, S.L. Antiarthritic activity of ethanolic seed extracts of Diplocyclos palmatus (L) C. Jeffrey in experimental animals. Der. Pharm. Lett. 2013, 5, 233-242.</mixed-citation></citation-alternatives></ref><ref id="cit156"><label>156</label><citation-alternatives><mixed-citation xml:lang="ru">Chakraborty, M.; Bhattacharya, S.; Bhattacharjee, P.; Das, R.; Mishra, R. Prevention of the progression of adjuvant induced arthritis by oral supplementation of Indian fresh water mussel (Lamellidens marginalis) aqueous extract in experimental rats. J. Ethnopharmacol. 2010, 132, 316-320. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2010.08.036.</mixed-citation><mixed-citation xml:lang="en">Chakraborty, M.; Bhattacharya, S.; Bhattacharjee, P.; Das, R.; Mishra, R. Prevention of the progression of adjuvant induced arthritis by oral supplementation of Indian fresh water mussel (Lamellidens marginalis) aqueous extract in experimental rats. J. Ethnopharmacol. 2010, 132, 316-320. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2010.08.036.</mixed-citation></citation-alternatives></ref><ref id="cit157"><label>157</label><citation-alternatives><mixed-citation xml:lang="ru">Badami, S.; Gupta, M.K.; Suresh, B. Antioxidant activity of ethanolic extract of Striga orobanchioides. J. Ethnopharmacol. 2003, 85, 227-230. https://doi.org/10.1007/s10787-019-00642-0.10.1016/s0378-8741(03)00021-7.</mixed-citation><mixed-citation xml:lang="en">Badami, S.; Gupta, M.K.; Suresh, B. Antioxidant activity of ethanolic extract of Striga orobanchioides. J. Ethnopharmacol. 2003, 85, 227-230. https://doi.org/10.1007/s10787-019-00642-0.10.1016/s0378-8741(03)00021-7.</mixed-citation></citation-alternatives></ref><ref id="cit158"><label>158</label><citation-alternatives><mixed-citation xml:lang="ru">Aiyegoro, O.A.; Okohm, A.I. Preliminary phytochemical screening and in vitro antioxidant activities of the aqueous extract of Helichrysum longifolium DC. BMC Complement. Altern. Med. 2010, 10, 21. https://doi.org/10.1007/s10787-019-00642-0.10.1186/1472-6882-10-21.</mixed-citation><mixed-citation xml:lang="en">Aiyegoro, O.A.; Okohm, A.I. Preliminary phytochemical screening and in vitro antioxidant activities of the aqueous extract of Helichrysum longifolium DC. BMC Complement. Altern. Med. 2010, 10, 21. https://doi.org/10.1007/s10787-019-00642-0.10.1186/1472-6882-10-21.</mixed-citation></citation-alternatives></ref><ref id="cit159"><label>159</label><citation-alternatives><mixed-citation xml:lang="ru">Kumaraswamy, M.V.; Satish, S. Antioxidant and Anti-Lipoxygenase activity of Thespesia lampas Dalz &amp; Gibs. Adv. Biol. Res. 2008, 2, 56-59.</mixed-citation><mixed-citation xml:lang="en">Kumaraswamy, M.V.; Satish, S. Antioxidant and Anti-Lipoxygenase activity of Thespesia lampas Dalz &amp; Gibs. Adv. Biol. Res. 2008, 2, 56-59.</mixed-citation></citation-alternatives></ref><ref id="cit160"><label>160</label><citation-alternatives><mixed-citation xml:lang="ru">Alonso-Castro, A.J.; Zapata-Morales, J.R.; Arana-Argáez, V.; Torres-Romero, J.C.; Ramírez-Villanueva, E.; Pérez-Medina, S.E.; Ramírez-Morales, M.A.; Juárez-Méndez, M.A.; Infante-Barrios, Y.P.; Martínez-Gutiérrez, F.; Carranza-Álvarez, C.; Isiordia-Espinoza, M.A.; Flores-Santos, A. Pharmacological and toxicological study of a chemical-standardized ethanol extract of the branches and leaves from Eysenhardtia polystachya (Ortega) Sarg. (Fabaceae). J Ethnopharmacol. 2018, 224, 314–322. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2018.06.016.</mixed-citation><mixed-citation xml:lang="en">Alonso-Castro, A.J.; Zapata-Morales, J.R.; Arana-Argáez, V.; Torres-Romero, J.C.; Ramírez-Villanueva, E.; Pérez-Medina, S.E.; Ramírez-Morales, M.A.; Juárez-Méndez, M.A.; Infante-Barrios, Y.P.; Martínez-Gutiérrez, F.; Carranza-Álvarez, C.; Isiordia-Espinoza, M.A.; Flores-Santos, A. Pharmacological and toxicological study of a chemical-standardized ethanol extract of the branches and leaves from Eysenhardtia polystachya (Ortega) Sarg. (Fabaceae). J Ethnopharmacol. 2018, 224, 314–322. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2018.06.016.</mixed-citation></citation-alternatives></ref><ref id="cit161"><label>161</label><citation-alternatives><mixed-citation xml:lang="ru">Pablo-Perez, S.S.; Parada-Cruz, B.; Barbier, O.C.; Meléndez-Camargo, M.E. The ethanolic extract of Eysenhardtia polystachya (Ort.)Sarg. bark and its fractions delay the progression of rheumatoid arthritis and show antinociceptive activity in murine models. Iran J Pharm Res. 2018, 17, 236-48.</mixed-citation><mixed-citation xml:lang="en">Pablo-Perez, S.S.; Parada-Cruz, B.; Barbier, O.C.; Meléndez-Camargo, M.E. The ethanolic extract of Eysenhardtia polystachya (Ort.)Sarg. bark and its fractions delay the progression of rheumatoid arthritis and show antinociceptive activity in murine models. Iran J Pharm Res. 2018, 17, 236-48.</mixed-citation></citation-alternatives></ref><ref id="cit162"><label>162</label><citation-alternatives><mixed-citation xml:lang="ru">Pan, F.; Chen, L.; Jiang, Y.; Xiong, L.; Min, L.; Xie, J.; Qi, J.; Xiao, H.; Chen, Y.; De Hoop, C.F. Bio-based UV protective films prepared with polylactic acid (PLA) and Phoebe zhennan extractives. Int J Biol Macromol. 2018, 119, 582–587. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.ijbiomac.2018.07.189.</mixed-citation><mixed-citation xml:lang="en">Pan, F.; Chen, L.; Jiang, Y.; Xiong, L.; Min, L.; Xie, J.; Qi, J.; Xiao, H.; Chen, Y.; De Hoop, C.F. Bio-based UV protective films prepared with polylactic acid (PLA) and Phoebe zhennan extractives. Int J Biol Macromol. 2018, 119, 582–587. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.ijbiomac.2018.07.189.</mixed-citation></citation-alternatives></ref><ref id="cit163"><label>163</label><citation-alternatives><mixed-citation xml:lang="ru">Huang, R.Y.; Chu, Y.L.; Jiang, Z.B.; Chen, X.M.; Zhang, X.; Zeng, X. Glycyrrhizin suppresses lung adenocarcinoma cell growth through inhibition of thromboxane synthase. Cell Physiol Biochem. 2014, 33, 375–388. https://doi.org/10.1007/s10787-019-00642-0.10.1159/000356677.</mixed-citation><mixed-citation xml:lang="en">Huang, R.Y.; Chu, Y.L.; Jiang, Z.B.; Chen, X.M.; Zhang, X.; Zeng, X. Glycyrrhizin suppresses lung adenocarcinoma cell growth through inhibition of thromboxane synthase. Cell Physiol Biochem. 2014, 33, 375–388. https://doi.org/10.1007/s10787-019-00642-0.10.1159/000356677.</mixed-citation></citation-alternatives></ref><ref id="cit164"><label>164</label><citation-alternatives><mixed-citation xml:lang="ru">169 Gao, S.; Wang, Q.; Tian, X.H.; Li, H.L.; Shen, Y.H.; Xu, X.K.; Wu, G.Z.; Hu, Z.L.; Zhang, W.D. Total sesquiterpene lactones prepared from Inula helenium L. has potentials in prevention and therapy of rheumatoid arthritis. J Ethnopharmacol. 2017, 196, 39–46. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2016.12.020.</mixed-citation><mixed-citation xml:lang="en">169 Gao, S.; Wang, Q.; Tian, X.H.; Li, H.L.; Shen, Y.H.; Xu, X.K.; Wu, G.Z.; Hu, Z.L.; Zhang, W.D. Total sesquiterpene lactones prepared from Inula helenium L. has potentials in prevention and therapy of rheumatoid arthritis. J Ethnopharmacol. 2017, 196, 39–46. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2016.12.020.</mixed-citation></citation-alternatives></ref><ref id="cit165"><label>165</label><citation-alternatives><mixed-citation xml:lang="ru">Chun, J.; Choi, R.J.; Khan, S.; Lee, D.S.; Kim, Y.C.; Nam, Y.J.; Lee, D.U.; Kim, Y.S. Alantolactone suppresses inducible nitric oxide synthase and cyclooxygenase-2 expression by down-regulating NFjB, MAPK and AP-1 via the MyD88 signaling pathway in LPS-activated RAW 264.7 cells. Int Immunopharmacol 2012, 14, 375–383. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.intimp.2012.08.011.</mixed-citation><mixed-citation xml:lang="en">Chun, J.; Choi, R.J.; Khan, S.; Lee, D.S.; Kim, Y.C.; Nam, Y.J.; Lee, D.U.; Kim, Y.S. Alantolactone suppresses inducible nitric oxide synthase and cyclooxygenase-2 expression by down-regulating NFjB, MAPK and AP-1 via the MyD88 signaling pathway in LPS-activated RAW 264.7 cells. Int Immunopharmacol 2012, 14, 375–383. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.intimp.2012.08.011.</mixed-citation></citation-alternatives></ref><ref id="cit166"><label>166</label><citation-alternatives><mixed-citation xml:lang="ru">Younis, T.; Khan, M.R.; Sajid, M.; Majid, M.; Zahra, Z.; Shah, N.A. Fraxinus xanthoxyloides leaves reduced the level of inflammatory mediators during in vitro and in vivo studies. BMC Complement Alt Med. 2016, 16, 230. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s12906-016-1189-7.</mixed-citation><mixed-citation xml:lang="en">Younis, T.; Khan, M.R.; Sajid, M.; Majid, M.; Zahra, Z.; Shah, N.A. Fraxinus xanthoxyloides leaves reduced the level of inflammatory mediators during in vitro and in vivo studies. BMC Complement Alt Med. 2016, 16, 230. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s12906-016-1189-7.</mixed-citation></citation-alternatives></ref><ref id="cit167"><label>167</label><citation-alternatives><mixed-citation xml:lang="ru">Majid, M.; Nasir, B.; Zahra, S.S.; Khan, M.R.; Mirza, B.; Haq, I.U. Ipomoea batatas L. Lam. ameliorates acute and chronic inflammations by suppressing inflammatory mediators, a comprehensive exploration using in vitro and in vivo models. BMC Complement Altern Med. 2018, 18, 216. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s12906-018-2279-5.</mixed-citation><mixed-citation xml:lang="en">Majid, M.; Nasir, B.; Zahra, S.S.; Khan, M.R.; Mirza, B.; Haq, I.U. Ipomoea batatas L. Lam. ameliorates acute and chronic inflammations by suppressing inflammatory mediators, a comprehensive exploration using in vitro and in vivo models. BMC Complement Altern Med. 2018, 18, 216. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s12906-018-2279-5.</mixed-citation></citation-alternatives></ref><ref id="cit168"><label>168</label><citation-alternatives><mixed-citation xml:lang="ru">Montserrat-De La Paz, S.; García-Giménez, M.D.; Ángel-Martín, M.; Pérez-Camino, M.C.; Fernández Arche, A. Longchain fatty alcohols from evening primrose oil inhibit the inflammatory response in murine peritoneal macrophages. J Ethnopharmacol. 2014, 151, 131–136. doi: 10.1016/j.jep.2013.10.012.</mixed-citation><mixed-citation xml:lang="en">Montserrat-De La Paz, S.; García-Giménez, M.D.; Ángel-Martín, M.; Pérez-Camino, M.C.; Fernández Arche, A. Longchain fatty alcohols from evening primrose oil inhibit the inflammatory response in murine peritoneal macrophages. J Ethnopharmacol. 2014, 151, 131–136. doi: 10.1016/j.jep.2013.10.012.</mixed-citation></citation-alternatives></ref><ref id="cit169"><label>169</label><citation-alternatives><mixed-citation xml:lang="ru">Voukeng, I.K.; Beng, V.P.; Kuete, V. Antibacterial activity of six medicinal Cameroonian plants against Gram-positive and Gram-negative multidrug resistant phenotypes. BMC Complement Altern Med. 2016, 16, 388. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s12906-016-1371-y.</mixed-citation><mixed-citation xml:lang="en">Voukeng, I.K.; Beng, V.P.; Kuete, V. Antibacterial activity of six medicinal Cameroonian plants against Gram-positive and Gram-negative multidrug resistant phenotypes. BMC Complement Altern Med. 2016, 16, 388. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s12906-016-1371-y.</mixed-citation></citation-alternatives></ref><ref id="cit170"><label>170</label><citation-alternatives><mixed-citation xml:lang="ru">Adeniyi, A.; Asase, A.; Ekpe, P.; Asitoakor, B.; Adu-Gyamfi, A.; Avekor, P. Ethnobotanical study of medicinal plants from Ghana; confirmation of ethnobotanical uses, and review of biological, and toxicological studies on medicinal plants used in Apra Hills Sacred Grove. J Herb Med. 2018, 14, 76–87. doi: 10.1016/j.hermed.2018.02.001</mixed-citation><mixed-citation xml:lang="en">Adeniyi, A.; Asase, A.; Ekpe, P.; Asitoakor, B.; Adu-Gyamfi, A.; Avekor, P. Ethnobotanical study of medicinal plants from Ghana; confirmation of ethnobotanical uses, and review of biological, and toxicological studies on medicinal plants used in Apra Hills Sacred Grove. J Herb Med. 2018, 14, 76–87. doi: 10.1016/j.hermed.2018.02.001</mixed-citation></citation-alternatives></ref><ref id="cit171"><label>171</label><citation-alternatives><mixed-citation xml:lang="ru">Soelberg, J.; Asase, A.; Akwetey, G.; Jäger, A.K. Historical versus contemporary medicinal plant uses in Ghana. J Ethnopharmacol. 2015, 160, 109–132. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2014.11.036.</mixed-citation><mixed-citation xml:lang="en">Soelberg, J.; Asase, A.; Akwetey, G.; Jäger, A.K. Historical versus contemporary medicinal plant uses in Ghana. J Ethnopharmacol. 2015, 160, 109–132. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2014.11.036.</mixed-citation></citation-alternatives></ref><ref id="cit172"><label>172</label><citation-alternatives><mixed-citation xml:lang="ru">Tseuguem, P.P.; Ngangoum, D.A.M.; Pouadjeu, J.M.; Piégang, B.N.; Sando, Z.; Kolber, B.J.; Tidgewell, K.J.; Nguelefack, T.B. Aqueous and methanol extracts of Paullinia pinnata L. (Sapindaceae) improve inflammation, pain and histological features in CFA-induced mono arthritis: evidence from in vivo and in vitro studies. J Ethnopharmacol. 2019, 236, 183–195. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2019.02.048.</mixed-citation><mixed-citation xml:lang="en">Tseuguem, P.P.; Ngangoum, D.A.M.; Pouadjeu, J.M.; Piégang, B.N.; Sando, Z.; Kolber, B.J.; Tidgewell, K.J.; Nguelefack, T.B. Aqueous and methanol extracts of Paullinia pinnata L. (Sapindaceae) improve inflammation, pain and histological features in CFA-induced mono arthritis: evidence from in vivo and in vitro studies. J Ethnopharmacol. 2019, 236, 183–195. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2019.02.048.</mixed-citation></citation-alternatives></ref><ref id="cit173"><label>173</label><citation-alternatives><mixed-citation xml:lang="ru">Mani, A.; Vasanthi, C.; Gopal, V.; Chellathai, D. Role of phyto-stabilised silver nanoparticles in suppressing adjuvant induced arthritis in rats. Int Immunopharmacol. 2016, 41, 17–23. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.intimp.2016.10.013.</mixed-citation><mixed-citation xml:lang="en">Mani, A.; Vasanthi, C.; Gopal, V.; Chellathai, D. Role of phyto-stabilised silver nanoparticles in suppressing adjuvant induced arthritis in rats. Int Immunopharmacol. 2016, 41, 17–23. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.intimp.2016.10.013.</mixed-citation></citation-alternatives></ref><ref id="cit174"><label>174</label><citation-alternatives><mixed-citation xml:lang="ru">Ch, M.I.; Ahmed, F.; Maqbool, M.; Hussain, T. Ethnomedicinal inventory of fora of maradori valley, district forward Khahuta, Azad Kashmir, Pakistan. Am J Res Commun. 2013, 1, 239–261.</mixed-citation><mixed-citation xml:lang="en">Ch, M.I.; Ahmed, F.; Maqbool, M.; Hussain, T. Ethnomedicinal inventory of fora of maradori valley, district forward Khahuta, Azad Kashmir, Pakistan. Am J Res Commun. 2013, 1, 239–261.</mixed-citation></citation-alternatives></ref><ref id="cit175"><label>175</label><citation-alternatives><mixed-citation xml:lang="ru">Saleem, A.; Saleem, M.; Akhtar, M.F.; Sharif, A.; Javaid, Z.; Sohail, K. In vitro and in vivo anti-arthritic evaluation of Polystichum braunii to validate its folkloric claim. Pak J Pharm Sci. 2019a, 32, 1167–1173.</mixed-citation><mixed-citation xml:lang="en">Saleem, A.; Saleem, M.; Akhtar, M.F.; Sharif, A.; Javaid, Z.; Sohail, K. In vitro and in vivo anti-arthritic evaluation of Polystichum braunii to validate its folkloric claim. Pak J Pharm Sci. 2019a, 32, 1167–1173.</mixed-citation></citation-alternatives></ref><ref id="cit176"><label>176</label><citation-alternatives><mixed-citation xml:lang="ru">Saleem, A.; Saleem, M.; Akhtar, M.F.; Shahzad, M.; Jahan, S. Polystichum braunii extracts inhibit Complete Freund's adjuvant-induced arthritis via upregulation of I-κB, IL-4, and IL-10, downregulation of COX-2, PGE2, IL-1β, IL-6, NF-κB, and TNF-α, and subsiding oxidative stress. Inflammopharmacology. 2020, 28(6), 1633-1648. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10787-020-00688-5.</mixed-citation><mixed-citation xml:lang="en">Saleem, A.; Saleem, M.; Akhtar, M.F.; Shahzad, M.; Jahan, S. Polystichum braunii extracts inhibit Complete Freund's adjuvant-induced arthritis via upregulation of I-κB, IL-4, and IL-10, downregulation of COX-2, PGE2, IL-1β, IL-6, NF-κB, and TNF-α, and subsiding oxidative stress. Inflammopharmacology. 2020, 28(6), 1633-1648. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10787-020-00688-5.</mixed-citation></citation-alternatives></ref><ref id="cit177"><label>177</label><citation-alternatives><mixed-citation xml:lang="ru">Shabbir, A.; Batool, S.A.; Basheer, M.I.; Shahzad, M.; Sultana, K.; Tareen, R.B.; Iqbal, J. Ziziphora clinopodioides ameliorated rheumatoid arthritis and infammatory paw edema in diferent models of acute and chronic infammation. Biomed Pharmacother. 2018, 97, 1710–1721. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.biopha.2017.11.118.</mixed-citation><mixed-citation xml:lang="en">Shabbir, A.; Batool, S.A.; Basheer, M.I.; Shahzad, M.; Sultana, K.; Tareen, R.B.; Iqbal, J. Ziziphora clinopodioides ameliorated rheumatoid arthritis and infammatory paw edema in diferent models of acute and chronic infammation. Biomed Pharmacother. 2018, 97, 1710–1721. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.biopha.2017.11.118.</mixed-citation></citation-alternatives></ref><ref id="cit178"><label>178</label><citation-alternatives><mixed-citation xml:lang="ru">Saleem, A.; Saleem, M.; Akhtar, M.F.; Shahzad, M.; Jahan, S. Moringa rivae leaf extracts attenuate Complete Freund’s adjuvantinduced arthritis in Wistar rats via modulation of infammatory and oxidative stress biomarkers. Infammopharmacology. 2020a, 28, 139–151. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10787-019-00596-3.</mixed-citation><mixed-citation xml:lang="en">Saleem, A.; Saleem, M.; Akhtar, M.F.; Shahzad, M.; Jahan, S. Moringa rivae leaf extracts attenuate Complete Freund’s adjuvantinduced arthritis in Wistar rats via modulation of infammatory and oxidative stress biomarkers. Infammopharmacology. 2020a, 28, 139–151. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10787-019-00596-3.</mixed-citation></citation-alternatives></ref><ref id="cit179"><label>179</label><citation-alternatives><mixed-citation xml:lang="ru">Kong, R.; Kang, O.H.; Seo, Y.S.; Zhou, T.; Kim, S.A.; Shin, D.W.; Kwon, D.Y. MAPKs and NF-κB pathway inhibitory efect of bisdemethoxycurcumin on phorbol-12-myristate-13-acetate and A23187-induced infammation in human mast cells. Mol Med Rep. 2018, 17, 630–635. https://doi.org/10.1007/s10787-019-00642-0.10.3892/mmr.2017.7852.</mixed-citation><mixed-citation xml:lang="en">Kong, R.; Kang, O.H.; Seo, Y.S.; Zhou, T.; Kim, S.A.; Shin, D.W.; Kwon, D.Y. MAPKs and NF-κB pathway inhibitory efect of bisdemethoxycurcumin on phorbol-12-myristate-13-acetate and A23187-induced infammation in human mast cells. Mol Med Rep. 2018, 17, 630–635. https://doi.org/10.1007/s10787-019-00642-0.10.3892/mmr.2017.7852.</mixed-citation></citation-alternatives></ref><ref id="cit180"><label>180</label><citation-alternatives><mixed-citation xml:lang="ru">Geng, Q.; Wei, Q.; Wang, S.; Qi, H.; Zhu, Q.; Liu, X.; Shi, X.; Wen, S. Physcion 8-O-β-glucopyranoside extracted from Polygonum cuspidatum exhibits anti-proliferative and anti-infammatory efects on MH7A rheumatoid arthritis-derived fbroblastlike synoviocytes through the TGF-β/MAPK pathway. Int J Mol Med. 2018, 42, 745–754. https://doi.org/10.1007/s10787-019-00642-0.10.3892/ijmm.2018.3649</mixed-citation><mixed-citation xml:lang="en">Geng, Q.; Wei, Q.; Wang, S.; Qi, H.; Zhu, Q.; Liu, X.; Shi, X.; Wen, S. Physcion 8-O-β-glucopyranoside extracted from Polygonum cuspidatum exhibits anti-proliferative and anti-infammatory efects on MH7A rheumatoid arthritis-derived fbroblastlike synoviocytes through the TGF-β/MAPK pathway. Int J Mol Med. 2018, 42, 745–754. https://doi.org/10.1007/s10787-019-00642-0.10.3892/ijmm.2018.3649</mixed-citation></citation-alternatives></ref><ref id="cit181"><label>181</label><citation-alternatives><mixed-citation xml:lang="ru">Perumal, S.S.; Ekambaram, S.P.; Dhanam, T. In vivo antiarthritic activity of the ethanol extracts of stem bark and seeds of Calophyllum inophyllum in Freund’s complete adjuvant induced arthritis. Pharm Biol. 2017, 55, 1330–1336. https://doi.org/10.1007/s10787-019-00642-0.10.1080/13880209.2016.1226346.</mixed-citation><mixed-citation xml:lang="en">Perumal, S.S.; Ekambaram, S.P.; Dhanam, T. In vivo antiarthritic activity of the ethanol extracts of stem bark and seeds of Calophyllum inophyllum in Freund’s complete adjuvant induced arthritis. Pharm Biol. 2017, 55, 1330–1336. https://doi.org/10.1007/s10787-019-00642-0.10.1080/13880209.2016.1226346.</mixed-citation></citation-alternatives></ref><ref id="cit182"><label>182</label><citation-alternatives><mixed-citation xml:lang="ru">Mirończuk-Chodakowska, I.; Witkowska, A.M.; Zujko, M.E. Endogenous non-enzymatic antioxidants in the human body. Adv Med Sci. 2018, 63, 68–78. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.advms.2017.05.005.</mixed-citation><mixed-citation xml:lang="en">Mirończuk-Chodakowska, I.; Witkowska, A.M.; Zujko, M.E. Endogenous non-enzymatic antioxidants in the human body. Adv Med Sci. 2018, 63, 68–78. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.advms.2017.05.005.</mixed-citation></citation-alternatives></ref><ref id="cit183"><label>183</label><citation-alternatives><mixed-citation xml:lang="ru">Foyet, H.S.; Tsala, D.E.; Bodo, J.Z.E.; Carine, A.N.; Heroyne, L.T.; Oben, E.K. Anti-infammatory and anti-arthritic activity of a methanol extract from Vitellaria paradoxa stem bark. Pharmacognosy Res. 2015, 7, 367–377. doi: 10.4103/0974-8490.159569.</mixed-citation><mixed-citation xml:lang="en">Foyet, H.S.; Tsala, D.E.; Bodo, J.Z.E.; Carine, A.N.; Heroyne, L.T.; Oben, E.K. Anti-infammatory and anti-arthritic activity of a methanol extract from Vitellaria paradoxa stem bark. Pharmacognosy Res. 2015, 7, 367–377. doi: 10.4103/0974-8490.159569.</mixed-citation></citation-alternatives></ref><ref id="cit184"><label>184</label><citation-alternatives><mixed-citation xml:lang="ru">Saleem, A.; Saleem, M.; Akhtar, M.F. Antioxidant, anti-infammatory and antiarthritic potential of Moringa oleifera Lam: an ethnomedicinal plant of Moringaceae family. S Afr J Bot. 2020b, 128, 246–256. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.sajb.2019.11.023</mixed-citation><mixed-citation xml:lang="en">Saleem, A.; Saleem, M.; Akhtar, M.F. Antioxidant, anti-infammatory and antiarthritic potential of Moringa oleifera Lam: an ethnomedicinal plant of Moringaceae family. S Afr J Bot. 2020b, 128, 246–256. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.sajb.2019.11.023</mixed-citation></citation-alternatives></ref><ref id="cit185"><label>185</label><citation-alternatives><mixed-citation xml:lang="ru">Shukla, M.; Gupta, K.; Rasheed, Z.; Khan, K.A.; Haqqi, T.M. Consumption of hydrolyzable tannins-rich pomegranate ex-tract suppresses inflammation and joint damage in rheumatoid arthritis. Nutrition. 2008, 24, 733–743. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.nut.2008.03.013.</mixed-citation><mixed-citation xml:lang="en">Shukla, M.; Gupta, K.; Rasheed, Z.; Khan, K.A.; Haqqi, T.M. Consumption of hydrolyzable tannins-rich pomegranate ex-tract suppresses inflammation and joint damage in rheumatoid arthritis. Nutrition. 2008, 24, 733–743. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.nut.2008.03.013.</mixed-citation></citation-alternatives></ref><ref id="cit186"><label>186</label><citation-alternatives><mixed-citation xml:lang="ru">Von Linsingen, R.; Gelmini, G.F.; Bicalho, M.D.G.; De Carvalho, N.S. MICA-129 A/ G dimorphism, its relation to soluble mica plasma level and spontaneous preterm birth: a case-control study. J Reprod Immunol. 2018, 129, 9–14. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jri.2018.07.002.</mixed-citation><mixed-citation xml:lang="en">Von Linsingen, R.; Gelmini, G.F.; Bicalho, M.D.G.; De Carvalho, N.S. MICA-129 A/ G dimorphism, its relation to soluble mica plasma level and spontaneous preterm birth: a case-control study. J Reprod Immunol. 2018, 129, 9–14. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jri.2018.07.002.</mixed-citation></citation-alternatives></ref><ref id="cit187"><label>187</label><citation-alternatives><mixed-citation xml:lang="ru">Kendir, G.; Köroğlu, A. In vitro anti-oxidant effect of the leaf and branch extracts of Ribes L. species in Turkey. Int. J. Pharm. Sci. Res. 2015, 2, 108. https://doi.org/10.1007/s10787-019-00642-0.10.15344/2394-1502/2015/108.</mixed-citation><mixed-citation xml:lang="en">Kendir, G.; Köroğlu, A. In vitro anti-oxidant effect of the leaf and branch extracts of Ribes L. species in Turkey. Int. J. Pharm. Sci. Res. 2015, 2, 108. https://doi.org/10.1007/s10787-019-00642-0.10.15344/2394-1502/2015/108.</mixed-citation></citation-alternatives></ref><ref id="cit188"><label>188</label><citation-alternatives><mixed-citation xml:lang="ru">Khan, S.W.; Khatoon, S. Ethnobotanical studies on useful trees and shrubs of Haramosh and Bugrote valleys, in Gilgit Northern Areas of Pakistan. Pakistan J. Bot. 2007, 39, 699–710.</mixed-citation><mixed-citation xml:lang="en">Khan, S.W.; Khatoon, S. Ethnobotanical studies on useful trees and shrubs of Haramosh and Bugrote valleys, in Gilgit Northern Areas of Pakistan. Pakistan J. Bot. 2007, 39, 699–710.</mixed-citation></citation-alternatives></ref><ref id="cit189"><label>189</label><citation-alternatives><mixed-citation xml:lang="ru">Abotsi, W.K.M.; Ainooson, G.K.; Woode, E. Anti-inflammatory and anti-oxidant effects of an ethanolic extract of the aerial parts of Hilleria latifolia (Lam.) H. Walt. (Phytolaccaceae). Afr. J. Tradit. Complement. Altern. Med. 2012, 9, 138‐152. https://doi.org/10.1007/s10787-019-00642-0.10.4314/ajtcam.v9i1.19.</mixed-citation><mixed-citation xml:lang="en">Abotsi, W.K.M.; Ainooson, G.K.; Woode, E. Anti-inflammatory and anti-oxidant effects of an ethanolic extract of the aerial parts of Hilleria latifolia (Lam.) H. Walt. (Phytolaccaceae). Afr. J. Tradit. Complement. Altern. Med. 2012, 9, 138‐152. https://doi.org/10.1007/s10787-019-00642-0.10.4314/ajtcam.v9i1.19.</mixed-citation></citation-alternatives></ref><ref id="cit190"><label>190</label><citation-alternatives><mixed-citation xml:lang="ru">Daniel, D.; Dluya, T. In vitro biochemical assessments of methanol stem bark extracts of Ficus sycomorus plant. Jordan J. Biol. Sci. 2016, 9, 63–68. https://doi.org/10.1007/s10787-019-00642-0.10.12816/0027009</mixed-citation><mixed-citation xml:lang="en">Daniel, D.; Dluya, T. In vitro biochemical assessments of methanol stem bark extracts of Ficus sycomorus plant. Jordan J. Biol. Sci. 2016, 9, 63–68. https://doi.org/10.1007/s10787-019-00642-0.10.12816/0027009</mixed-citation></citation-alternatives></ref><ref id="cit191"><label>191</label><citation-alternatives><mixed-citation xml:lang="ru">Rosas, E.C.; Correa, L.B.; Pádua, Tde A.; Costa, T.E.; Mazzei, J.L.; Heringer, A.P.; Bizarro, C.A.; Kaplan, M.A.; Figueiredo, M.R.; Henriques, M.G. Anti-inflammatory effect of Schinus terebinthifolius raddi hydroalcoholic extract on neutrophil migration in zymosan-induced arthritis. J Ethnopharmacol. 2015, 175, 490–498. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2015.10.014.</mixed-citation><mixed-citation xml:lang="en">Rosas, E.C.; Correa, L.B.; Pádua, Tde A.; Costa, T.E.; Mazzei, J.L.; Heringer, A.P.; Bizarro, C.A.; Kaplan, M.A.; Figueiredo, M.R.; Henriques, M.G. Anti-inflammatory effect of Schinus terebinthifolius raddi hydroalcoholic extract on neutrophil migration in zymosan-induced arthritis. J Ethnopharmacol. 2015, 175, 490–498. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.jep.2015.10.014.</mixed-citation></citation-alternatives></ref><ref id="cit192"><label>192</label><citation-alternatives><mixed-citation xml:lang="ru">Correa, L.B.; Pádua, T.A.; Seito, L.N.; Costa, T.E.; Silva, M.A.; Candéa, A.L.; Rosas, E.C.; Henriques, M.G. Anti-inflammatory effect of methyl gallate on experimental arthritis: inhibition of neutrophil recruitment, production of inflammatory mediators, and activation of macrophages. J Nat Prod. 2016, 79, 1554–1566. https://doi.org/10.1007/s10787-019-00642-0.10.1021/acs.jnatprod.5b01115.</mixed-citation><mixed-citation xml:lang="en">Correa, L.B.; Pádua, T.A.; Seito, L.N.; Costa, T.E.; Silva, M.A.; Candéa, A.L.; Rosas, E.C.; Henriques, M.G. Anti-inflammatory effect of methyl gallate on experimental arthritis: inhibition of neutrophil recruitment, production of inflammatory mediators, and activation of macrophages. J Nat Prod. 2016, 79, 1554–1566. https://doi.org/10.1007/s10787-019-00642-0.10.1021/acs.jnatprod.5b01115.</mixed-citation></citation-alternatives></ref><ref id="cit193"><label>193</label><citation-alternatives><mixed-citation xml:lang="ru">Rocha, P.D.S.D.; Campos, J.F.; Nunes-Souza, V.; Vieira, M.D.C.; Boleti, A.P.A.; Rabelo, L.A.; Dos Santos, E.L.; de Picoli Souza, K. Antioxidant and protective effects of Schinus terebinthifolius Raddi against Doxorubicin-induced toxicity. Appl Biochem Biotechnol. 2018, 184(3), 869-884. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s12010-017-2589-y.</mixed-citation><mixed-citation xml:lang="en">Rocha, P.D.S.D.; Campos, J.F.; Nunes-Souza, V.; Vieira, M.D.C.; Boleti, A.P.A.; Rabelo, L.A.; Dos Santos, E.L.; de Picoli Souza, K. Antioxidant and protective effects of Schinus terebinthifolius Raddi against Doxorubicin-induced toxicity. Appl Biochem Biotechnol. 2018, 184(3), 869-884. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s12010-017-2589-y.</mixed-citation></citation-alternatives></ref><ref id="cit194"><label>194</label><citation-alternatives><mixed-citation xml:lang="ru">Plaza, A.; Perrone, A.; Balestrieri, C.; Balestrieri, L.; Bifulco, G.; Carbone, V.; Hamed, A.; Piacente, S. New antiproliferative 14 , 15-secopregnane glycosides from. Solenostemma argel. 2005a, 61, 7470–7480. https://doi.org/10.1016/j.tet.2005.05.048.</mixed-citation><mixed-citation xml:lang="en">Plaza, A.; Perrone, A.; Balestrieri, C.; Balestrieri, L.; Bifulco, G.; Carbone, V.; Hamed, A.; Piacente, S. New antiproliferative 14 , 15-secopregnane glycosides from. Solenostemma argel. 2005a, 61, 7470–7480. https://doi.org/10.1016/j.tet.2005.05.048.</mixed-citation></citation-alternatives></ref><ref id="cit195"><label>195</label><citation-alternatives><mixed-citation xml:lang="ru">Innocenti, G.; Dall’Acqua, S.; Minesso, P.; Budriesi, R.; Micucci, M.; Chiarini, A. Evaluation of muscarinic M3-receptor antagonism of Solenostemma argel leaves. Planta Med. 2010, 76, 634. https://doi.org/10.1055/s-0030-1264932.</mixed-citation><mixed-citation xml:lang="en">Innocenti, G.; Dall’Acqua, S.; Minesso, P.; Budriesi, R.; Micucci, M.; Chiarini, A. Evaluation of muscarinic M3-receptor antagonism of Solenostemma argel leaves. Planta Med. 2010, 76, 634. https://doi.org/10.1055/s-0030-1264932.</mixed-citation></citation-alternatives></ref><ref id="cit196"><label>196</label><citation-alternatives><mixed-citation xml:lang="ru">Al-Jaber, N.A.; Awaad, A.S.; Moses, J.E. Review on some antioxidant plants growing in Arab world. J. Saudi Chem. Soc. 2011, 15, 293–307. https://doi.org/10.1016/j. jscs.2011.07.004.</mixed-citation><mixed-citation xml:lang="en">Al-Jaber, N.A.; Awaad, A.S.; Moses, J.E. Review on some antioxidant plants growing in Arab world. J. Saudi Chem. Soc. 2011, 15, 293–307. https://doi.org/10.1016/j. jscs.2011.07.004.</mixed-citation></citation-alternatives></ref><ref id="cit197"><label>197</label><citation-alternatives><mixed-citation xml:lang="ru">Ibrahim, E.; Gaafar, A.; Salama, D.Z.; El-Baz, F. Anti-inflammatory and antioxidant activity of Solenostemma argel extract. IJPPR. 2015, 7, 635–641.</mixed-citation><mixed-citation xml:lang="en">Ibrahim, E.; Gaafar, A.; Salama, D.Z.; El-Baz, F. Anti-inflammatory and antioxidant activity of Solenostemma argel extract. IJPPR. 2015, 7, 635–641.</mixed-citation></citation-alternatives></ref><ref id="cit198"><label>198</label><citation-alternatives><mixed-citation xml:lang="ru">Angela, P.; Alberto, P.; Arafa, H.; Cosimo, P.; Sonia, P. Solenostemma argel: a rich source of very unusual pregnane and 14,15- secopregnane glycosides with antiproliferative activity. Curr. Org. Chem. 2008, 12 (18), 1648–1660. https://doi.org/10.1007/s10787-019-00642-0.10.2174/138527208786786282.</mixed-citation><mixed-citation xml:lang="en">Angela, P.; Alberto, P.; Arafa, H.; Cosimo, P.; Sonia, P. Solenostemma argel: a rich source of very unusual pregnane and 14,15- secopregnane glycosides with antiproliferative activity. Curr. Org. Chem. 2008, 12 (18), 1648–1660. https://doi.org/10.1007/s10787-019-00642-0.10.2174/138527208786786282.</mixed-citation></citation-alternatives></ref><ref id="cit199"><label>199</label><citation-alternatives><mixed-citation xml:lang="ru">Demmak, R.; Bordage, S.; Bensegueni, A.; Boutaghane, N.; Hennebelle, T.; Mokrani, E.; Sahpaz, S. Chemical constituents from Solenostemma argel and their cholinesterase inhibitory activity. Nat. Prod. Sci. 2019, 25, 115. https://doi.org/10.20307/ nps.2019.25.2.115.</mixed-citation><mixed-citation xml:lang="en">Demmak, R.; Bordage, S.; Bensegueni, A.; Boutaghane, N.; Hennebelle, T.; Mokrani, E.; Sahpaz, S. Chemical constituents from Solenostemma argel and their cholinesterase inhibitory activity. Nat. Prod. Sci. 2019, 25, 115. https://doi.org/10.20307/ nps.2019.25.2.115.</mixed-citation></citation-alternatives></ref><ref id="cit200"><label>200</label><citation-alternatives><mixed-citation xml:lang="ru">Navarro, M.; Arnaez, E.; Moreira, I.; Hurtado, A.; Monge, D.; Monagas, M. Polyphenolic composition and antioxidant activity of Uncaria tomentosa commercial bark products. Antioxidants. 2019, 8, 339. https://doi.org/10.1007/s10787-019-00642-0.10.3390/antiox8090339.</mixed-citation><mixed-citation xml:lang="en">Navarro, M.; Arnaez, E.; Moreira, I.; Hurtado, A.; Monge, D.; Monagas, M. Polyphenolic composition and antioxidant activity of Uncaria tomentosa commercial bark products. Antioxidants. 2019, 8, 339. https://doi.org/10.1007/s10787-019-00642-0.10.3390/antiox8090339.</mixed-citation></citation-alternatives></ref><ref id="cit201"><label>201</label><citation-alternatives><mixed-citation xml:lang="ru">Sordi, R.; Castro, S.N.; Lera, A.T.; Irene, M.N.; Farinazzo, M. de M.; Sette, C.; Cubero, D. de I. G.; Baccarin, A.L. de C.; Giglio, A. del. Randomized, doubleblind, placebo-controlled phase II clinical trial on the use of Uncaria tomentosa (Cat’s Claw) for aromatase inhibitor-induced arthralgia: a pilot study. J Nat Remed. 2019, 19, 24–31. https://doi.org/10.1007/s10787-019-00642-0.10.18311/jnr/2019/22867</mixed-citation><mixed-citation xml:lang="en">Sordi, R.; Castro, S.N.; Lera, A.T.; Irene, M.N.; Farinazzo, M. de M.; Sette, C.; Cubero, D. de I. G.; Baccarin, A.L. de C.; Giglio, A. del. Randomized, doubleblind, placebo-controlled phase II clinical trial on the use of Uncaria tomentosa (Cat’s Claw) for aromatase inhibitor-induced arthralgia: a pilot study. J Nat Remed. 2019, 19, 24–31. https://doi.org/10.1007/s10787-019-00642-0.10.18311/jnr/2019/22867</mixed-citation></citation-alternatives></ref><ref id="cit202"><label>202</label><citation-alternatives><mixed-citation xml:lang="ru">Mur, E.; Hartig, F.; Eibl, G.; Schirmer, M. Randomized double blind trial of an extract from the pentacyclic alkaloid-chemotype of uncaria tomentosa for the treatment of rheumatoid arthritis. J Rheumatol. 2002, 29, 678–681.</mixed-citation><mixed-citation xml:lang="en">Mur, E.; Hartig, F.; Eibl, G.; Schirmer, M. Randomized double blind trial of an extract from the pentacyclic alkaloid-chemotype of uncaria tomentosa for the treatment of rheumatoid arthritis. J Rheumatol. 2002, 29, 678–681.</mixed-citation></citation-alternatives></ref><ref id="cit203"><label>203</label><citation-alternatives><mixed-citation xml:lang="ru">Singh, S.; Singh, T.G.; Mahajan, K.; Dhiman, S. Medicinal plants used against various inflammatory biomarkers for the management of rheumatoid arthritis. J Pharm Pharmacol. 2020, 72(10), 1306-1327. https://doi.org/10.1007/s10787-019-00642-0.10.1111/jphp.13326.</mixed-citation><mixed-citation xml:lang="en">Singh, S.; Singh, T.G.; Mahajan, K.; Dhiman, S. Medicinal plants used against various inflammatory biomarkers for the management of rheumatoid arthritis. J Pharm Pharmacol. 2020, 72(10), 1306-1327. https://doi.org/10.1007/s10787-019-00642-0.10.1111/jphp.13326.</mixed-citation></citation-alternatives></ref><ref id="cit204"><label>204</label><citation-alternatives><mixed-citation xml:lang="ru">Wang, H.; Jiang, Z.; Pang, Z.; Zhou, T.; Gu, Y. Acacetin alleviates inflammation and matrix degradation in nucleus pulposus cells and ameliorates intervertebral disc degeneration in vivo. Drug Des Devel Ther. 2020, 14, 4801-4813. https://doi.org/10.1007/s10787-019-00642-0.10.2147/DDDT.S274812.</mixed-citation><mixed-citation xml:lang="en">Wang, H.; Jiang, Z.; Pang, Z.; Zhou, T.; Gu, Y. Acacetin alleviates inflammation and matrix degradation in nucleus pulposus cells and ameliorates intervertebral disc degeneration in vivo. Drug Des Devel Ther. 2020, 14, 4801-4813. https://doi.org/10.1007/s10787-019-00642-0.10.2147/DDDT.S274812.</mixed-citation></citation-alternatives></ref><ref id="cit205"><label>205</label><citation-alternatives><mixed-citation xml:lang="ru">Gao, F.; Liu, X.; Shen, Z.Y.; Jia, X.H.; He, H.; Gao, J.; Wu, J.H.; Jiang, C.H.; Zhou, H.; Wang, Y.P. Andrographolide sulfonate attenuates acute lung injury by reducing expression of myeloperoxidase and neutrophil-derived proteases in mice. Front. Physiol. 2018, 9, 939. https://doi.org/10.1007/s10787-019-00642-0.10.3389/fphys.2018.00939.</mixed-citation><mixed-citation xml:lang="en">Gao, F.; Liu, X.; Shen, Z.Y.; Jia, X.H.; He, H.; Gao, J.; Wu, J.H.; Jiang, C.H.; Zhou, H.; Wang, Y.P. Andrographolide sulfonate attenuates acute lung injury by reducing expression of myeloperoxidase and neutrophil-derived proteases in mice. Front. Physiol. 2018, 9, 939. https://doi.org/10.1007/s10787-019-00642-0.10.3389/fphys.2018.00939.</mixed-citation></citation-alternatives></ref><ref id="cit206"><label>206</label><citation-alternatives><mixed-citation xml:lang="ru">Peng, S.; Gao, J.; Liu, W.; Jiang, C.; Yang, X.; Sun, Y.; Guo, W.; Xu, Q. Andrographolide ameliorates OVA-induced lung injury in mice by suppressing ROS-mediated NF-κB signaling and NLRP3 inflammasome activation. Oncotarget 2016, 7, 80262–80274. https://doi.org/10.1007/s10787-019-00642-0.10.18632/oncotarget.12918.</mixed-citation><mixed-citation xml:lang="en">Peng, S.; Gao, J.; Liu, W.; Jiang, C.; Yang, X.; Sun, Y.; Guo, W.; Xu, Q. Andrographolide ameliorates OVA-induced lung injury in mice by suppressing ROS-mediated NF-κB signaling and NLRP3 inflammasome activation. Oncotarget 2016, 7, 80262–80274. https://doi.org/10.1007/s10787-019-00642-0.10.18632/oncotarget.12918.</mixed-citation></citation-alternatives></ref><ref id="cit207"><label>207</label><citation-alternatives><mixed-citation xml:lang="ru">Chen, H.W.; Huang, C.S.; Li, C.C.; Lin, A.H.; Huang, Y.J.; Wang, T.S.; Yao, H.T.; Lii, C. K. Bioavailability of andrographolide and protection against carbon tetrachloride-induced oxidative damage in rats. Toxicol. Appl. Pharmacol. 2014, 280, 1–9. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.taap.2014.07.024.</mixed-citation><mixed-citation xml:lang="en">Chen, H.W.; Huang, C.S.; Li, C.C.; Lin, A.H.; Huang, Y.J.; Wang, T.S.; Yao, H.T.; Lii, C. K. Bioavailability of andrographolide and protection against carbon tetrachloride-induced oxidative damage in rats. Toxicol. Appl. Pharmacol. 2014, 280, 1–9. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.taap.2014.07.024.</mixed-citation></citation-alternatives></ref><ref id="cit208"><label>208</label><citation-alternatives><mixed-citation xml:lang="ru">Li Z.; Tan J.; Wang L.; Li Q. Andrographolide benefits rheumatoid arthritis via inhibiting MAPK pathways. Inflammation 2017, 40, 1599–1605. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10753-017-0600-y.</mixed-citation><mixed-citation xml:lang="en">Li Z.; Tan J.; Wang L.; Li Q. Andrographolide benefits rheumatoid arthritis via inhibiting MAPK pathways. Inflammation 2017, 40, 1599–1605. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10753-017-0600-y.</mixed-citation></citation-alternatives></ref><ref id="cit209"><label>209</label><citation-alternatives><mixed-citation xml:lang="ru">Luo, S.; Li, H.; Liu, J.; Xie, X.; Wan, Z.; Wang, Y.; Zhao, Z.; Wu, X.; Li, X.; Yang, M.; Li, X. Andrographolide ameliorates oxidative stress, inflammation and histological outcome in complete Freund's adjuvant-induced arthritis. Chem Biol Interact. 2020, 319, 108984. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.cbi.2020.108984.</mixed-citation><mixed-citation xml:lang="en">Luo, S.; Li, H.; Liu, J.; Xie, X.; Wan, Z.; Wang, Y.; Zhao, Z.; Wu, X.; Li, X.; Yang, M.; Li, X. Andrographolide ameliorates oxidative stress, inflammation and histological outcome in complete Freund's adjuvant-induced arthritis. Chem Biol Interact. 2020, 319, 108984. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.cbi.2020.108984.</mixed-citation></citation-alternatives></ref><ref id="cit210"><label>210</label><citation-alternatives><mixed-citation xml:lang="ru">Suh, N.J.; Shim, C.K.; Lee, M.H.; Kim, S.K.; Chang, I.M. Pharmacokinetic study of an iridoid glucoside: aucubin. Pharm Res. 1991,8(8),1059-63. https://doi.org/10.1007/s10787-019-00642-0.10.1023/a:1015821527621.</mixed-citation><mixed-citation xml:lang="en">Suh, N.J.; Shim, C.K.; Lee, M.H.; Kim, S.K.; Chang, I.M. Pharmacokinetic study of an iridoid glucoside: aucubin. Pharm Res. 1991,8(8),1059-63. https://doi.org/10.1007/s10787-019-00642-0.10.1023/a:1015821527621.</mixed-citation></citation-alternatives></ref><ref id="cit211"><label>211</label><citation-alternatives><mixed-citation xml:lang="ru">Jin, H.; Wang, Q.; Wu, J.; Han, X.; Qian, T.; Zhang, Z.; Wang, J.; Pan, X.; Wu, A.; Wang, X. Baicalein inhibits the IL-1β-induced inflammatory response in nucleus pulposus cells and attenuates disc degeneration In vivo. Inflammation. 2019, 42(3), 1032-1044. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10753-019-00965-8.</mixed-citation><mixed-citation xml:lang="en">Jin, H.; Wang, Q.; Wu, J.; Han, X.; Qian, T.; Zhang, Z.; Wang, J.; Pan, X.; Wu, A.; Wang, X. Baicalein inhibits the IL-1β-induced inflammatory response in nucleus pulposus cells and attenuates disc degeneration In vivo. Inflammation. 2019, 42(3), 1032-1044. https://doi.org/10.1007/s10787-019-00642-0.10.1007/s10753-019-00965-8.</mixed-citation></citation-alternatives></ref><ref id="cit212"><label>212</label><citation-alternatives><mixed-citation xml:lang="ru">Wang, X.H.; Jiang, S.M.; Sun, Q.W. Effects of berberine on human rheumatoid arthritis fibroblast-like synoviocytes. Exp Biol Med (Maywood.) 2011, 236, 859–866. https://doi.org/10.1007/s10787-019-00642-0.10.1258/ebm.2011.010366.</mixed-citation><mixed-citation xml:lang="en">Wang, X.H.; Jiang, S.M.; Sun, Q.W. Effects of berberine on human rheumatoid arthritis fibroblast-like synoviocytes. Exp Biol Med (Maywood.) 2011, 236, 859–866. https://doi.org/10.1007/s10787-019-00642-0.10.1258/ebm.2011.010366.</mixed-citation></citation-alternatives></ref><ref id="cit213"><label>213</label><citation-alternatives><mixed-citation xml:lang="ru">Ren, Y.; Lu, L.; Guo, T.B.; Qiu, J.; Yang, Y.; Liu, A.; Zhang, J.Z. Novel immunomodulatory properties of berbamine through selective down-regulation of STAT4 and action of IFN gamma in experimental autoimmune encephalomyelitis. J Immunol. 2008, 181, 1491–1498. https://doi.org/10.1007/s10787-019-00642-0.10.4049/jimmunol.181.2.1491.</mixed-citation><mixed-citation xml:lang="en">Ren, Y.; Lu, L.; Guo, T.B.; Qiu, J.; Yang, Y.; Liu, A.; Zhang, J.Z. Novel immunomodulatory properties of berbamine through selective down-regulation of STAT4 and action of IFN gamma in experimental autoimmune encephalomyelitis. J Immunol. 2008, 181, 1491–1498. https://doi.org/10.1007/s10787-019-00642-0.10.4049/jimmunol.181.2.1491.</mixed-citation></citation-alternatives></ref><ref id="cit214"><label>214</label><citation-alternatives><mixed-citation xml:lang="ru">Shirwaikar, A.; Shirwaikar, A.; Rajendran, K.; Punitha, I.S.R. In vitro anti-oxidant studies on the benzyl tetra isoquinoline alkaloid berberine. Biol Pharm Bull. 2006, 29, 1906–1910. https://doi.org/10.1007/s10787-019-00642-0.10.1248/bpb.29.1906.</mixed-citation><mixed-citation xml:lang="en">Shirwaikar, A.; Shirwaikar, A.; Rajendran, K.; Punitha, I.S.R. In vitro anti-oxidant studies on the benzyl tetra isoquinoline alkaloid berberine. Biol Pharm Bull. 2006, 29, 1906–1910. https://doi.org/10.1007/s10787-019-00642-0.10.1248/bpb.29.1906.</mixed-citation></citation-alternatives></ref><ref id="cit215"><label>215</label><citation-alternatives><mixed-citation xml:lang="ru">Xie, C.; Ma, H.; Shi, Y.; Li, J.; Wu, H.; Wang, B.; Shao, Z.; Huang, C.; Chen, J.; Sun, L.; Zhou, Y.; Tian, N.; Wu, Y.; Gao, W.; Wu, A.; Wang, X.; Zhang, X. Cardamonin protects nucleus pulposus cells against IL-1β-induced inflammation and catabolism via Nrf2/NF-κB axis. Food Funct. 2021, 12(6), 2703-2714. https://doi.org/10.1007/s10787-019-00642-0.10.1039/d0fo03353g.</mixed-citation><mixed-citation xml:lang="en">Xie, C.; Ma, H.; Shi, Y.; Li, J.; Wu, H.; Wang, B.; Shao, Z.; Huang, C.; Chen, J.; Sun, L.; Zhou, Y.; Tian, N.; Wu, Y.; Gao, W.; Wu, A.; Wang, X.; Zhang, X. Cardamonin protects nucleus pulposus cells against IL-1β-induced inflammation and catabolism via Nrf2/NF-κB axis. Food Funct. 2021, 12(6), 2703-2714. https://doi.org/10.1007/s10787-019-00642-0.10.1039/d0fo03353g.</mixed-citation></citation-alternatives></ref><ref id="cit216"><label>216</label><citation-alternatives><mixed-citation xml:lang="ru">Morita, T. Celastrol: a new therapeutic potential of traditional Chinese medicine. Am. J. Hypertens. 2010, 23(8), 821. https://doi.org/10.1007/s10787-019-00642-0.10.1038/ajh.2010.87.</mixed-citation><mixed-citation xml:lang="en">Morita, T. Celastrol: a new therapeutic potential of traditional Chinese medicine. Am. J. Hypertens. 2010, 23(8), 821. https://doi.org/10.1007/s10787-019-00642-0.10.1038/ajh.2010.87.</mixed-citation></citation-alternatives></ref><ref id="cit217"><label>217</label><citation-alternatives><mixed-citation xml:lang="ru">Pinna, G.F.; Fiorucci, M.; Reimund, J.M.; Taquet, N.; Arondel, Y.; Muller, C.D. Celastrol inhibits pro-inflammatory cytokine secretion in Crohn’s disease biopsies, Biochem. Biophys. Res. Commun. 2004, 322(3), 778–786. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.bbrc.2004.07.186.</mixed-citation><mixed-citation xml:lang="en">Pinna, G.F.; Fiorucci, M.; Reimund, J.M.; Taquet, N.; Arondel, Y.; Muller, C.D. Celastrol inhibits pro-inflammatory cytokine secretion in Crohn’s disease biopsies, Biochem. Biophys. Res. Commun. 2004, 322(3), 778–786. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.bbrc.2004.07.186.</mixed-citation></citation-alternatives></ref><ref id="cit218"><label>218</label><citation-alternatives><mixed-citation xml:lang="ru">Nabekura, T.; Hiroi, T.; Kawasaki, T.; Uwai, Y. Effects of natural nuclear factorkappa B inhibitors on anticancer drug efflux transporter human Pglycoprotein. Biomed. Pharmacother. 2015, 70, 140–145. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.biopha.2015.01.007.</mixed-citation><mixed-citation xml:lang="en">Nabekura, T.; Hiroi, T.; Kawasaki, T.; Uwai, Y. Effects of natural nuclear factorkappa B inhibitors on anticancer drug efflux transporter human Pglycoprotein. Biomed. Pharmacother. 2015, 70, 140–145. https://doi.org/10.1007/s10787-019-00642-0.10.1016/j.biopha.2015.01.007.</mixed-citation></citation-alternatives></ref><ref id="cit219"><label>219</label><citation-alternatives><mixed-citation xml:lang="ru">Chen, J.; Xuan, J.; Gu, Y.T.; Shi, K.S.; Xie, J.J.; Chen, J.X.; Zheng, Z.M.; Chen, Y.; Chen, X.B.; Wu, Y.S.; Zhang, X.L.; Wang, X.Y. Celastrol reduces IL-1β induced matrix catabolism, oxidative stress and inflammation in human nucleus pulposus cells and attenuates rat intervertebral disc degeneration in vivo. Biomed Pharmacother. 2017, 91, 208-219. https://doi.org/10.1007/s10787-019-00642-0. 10.1016/j.biopha.2017.04.093.</mixed-citation><mixed-citation xml:lang="en">Chen, J.; Xuan, J.; Gu, Y.T.; Shi, K.S.; Xie, J.J.; Chen, J.X.; Zheng, Z.M.; Chen, Y.; Chen, X.B.; Wu, Y.S.; Zhang, X.L.; Wang, X.Y. Celastrol reduces IL-1β induced matrix catabolism, oxidative stress and inflammation in human nucleus pulposus cells and attenuates rat intervertebral disc degeneration in vivo. Biomed Pharmacother. 2017, 91, 208-219. https://doi.org/10.1007/s10787-019-00642-0. 10.1016/j.biopha.2017.04.093.</mixed-citation></citation-alternatives></ref><ref id="cit220"><label>220</label><citation-alternatives><mixed-citation xml:lang="ru">Muravyova D. A. Medicinal plants. Great Medical Encyclopedia: in 30 volumes, ch. ed. B.V. Petrovsky. — 3rd ed. - M.: Soviet Encyclopedia, 1980, 12: Cryosurgery, Lenegr., 536 p.</mixed-citation><mixed-citation xml:lang="en">Muravyova D. A. Medicinal plants. Great Medical Encyclopedia: in 30 volumes, ch. ed. B.V. Petrovsky. — 3rd ed. - M.: Soviet Encyclopedia, 1980, 12: Cryosurgery, Lenegr., 536 p.</mixed-citation></citation-alternatives></ref><ref id="cit221"><label>221</label><citation-alternatives><mixed-citation xml:lang="ru">Alam, M.A.; Subhan, N.; Hossain, H.; Hossain, M.; Reza, H.M.; Rahman, M.M.; Ullah, M.O. Hydroxycinnamic acid derivatives: a potential class of natural compounds for the management of lipid metabolism and obesity. Nutr. Metab. 2016, 13, 27. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s12986-016-0080-3.</mixed-citation><mixed-citation xml:lang="en">Alam, M.A.; Subhan, N.; Hossain, H.; Hossain, M.; Reza, H.M.; Rahman, M.M.; Ullah, M.O. Hydroxycinnamic acid derivatives: a potential class of natural compounds for the management of lipid metabolism and obesity. Nutr. Metab. 2016, 13, 27. https://doi.org/10.1007/s10787-019-00642-0.10.1186/s12986-016-0080-3.</mixed-citation></citation-alternatives></ref><ref id="cit222"><label>222</label><citation-alternatives><mixed-citation xml:lang="ru">Li, K.; Li, Y.; Ma, Z.; Zhao, J. Crocin exerts anti-inflammatory and anti-catabolic effects on rat intervertebral discs by suppressing the activation of JNK. Int J Mol Med. 2015, 36(5), 1291-9. doi: 10.3892/ijmm.2015.2359.</mixed-citation><mixed-citation xml:lang="en">Li, K.; Li, Y.; Ma, Z.; Zhao, J. Crocin exerts anti-inflammatory and anti-catabolic effects on rat intervertebral discs by suppressing the activation of JNK. Int J Mol Med. 2015, 36(5), 1291-9. doi: 10.3892/ijmm.2015.2359.</mixed-citation></citation-alternatives></ref><ref id="cit223"><label>223</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu, L.; Zhang, Z.; Xia, N.; Zhang, W.; Wei, Y.; Huang, J.; Ren, Z.; Meng, F.; Yang, L. Anti-arthritic activity of ferulic acid in complete Freund's adjuvant (CFA)-induced arthritis in rats: JAK2 inhibition. Inflammopharmacology. 2020, 28(2), 463-473. https://doi.org/10.1007/s10787-019-00642-0.</mixed-citation><mixed-citation xml:lang="en">Zhu, L.; Zhang, Z.; Xia, N.; Zhang, W.; Wei, Y.; Huang, J.; Ren, Z.; Meng, F.; Yang, L. Anti-arthritic activity of ferulic acid in complete Freund's adjuvant (CFA)-induced arthritis in rats: JAK2 inhibition. Inflammopharmacology. 2020, 28(2), 463-473. https://doi.org/10.1007/s10787-019-00642-0.</mixed-citation></citation-alternatives></ref><ref id="cit224"><label>224</label><citation-alternatives><mixed-citation xml:lang="ru">Lee, J.H.; Kim, G.H. Evaluation of antioxidant and inhibitory activities for different subclasses flavonoids on enzymes for rheumatoid arthritis. J. Food Sci. 2010, 75, 212–217. https://doi.org/10.1111/j.1750-3841.2010.01755.x.</mixed-citation><mixed-citation xml:lang="en">Lee, J.H.; Kim, G.H. Evaluation of antioxidant and inhibitory activities for different subclasses flavonoids on enzymes for rheumatoid arthritis. J. Food Sci. 2010, 75, 212–217. https://doi.org/10.1111/j.1750-3841.2010.01755.x.</mixed-citation></citation-alternatives></ref><ref id="cit225"><label>225</label><citation-alternatives><mixed-citation xml:lang="ru">Gautam, R.; Jachak, S.M. Recent developments in anti-inflammatory natural products. Med. Res. Rev. 2009, 29, 767–820. https://doi.org/10.1002/med.20156.</mixed-citation><mixed-citation xml:lang="en">Gautam, R.; Jachak, S.M. Recent developments in anti-inflammatory natural products. Med. Res. Rev. 2009, 29, 767–820. https://doi.org/10.1002/med.20156.</mixed-citation></citation-alternatives></ref><ref id="cit226"><label>226</label><citation-alternatives><mixed-citation xml:lang="ru">Patel, K.; Jain, A.; Patel, D.K. Medicinal significance, pharmacological activities, and analytical aspects of anthocyanidins ‘delphinidin’ : a concise report. J. Acute Dis. 2013, 2, 169–178. https://doi.org/10.1016/S2221-6189(13)60123-7.</mixed-citation><mixed-citation xml:lang="en">Patel, K.; Jain, A.; Patel, D.K. Medicinal significance, pharmacological activities, and analytical aspects of anthocyanidins ‘delphinidin’ : a concise report. J. Acute Dis. 2013, 2, 169–178. https://doi.org/10.1016/S2221-6189(13)60123-7.</mixed-citation></citation-alternatives></ref><ref id="cit227"><label>227</label><citation-alternatives><mixed-citation xml:lang="ru">Sarkar, A.; Tripathi, V.D.; Sahu, R.K. Anti-inflammatory and anti-arthritis activity of flavonoids fractions isolated from Centipeda minima leaves extracts in rats. Clin. Exp. Pharmacol. 2017, 7(2), 1–8. https://doi.org/10.4172/2161-1459.1000231.</mixed-citation><mixed-citation xml:lang="en">Sarkar, A.; Tripathi, V.D.; Sahu, R.K. Anti-inflammatory and anti-arthritis activity of flavonoids fractions isolated from Centipeda minima leaves extracts in rats. Clin. Exp. Pharmacol. 2017, 7(2), 1–8. https://doi.org/10.4172/2161-1459.1000231.</mixed-citation></citation-alternatives></ref><ref id="cit228"><label>228</label><citation-alternatives><mixed-citation xml:lang="ru">Ambriz-P´erez, D.L.; Leyva-Lopez, ´ N.; Gutierrez-Grijalva, E.P.; Heredia, J.B.; Yildiz, F. Phenolic compounds: natural alternative in inflammation treatment. A Review. Cogent Food Agric. 2016, 2(1), 1–14. https://doi.org/10.1080/ 23311932.2015.1131412.</mixed-citation><mixed-citation xml:lang="en">Ambriz-P´erez, D.L.; Leyva-Lopez, ´ N.; Gutierrez-Grijalva, E.P.; Heredia, J.B.; Yildiz, F. Phenolic compounds: natural alternative in inflammation treatment. A Review. Cogent Food Agric. 2016, 2(1), 1–14. https://doi.org/10.1080/ 23311932.2015.1131412.</mixed-citation></citation-alternatives></ref><ref id="cit229"><label>229</label><citation-alternatives><mixed-citation xml:lang="ru">Abdel Motaal, A.; Ezzat, S.M.; Tadros, M.G.; El-Askary, H.I. In vivo antiinflammatory activity of caffeoylquinic acid derivatives from Solidago virgaurea in rats. Pharm. Biol. 2016, 54(12), 2864–2870. https://doi.org/10.1080/ 13880209.2016.1190381.</mixed-citation><mixed-citation xml:lang="en">Abdel Motaal, A.; Ezzat, S.M.; Tadros, M.G.; El-Askary, H.I. In vivo antiinflammatory activity of caffeoylquinic acid derivatives from Solidago virgaurea in rats. Pharm. Biol. 2016, 54(12), 2864–2870. https://doi.org/10.1080/ 13880209.2016.1190381.</mixed-citation></citation-alternatives></ref><ref id="cit230"><label>230</label><citation-alternatives><mixed-citation xml:lang="ru">Liang, N.; Kitts, D.D. Role of chlorogenic acids in controlling oxidative and inflammatory stress conditions. Nutrients. 2015, 8(1). https://doi.org/10.3390/ nu8010016.</mixed-citation><mixed-citation xml:lang="en">Liang, N.; Kitts, D.D. Role of chlorogenic acids in controlling oxidative and inflammatory stress conditions. Nutrients. 2015, 8(1). https://doi.org/10.3390/ nu8010016.</mixed-citation></citation-alternatives></ref><ref id="cit231"><label>231</label><citation-alternatives><mixed-citation xml:lang="ru">Niazi, J.; Sachdeva, R.; Bansal, Y.; Gupta, V.; Kaur, N. Anti-inflammatory and antinociceptive activity of vanillin. Drug Des. Dev. Ther. 2014, 5(2), 145. https://doi.org/ 10.4103/2394-2002.139630.</mixed-citation><mixed-citation xml:lang="en">Niazi, J.; Sachdeva, R.; Bansal, Y.; Gupta, V.; Kaur, N. Anti-inflammatory and antinociceptive activity of vanillin. Drug Des. Dev. Ther. 2014, 5(2), 145. https://doi.org/ 10.4103/2394-2002.139630.</mixed-citation></citation-alternatives></ref><ref id="cit232"><label>232</label><citation-alternatives><mixed-citation xml:lang="ru">Ounaissia, K.; Pertuit, D.; Mitaine-Offer, A.C.; Miyamoto, T.; Tanaka, C.; Delemasure, S.; Dutartre, P.; Smati, D.; Lacaille-Dubois, M.A. New pregnane and phenolic glycosides from Solenostemma argel. Fitoterapia. 2016, 114, 98–104. https://doi.org/ 10.1016/j.fitote.2016.08.002.</mixed-citation><mixed-citation xml:lang="en">Ounaissia, K.; Pertuit, D.; Mitaine-Offer, A.C.; Miyamoto, T.; Tanaka, C.; Delemasure, S.; Dutartre, P.; Smati, D.; Lacaille-Dubois, M.A. New pregnane and phenolic glycosides from Solenostemma argel. Fitoterapia. 2016, 114, 98–104. https://doi.org/ 10.1016/j.fitote.2016.08.002.</mixed-citation></citation-alternatives></ref><ref id="cit233"><label>233</label><citation-alternatives><mixed-citation xml:lang="ru">Innocenti, G.; Dall’Acqua, S.; Sosa, S.; Altinier, G.; Della Loggia, R. Topical antiinflammatory activity of Solenostemma argel leaves. J. Ethnopharmacol. 2005, 102(2), 307–310. https://doi.org/10.1016/j.jep.2005.06.007.</mixed-citation><mixed-citation xml:lang="en">Innocenti, G.; Dall’Acqua, S.; Sosa, S.; Altinier, G.; Della Loggia, R. Topical antiinflammatory activity of Solenostemma argel leaves. J. Ethnopharmacol. 2005, 102(2), 307–310. https://doi.org/10.1016/j.jep.2005.06.007.</mixed-citation></citation-alternatives></ref><ref id="cit234"><label>234</label><citation-alternatives><mixed-citation xml:lang="ru">Perrone, A.; Plaza, A.; Ercolino, S.F.; Hamed, A.I.; Parente, L.; Pizza, C.; Piacente, S. 14,15-Secopregnane derivatives from the leaves of Solenostemma argel. J. Nat. Prod. 2006, 69(1), 50–54. https://doi.org/10.1021/np050263c.</mixed-citation><mixed-citation xml:lang="en">Perrone, A.; Plaza, A.; Ercolino, S.F.; Hamed, A.I.; Parente, L.; Pizza, C.; Piacente, S. 14,15-Secopregnane derivatives from the leaves of Solenostemma argel. J. Nat. Prod. 2006, 69(1), 50–54. https://doi.org/10.1021/np050263c.</mixed-citation></citation-alternatives></ref><ref id="cit235"><label>235</label><citation-alternatives><mixed-citation xml:lang="ru">Liu, B.; Xu, C.; Wu, X.; Liu, F.; Du, Y.; Sun, J.; Tao, J.; Dong, J. Icariin exerts an antidepressant effect in an unpredictable chronic mild stress model of depression in rats and is associated with the regulation of hippocampal neuroinflammation. Neuroscience. 2015, 294, 193–205. https://doi.org/10.1016/j.neuroscience.2015.02.053.</mixed-citation><mixed-citation xml:lang="en">Liu, B.; Xu, C.; Wu, X.; Liu, F.; Du, Y.; Sun, J.; Tao, J.; Dong, J. Icariin exerts an antidepressant effect in an unpredictable chronic mild stress model of depression in rats and is associated with the regulation of hippocampal neuroinflammation. Neuroscience. 2015, 294, 193–205. https://doi.org/10.1016/j.neuroscience.2015.02.053.</mixed-citation></citation-alternatives></ref><ref id="cit236"><label>236</label><citation-alternatives><mixed-citation xml:lang="ru">Yang, A.; Yu, C.; Lu, Q.; Li, H.; Li, Z.; He, C. Mechanism of action of icariin in bone marrow mesenchymal stem cells. Stem Cells International. 2019, 2019, 5747298. https://doi.org/10.1155/2019/5747298.</mixed-citation><mixed-citation xml:lang="en">Yang, A.; Yu, C.; Lu, Q.; Li, H.; Li, Z.; He, C. Mechanism of action of icariin in bone marrow mesenchymal stem cells. Stem Cells International. 2019, 2019, 5747298. https://doi.org/10.1155/2019/5747298.</mixed-citation></citation-alternatives></ref><ref id="cit237"><label>237</label><citation-alternatives><mixed-citation xml:lang="ru">Qin, S.; Zhou, W.; Liu, S.; Chen, P.; Wu, H. Icariin stimulates the proliferation of rat bone mesenchymal stem cells via ERK and p38 MAPK signaling. Int J Clin Exp Med. 2015, 8(5), 7125–7133.</mixed-citation><mixed-citation xml:lang="en">Qin, S.; Zhou, W.; Liu, S.; Chen, P.; Wu, H. Icariin stimulates the proliferation of rat bone mesenchymal stem cells via ERK and p38 MAPK signaling. Int J Clin Exp Med. 2015, 8(5), 7125–7133.</mixed-citation></citation-alternatives></ref><ref id="cit238"><label>238</label><citation-alternatives><mixed-citation xml:lang="ru">Yang, P.; Guan, Y.Q.; Li, Y.L.; Zhang, L.; Zhang, L.; Li, L. Icariin promotes cell proliferation and regulates gene expression in human neural stem cells in vitro. Mol Med Rep. 2016, 14(2), 1316–1322. https://doi.org/10.3892/mmr.2016.5377.</mixed-citation><mixed-citation xml:lang="en">Yang, P.; Guan, Y.Q.; Li, Y.L.; Zhang, L.; Zhang, L.; Li, L. Icariin promotes cell proliferation and regulates gene expression in human neural stem cells in vitro. Mol Med Rep. 2016, 14(2), 1316–1322. https://doi.org/10.3892/mmr.2016.5377.</mixed-citation></citation-alternatives></ref><ref id="cit239"><label>239</label><citation-alternatives><mixed-citation xml:lang="ru">Chen, S.; Deng, X.; Ma, K.; Zhao, L.; Huang, D.; Li, Z.; Shao, Z. Icariin improves the viability and function of cryopreserved human nucleus pulposus-derived mesenchymal stem cells. Oxidative Medicine and Cellular Longevity. 2018, 2018, 3459612. https://doi.org/10.1155/2018/3459612.</mixed-citation><mixed-citation xml:lang="en">Chen, S.; Deng, X.; Ma, K.; Zhao, L.; Huang, D.; Li, Z.; Shao, Z. Icariin improves the viability and function of cryopreserved human nucleus pulposus-derived mesenchymal stem cells. Oxidative Medicine and Cellular Longevity. 2018, 2018, 3459612. https://doi.org/10.1155/2018/3459612.</mixed-citation></citation-alternatives></ref><ref id="cit240"><label>240</label><citation-alternatives><mixed-citation xml:lang="ru">Hua, W.; Li, S.; Luo, R.; Wu, X.; Zhang, Y.; Liao, Z.; Song, Y.; Wang, K.; Zhao, K.; Yang, S.; Yang, C. Icariin protects human nucleus pulposus cells from hydrogen peroxide-induced mitochondria-mediated apoptosis by activating nuclear factor erythroid 2-related factor 2. Biochim Biophys Acta Mol Basis Dis. 2020, 1866(1), 165575. https://doi.org/10.1016/j.bbadis.2019.165575.</mixed-citation><mixed-citation xml:lang="en">Hua, W.; Li, S.; Luo, R.; Wu, X.; Zhang, Y.; Liao, Z.; Song, Y.; Wang, K.; Zhao, K.; Yang, S.; Yang, C. Icariin protects human nucleus pulposus cells from hydrogen peroxide-induced mitochondria-mediated apoptosis by activating nuclear factor erythroid 2-related factor 2. Biochim Biophys Acta Mol Basis Dis. 2020, 1866(1), 165575. https://doi.org/10.1016/j.bbadis.2019.165575.</mixed-citation></citation-alternatives></ref><ref id="cit241"><label>241</label><citation-alternatives><mixed-citation xml:lang="ru">Hua, W.; Zhang, Y.; Wu, X.; Kang, L.; Tu, J.; Zhao, K.; Li, S.; Wang, K.; Song, Y.; Luo, R.; Shao, Z.; Yang, S.; Yang, C. Icariin attenuates Interleukin-1β-induced inflammatory response in human nucleus pulposus cells. Curr Pharm Des. 2018, 23(39), 6071–6078. https://doi.org/10.2174/1381612823666170615112158.</mixed-citation><mixed-citation xml:lang="en">Hua, W.; Zhang, Y.; Wu, X.; Kang, L.; Tu, J.; Zhao, K.; Li, S.; Wang, K.; Song, Y.; Luo, R.; Shao, Z.; Yang, S.; Yang, C. Icariin attenuates Interleukin-1β-induced inflammatory response in human nucleus pulposus cells. Curr Pharm Des. 2018, 23(39), 6071–6078. https://doi.org/10.2174/1381612823666170615112158.</mixed-citation></citation-alternatives></ref><ref id="cit242"><label>242</label><citation-alternatives><mixed-citation xml:lang="ru">Wu, H.; Zha, Z.G.; Yao, P. Experimental study of icariin in inducing bone marrow mesenchymal stem cell differentiation. Zhongguo Zhong Xi Yi Jie He Za Zhi. 2010, 30(4), 410–415.</mixed-citation><mixed-citation xml:lang="en">Wu, H.; Zha, Z.G.; Yao, P. Experimental study of icariin in inducing bone marrow mesenchymal stem cell differentiation. Zhongguo Zhong Xi Yi Jie He Za Zhi. 2010, 30(4), 410–415.</mixed-citation></citation-alternatives></ref><ref id="cit243"><label>243</label><citation-alternatives><mixed-citation xml:lang="ru">Su, Y.S.; Fan, Z.X.; Xiao, S.E.; Lin, B.J.; Miao, Y.; Hu, Z.Q.; Liu, H. Icariin promotes mouse hair follicle growth by increasing insulin-like growth factor 1 expression in dermal papillary cells. Clin Exp Dermatol. 2017, 42(3), 287–294. https://doi.org/10.1111/ced.13043.</mixed-citation><mixed-citation xml:lang="en">Su, Y.S.; Fan, Z.X.; Xiao, S.E.; Lin, B.J.; Miao, Y.; Hu, Z.Q.; Liu, H. Icariin promotes mouse hair follicle growth by increasing insulin-like growth factor 1 expression in dermal papillary cells. Clin Exp Dermatol. 2017, 42(3), 287–294. https://doi.org/10.1111/ced.13043.</mixed-citation></citation-alternatives></ref><ref id="cit244"><label>244</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang, Z.; Qin, F.; Feng, Y.; Zhang, S.; Xie, C.; Huang, H.; Sang, C.; Hu, S.; Jiao, F.; Jiang, J.; Qin, Y. Icariin regulates stem cell migration for endogenous repair of intervertebral disc degeneration by increasing the expression of chemotactic cytokines. BMC Complement Med Ther. 2022, 22, 63. https://doi.org/10.1186/s12906-022-03544-x.</mixed-citation><mixed-citation xml:lang="en">Zhang, Z.; Qin, F.; Feng, Y.; Zhang, S.; Xie, C.; Huang, H.; Sang, C.; Hu, S.; Jiao, F.; Jiang, J.; Qin, Y. Icariin regulates stem cell migration for endogenous repair of intervertebral disc degeneration by increasing the expression of chemotactic cytokines. BMC Complement Med Ther. 2022, 22, 63. https://doi.org/10.1186/s12906-022-03544-x.</mixed-citation></citation-alternatives></ref><ref id="cit245"><label>245</label><citation-alternatives><mixed-citation xml:lang="ru">Choi, E.S.; Yoon, J.J.; Han, B.H.; Jeong, D.H.; Lee, Y.J.; Kang, D.G.; Lee, H.S. Ligustilide attenuates vascular inflammation and activates Nrf2/HO-1 induction and, NO synthesis in HUVECs, Phytomedicine. 2018, 38, 12–23. https://doi.org/10.1016/j.phymed.2017.09.022.</mixed-citation><mixed-citation xml:lang="en">Choi, E.S.; Yoon, J.J.; Han, B.H.; Jeong, D.H.; Lee, Y.J.; Kang, D.G.; Lee, H.S. Ligustilide attenuates vascular inflammation and activates Nrf2/HO-1 induction and, NO synthesis in HUVECs, Phytomedicine. 2018, 38, 12–23. https://doi.org/10.1016/j.phymed.2017.09.022.</mixed-citation></citation-alternatives></ref><ref id="cit246"><label>246</label><citation-alternatives><mixed-citation xml:lang="ru">Su, Y.W.; Chiou, W.F.; Chao, S.H.; Lee, M.H.; Chen, C.C.; Tsai, Y.C. Ligustilide prevents LPS-induced iNOS expression in RAW 264.7 macrophages by preventing ROS production and down-regulating the MAPK, NF-κB and AP-1 signaling pathways, Int. Immunopharmacol. 2011, 11(9), 1166–1172. https://doi.org/10.1016/j.intimp.2011.03.014.</mixed-citation><mixed-citation xml:lang="en">Su, Y.W.; Chiou, W.F.; Chao, S.H.; Lee, M.H.; Chen, C.C.; Tsai, Y.C. Ligustilide prevents LPS-induced iNOS expression in RAW 264.7 macrophages by preventing ROS production and down-regulating the MAPK, NF-κB and AP-1 signaling pathways, Int. Immunopharmacol. 2011, 11(9), 1166–1172. https://doi.org/10.1016/j.intimp.2011.03.014.</mixed-citation></citation-alternatives></ref><ref id="cit247"><label>247</label><citation-alternatives><mixed-citation xml:lang="ru">Wang, K.; Chen, T.; Ying, X.; Zhang, Z.; Shao, Z.; Lin, J.; Xu, T.; Chen, Y.; Wang, X.; Chen, J.; Sheng, S. Ligustilide alleviated IL-1β induced apoptosis and extracellular matrix degradation of nucleus pulposus cells and attenuates intervertebral disc degeneration in vivo. Int Immunopharmacol. 2019, 69, 398-407. https://doi.org/10.1016/j.intimp.2019.01.004.</mixed-citation><mixed-citation xml:lang="en">Wang, K.; Chen, T.; Ying, X.; Zhang, Z.; Shao, Z.; Lin, J.; Xu, T.; Chen, Y.; Wang, X.; Chen, J.; Sheng, S. Ligustilide alleviated IL-1β induced apoptosis and extracellular matrix degradation of nucleus pulposus cells and attenuates intervertebral disc degeneration in vivo. Int Immunopharmacol. 2019, 69, 398-407. https://doi.org/10.1016/j.intimp.2019.01.004.</mixed-citation></citation-alternatives></ref><ref id="cit248"><label>248</label><citation-alternatives><mixed-citation xml:lang="ru">Gao, G.; Chang, F.; Zhang, T.; Huang, X.; Yu, C.; Hu, Z.; Ji, M.; Duan, Y. Naringin protects against Interleukin 1β (IL-1β)-induced human nucleus pulposus cells degeneration via downregulation nuclear factor kappa B (NF-κB) Pathway and p53 Expression. Med Sci Monit. 2019, 25, 9963-9972. https://doi.org/10.12659/MSM.918597.</mixed-citation><mixed-citation xml:lang="en">Gao, G.; Chang, F.; Zhang, T.; Huang, X.; Yu, C.; Hu, Z.; Ji, M.; Duan, Y. Naringin protects against Interleukin 1β (IL-1β)-induced human nucleus pulposus cells degeneration via downregulation nuclear factor kappa B (NF-κB) Pathway and p53 Expression. Med Sci Monit. 2019, 25, 9963-9972. https://doi.org/10.12659/MSM.918597.</mixed-citation></citation-alternatives></ref><ref id="cit249"><label>249</label><citation-alternatives><mixed-citation xml:lang="ru">Li, Y.; Li, K.; Hu, Y.; Xu, B.; Zhao, J. Piperine mediates LPS induced inflammatory and catabolic effects in rat intervertebral disc. Int J Clin Exp Pathol. 2015, 8(6), 6203-13.</mixed-citation><mixed-citation xml:lang="en">Li, Y.; Li, K.; Hu, Y.; Xu, B.; Zhao, J. Piperine mediates LPS induced inflammatory and catabolic effects in rat intervertebral disc. Int J Clin Exp Pathol. 2015, 8(6), 6203-13.</mixed-citation></citation-alternatives></ref><ref id="cit250"><label>250</label><citation-alternatives><mixed-citation xml:lang="ru">Liu, H.B.; Meng, Q.H.; Huang, J.B.; Wang, C.; Liu X.W. Nephroprotective effects of polydatin against ischemia / reperfusion injury: A role for the PI3K / Akt signal pathway. Oxidative Medicine and Cellular Longevity. 2015, 2015, 1–13. https://doi.org/10.1155/2015/ 362158.</mixed-citation><mixed-citation xml:lang="en">Liu, H.B.; Meng, Q.H.; Huang, J.B.; Wang, C.; Liu X.W. Nephroprotective effects of polydatin against ischemia / reperfusion injury: A role for the PI3K / Akt signal pathway. Oxidative Medicine and Cellular Longevity. 2015, 2015, 1–13. https://doi.org/10.1155/2015/ 362158.</mixed-citation></citation-alternatives></ref><ref id="cit251"><label>251</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang, Q.; Yi, M.; Guo, Q.; Wang, C.; Wang, H.; Meng, S.; Liu, C.; Fu, Y.; Ji, H.; Chen, T. Protective effects of polydatin on lipopolysaccharide-induced acute lung injury through TLR4-MyD88-NF-κB pathway. Int Immunopharmacol. 2015, 29(2), 370-376. https://doi.org/10.1016/j.intimp.2015.10.027.</mixed-citation><mixed-citation xml:lang="en">Jiang, Q.; Yi, M.; Guo, Q.; Wang, C.; Wang, H.; Meng, S.; Liu, C.; Fu, Y.; Ji, H.; Chen, T. Protective effects of polydatin on lipopolysaccharide-induced acute lung injury through TLR4-MyD88-NF-κB pathway. Int Immunopharmacol. 2015, 29(2), 370-376. https://doi.org/10.1016/j.intimp.2015.10.027.</mixed-citation></citation-alternatives></ref><ref id="cit252"><label>252</label><citation-alternatives><mixed-citation xml:lang="ru">Lanzilli, G.; Cottarelli, A.; Nicotera, G.; Guida, S.; Ravagnan, G.; Fuggetta, M.P. Anti-inflammatory effect of resveratrol and polydatin by in vitro IL-17 modulation. Inflammation. 2012, 35(1), 240-8. https://doi.org/10.1007/s10753-011-9310-z.</mixed-citation><mixed-citation xml:lang="en">Lanzilli, G.; Cottarelli, A.; Nicotera, G.; Guida, S.; Ravagnan, G.; Fuggetta, M.P. Anti-inflammatory effect of resveratrol and polydatin by in vitro IL-17 modulation. Inflammation. 2012, 35(1), 240-8. https://doi.org/10.1007/s10753-011-9310-z.</mixed-citation></citation-alternatives></ref><ref id="cit253"><label>253</label><citation-alternatives><mixed-citation xml:lang="ru">Ravagnan, G.; De Filippis, A.; Cartenì, M.; De Maria, S.; Cozza, V.; Petrazzuolo, M.; Tufano, M.A.; Donnarumma, G. Polydatin, a natural precursor of resveratrol, induces β-defensin production and reduces inflammatory response. Inflammation. 2013, 36(1), 26-34. https://doi.org/10.1007/s10753-012-9516-8.</mixed-citation><mixed-citation xml:lang="en">Ravagnan, G.; De Filippis, A.; Cartenì, M.; De Maria, S.; Cozza, V.; Petrazzuolo, M.; Tufano, M.A.; Donnarumma, G. Polydatin, a natural precursor of resveratrol, induces β-defensin production and reduces inflammatory response. Inflammation. 2013, 36(1), 26-34. https://doi.org/10.1007/s10753-012-9516-8.</mixed-citation></citation-alternatives></ref><ref id="cit254"><label>254</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou, L.; Ivanov, I.I.; Spolski, R.; Min, R.; Shenderov, K.; Egawa, T.; Levy, D.E.; Leonard, W.J.; Littman, D.R. IL-6 programs T(H)-17 cell differentiation by promoting sequential engagement of the IL-21 and IL-23 pathways. Nat Immunol. 2007, 8(9), 967-74. https://doi.org/10.1038/ni1488.</mixed-citation><mixed-citation xml:lang="en">Zhou, L.; Ivanov, I.I.; Spolski, R.; Min, R.; Shenderov, K.; Egawa, T.; Levy, D.E.; Leonard, W.J.; Littman, D.R. IL-6 programs T(H)-17 cell differentiation by promoting sequential engagement of the IL-21 and IL-23 pathways. Nat Immunol. 2007, 8(9), 967-74. https://doi.org/10.1038/ni1488.</mixed-citation></citation-alternatives></ref><ref id="cit255"><label>255</label><citation-alternatives><mixed-citation xml:lang="ru">Cho, M.L.; Kang, J.W.; Moon, Y.M.; Nam, H.J.; Jhun, J.Y.; Heo, S.B.; Jin, H.T.; Min, S.Y.; Ju, J.H.; Park, K.S.; Cho, Y.G.; Yoon, C.H.; Park, S.H.; Sung, Y.C.; Kim, H.Y. STAT3 and NF-kappaB signal pathway is required for IL-23-mediated IL-17 production in spontaneous arthritis animal model IL-1 receptor antagonist-deficient mice. J Immunol. 2006, 176(9), 5652-61. https://doi.org/10.4049/jimmunol.176.9.5652.</mixed-citation><mixed-citation xml:lang="en">Cho, M.L.; Kang, J.W.; Moon, Y.M.; Nam, H.J.; Jhun, J.Y.; Heo, S.B.; Jin, H.T.; Min, S.Y.; Ju, J.H.; Park, K.S.; Cho, Y.G.; Yoon, C.H.; Park, S.H.; Sung, Y.C.; Kim, H.Y. STAT3 and NF-kappaB signal pathway is required for IL-23-mediated IL-17 production in spontaneous arthritis animal model IL-1 receptor antagonist-deficient mice. J Immunol. 2006, 176(9), 5652-61. https://doi.org/10.4049/jimmunol.176.9.5652.</mixed-citation></citation-alternatives></ref><ref id="cit256"><label>256</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang, J.; Tan, Y.; Yao, F.; Zhang, Q. Polydatin alleviates non-alcoholic fatty liver disease in rats by inhibiting the expression of TNF-α and SREBP-1c. Mol Med Rep. 2012, 6(4), 815-20. https://doi.org/10.3892/mmr.2012.1015.</mixed-citation><mixed-citation xml:lang="en">Zhang, J.; Tan, Y.; Yao, F.; Zhang, Q. Polydatin alleviates non-alcoholic fatty liver disease in rats by inhibiting the expression of TNF-α and SREBP-1c. Mol Med Rep. 2012, 6(4), 815-20. https://doi.org/10.3892/mmr.2012.1015.</mixed-citation></citation-alternatives></ref><ref id="cit257"><label>257</label><citation-alternatives><mixed-citation xml:lang="ru">Hogg, S.J.; Chitcholtan, K.; Hassan, W.; Sykes, P.H.; Garrill, A. Resveratrol, Acetyl-Resveratrol, and Polydatin exhibit antigrowth activity against 3D Cell aggregates of the SKOV-3 and OVCAR-8 Ovarian cancer cell lines. Obstet Gynecol Int. 2015, 2015, 279591. https://doi.org/10.1155/2015/279591.</mixed-citation><mixed-citation xml:lang="en">Hogg, S.J.; Chitcholtan, K.; Hassan, W.; Sykes, P.H.; Garrill, A. Resveratrol, Acetyl-Resveratrol, and Polydatin exhibit antigrowth activity against 3D Cell aggregates of the SKOV-3 and OVCAR-8 Ovarian cancer cell lines. Obstet Gynecol Int. 2015, 2015, 279591. https://doi.org/10.1155/2015/279591.</mixed-citation></citation-alternatives></ref><ref id="cit258"><label>258</label><citation-alternatives><mixed-citation xml:lang="ru">Kamel, K.M.; Gad, A.M.; Mansour, S.M.; Safar, M.M.; Fawzy, H.M. Novel anti-arthritic mechanisms of Polydatin in Complete Freund's Adjuvant-induced arthritis in Rats: Involvement of IL-6, STAT-3, IL-17, and NF-кB. Inflammation. 2018, 41(5), 1974-1986. https://doi.org/10.1007/s10753-018-0841-4.</mixed-citation><mixed-citation xml:lang="en">Kamel, K.M.; Gad, A.M.; Mansour, S.M.; Safar, M.M.; Fawzy, H.M. Novel anti-arthritic mechanisms of Polydatin in Complete Freund's Adjuvant-induced arthritis in Rats: Involvement of IL-6, STAT-3, IL-17, and NF-кB. Inflammation. 2018, 41(5), 1974-1986. https://doi.org/10.1007/s10753-018-0841-4.</mixed-citation></citation-alternatives></ref><ref id="cit259"><label>259</label><citation-alternatives><mixed-citation xml:lang="ru">Li, B.; Wang, X.L. Effective treatment of polydatin weakens the symptoms of collagen-induced arthritis in mice through its anti-oxidative and anti-inflammatory effects and the activation of MMP-9. Mol Med Rep. 2016, 14(6), 5357-5362. https://doi.org/10.3892/mmr.2016.5903.</mixed-citation><mixed-citation xml:lang="en">Li, B.; Wang, X.L. Effective treatment of polydatin weakens the symptoms of collagen-induced arthritis in mice through its anti-oxidative and anti-inflammatory effects and the activation of MMP-9. Mol Med Rep. 2016, 14(6), 5357-5362. https://doi.org/10.3892/mmr.2016.5903.</mixed-citation></citation-alternatives></ref><ref id="cit260"><label>260</label><citation-alternatives><mixed-citation xml:lang="ru">Gauthaman, K.; Adaikan, P.G.; Prasad, R.N.V. Aphrodisiac properties of Tribulus terrestris extract (Protodioscin) in normal and castrated rats. Life Sci. 2002, 71(12), 1385–1396. https://doi.org/10.1016/s0024-3205(02)01858-1.</mixed-citation><mixed-citation xml:lang="en">Gauthaman, K.; Adaikan, P.G.; Prasad, R.N.V. Aphrodisiac properties of Tribulus terrestris extract (Protodioscin) in normal and castrated rats. Life Sci. 2002, 71(12), 1385–1396. https://doi.org/10.1016/s0024-3205(02)01858-1.</mixed-citation></citation-alternatives></ref><ref id="cit261"><label>261</label><citation-alternatives><mixed-citation xml:lang="ru">Hu, K.; Yao, X. Protodioscin (NSC-698 796): its spectrum of cytotoxicity against sixty human cancer cell lines in an anticancer drug screen panel. Planta Med. 2002, 68(4), 297–301. https://doi.org/10.1055/s-2002-26743.</mixed-citation><mixed-citation xml:lang="en">Hu, K.; Yao, X. Protodioscin (NSC-698 796): its spectrum of cytotoxicity against sixty human cancer cell lines in an anticancer drug screen panel. Planta Med. 2002, 68(4), 297–301. https://doi.org/10.1055/s-2002-26743.</mixed-citation></citation-alternatives></ref><ref id="cit262"><label>262</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang, R.; Gilbert, S.; Yao, X.; Vallance, J.; Steinbrecher, K.; Moriggl, R.; Zhang, D.; Eluri, M.; Chen, H.; Cao, H.; Shroyer, N.; Denson, L.; Han, X. Natural compound methyl protodioscin protects against intestinal inflammation through modulation of intestinal immune responses. Pharmacol Res Perspect. 2015, 3(2), e00118. https://doi.org/10.1002/prp2.118.</mixed-citation><mixed-citation xml:lang="en">Zhang, R.; Gilbert, S.; Yao, X.; Vallance, J.; Steinbrecher, K.; Moriggl, R.; Zhang, D.; Eluri, M.; Chen, H.; Cao, H.; Shroyer, N.; Denson, L.; Han, X. Natural compound methyl protodioscin protects against intestinal inflammation through modulation of intestinal immune responses. Pharmacol Res Perspect. 2015, 3(2), e00118. https://doi.org/10.1002/prp2.118.</mixed-citation></citation-alternatives></ref><ref id="cit263"><label>263</label><citation-alternatives><mixed-citation xml:lang="ru">Lee, J.H.; Lim, H.J.; Lee, C.W.; Son, K.H.; Son, J.K.; Lee, S.K.; Kim, H.P.Methyl protodioscin from the roots of Asparagus cochinchinensis attenuates airway inflammation by inhibiting cytokine production. Evid Based Complement Altern Med. 2015, 2015, 640846. https://doi.org/10.1155/2015/640846.</mixed-citation><mixed-citation xml:lang="en">Lee, J.H.; Lim, H.J.; Lee, C.W.; Son, K.H.; Son, J.K.; Lee, S.K.; Kim, H.P.Methyl protodioscin from the roots of Asparagus cochinchinensis attenuates airway inflammation by inhibiting cytokine production. Evid Based Complement Altern Med. 2015, 2015, 640846. https://doi.org/10.1155/2015/640846.</mixed-citation></citation-alternatives></ref><ref id="cit264"><label>264</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang, X.; Xue, X.; Xian, L.; Guo, Z.; Ito, Y.; Sun, W. Potential neuroprotection of protodioscin against cerebral ischemia-reperfusion injury in rats through intervening inflammation and apoptosis. Steroids. 2016, 113, 52–63. https://doi.org/10.1016/j.steroids.2016.06.008.</mixed-citation><mixed-citation xml:lang="en">Zhang, X.; Xue, X.; Xian, L.; Guo, Z.; Ito, Y.; Sun, W. Potential neuroprotection of protodioscin against cerebral ischemia-reperfusion injury in rats through intervening inflammation and apoptosis. Steroids. 2016, 113, 52–63. https://doi.org/10.1016/j.steroids.2016.06.008.</mixed-citation></citation-alternatives></ref><ref id="cit265"><label>265</label><citation-alternatives><mixed-citation xml:lang="ru">Liu, J.Y.; Hou, Y.L.; Cao, R.; Qiu, H.X.; Cheng, G.H.; Tu, R.; Wang, L.; Zhang, J.L.; Liu, D. Protodioscin ameliorates oxidative stress, inflammation and histology outcome in Complete Freund's adjuvant induced arthritis rats. Apoptosis. 2017, 22(11), 1454-1460. https://doi.org/10.1007/s10495-017-1420-0.</mixed-citation><mixed-citation xml:lang="en">Liu, J.Y.; Hou, Y.L.; Cao, R.; Qiu, H.X.; Cheng, G.H.; Tu, R.; Wang, L.; Zhang, J.L.; Liu, D. Protodioscin ameliorates oxidative stress, inflammation and histology outcome in Complete Freund's adjuvant induced arthritis rats. Apoptosis. 2017, 22(11), 1454-1460. https://doi.org/10.1007/s10495-017-1420-0.</mixed-citation></citation-alternatives></ref><ref id="cit266"><label>266</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao, Y.; Liu, J.; Liu, C.; Zeng, X.; Li, X.; Zhao, J. Anti-inflammatory effects of pcoumaric acid in LPS-stimulated RAW264.7 cells: involvement of NF-κB and MAPKs Pathways. Med Chem (Los Angeles). 2016, 6, 327–330. https://doi.org/10.4172/2161-0444.1000365.</mixed-citation><mixed-citation xml:lang="en">Zhao, Y.; Liu, J.; Liu, C.; Zeng, X.; Li, X.; Zhao, J. Anti-inflammatory effects of pcoumaric acid in LPS-stimulated RAW264.7 cells: involvement of NF-κB and MAPKs Pathways. Med Chem (Los Angeles). 2016, 6, 327–330. https://doi.org/10.4172/2161-0444.1000365.</mixed-citation></citation-alternatives></ref><ref id="cit267"><label>267</label><citation-alternatives><mixed-citation xml:lang="ru">Warren, C.A.; Paulhill, K.J.; Davidson, L.A.; Lupton, J.R.; Taddeo, S.S.; Hong, M.Y.; Carroll, R.J.; Chapkin, R.S.; Turner, N.D. Quercetin may suppress rat aberrant crypt foci formation by suppressing inflammatory mediators that influence proliferation and apoptosis. J. Nutr. 2009, 139, 101–105. https://doi.org/10.3945/jn.108.096271.</mixed-citation><mixed-citation xml:lang="en">Warren, C.A.; Paulhill, K.J.; Davidson, L.A.; Lupton, J.R.; Taddeo, S.S.; Hong, M.Y.; Carroll, R.J.; Chapkin, R.S.; Turner, N.D. Quercetin may suppress rat aberrant crypt foci formation by suppressing inflammatory mediators that influence proliferation and apoptosis. J. Nutr. 2009, 139, 101–105. https://doi.org/10.3945/jn.108.096271.</mixed-citation></citation-alternatives></ref><ref id="cit268"><label>268</label><citation-alternatives><mixed-citation xml:lang="ru">Li, Y.; Yao, J.; Han, C.; Yang, J.; Chaudhry, M.; Wang, S.; Liu, H.; Yin, Y. Quercetin, infammation and immunity. Nutrients. 2016, 8(3), 167. https://doi.org/10.3390/nu8030167.</mixed-citation><mixed-citation xml:lang="en">Li, Y.; Yao, J.; Han, C.; Yang, J.; Chaudhry, M.; Wang, S.; Liu, H.; Yin, Y. Quercetin, infammation and immunity. Nutrients. 2016, 8(3), 167. https://doi.org/10.3390/nu8030167.</mixed-citation></citation-alternatives></ref><ref id="cit269"><label>269</label><citation-alternatives><mixed-citation xml:lang="ru">Taylor, P.; Gartemann, J.; Hsieh, J.; Creeden, J. A systematic review of serum biomarkers anti-cyclic citrullinated peptide and rheumatoid factor as tests for rheumatoid arthritis. Autoimmune Dis. 2011, 2011, 815038. https://doi.org/10.4061/2011/ 815038.</mixed-citation><mixed-citation xml:lang="en">Taylor, P.; Gartemann, J.; Hsieh, J.; Creeden, J. A systematic review of serum biomarkers anti-cyclic citrullinated peptide and rheumatoid factor as tests for rheumatoid arthritis. Autoimmune Dis. 2011, 2011, 815038. https://doi.org/10.4061/2011/ 815038.</mixed-citation></citation-alternatives></ref><ref id="cit270"><label>270</label><citation-alternatives><mixed-citation xml:lang="ru">Li, K.; Li, Y.; Xu, B.; Mao, L.; Zhao, J. Sesamin inhibits lipopolysaccharide-induced inflammation and extracellular matrix catabolism in rat intervertebral disc. Connect Tissue Res. 2016, 57(5), 347-59. https://doi.org/10.1080/03008207.2016.1182998.</mixed-citation><mixed-citation xml:lang="en">Li, K.; Li, Y.; Xu, B.; Mao, L.; Zhao, J. Sesamin inhibits lipopolysaccharide-induced inflammation and extracellular matrix catabolism in rat intervertebral disc. Connect Tissue Res. 2016, 57(5), 347-59. https://doi.org/10.1080/03008207.2016.1182998.</mixed-citation></citation-alternatives></ref><ref id="cit271"><label>271</label><citation-alternatives><mixed-citation xml:lang="ru">Yun, K.J.; Koh, D.J.; Kim, S.H.; Park, S.J.; Ryu, J.H.; Kim, D.G.; Lee, J.Y.; Lee, K.T. Anti-inflammatory effects of sinapic acid through the suppression of inducible nitric oxide synthase, cyclooxygase-2, and proinflammatory cytokines expressions via nuclear factor-kappaB inactivation. J Agric Food Chem. 2008, 56(21), 10265-72. https://doi.org/10.1021/jf802095g.</mixed-citation><mixed-citation xml:lang="en">Yun, K.J.; Koh, D.J.; Kim, S.H.; Park, S.J.; Ryu, J.H.; Kim, D.G.; Lee, J.Y.; Lee, K.T. Anti-inflammatory effects of sinapic acid through the suppression of inducible nitric oxide synthase, cyclooxygase-2, and proinflammatory cytokines expressions via nuclear factor-kappaB inactivation. J Agric Food Chem. 2008, 56(21), 10265-72. https://doi.org/10.1021/jf802095g.</mixed-citation></citation-alternatives></ref><ref id="cit272"><label>272</label><citation-alternatives><mixed-citation xml:lang="ru">di Meglio, P.; Ianaro, A.; Ghosh, S. Amelioration of acute inflammation by systemic administration of a cell-permeable peptide inhibitor of NF-kappaB activation. Arthritis Rheum. 2005, 52(3), 951–958. https://doi.org/10.1002/art.20960.</mixed-citation><mixed-citation xml:lang="en">di Meglio, P.; Ianaro, A.; Ghosh, S. Amelioration of acute inflammation by systemic administration of a cell-permeable peptide inhibitor of NF-kappaB activation. Arthritis Rheum. 2005, 52(3), 951–958. https://doi.org/10.1002/art.20960.</mixed-citation></citation-alternatives></ref><ref id="cit273"><label>273</label><citation-alternatives><mixed-citation xml:lang="ru">Lee, Y.R.; Kweon, S.H.; Kwon, K.B.; Park, J.W.; Yoon, T.R.; Park, B.H. Inhibition of IL1 beta-mediated inflammatory responses by the IkappaB alpha super-repressor in human fibroblast-like synoviocytes. Biochem. Biophys. Res. Commun. 2009, 378(1), 90–94. https://doi.org/10.1016/j.bbrc.2008.11.002.</mixed-citation><mixed-citation xml:lang="en">Lee, Y.R.; Kweon, S.H.; Kwon, K.B.; Park, J.W.; Yoon, T.R.; Park, B.H. Inhibition of IL1 beta-mediated inflammatory responses by the IkappaB alpha super-repressor in human fibroblast-like synoviocytes. Biochem. Biophys. Res. Commun. 2009, 378(1), 90–94. https://doi.org/10.1016/j.bbrc.2008.11.002.</mixed-citation></citation-alternatives></ref><ref id="cit274"><label>274</label><citation-alternatives><mixed-citation xml:lang="ru">Xia, T.; Gao, R.; Zhou, G.; Liu, J.; Li, J.; Shen, J. Trans-cinnamaldehyde inhibits IL-1β-stimulated inflammation in chondrocytes by suppressing NF-κB and p38-JNK pathways and exerts chondrocyte protective effects in a rat model of osteoarthritis. BioMed Res Int. 2019, 2019, 4039472. https://doi.org/10.1155/2019/4039472.</mixed-citation><mixed-citation xml:lang="en">Xia, T.; Gao, R.; Zhou, G.; Liu, J.; Li, J.; Shen, J. Trans-cinnamaldehyde inhibits IL-1β-stimulated inflammation in chondrocytes by suppressing NF-κB and p38-JNK pathways and exerts chondrocyte protective effects in a rat model of osteoarthritis. BioMed Res Int. 2019, 2019, 4039472. https://doi.org/10.1155/2019/4039472.</mixed-citation></citation-alternatives></ref><ref id="cit275"><label>275</label><citation-alternatives><mixed-citation xml:lang="ru">Pahan, S.; Pahan, K. Can cinnamon spice down autoimmune diseases? J Clin Exp Immunol. 2020, 5(6), 252-8. https://doi.org/10.33140/jcei.05.06.01.</mixed-citation><mixed-citation xml:lang="en">Pahan, S.; Pahan, K. Can cinnamon spice down autoimmune diseases? J Clin Exp Immunol. 2020, 5(6), 252-8. https://doi.org/10.33140/jcei.05.06.01.</mixed-citation></citation-alternatives></ref><ref id="cit276"><label>276</label><citation-alternatives><mixed-citation xml:lang="ru">El-Tanbouly, G.S.; Abdelrahman, R.S. Novel anti-arthritic mechanisms of trans-cinnamaldehyde against complete Freund's adjuvant-induced arthritis in mice: involvement of NF-кB/TNF-α and IL-6/IL-23/ IL-17 pathways in the immuno-inflammatory responses. Inflammopharmacology. 2022, 30(5), 1769-1780. https://doi.org/10.1007/s10787-022-01005-y.</mixed-citation><mixed-citation xml:lang="en">El-Tanbouly, G.S.; Abdelrahman, R.S. Novel anti-arthritic mechanisms of trans-cinnamaldehyde against complete Freund's adjuvant-induced arthritis in mice: involvement of NF-кB/TNF-α and IL-6/IL-23/ IL-17 pathways in the immuno-inflammatory responses. Inflammopharmacology. 2022, 30(5), 1769-1780. https://doi.org/10.1007/s10787-022-01005-y.</mixed-citation></citation-alternatives></ref><ref id="cit277"><label>277</label><citation-alternatives><mixed-citation xml:lang="ru">Liu, P.; Wang, J.; Wen, W.; Pan, T.; Chen, H.; Fu, Y.; Wang, F.; Huang, J.H.; Xu, S. Cinnamaldehyde suppresses NLRP3 derived IL-1β via activating succinate/HIF-1 in rheumatoid arthritis rats. Int Immunopharmacol. 2020, 84, 106570. https://doi.org/10.1016/j.intimp.2020.106570.</mixed-citation><mixed-citation xml:lang="en">Liu, P.; Wang, J.; Wen, W.; Pan, T.; Chen, H.; Fu, Y.; Wang, F.; Huang, J.H.; Xu, S. Cinnamaldehyde suppresses NLRP3 derived IL-1β via activating succinate/HIF-1 in rheumatoid arthritis rats. Int Immunopharmacol. 2020, 84, 106570. https://doi.org/10.1016/j.intimp.2020.106570.</mixed-citation></citation-alternatives></ref><ref id="cit278"><label>278</label><citation-alternatives><mixed-citation xml:lang="ru">Cheng, W.X.; Zhong, S.; Meng, X.B.; Zheng, N.Y.; Zhang, P.; Wang, Y.; Qin, L.; Wang, X.L. Cinnamaldehyde inhibits inflammation of human synoviocyte cells through regulation of Jak/Stat pathway and ameliorates collagen-induced arthritis in rats. J Pharmacol Exp Ther. 2020, 373(2), 302–310. https://doi.org/10.1124/jpet.119.262907.</mixed-citation><mixed-citation xml:lang="en">Cheng, W.X.; Zhong, S.; Meng, X.B.; Zheng, N.Y.; Zhang, P.; Wang, Y.; Qin, L.; Wang, X.L. Cinnamaldehyde inhibits inflammation of human synoviocyte cells through regulation of Jak/Stat pathway and ameliorates collagen-induced arthritis in rats. J Pharmacol Exp Ther. 2020, 373(2), 302–310. https://doi.org/10.1124/jpet.119.262907.</mixed-citation></citation-alternatives></ref><ref id="cit279"><label>279</label><citation-alternatives><mixed-citation xml:lang="ru">Fang, W.; Zhou, X.; Wang, J.; Xu, L.; Zhou, L.; Yu, W.; Tao, Y.; Zhu, J.; Hu, B.; Liang, C.; Li, F.; Hua, J.; Chen, Q. Wogonin mitigates intervertebral disc degeneration through the Nrf2/ARE and MAPK signaling pathways. Int Immunopharmacol. 2018, 65, 539-549. https://doi.org/10.1016/j.intimp.2018.10.024.</mixed-citation><mixed-citation xml:lang="en">Fang, W.; Zhou, X.; Wang, J.; Xu, L.; Zhou, L.; Yu, W.; Tao, Y.; Zhu, J.; Hu, B.; Liang, C.; Li, F.; Hua, J.; Chen, Q. Wogonin mitigates intervertebral disc degeneration through the Nrf2/ARE and MAPK signaling pathways. Int Immunopharmacol. 2018, 65, 539-549. https://doi.org/10.1016/j.intimp.2018.10.024.</mixed-citation></citation-alternatives></ref><ref id="cit280"><label>280</label><citation-alternatives><mixed-citation xml:lang="ru">Shnayder, N.A.; Ashhotov, A.V.; Trefilova, V.V.; Novitsky, M.A.; Medvedev, G.V.; Petrova, M.M.; Narodova, E.A.; Kaskaeva, D.S.; Chumakova, G.A.; Garganeeva, N.P.; Lareva, N.V.; Al-Zamil, M.; Asadullin, A.R.; Nasyrova, R.F. High-Tech Methods of Cytokine Imbalance Correction in Intervertebral Disc Degeneration. Int J Mol Sci. 2023; 24(9): 7692. https://doi.org/ 10.3390/ijms24097692.</mixed-citation><mixed-citation xml:lang="en">Shnayder, N.A.; Ashhotov, A.V.; Trefilova, V.V.; Novitsky, M.A.; Medvedev, G.V.; Petrova, M.M.; Narodova, E.A.; Kaskaeva, D.S.; Chumakova, G.A.; Garganeeva, N.P.; Lareva, N.V.; Al-Zamil, M.; Asadullin, A.R.; Nasyrova, R.F. High-Tech Methods of Cytokine Imbalance Correction in Intervertebral Disc Degeneration. Int J Mol Sci. 2023; 24(9): 7692. https://doi.org/ 10.3390/ijms24097692.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
