<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="review-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="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">sibmed</journal-id><journal-title-group><journal-title xml:lang="ru">Сибирский научный медицинский журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Сибирский научный медицинский журнал</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2410-2512</issn><issn pub-type="epub">2410-2520</issn><publisher><publisher-name>ИЦиГ СО РАН</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18699/SSMJ20250303</article-id><article-id custom-type="elpub" pub-id-type="custom">sibmed-2228</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="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Перспективы применения флавоноидов при остеопорозе</article-title><trans-title-group xml:lang="en"><trans-title>Prospects for the use of flavonoids in osteoporosis</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8101-103X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зверев</surname><given-names>Я. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Zverev</surname><given-names>Ya. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Яков Федорович Зверев, д. м. н., проф.</p><p>656038; пр. Ленина, 40; Барнаул</p></bio><bio xml:lang="en"><p>Yakov F. Zverev, doctor of medical science, professor</p><p>656038; Lenina ave., 40; Barnaul</p></bio><email xlink:type="simple">zveryasha@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5889-7071</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рыкунова</surname><given-names>А. Я.</given-names></name><name name-style="western" xml:lang="en"><surname>Rykunova</surname><given-names>A. Ya.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Анна Яковлевна Рыкунова, к. м. н.</p><p>656038; пр. Ленина, 40; Барнаул</p></bio><bio xml:lang="en"><p>Anna Ya. Rykunova, candidate of medical sciences</p><p>656038; Lenina ave., 40; Barnaul</p></bio><email xlink:type="simple">zveranna@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Алтайский государственный медицинский университет Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Altai State Medical University of Minzdrav of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>13</day><month>07</month><year>2025</year></pub-date><volume>45</volume><issue>3</issue><fpage>26</fpage><lpage>42</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Зверев Я.Ф., Рыкунова А.Я., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Зверев Я.Ф., Рыкунова А.Я.</copyright-holder><copyright-holder xml:lang="en">Zverev Y.F., Rykunova A.Y.</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://sibmed.elpub.ru/jour/article/view/2228">https://sibmed.elpub.ru/jour/article/view/2228</self-uri><abstract><p>   Обзор посвящен целесообразности применения флавоноидов в комплексной терапии остеопороза. Многочисленные виды фармакологической активности, присущие этим полифенольным соединениям растительного происхождения, в том числе противовоспалительная, антиоксидантная, антипролиферативная, иммуномодулирующая, противоопухолевая, антикоагулянтная и другие, заставили с вниманием подойти к возможности их клинической эффективности при костной патологии. Экспериментальные исследования последних лет позволили установить, что протективное действие флавоноидов, препятствующее патологической потере кости, обусловлено, прежде всего, активацией формирования новой костной ткани путем стимуляции пролиферации и дифференцировки остеобластов, а также ослаблением процесса резорбции кости за счет угнетения остеокластогенеза. Обсуждаются возможные механизмы отмеченных эффектов с учетом воздействия на процессы внутриклеточного сигнализирования. Отмечается положительное влияние на процесс остеогенеза эстрогеноподобных свойств ряда флавоноидов. В обзоре рассмотрены многообещающие свойства наиболее широко встречающихся флавонолов, флавонов, флаванонов, флаван-3-одов (катехинов), антоцианидинов, изофлавонов, позволяющие с оптимизмом смотреть на их клиническое применение в будущем. Как полагают многие авторы, дальнейшие углубленные доклинические исследования должны ответить на многие сохраняющиеся вопросы, касающиеся механизмов действия флавоноидов, а также решить проблему их биодоступности.</p></abstract><trans-abstract xml:lang="en"><p>   The review is devoted to the feasibility of using flavonoids in the complex therapy of osteoporosis. Numerous types of pharmacological activity inherent in these polyphenolic compounds of plant origin, including anti-inflammatory, antioxidant, antiproliferative, immunomodulatory, antitumor, anticoagulant and others, forced us to carefully approach the possibility of their clinical effectiveness in bone pathology. Experimental studies of recent years have shown that the protective effect of flavonoids preventing pathological bone loss is primarily due to activation of new bone tissue formation by stimulating proliferation and differentiation of osteoblasts, as well as weakening the bone resorption process by inhibiting osteoclastogenesis. Possible mechanisms of the noted effects are discussed taking into account the impact on intracellular signaling processes. A positive effect of estrogen-like properties of a number of flavonoids on the osteogenesis process is noted. The review considers the promising properties of the most widely encountered flavonols, flavones, flavanones, flavan-3-ods (catechins), anthocyanidins, and isoflavones, allowing one to look with optimism at their clinical application in the future. As many authors believe, further in-depth preclinical studies should answer many remaining questions regarding the mechanisms of action of flavonoids, as well as solve the problem of their bioavailability.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>остеопороз</kwd><kwd>флавоноиды</kwd><kwd>остеобластогенез</kwd><kwd>остеокластогенез</kwd><kwd>механизмы действия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>оsteoporosis</kwd><kwd>flavonoids</kwd><kwd>osteoblastogenesis</kwd><kwd>osteoclastogenesis</kwd><kwd>mechanisms of action</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">Нуруллина Г.М., Ахмадуллина Г.И. Костное ремоделирование в норме и при первичном остеопорозе: значение маркеров костного ремоделирования. Арх. внутр. мед. 2018;8(2):100–110. doi: 10.20514/2226-6704-2018-8-2-100-110</mixed-citation><mixed-citation xml:lang="en">Nurullina G.M., Akhmadullina G.I. Bone remodeling in norm and in primary osteoporosis: the significance of bone remodeling markers. Arkhiv vnutrenney meditsiny = Archive of Internal Medicine. 2018;8(2):100–110. [In Russian]. doi: 10.20514/2226-6704-2018-8-2-100-110</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Игнатенко Г.А., Немсадзе И.Г., Мирович Е.Д., Чурилов А.В., Майлян Э.А., Глазков И.С., Румянцева З.С. Роль цитокинов в ремоделировании костной ткани и патогенез постменопаузального остеопороза. Мед. вестн. Юга России. 2020;11(2):6–18. doi: 10.21886/2219-8075-2020-11-2-6-18</mixed-citation><mixed-citation xml:lang="en">Ignatenko G.A., Nemsadze I.G., Mirovich E.D., Churilov A.V., Maylyan E.A., Glazkov A.E., Rumyantceva Z.S. The role of cytokines in bone remodeling and the pathogenesis of postmenopausal osteoporosis. Meditsinskiy vestnik Yuga Rossii = Medical Herald of the South of Russia. 2020;11(2):6–18. [In Russian]. doi: 10.21886/2219-8075-2020-11-2-6-18</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Ялаев Б.И., Хусаинова P.И. Эпигенетическая регуляция ремоделирования костной ткани и ее роль в патогенезе первичного остеопороза. Вавил. ж. генетики и селекции. 2023;27(4):401–410. doi: 10.18699/VJGB-23-48</mixed-citation><mixed-citation xml:lang="en">Yalaev B.I., Khusainova R.I. Epigenetic regulation of bone remodeling and its role in the pathogenesis of primary osteoporosis. Vavilovskiy zhurnal genetiki i selektsii = Vavilov Journal of Genetics and Breeding. 2023;27(4):401–410. [In Russian]. doi: 10.18699/VJGB-23-48</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Kim J.M., Lin C., Stavre Z., Greenblatt M.B., Shim J.H. Osteoblast-osteoclast communications and bone homeostasis. Cells. 2020;9(19):2073. doi: 10.3390/cells9092073</mixed-citation><mixed-citation xml:lang="en">Kim J.M., Lin C., Stavre Z., Greenblatt M.B., Shim J.H. Osteoblast-osteoclast communications and bone homeostasis. Cells. 2020;9(19):2073. doi: 10.3390/cells9092073</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Yang R., Li J., Zhang J., Xue Q., Qin R., Wang R., Goltzman D., Miao D. 17β-estradiol plays the anti-osteoporosis role via a novel ESR1-Keap1-Nrf2 axismediated stress response activation and Tmem119 up-regulation. Free Radic. Biol. Med. 2023;195:231–244. doi: 10.1016/j.freeradbiomed.2022.12.102</mixed-citation><mixed-citation xml:lang="en">Yang R., Li J., Zhang J., Xue Q., Qin R., Wang R., Goltzman D., Miao D. 17β-estradiol plays the anti-osteoporosis role via a novel ESR1-Keap1-Nrf2 axismediated stress response activation and Tmem119 up-regulation. Free Radic. Biol. Med. 2023;195:231–244. doi: 10.1016/j.freeradbiomed.2022.12.102</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Li Q., Tian C., Liu X., Li D., Liu H. Anti-inflammatory and antioxidant traditional Chinese Medicine in treatment and prevention of osteoporosis. Front. Pharmacol. 2023;14:1203767. doi: 10.3389/fphar.2023.1203767</mixed-citation><mixed-citation xml:lang="en">Li Q., Tian C., Liu X., Li D., Liu H. Anti-inflammatory and antioxidant traditional Chinese Medicine in treatment and prevention of osteoporosis. Front. Pharmacol. 2023;14:1203767. doi: 10.3389/fphar.2023.1203767</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Gu Z., Zhou G., Zhang X., Liang G., Xiao X., Dou Y. Research progress of plant medicine and Chinese herbal compounds in the treatment of rheumatoid arthritis combined with osteoporosis. Front. Med. (Lausanne). 2024;10:1288591. doi: 10.3389/fmed.2023.1288591</mixed-citation><mixed-citation xml:lang="en">Gu Z., Zhou G., Zhang X., Liang G., Xiao X., Dou Y. Research progress of plant medicine and Chinese herbal compounds in the treatment of rheumatoid arthritis combined with osteoporosis. Front. Med. (Lausanne). 2024;10:1288591. doi: 10.3389/fmed.2023.1288591</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou C., Shen S., Zhang M., Luo H., Zhang Y., Wu C., Zeng L., Ruan H. Mechanisms of action and synergetic formulas of plant-based natural compounds from traditional Chinese Medicine for managing osteoporosis: a literature review. Front. Med. (Lausanne). 2023;10:1235081. doi: 10.3389/fmed.2023.1235081</mixed-citation><mixed-citation xml:lang="en">Zhou C., Shen S., Zhang M., Luo H., Zhang Y., Wu C., Zeng L., Ruan H. Mechanisms of action and synergetic formulas of plant-based natural compounds from traditional Chinese Medicine for managing osteoporosis: a literature review. Front. Med. (Lausanne). 2023;10:1235081. doi: 10.3389/fmed.2023.1235081</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Cao G., Hu S.Q., Ning Y., Dou X., Ding C., Wang L., Wang Z., Sang X., Yang Q., Shi J., Hao M., Han X. Traditional Chinese medicine in osteoporosis: from pathogenesis to potential activity. Front. Pharmacol. 2024;15:1370900. doi: 10.3389/fphar.2024.1370900</mixed-citation><mixed-citation xml:lang="en">Cao G., Hu S.Q., Ning Y., Dou X., Ding C., Wang L., Wang Z., Sang X., Yang Q., Shi J., Hao M., Han X. Traditional Chinese medicine in osteoporosis: from pathogenesis to potential activity. Front. Pharmacol. 2024;15:1370900. doi: 10.3389/fphar.2024.1370900</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Зверев Я.Ф., Рыкунова А.Я. Фармакология флавоноидов. Барнаул, 2023. 178 c. – Zverev Ya.F., Rykunova A.Ya. Pharmacology of flavonoids. Barnaul, 2023. 178 p. [In Russian].</mixed-citation><mixed-citation xml:lang="en">Зверев Я.Ф., Рыкунова А.Я. Фармакология флавоноидов. Барнаул, 2023. 178 c. – Zverev Ya.F., Rykunova A.Ya. Pharmacology of flavonoids. Barnaul, 2023. 178 p. [In Russian].</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Ramesh P., Jagadeesan R., Sekaran S., Dhanasekaran A., Vimalraj S. Flavonoids: classification, function, and molecular mechanisms involved in bone remodeling. Front. Endocrinol. (Lausanne). 2021;12:779638. doi: 10.3389/fendo.2021.779638</mixed-citation><mixed-citation xml:lang="en">Ramesh P., Jagadeesan R., Sekaran S., Dhanasekaran A., Vimalraj S. Flavonoids: classification, function, and molecular mechanisms involved in bone remodeling. Front. Endocrinol. (Lausanne). 2021;12:779638. doi: 10.3389/fendo.2021.779638</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Bellavia D., Dimarco E., Costa V., Carina V., de Luca A., Raimondi L., Fini M., Gentile C., Caradonna F., Giavaresi G. Flavonoids in bone erosive diseases: perspectives in osteoporosis treatments. Trends Endocrinol. Metab. 2021;32(2):76–94. doi: 10.1016/j.tem.2020.11.007</mixed-citation><mixed-citation xml:lang="en">Bellavia D., Dimarco E., Costa V., Carina V., de Luca A., Raimondi L., Fini M., Gentile C., Caradonna F., Giavaresi G. Flavonoids in bone erosive diseases: perspectives in osteoporosis treatments. Trends Endocrinol. Metab. 2021;32(2):76–94. doi: 10.1016/j.tem.2020.11.007</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Sharma A.R., Lee Y.H., Bat-Ulzii A., Chatterjee S., Bhattacharya M., Chakraborty C., Lee S.S. Bioactivity, molecular mechanism, and targeted delivery of flavonoids for bone loss. Nutrients. 2023;15(4):919. doi: 10.3390/nu15040919</mixed-citation><mixed-citation xml:lang="en">Sharma A.R., Lee Y.H., Bat-Ulzii A., Chatterjee S., Bhattacharya M., Chakraborty C., Lee S.S. Bioactivity, molecular mechanism, and targeted delivery of flavonoids for bone loss. Nutrients. 2023;15(4):919. doi: 10.3390/nu15040919</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Guan F., Wang Q., Bao T., Chao Y. Anti-rheumatic effect of quercetin and recent developments in nano formulation. RSC Adv. 2021;11(13):7280–7293. doi: 10.1039/d0ra08817j</mixed-citation><mixed-citation xml:lang="en">Guan F., Wang Q., Bao T., Chao Y. Anti-rheumatic effect of quercetin and recent developments in nano formulation. RSC Adv. 2021;11(13):7280–7293. doi: 10.1039/d0ra08817j</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Tang M., Zeng Y., Peng W., Xie X., Yang Y., Ji B., Li F. Pharmacological aspects of natural quercetin in rheumatoid arthritis. Drug Des. Devel. Ther. 2022;16:2043–2053. doi: 10.2147/DDDT.S364759</mixed-citation><mixed-citation xml:lang="en">Tang M., Zeng Y., Peng W., Xie X., Yang Y., Ji B., Li F. Pharmacological aspects of natural quercetin in rheumatoid arthritis. Drug Des. Devel. Ther. 2022;16:2043–2053. doi: 10.2147/DDDT.S364759</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Loukas A.T., Papadourakis M., Panagiotopoulos V., Zarmpala A., Chontzopoulou E., Christodoulou S., Katsila T., Zoumpoulakis P., Matsoukas M.T. Natural compounds for bone remodeling: a computational and experimental approach targeting bone metabolism-related proteins. Int. J. Mol. Sci. 2024;25(9):5047. doi: 10.3390/ijms25095047</mixed-citation><mixed-citation xml:lang="en">Loukas A.T., Papadourakis M., Panagiotopoulos V., Zarmpala A., Chontzopoulou E., Christodoulou S., Katsila T., Zoumpoulakis P., Matsoukas M.T. Natural compounds for bone remodeling: a computational and experimental approach targeting bone metabolism-related proteins. Int. J. Mol. Sci. 2024;25(9):5047. doi: 10.3390/ijms25095047</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Wei Q., Ouyang M., GuoX., Fu X., Liu T., Luo Y., Tang H., Yang Y., Gao X., Mao H. Effect of hyperoside on osteoporosis in ovariectomized mice through estrogen receptor α/ITGβ3 signaling pathway. Eur. J. Pharmacol. 2024;977:176666. doi: 10.1016/j.ejphar.2024.176666</mixed-citation><mixed-citation xml:lang="en">Wei Q., Ouyang M., GuoX., Fu X., Liu T., Luo Y., Tang H., Yang Y., Gao X., Mao H. Effect of hyperoside on osteoporosis in ovariectomized mice through estrogen receptor α/ITGβ3 signaling pathway. Eur. J. Pharmacol. 2024;977:176666. doi: 10.1016/j.ejphar.2024.176666</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Pang X.G., Cong Y., Bao N.R., Li Y.G., Zhao J.N. Quercetin stimulates bone marrow mesenchymal stem cell differentiation through an estrogen receptor-mediated pathway. Bio. Med. Res. Int. 2018;2018:4178021. doi: 10.1155/2018/4178021</mixed-citation><mixed-citation xml:lang="en">Pang X.G., Cong Y., Bao N.R., Li Y.G., Zhao J.N. Quercetin stimulates bone marrow mesenchymal stem cell differentiation through an estrogen receptor-mediated pathway. Bio. Med. Res. Int. 2018;2018:4178021. doi: 10.1155/2018/4178021</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao J., Wu J., Xu B., Yuan Z., Leng Y., Min J., Lan X., Luo J. Kaempferol promotes bone formation in part via the mTOR signaling pathway. Mol. Med. Rep. 2019;20(6):5197–5207. doi: 10.3892/mmr.2019.10747</mixed-citation><mixed-citation xml:lang="en">Zhao J., Wu J., Xu B., Yuan Z., Leng Y., Min J., Lan X., Luo J. Kaempferol promotes bone formation in part via the mTOR signaling pathway. Mol. Med. Rep. 2019;20(6):5197–5207. doi: 10.3892/mmr.2019.10747</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Liu H., Yi X., Tu S., Cheng C., Luo J. Kaempferol promotes BMSC osteogenic differentiation and improves osteoporosis by downregulation miR-10a-3p and upregulating CXCL12. Mol. Cell. Endocrinol. 2021;520:111074. doi: 10.1016/j.mce.2020.111074</mixed-citation><mixed-citation xml:lang="en">Liu H., Yi X., Tu S., Cheng C., Luo J. Kaempferol promotes BMSC osteogenic differentiation and improves osteoporosis by downregulation miR-10a-3p and upregulating CXCL12. Mol. Cell. Endocrinol. 2021;520:111074. doi: 10.1016/j.mce.2020.111074</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Nowak B., Matuszewska A., Nikodem A., Filipiak J., Landwójtowicz M., Sadanowicz E., Jędrzejuk D., Rzeszutko M., Zduniak K., Piasecki T., … Szelag A. Oral administration of kaempferol inhibits bone loss in rat model of ovariectomy-induced osteopenia. Pharmacol. Rep. 2017;69(5):1113–1119. doi: 10.1016/j.pharep.2017.05.002</mixed-citation><mixed-citation xml:lang="en">Nowak B., Matuszewska A., Nikodem A., Filipiak J., Landwójtowicz M., Sadanowicz E., Jędrzejuk D., Rzeszutko M., Zduniak K., Piasecki T., … Szelag A. Oral administration of kaempferol inhibits bone loss in rat model of ovariectomy-induced osteopenia. Pharmacol. Rep. 2017;69(5):1113–1119. doi: 10.1016/j.pharep.2017.05.002</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Lee C.J., Moon S.J., Jeong J.H., Lee S., Lee M.H., Yoo S.M., Lee H.S., Kang H.C., Lee J.Y., Lee W.S., … Cho Y.Y. Kaempferol targeting on the fibroblast growth factor receptor 3-ribosomal S6 kinase 2 signaling axis prevents the development of rheumatoid arthritis. Cell. Death Dis. 2018;9(3):401. doi: 10.1038/s41419-018-0433-0</mixed-citation><mixed-citation xml:lang="en">Lee C.J., Moon S.J., Jeong J.H., Lee S., Lee M.H., Yoo S.M., Lee H.S., Kang H.C., Lee J.Y., Lee W.S., … Cho Y.Y. Kaempferol targeting on the fibroblast growth factor receptor 3-ribosomal S6 kinase 2 signaling axis prevents the development of rheumatoid arthritis. Cell. Death Dis. 2018;9(3):401. doi: 10.1038/s41419-018-0433-0</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang Z., Xu W., Zhang Z., Chen X., Jin H., Jiang N., Xu H. The bone-protective benefits of kaempferol combined with metformin by regulation of osteogenesis-angiogenesis coupling in OVX rats. Biomed. Pharmacother. 2024;173:116364. doi: 10.1016/j.biopha.2024.116364</mixed-citation><mixed-citation xml:lang="en">Zhang Z., Xu W., Zhang Z., Chen X., Jin H., Jiang N., Xu H. The bone-protective benefits of kaempferol combined with metformin by regulation of osteogenesis-angiogenesis coupling in OVX rats. Biomed. Pharmacother. 2024;173:116364. doi: 10.1016/j.biopha.2024.116364</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Kelepouri D., Mavropoulos A., Bogdanos D.P., Sakkas L.I. The role of flavonoids in inhibitory Th17 responses in inflammatory arthritis. J. Immunol. Res. 2018;2018:9324357. doi: 10.1155/2018/9324357</mixed-citation><mixed-citation xml:lang="en">Kelepouri D., Mavropoulos A., Bogdanos D.P., Sakkas L.I. The role of flavonoids in inhibitory Th17 responses in inflammatory arthritis. J. Immunol. Res. 2018;2018:9324357. doi: 10.1155/2018/9324357</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Huang Z., Cheng C., Cao B., Wang J., Wei H., Liu X., Han Y., Yang S., Wang X. Icariin protects against glucocorticoid-induced osteonecrosis of the femoral head of rats. Cell. Physiol. Biochem. 2018;47(2):694–706. doi: 10.1159/000490023</mixed-citation><mixed-citation xml:lang="en">Huang Z., Cheng C., Cao B., Wang J., Wei H., Liu X., Han Y., Yang S., Wang X. Icariin protects against glucocorticoid-induced osteonecrosis of the femoral head of rats. Cell. Physiol. Biochem. 2018;47(2):694–706. doi: 10.1159/000490023</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Xu H., Zhou S., Qu R., Yang Y., Gong Y., Hong Y., Jin A., Huang X., Dai Q., Jiang L. Icariin prevents oestrogen deficiency-induced alveolar bone loss through promoting osteogenesis via STAT3. Cell. Prolif. 2020;53(2):e12743. doi: 10.1111/cpr.12743</mixed-citation><mixed-citation xml:lang="en">Xu H., Zhou S., Qu R., Yang Y., Gong Y., Hong Y., Jin A., Huang X., Dai Q., Jiang L. Icariin prevents oestrogen deficiency-induced alveolar bone loss through promoting osteogenesis via STAT3. Cell. Prolif. 2020;53(2):e12743. doi: 10.1111/cpr.12743</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Xu Q., Chen G., Liu X., Dai M., Zhang B. Icariin inhibits RANKL-induced osteoclastogenesis via modulation of the NF-kappa B and MAPK signaling pathways. Biochem. Biophys. Res. Commun. 2019;508(3):902–906. doi: 10.1016/j.bbrc.2018.11.201</mixed-citation><mixed-citation xml:lang="en">Xu Q., Chen G., Liu X., Dai M., Zhang B. Icariin inhibits RANKL-induced osteoclastogenesis via modulation of the NF-kappa B and MAPK signaling pathways. Biochem. Biophys. Res. Commun. 2019;508(3):902–906. doi: 10.1016/j.bbrc.2018.11.201</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Chi L., Gao W., Shu X., Lu X. A natural flavonoid glucoside, icariin, regulates Th17 and alleviates rheumatoid arthritis in a murine model. Mediators Inflamm. 2014;2014:392062. doi: 10.1155/2014/392062</mixed-citation><mixed-citation xml:lang="en">Chi L., Gao W., Shu X., Lu X. A natural flavonoid glucoside, icariin, regulates Th17 and alleviates rheumatoid arthritis in a murine model. Mediators Inflamm. 2014;2014:392062. doi: 10.1155/2014/392062</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Sun P., Liu Y., Deng X., Yu C., Dai N., Yuan X., Chen L., Yu S., Si W., Wang X., … Pang H. An inhibitor of cathepsin K, icariin suppresses cartilage and bone degradation in mice of collagen-induced arthritis. Phytomedicine. 2013;20(11):975–979. doi: 10.1016/j.phymed.2013.04.019</mixed-citation><mixed-citation xml:lang="en">Sun P., Liu Y., Deng X., Yu C., Dai N., Yuan X., Chen L., Yu S., Si W., Wang X., … Pang H. An inhibitor of cathepsin K, icariin suppresses cartilage and bone degradation in mice of collagen-induced arthritis. Phytomedicine. 2013;20(11):975–979. doi: 10.1016/j.phymed.2013.04.019</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Xue L., Jiang Y., Han T., Zhang N., Qin L., Xin H., Zhang Q. Comparative proteomic and metabolomic analysis reveal the antiosteoporotic molecular mechanism of icariin from Epimedium brevicornu maxim. J. Ethnopharmacol. 2016;192:370–381. doi: 10.1016/j.jep.2016.07.037</mixed-citation><mixed-citation xml:lang="en">Xue L., Jiang Y., Han T., Zhang N., Qin L., Xin H., Zhang Q. Comparative proteomic and metabolomic analysis reveal the antiosteoporotic molecular mechanism of icariin from Epimedium brevicornu maxim. J. Ethnopharmacol. 2016;192:370–381. doi: 10.1016/j.jep.2016.07.037</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Hughes S.D., Ketheesan N., Haleagrahara N. The therapeutic potential of plant flavonoids on rheumatoid arthritis. Crit. Rev. Food Sci. Nutr. 2017;57(17):3601–3613. doi: 10.1080/10408398.2016.1246413</mixed-citation><mixed-citation xml:lang="en">Hughes S.D., Ketheesan N., Haleagrahara N. The therapeutic potential of plant flavonoids on rheumatoid arthritis. Crit. Rev. Food Sci. Nutr. 2017;57(17):3601–3613. doi: 10.1080/10408398.2016.1246413</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang X., Zhou C., Zha X., Xu Z., Li L., Liu Y., Xu L., Cui L., Xu D., Zhu B. Apigenin promotes osteogenic differentiation of human mesenchymal stem cells through JNK and P38 MAPK pathways. Mol. Cell. Biochem. 2015;407(1-2):41–50. doi: 10.1007/s11010-015-2452-9</mixed-citation><mixed-citation xml:lang="en">Zhang X., Zhou C., Zha X., Xu Z., Li L., Liu Y., Xu L., Cui L., Xu D., Zhu B. Apigenin promotes osteogenic differentiation of human mesenchymal stem cells through JNK and P38 MAPK pathways. Mol. Cell. Biochem. 2015;407(1-2):41–50. doi: 10.1007/s11010-015-2452-9</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Lorusso F., Scarano A., Fulle S., Valbonetti L., Mancinelli R., di Filippo E.S. Effectiveness of apigenin, resveratrol, and curcumin as adjuvant nutraceuticals for calvarial bone defect healing: an in vitro and histological study on rats. Nutrients. 2023;15(5):1235. doi: 10.3390/nu15051235</mixed-citation><mixed-citation xml:lang="en">Lorusso F., Scarano A., Fulle S., Valbonetti L., Mancinelli R., di Filippo E.S. Effectiveness of apigenin, resveratrol, and curcumin as adjuvant nutraceuticals for calvarial bone defect healing: an in vitro and histological study on rats. Nutrients. 2023;15(5):1235. doi: 10.3390/nu15051235</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Ali D., Okla M., Abuelreich S., Vishnabalaji R., Ditzel N., Hamam R., Kowal J.M., Sayed A., Aldahmash A., Alajez N.M., Kassem M. Apigenin and rutaecarpine reduce the burden of cellular senescence in bone morrow stromal stem cells. Front. Endocrinol. (Lausanne). 2024;15:1360054. doi: 10.3389/fendo.2024.1360054</mixed-citation><mixed-citation xml:lang="en">Ali D., Okla M., Abuelreich S., Vishnabalaji R., Ditzel N., Hamam R., Kowal J.M., Sayed A., Aldahmash A., Alajez N.M., Kassem M. Apigenin and rutaecarpine reduce the burden of cellular senescence in bone morrow stromal stem cells. Front. Endocrinol. (Lausanne). 2024;15:1360054. doi: 10.3389/fendo.2024.1360054</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">d’Amico E., Pierfelice T.V., Iezzi G., di Pietro N., Lepore S., Lorusso F., Scarano A., Pandolfi A., Piattelli A., Petrini M. Apigenin promotes proliferation and mineralization human osteoblasts and up-regulates osteogenic markers. Appl. Sci. 2022;12:8510. doi: 10.3390/app12178510</mixed-citation><mixed-citation xml:lang="en">d’Amico E., Pierfelice T.V., Iezzi G., di Pietro N., Lepore S., Lorusso F., Scarano A., Pandolfi A., Piattelli A., Petrini M. Apigenin promotes proliferation and mineralization human osteoblasts and up-regulates osteogenic markers. Appl. Sci. 2022;12:8510. doi: 10.3390/app12178510</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Asadi A., Goudarzi F., Ghanadian M., Mohammadalipour A. Evaluation of the osteogenic effect of apigenin on human mesenchymal stem cells by inhibiting inflammation through modulation of NF-κB/IκBα. Res. Pharm. Sci. 2022;17(6):697–706. doi: 10.4103/1735-5362.359436</mixed-citation><mixed-citation xml:lang="en">Asadi A., Goudarzi F., Ghanadian M., Mohammadalipour A. Evaluation of the osteogenic effect of apigenin on human mesenchymal stem cells by inhibiting inflammation through modulation of NF-κB/IκBα. Res. Pharm. Sci. 2022;17(6):697–706. doi: 10.4103/1735-5362.359436</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Jung W.W. Protective effect of apigenin against oxidative stress-induced damage in osteoblastic cells. Int. J. Mol. Med. 2014;33(5):1327–1334. doi: 10.3892/ijmm.2014.1666</mixed-citation><mixed-citation xml:lang="en">Jung W.W. Protective effect of apigenin against oxidative stress-induced damage in osteoblastic cells. Int. J. Mol. Med. 2014;33(5):1327–1334. doi: 10.3892/ijmm.2014.1666</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Bandyopadhyay S., Lion J.M., Mentaverri R., Ricupero D.A., Kamel S., Romero J., Chattopadhyay N. Attenuation of osteoclastogenesis and osteoclast function by apigenin. Biochem. Pharmacol. 2006;72(2):184–197. doi: 10.1016/j.bcp.2006.04.018</mixed-citation><mixed-citation xml:lang="en">Bandyopadhyay S., Lion J.M., Mentaverri R., Ricupero D.A., Kamel S., Romero J., Chattopadhyay N. Attenuation of osteoclastogenesis and osteoclast function by apigenin. Biochem. Pharmacol. 2006;72(2):184–197. doi: 10.1016/j.bcp.2006.04.018</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Li Y., Yang B., Bai Y.U., Xia S., Mao M., Li X., Li N., Chen L. The roles of synovial hyperplasia, angiogenesis and osteoclastogenesis in the protective effect of apigenin in collagen-induced arthritis. Int. Immunopharmacol. 2019;73:362–369. doi: 10.1016/j.intimp.2019.05.024</mixed-citation><mixed-citation xml:lang="en">Li Y., Yang B., Bai Y.U., Xia S., Mao M., Li X., Li N., Chen L. The roles of synovial hyperplasia, angiogenesis and osteoclastogenesis in the protective effect of apigenin in collagen-induced arthritis. Int. Immunopharmacol. 2019;73:362–369. doi: 10.1016/j.intimp.2019.05.024</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Goto T., Hagiwara K., Shirai N., Yoshida K., Hagiwara H. Apigenin inhibits osteoblastogenesis and osteoclastogenesis and prevents bone loss in ovariectomized mice. Cytotechnology. 2015;67(2):357–362. doi: 10.1007/s10616-014-9694-3</mixed-citation><mixed-citation xml:lang="en">Goto T., Hagiwara K., Shirai N., Yoshida K., Hagiwara H. Apigenin inhibits osteoblastogenesis and osteoclastogenesis and prevents bone loss in ovariectomized mice. Cytotechnology. 2015;67(2):357–362. doi: 10.1007/s10616-014-9694-3</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Choi E.M. Luteolin protects osteoblastic MC3T3-E1 cells from antimycin A-induced cytototoxicity through the improved mitochondrial function and activation of PI3K/Akt/CREB. Toxicol. In Vitro. 2011;25(8):1671–1679. doi: 10.1016/j.tiv.2011.07.004</mixed-citation><mixed-citation xml:lang="en">Choi E.M. Luteolin protects osteoblastic MC3T3-E1 cells from antimycin A-induced cytototoxicity through the improved mitochondrial function and activation of PI3K/Akt/CREB. Toxicol. In Vitro. 2011;25(8):1671–1679. doi: 10.1016/j.tiv.2011.07.004</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Zheng L. Luteolin stimulates proliferation and inhibits late differentiation of primary rat calvarial osteoblast induced by high-dose dexamethasone via Sema3A/NRP1/Plexin A1. Curr. Pharm. Biotechnol. 2021;22(11):1538–1545. doi: 10.2174/1389201021666201216150442</mixed-citation><mixed-citation xml:lang="en">Zheng L. Luteolin stimulates proliferation and inhibits late differentiation of primary rat calvarial osteoblast induced by high-dose dexamethasone via Sema3A/NRP1/Plexin A1. Curr. Pharm. Biotechnol. 2021;22(11):1538–1545. doi: 10.2174/1389201021666201216150442</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Jing Z., Wang C., Yang Q., Wei X., Jin Y., Meng Q., Liu Q., Liu Z., Ma X., Liu K., Sun H., Liu M. Luteolin attenuates glucocorticoid-induced osteoporosis by regulating ERK/Lrp-5/GSK-3β signaling pathway in vivo and in vitro. J. Cell. Physiol. 2019;234(4):4472–4490. doi: 10.1002/jcp.27252</mixed-citation><mixed-citation xml:lang="en">Jing Z., Wang C., Yang Q., Wei X., Jin Y., Meng Q., Liu Q., Liu Z., Ma X., Liu K., Sun H., Liu M. Luteolin attenuates glucocorticoid-induced osteoporosis by regulating ERK/Lrp-5/GSK-3β signaling pathway in vivo and in vitro. J. Cell. Physiol. 2019;234(4):4472–4490. doi: 10.1002/jcp.27252</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Lee J.W., Ahn J.Y., Hasegawa S.I., Cha B.Y., Yonezawa T., Nagai K., Seo H.J., Jeon W.B., Wao J.T. Inhibitory effect of luteolin on osteoclast differentiation and function. Cytotechnology. 2009;61(3):125–134. doi: 10.1007/s10616-010-9253-5</mixed-citation><mixed-citation xml:lang="en">Lee J.W., Ahn J.Y., Hasegawa S.I., Cha B.Y., Yonezawa T., Nagai K., Seo H.J., Jeon W.B., Wao J.T. Inhibitory effect of luteolin on osteoclast differentiation and function. Cytotechnology. 2009;61(3):125–134. doi: 10.1007/s10616-010-9253-5</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Chai S., Yang Y., Wei L., Cao Y., Ma J., Zheng X., Teng J., Qin N. Luteolin rescues postmenopausal osteoporosis elicited by OVX through alleviating osteoblast pyroptosis via activating PI3K-AKT signaling. Phytomedicine. 2024;128:155516. doi: 10.1016/j.phymed.2024.155516</mixed-citation><mixed-citation xml:lang="en">Chai S., Yang Y., Wei L., Cao Y., Ma J., Zheng X., Teng J., Qin N. Luteolin rescues postmenopausal osteoporosis elicited by OVX through alleviating osteoblast pyroptosis via activating PI3K-AKT signaling. Phytomedicine. 2024;128:155516. doi: 10.1016/j.phymed.2024.155516</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Song F., Wei C., Zhou L., Qin A., Yang M., Tickner J., Huang Y., Zhao J., Xu J. Luteoloside prevents lipopolysaccharide-induced osteolysis and suppresses RANKL-induced osteoclastogenesis through attenuating RANKL signaling cascades. J. Cell. Physiol. 2018;233(2):1723–1735. doi: 10.1002/jcp.26084</mixed-citation><mixed-citation xml:lang="en">Song F., Wei C., Zhou L., Qin A., Yang M., Tickner J., Huang Y., Zhao J., Xu J. Luteoloside prevents lipopolysaccharide-induced osteolysis and suppresses RANKL-induced osteoclastogenesis through attenuating RANKL signaling cascades. J. Cell. Physiol. 2018;233(2):1723–1735. doi: 10.1002/jcp.26084</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Kim J.M., Lee S.U., Kim Y.S., Min Y.K., Kim S.H. Baicalein stimulates osteoblast differentiation via coordinating activation MAP kinases and transcription factors. J. Cell. Biochem. 2008;104(5):1906–1917. doi: 10.1002/jcb.21760</mixed-citation><mixed-citation xml:lang="en">Kim J.M., Lee S.U., Kim Y.S., Min Y.K., Kim S.H. Baicalein stimulates osteoblast differentiation via coordinating activation MAP kinases and transcription factors. J. Cell. Biochem. 2008;104(5):1906–1917. doi: 10.1002/jcb.21760</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Li S., Tang J., Chen J., Zhang P., Wang T., Chen T., Yan B., Huang B., Wang L., Huang M., Zhang Z., Jin D. Regulation of bone formation by baicalein via the mTORC1 pathway. Drug Des. Des. Devel. Ther. 2015;9:5169–5183. doi: 10.2147/DDDT.S81578</mixed-citation><mixed-citation xml:lang="en">Li S., Tang J., Chen J., Zhang P., Wang T., Chen T., Yan B., Huang B., Wang L., Huang M., Zhang Z., Jin D. Regulation of bone formation by baicalein via the mTORC1 pathway. Drug Des. Des. Devel. Ther. 2015;9:5169–5183. doi: 10.2147/DDDT.S81578</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Wang Q., Shi D., Geng Y., Huang Q., Xiang L. Baicalin augments the differentiation of osteoblasts via enhancement of microRNA-217. Mol. Cell. Biochem. 2020;463(1-2):91–100. doi: 10.1007/s11010-019-03632-6</mixed-citation><mixed-citation xml:lang="en">Wang Q., Shi D., Geng Y., Huang Q., Xiang L. Baicalin augments the differentiation of osteoblasts via enhancement of microRNA-217. Mol. Cell. Biochem. 2020;463(1-2):91–100. doi: 10.1007/s11010-019-03632-6</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Kim M.H., Ryu S.Y., Bae M.A., Choi J.S., Min Y.K., Kim S.H. Baicalein inhibits osteoclast differentiation and induces mature osteoclast apoptosis. Food Chem. Toxicol. 2008;46(11):3375–3382. doi: 10.1016/j.fct.2008.08.016</mixed-citation><mixed-citation xml:lang="en">Kim M.H., Ryu S.Y., Bae M.A., Choi J.S., Min Y.K., Kim S.H. Baicalein inhibits osteoclast differentiation and induces mature osteoclast apoptosis. Food Chem. Toxicol. 2008;46(11):3375–3382. doi: 10.1016/j.fct.2008.08.016</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Cai P., Lu Y., Yin Z., Wang X., Zhou X., Li Z. Baicalein ameliorates osteoporosis via AKT/FOXO1 signaling. Aging (Albany NY). 2021;13(13):17370–17379. doi: 10.18632/aging.203227</mixed-citation><mixed-citation xml:lang="en">Cai P., Lu Y., Yin Z., Wang X., Zhou X., Li Z. Baicalein ameliorates osteoporosis via AKT/FOXO1 signaling. Aging (Albany NY). 2021;13(13):17370–17379. doi: 10.18632/aging.203227</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Saul D., Weber M., Zimmermann M.H., Kosinsky R.L., Hoffman D.B., Menger B., Taudien S., Lehmann W., Komrakova M., Sehmisch S. Effect of the lioxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats. Nutr. Metab. (Lond). 2019;16:4. doi: 10.1186/s12986-018-0327-2</mixed-citation><mixed-citation xml:lang="en">Saul D., Weber M., Zimmermann M.H., Kosinsky R.L., Hoffman D.B., Menger B., Taudien S., Lehmann W., Komrakova M., Sehmisch S. Effect of the lioxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats. Nutr. Metab. (Lond). 2019;16:4. doi: 10.1186/s12986-018-0327-2</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Li Y., Wang X. Chrysin attenuates high glucose-induced BMSc dysfunction via the activation of the PI3K/AKT/Nrf2 signaling pathway. Drug Des. Devel. Ther. 2022;16:165–182. doi: 10.2147/DDDT.S335024</mixed-citation><mixed-citation xml:lang="en">Li Y., Wang X. Chrysin attenuates high glucose-induced BMSc dysfunction via the activation of the PI3K/AKT/Nrf2 signaling pathway. Drug Des. Devel. Ther. 2022;16:165–182. doi: 10.2147/DDDT.S335024</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Oršolić N., Nemrava J., Jeleč Ž., Kukolj M., Odeh D., Jakopović B., Jembrek M.J., Bagatin T., Fureš R., Bagatin D. Antioxidative and anti-inflammatory activities of chrysin and naringenin in a drug-induced bone loss model in rats. Int. J. Mol. Sci. 2022;23(5):2872. doi: 10.3390/ijms23052872</mixed-citation><mixed-citation xml:lang="en">Oršolić N., Nemrava J., Jeleč Ž., Kukolj M., Odeh D., Jakopović B., Jembrek M.J., Bagatin T., Fureš R., Bagatin D. Antioxidative and anti-inflammatory activities of chrysin and naringenin in a drug-induced bone loss model in rats. Int. J. Mol. Sci. 2022;23(5):2872. doi: 10.3390/ijms23052872</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Wu Z., Li C., Chen Y., Liu Q., Li N., He X., Li W., Shen R., Li L., Wei C., … Xu F. Chrysin protects against titanium particle-induced osteolysis by attenuating osteoclast formation and function by inhibiting NF-κB and MAPK signaling. Front. Pharmacol. 2022;13:793087. doi: 10.3389/fphar.2022.793087</mixed-citation><mixed-citation xml:lang="en">Wu Z., Li C., Chen Y., Liu Q., Li N., He X., Li W., Shen R., Li L., Wei C., … Xu F. Chrysin protects against titanium particle-induced osteolysis by attenuating osteoclast formation and function by inhibiting NF-κB and MAPK signaling. Front. Pharmacol. 2022;13:793087. doi: 10.3389/fphar.2022.793087</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Ortiz A.C., Fideles S.O.M., Reis C.H.B., Bellini M.Z., Pereira E.S.B.M., Pilon J.P.G., de Marchi M.A., Detregiachi C.R.P., Flato U.A.P., de Moraes Triazzi B.F., … Buchaim R.L. Therapeutic effects of citrus flavonoids neohesperidin, hesperidin and its aglycone, hesperetin on bone health. Biomolecules. 2022;12(5):626. doi: 10.3390/biom12050626</mixed-citation><mixed-citation xml:lang="en">Ortiz A.C., Fideles S.O.M., Reis C.H.B., Bellini M.Z., Pereira E.S.B.M., Pilon J.P.G., de Marchi M.A., Detregiachi C.R.P., Flato U.A.P., de Moraes Triazzi B.F., … Buchaim R.L. Therapeutic effects of citrus flavonoids neohesperidin, hesperidin and its aglycone, hesperetin on bone health. Biomolecules. 2022;12(5):626. doi: 10.3390/biom12050626</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Hong W., Zhang W. Hesperidin promotes differentiation of alveolar osteoblasts via Wnt/β-catenin signaling pathway. J. Recept. Signal. Transduct. Res. 2020;40(5):442–448. doi: 10.1080/10799893.2020.1752718</mixed-citation><mixed-citation xml:lang="en">Hong W., Zhang W. Hesperidin promotes differentiation of alveolar osteoblasts via Wnt/β-catenin signaling pathway. J. Recept. Signal. Transduct. Res. 2020;40(5):442–448. doi: 10.1080/10799893.2020.1752718</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Miguez P.A., Tuin S.A., Robinson A.G., Belcher J., Longwattanapisan P., Perley K., de Paiva Gonçalves, Hanifi A., Pleshko N., Barton E.R. Hesperidin promotes osteogenesis and modulates collagen matrix organization and mineralization in vitro and in vivo. Int. J. Mol. Sci. 2021;22(6):3223. doi: 10.3390/ijms22063223</mixed-citation><mixed-citation xml:lang="en">Miguez P.A., Tuin S.A., Robinson A.G., Belcher J., Longwattanapisan P., Perley K., de Paiva Gonçalves, Hanifi A., Pleshko N., Barton E.R. Hesperidin promotes osteogenesis and modulates collagen matrix organization and mineralization in vitro and in vivo. Int. J. Mol. Sci. 2021;22(6):3223. doi: 10.3390/ijms22063223</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Liu L., Zheng J., Yang Y.Z., Ni L., Chen H., Yu D. Hesperetin alleviated glucocorticoid-induced inhibition of osteogenic differentiation of BMSCs through regulating the ERK signaling pathway. Med. Mol. Morphol. 2021;54(1):1–7. doi: 10.1007/s00795-020-00251-9</mixed-citation><mixed-citation xml:lang="en">Liu L., Zheng J., Yang Y.Z., Ni L., Chen H., Yu D. Hesperetin alleviated glucocorticoid-induced inhibition of osteogenic differentiation of BMSCs through regulating the ERK signaling pathway. Med. Mol. Morphol. 2021;54(1):1–7. doi: 10.1007/s00795-020-00251-9</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Hu H.Y., Zhang Z.Z., Jiang X.Y., Duan T.H., Feng W., Wang X.G. Hesperidin anti-osteoporosis by regulating estrogen signaling pathways. Molecules. 2023;28(19):6987. doi: 10.3390/molecules28196987</mixed-citation><mixed-citation xml:lang="en">Hu H.Y., Zhang Z.Z., Jiang X.Y., Duan T.H., Feng W., Wang X.G. Hesperidin anti-osteoporosis by regulating estrogen signaling pathways. Molecules. 2023;28(19):6987. doi: 10.3390/molecules28196987</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang M., Chen D., Zeng N., Liu Z., Chen X., Xiao H., Xiao L., Liu Z., Dong Y., Zheng J. Hesperidin ameliorates dexamethasone-induced osteoporosis by inhibiting p53. Front. Cell. Dev. Biol. 2022;10:820922. doi: 10.3389/fcell.2022.820922</mixed-citation><mixed-citation xml:lang="en">Zhang M., Chen D., Zeng N., Liu Z., Chen X., Xiao H., Xiao L., Liu Z., Dong Y., Zheng J. Hesperidin ameliorates dexamethasone-induced osteoporosis by inhibiting p53. Front. Cell. Dev. Biol. 2022;10:820922. doi: 10.3389/fcell.2022.820922</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Uehara M. Prevention of osteoporosis by foods and dietary supplements. Hesperidin and bone metabolism. Clin. Calcium. 2006;16(10):1669–1676.</mixed-citation><mixed-citation xml:lang="en">Uehara M. Prevention of osteoporosis by foods and dietary supplements. Hesperidin and bone metabolism. Clin. Calcium. 2006;16(10):1669–1676.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Shehata A.S., Amer M.G., Abd El-Haleem M.R., Karam R.A. The ability of hesperidin compared to that of insulin for preventing osteoporosis induced by type I diabetes in young male albino rats: a histological and biochemical study. Exp. Toxicol. Pathol. 2017;69(4):203–212. doi: 10.1016/j.etp.2017.01.008</mixed-citation><mixed-citation xml:lang="en">Shehata A.S., Amer M.G., Abd El-Haleem M.R., Karam R.A. The ability of hesperidin compared to that of insulin for preventing osteoporosis induced by type I diabetes in young male albino rats: a histological and biochemical study. Exp. Toxicol. Pathol. 2017;69(4):203–212. doi: 10.1016/j.etp.2017.01.008</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Aihaiti Y., Cai Y.S., Tuerhong X., Yang Y.N., Ma Y., Zheng H.S., Xu K., Xu P. Therapeutic effects of naringin in rheumatoid asthritis: network pharmacology and experimental validation. Front. Pharmacol. 2021;12:672054. doi: 10.3389/fphar.2021.672054</mixed-citation><mixed-citation xml:lang="en">Aihaiti Y., Cai Y.S., Tuerhong X., Yang Y.N., Ma Y., Zheng H.S., Xu K., Xu P. Therapeutic effects of naringin in rheumatoid asthritis: network pharmacology and experimental validation. Front. Pharmacol. 2021;12:672054. doi: 10.3389/fphar.2021.672054</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Yu X., Zhang P., Tang K., Shen H., Chen H., Zhang Z., Zhao W., Shang Q., Zhu G., Tan R., … Zhou B. Network pharmacology integrated with molecular docking explores the mechanisms of naringin against osteoporotic fracture by regulating oxidative stress. Evid. Based Complement. Alternat. Med. 2021;2021:6421122. doi: 10.1155/2021/6421122</mixed-citation><mixed-citation xml:lang="en">Yu X., Zhang P., Tang K., Shen H., Chen H., Zhang Z., Zhao W., Shang Q., Zhu G., Tan R., … Zhou B. Network pharmacology integrated with molecular docking explores the mechanisms of naringin against osteoporotic fracture by regulating oxidative stress. Evid. Based Complement. Alternat. Med. 2021;2021:6421122. doi: 10.1155/2021/6421122</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Nor Muhamad M.L., Ekeuku S.O., Wong S.K., Chin K.Y. A scoping review of the skeletal effects of naringenin. Nutrients. 2022;14(22):4851. doi: 10.3390/nu14224851</mixed-citation><mixed-citation xml:lang="en">Nor Muhamad M.L., Ekeuku S.O., Wong S.K., Chin K.Y. A scoping review of the skeletal effects of naringenin. Nutrients. 2022;14(22):4851. doi: 10.3390/nu14224851</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Gan J., Deng X., Le Y., Lai J., Liao A. The development of naringin for use against bone and cartilage disorders. Molecules. 2023;28(9):3716. doi: 10.3390/molecules28093716</mixed-citation><mixed-citation xml:lang="en">Gan J., Deng X., Le Y., Lai J., Liao A. The development of naringin for use against bone and cartilage disorders. Molecules. 2023;28(9):3716. doi: 10.3390/molecules28093716</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Ang E.S.M., Yang X., Chen H., Liu Q., Zheng M.H., Xu J. Naringin abrogates osteoclastogenesis and bone resorption via the inhibition of RANKL-induced NF-κB and ERK activation. FEBS Lett. 2011;585(17):2755–2762. doi: 10.1016/j.febslet.2011.07.046</mixed-citation><mixed-citation xml:lang="en">Ang E.S.M., Yang X., Chen H., Liu Q., Zheng M.H., Xu J. Naringin abrogates osteoclastogenesis and bone resorption via the inhibition of RANKL-induced NF-κB and ERK activation. FEBS Lett. 2011;585(17):2755–2762. doi: 10.1016/j.febslet.2011.07.046</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Wang W., Li M., Luo M., Shen M., Xu C., Xu G., Chen Y., Xia L. Naringenin inhibits osteoclastogenesis through modulation of helper T cells-secreted IL-4. J. Cell. Biochem. 2018;119(2):2084–2093. doi: 10.1002/jcb.26370</mixed-citation><mixed-citation xml:lang="en">Wang W., Li M., Luo M., Shen M., Xu C., Xu G., Chen Y., Xia L. Naringenin inhibits osteoclastogenesis through modulation of helper T cells-secreted IL-4. J. Cell. Biochem. 2018;119(2):2084–2093. doi: 10.1002/jcb.26370</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Wang W., Wu C., Tian B., Liu X., Zhai Z., Qu X., Jiang C., Ouyang Z., Mao Y., Tang T., Qin A., Zhu Z. The inhibition of RANKL-induced osteoclastogenesis through the suppression of p38 signaling pathway by naringenin and attenuation of titanium-particle-induced osteolysis. Int. J. Mol. Sci. 2014;15(12):21913–21934. doi: 10.3390/ijms151221913</mixed-citation><mixed-citation xml:lang="en">Wang W., Wu C., Tian B., Liu X., Zhai Z., Qu X., Jiang C., Ouyang Z., Mao Y., Tang T., Qin A., Zhu Z. The inhibition of RANKL-induced osteoclastogenesis through the suppression of p38 signaling pathway by naringenin and attenuation of titanium-particle-induced osteolysis. Int. J. Mol. Sci. 2014;15(12):21913–21934. doi: 10.3390/ijms151221913</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Oršolić N., Goluža E., Dikić D., Lisičić D., Sašilo K., Rođ E., Jeleć Ž., Lazarus M.V., Orct T. Role of flavonoids on oxidative stress and mineral contents in the retinoic acid-induced bone loss model of rat. Eur. J. Nutr. 2014;53(5):1217–1227. doi: 10.1007/s00394-013-0622-7</mixed-citation><mixed-citation xml:lang="en">Oršolić N., Goluža E., Dikić D., Lisičić D., Sašilo K., Rođ E., Jeleć Ž., Lazarus M.V., Orct T. Role of flavonoids on oxidative stress and mineral contents in the retinoic acid-induced bone loss model of rat. Eur. J. Nutr. 2014;53(5):1217–1227. doi: 10.1007/s00394-013-0622-7</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Bussmann A.J.C., Borghi S.M., Zaninelli T.H., Dos Santos T.S., Guazelli C.F.S., Fattori V., Domiciano T.P., Pinho-Ribeiro F.A., Ruiz-Miyazawa K.W., Casella A.M.B., … Verri W.A. The citrus flavanone naringenin attenuates zymosan-induced mouse joint inflammation: induction of Nrf2 expression in recruited CD45 hematopoietic cells. Inflammopharmacology. 2019;27(6):1229–1242. doi: 10.1007/s10787-018-00561-6</mixed-citation><mixed-citation xml:lang="en">Bussmann A.J.C., Borghi S.M., Zaninelli T.H., Dos Santos T.S., Guazelli C.F.S., Fattori V., Domiciano T.P., Pinho-Ribeiro F.A., Ruiz-Miyazawa K.W., Casella A.M.B., … Verri W.A. The citrus flavanone naringenin attenuates zymosan-induced mouse joint inflammation: induction of Nrf2 expression in recruited CD45 hematopoietic cells. Inflammopharmacology. 2019;27(6):1229–1242. doi: 10.1007/s10787-018-00561-6</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Jagetia G.C., Venkatesha V.A., Reddy T.K. Naringin, a citrus flavonone, protects against radiation-induced chromosome damage in mouse bone marrow. Mutagenesis. 2003;18(4):337–343. doi: 10.1093/mutage/geg001</mixed-citation><mixed-citation xml:lang="en">Jagetia G.C., Venkatesha V.A., Reddy T.K. Naringin, a citrus flavonone, protects against radiation-induced chromosome damage in mouse bone marrow. Mutagenesis. 2003;18(4):337–343. doi: 10.1093/mutage/geg001</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Swarnkar G., Sharan K., Siddiqui J.A., Mishra J.S., Khan K., Gupta V., Rawat R., Maurya R., Dwivedi A.K., Sanyal S., Chattopadhyay N. A naturally occurring derivative exerts potent bone anabolic effects by mimicking oestrogen action on osteoblasts. Br. J. Pharmacol. 2012;165(5):1526–1542. doi: 10.1111/j.1476-5381.2011.01637.x</mixed-citation><mixed-citation xml:lang="en">Swarnkar G., Sharan K., Siddiqui J.A., Mishra J.S., Khan K., Gupta V., Rawat R., Maurya R., Dwivedi A.K., Sanyal S., Chattopadhyay N. A naturally occurring derivative exerts potent bone anabolic effects by mimicking oestrogen action on osteoblasts. Br. J. Pharmacol. 2012;165(5):1526–1542. doi: 10.1111/j.1476-5381.2011.01637.x</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Xie X., Fu J., Gou W., Qin Y., Wang D., Huang Z., Wang L., Li X. Potential mechanism of tea for treating osteoporosis, osteoarthritis, and rheumatoid arthritis. Front. Med. (Lausanne). 2024;11:1289777. doi: 10.3389/fmed.2024.1289777</mixed-citation><mixed-citation xml:lang="en">Xie X., Fu J., Gou W., Qin Y., Wang D., Huang Z., Wang L., Li X. Potential mechanism of tea for treating osteoporosis, osteoarthritis, and rheumatoid arthritis. Front. Med. (Lausanne). 2024;11:1289777. doi: 10.3389/fmed.2024.1289777</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Kaida K., Honda Y., Hashimoto Y., Tanaka M., Baba S. Application of green tea catechin for inducing the osteogenic differentiation of human differentiated fat cells in vitro. Int. J. Mol. Sci. 2015;16(12):27988–28000. doi: 10.3390/ijms161226081</mixed-citation><mixed-citation xml:lang="en">Kaida K., Honda Y., Hashimoto Y., Tanaka M., Baba S. Application of green tea catechin for inducing the osteogenic differentiation of human differentiated fat cells in vitro. Int. J. Mol. Sci. 2015;16(12):27988–28000. doi: 10.3390/ijms161226081</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Sakai G., Otsuka T., Fujita K., Kainuma S., Kuroyanagi G., Kawabata T., Matsushima-Nishiwaki R., Kozawa O., Tokuda H. Amplification by (-)-epigallocatechin gallate of prostaglandin F2α-stimulated synthesis of osteoprotegerin in osteoblasts. Mol. Med. Rep. 2017;16(5):6376–6381. doi: 10.3892/mmr.2017.7354</mixed-citation><mixed-citation xml:lang="en">Sakai G., Otsuka T., Fujita K., Kainuma S., Kuroyanagi G., Kawabata T., Matsushima-Nishiwaki R., Kozawa O., Tokuda H. Amplification by (-)-epigallocatechin gallate of prostaglandin F2α-stimulated synthesis of osteoprotegerin in osteoblasts. Mol. Med. Rep. 2017;16(5):6376–6381. doi: 10.3892/mmr.2017.7354</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Wong K.C., Cao S., Dong X., Law M.C., Chan T.H., Wong M.S. (-)-Epiafzelechin protects against ovariectomy-induced bone loss in adult mice and modulate osteoblastic and osteoclastic functions in vitro. Nutrients. 2017;9(5):530. doi: 10.3390/nu9050530</mixed-citation><mixed-citation xml:lang="en">Wong K.C., Cao S., Dong X., Law M.C., Chan T.H., Wong M.S. (-)-Epiafzelechin protects against ovariectomy-induced bone loss in adult mice and modulate osteoblastic and osteoclastic functions in vitro. Nutrients. 2017;9(5):530. doi: 10.3390/nu9050530</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Morinobu A., Biao W., Tanaka S., Horiuchi M., Jun L., Tsuji G., Sakai Y., Kurosaka M., Kumagai S. (-)-Epigallocatechin-3-gallate suppresses osteoclast differentiation and ameliorates experimental arthritis in mice. Arthritis Rheum. 2008;58(7):2012–2018. doi: 10.1002/art.23594</mixed-citation><mixed-citation xml:lang="en">Morinobu A., Biao W., Tanaka S., Horiuchi M., Jun L., Tsuji G., Sakai Y., Kurosaka M., Kumagai S. (-)-Epigallocatechin-3-gallate suppresses osteoclast differentiation and ameliorates experimental arthritis in mice. Arthritis Rheum. 2008;58(7):2012–2018. doi: 10.1002/art.23594</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Park K.H., Gu D.R., So H.S., Kim K.J., Lee S.H. Dual role of cyanide-3-glycoside on the differentiation of bone cells. J. Dent. Res. 2015;94(12):1676–1683. doi: 10.1177/0022034515604620</mixed-citation><mixed-citation xml:lang="en">Park K.H., Gu D.R., So H.S., Kim K.J., Lee S.H. Dual role of cyanide-3-glycoside on the differentiation of bone cells. J. Dent. Res. 2015;94(12):1676–1683. doi: 10.1177/0022034515604620</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Saulite L., Jekabsons K., Klavins M., Muceniece R., Riekstina U. Effects of malvidin, cyaniding and delphinidin on human adipose mesenchymal stem cell differentiation into adipocytes, chondrocytes and osteocytes. Phytomedicine. 2019;53:86–95. doi: 10.1016/j.phymed.2018.09.029</mixed-citation><mixed-citation xml:lang="en">Saulite L., Jekabsons K., Klavins M., Muceniece R., Riekstina U. Effects of malvidin, cyaniding and delphinidin on human adipose mesenchymal stem cell differentiation into adipocytes, chondrocytes and osteocytes. Phytomedicine. 2019;53:86–95. doi: 10.1016/j.phymed.2018.09.029</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Moriwaki S., Suzuki K., Muramatsu M., Nomura A., Inoue F., Into T., Yoshiko Y., Niida S. Delphinidin, one of the major anthocyanidins, prevents bone loss through the inhibition of excessive osteoclastogenesis in osteoposis model mice. PLoS One. 2014;9(5):e97177. doi: 10.1371/journal.pone.0097177</mixed-citation><mixed-citation xml:lang="en">Moriwaki S., Suzuki K., Muramatsu M., Nomura A., Inoue F., Into T., Yoshiko Y., Niida S. Delphinidin, one of the major anthocyanidins, prevents bone loss through the inhibition of excessive osteoclastogenesis in osteoposis model mice. PLoS One. 2014;9(5):e97177. doi: 10.1371/journal.pone.0097177</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Nagaoka M., Maeda T., Moriwaki S., Nomura A., Kato Y., Niida S., Kruger M.C., Suzuki K. Petunidin, a B-ring 5’-O-methylated derivative of delphinidin, stimulates osteoblastogenesis and reduces sRANKL-induced bone loss. Int. J. Mol. Sci. 2019;20(11):2795. doi: 10.3390/ijms20112795</mixed-citation><mixed-citation xml:lang="en">Nagaoka M., Maeda T., Moriwaki S., Nomura A., Kato Y., Niida S., Kruger M.C., Suzuki K. Petunidin, a B-ring 5’-O-methylated derivative of delphinidin, stimulates osteoblastogenesis and reduces sRANKL-induced bone loss. Int. J. Mol. Sci. 2019;20(11):2795. doi: 10.3390/ijms20112795</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Chen G.D., Liang S.J., Huang L., Yu H.R., Wu Y.L., Wei Q.Z., Zhang Z.Q. Association of dietary anthocyanidins intake with bone health in children: a cross-sectional study. Calif. Tissue Int. 2023;113(4):393–402. doi: 10.1007/s00223-023-01128-6</mixed-citation><mixed-citation xml:lang="en">Chen G.D., Liang S.J., Huang L., Yu H.R., Wu Y.L., Wei Q.Z., Zhang Z.Q. Association of dietary anthocyanidins intake with bone health in children: a cross-sectional study. Calif. Tissue Int. 2023;113(4):393–402. doi: 10.1007/s00223-023-01128-6</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Филиппова О.В. Фитоэстрогены: перспективы применения. Эффектив. фармакотерапия. 2020;16(22):30–36. doi: 10.33978/2307-3586-2020-16-22-30-36</mixed-citation><mixed-citation xml:lang="en">Filippova O.V. Phytoestrogens: prospects of use. Effektivnaya farmakoterapiya = Effective Pharmacotherapy. 2020;16(22):30–36. [In Russian]. doi: 10.33978/2307-3586-2020-16-22-30-36</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Mohapatra S., Kumar P.A., Aggarwal A., Iqubal A., Mirza M.A., Iqbal Z. Phytotherapeutic approach for conquering menopausal syndrome and osteoporosis. Phytother. Res. 2024;38(6):2728–2763. doi: 10.1002/ptr.8172</mixed-citation><mixed-citation xml:lang="en">Mohapatra S., Kumar P.A., Aggarwal A., Iqubal A., Mirza M.A., Iqbal Z. Phytotherapeutic approach for conquering menopausal syndrome and osteoporosis. Phytother. Res. 2024;38(6):2728–2763. doi: 10.1002/ptr.8172</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Liao M.H., Tai Y.T., Cherng Y.G., Liu S.H., Chang Y.A., Lin P.I., Chen R.M. Genistein induces oestrogen receptor-α gene expression in osteoblasts through the activation of mitogen-activated protein kinase/NF-κB/activator protein-1 and promotes cell mineralization. Br. J. Nutr. 2014;111(1):55–63. doi: 10.1017/S0007114513002043</mixed-citation><mixed-citation xml:lang="en">Liao M.H., Tai Y.T., Cherng Y.G., Liu S.H., Chang Y.A., Lin P.I., Chen R.M. Genistein induces oestrogen receptor-α gene expression in osteoblasts through the activation of mitogen-activated protein kinase/NF-κB/activator protein-1 and promotes cell mineralization. Br. J. Nutr. 2014;111(1):55–63. doi: 10.1017/S0007114513002043</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Kim M., Lim J., Lee J.H., Lee K.M., Kim S., Park K.W., Nho C.W., Cho Y.C. Understanding the functional role of genistein in the bone differentiation in mouse osteoblastic cell line MC3T3-E1 by RNA-Seq analysis. Sci. Rep. 2018;8(1):1–12. doi: 10.1038/s41598-018-21601-9</mixed-citation><mixed-citation xml:lang="en">Kim M., Lim J., Lee J.H., Lee K.M., Kim S., Park K.W., Nho C.W., Cho Y.C. Understanding the functional role of genistein in the bone differentiation in mouse osteoblastic cell line MC3T3-E1 by RNA-Seq analysis. Sci. Rep. 2018;8(1):1–12. doi: 10.1038/s41598-018-21601-9</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Cepeda S.B., Sandoval M.J., Crescitelli M.C., Rauschemberger M.B., Massheimer V.Z. The isoflavone genistein enhances osteoblastogenesis: signaling pathways involved. J. Physiol. Biochem. 2020;76(1):99–110. doi: 10.1007/s13105-019-00722-3</mixed-citation><mixed-citation xml:lang="en">Cepeda S.B., Sandoval M.J., Crescitelli M.C., Rauschemberger M.B., Massheimer V.Z. The isoflavone genistein enhances osteoblastogenesis: signaling pathways involved. J. Physiol. Biochem. 2020;76(1):99–110. doi: 10.1007/s13105-019-00722-3</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Chakraborty D., Gupta K., Biswas S. A mechanistic insights of phytoestrogens used for rheumatoid arthritis : an evidence-based review. Biomed. Pharmacother. 2021;133:111039. doi: 10.1016/j.biopha.2020.111039</mixed-citation><mixed-citation xml:lang="en">Chakraborty D., Gupta K., Biswas S. A mechanistic insights of phytoestrogens used for rheumatoid arthritis : an evidence-based review. Biomed. Pharmacother. 2021;133:111039. doi: 10.1016/j.biopha.2020.111039</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">Filipović B., Sošić-JurjevićB., Ajdžanović V., Živanović J., Manojlović-Stojanovski M., Nestorović N., Ristić N., Trifunović S., Milošević V. The phytoestrogen genistein prevents trabecular bone loss and affects thyroid follicular cells in a male rat model of osteoporosis. J. Anat. 2018;233(2):204–212. doi: 10.1111/joa.12828</mixed-citation><mixed-citation xml:lang="en">Filipović B., Sošić-JurjevićB., Ajdžanović V., Živanović J., Manojlović-Stojanovski M., Nestorović N., Ristić N., Trifunović S., Milošević V. The phytoestrogen genistein prevents trabecular bone loss and affects thyroid follicular cells in a male rat model of osteoporosis. J. Anat. 2018;233(2):204–212. doi: 10.1111/joa.12828</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">Karieb S., Fox S.W. Phytoestrogens directly inhibit TNF-α-induced bone resorption in RAW264.7 cells by suppressing c-fos-induced NFATc1 expression. J. Cell. Biochem. 2011;112(2):476–487. doi: 10.1002/jcb.22935</mixed-citation><mixed-citation xml:lang="en">Karieb S., Fox S.W. Phytoestrogens directly inhibit TNF-α-induced bone resorption in RAW264.7 cells by suppressing c-fos-induced NFATc1 expression. J. Cell. Biochem. 2011;112(2):476–487. doi: 10.1002/jcb.22935</mixed-citation></citation-alternatives></ref><ref id="cit93"><label>93</label><citation-alternatives><mixed-citation xml:lang="ru">Park K., Ju W.C., Jeo J.H., Kim J.Y., Seo H.S., Uchida Y., Cho Y. Increased OPG/RANKL ratio in the conditioned medium of soybean-treated osteoblasts suppresses RANKL-induced osteoclast differentiation. Int. J. Mol. Med. 2014;33(1):178–184. doi: 10.3892/ijmm.2013.1557</mixed-citation><mixed-citation xml:lang="en">Park K., Ju W.C., Jeo J.H., Kim J.Y., Seo H.S., Uchida Y., Cho Y. Increased OPG/RANKL ratio in the conditioned medium of soybean-treated osteoblasts suppresses RANKL-induced osteoclast differentiation. Int. J. Mol. Med. 2014;33(1):178–184. doi: 10.3892/ijmm.2013.1557</mixed-citation></citation-alternatives></ref><ref id="cit94"><label>94</label><citation-alternatives><mixed-citation xml:lang="ru">de Wilde A., Lieberherr M., Colin C., Pointillart A. A low dose of daidzein acts as an Erβ-selective agonist in trabecular osteoblasts of young female piglets. J. Cell. Physiol. 2004;200(2):253–262. doi: 10,1002/jcp.20008</mixed-citation><mixed-citation xml:lang="en">de Wilde A., Lieberherr M., Colin C., Pointillart A. A low dose of daidzein acts as an Erβ-selective agonist in trabecular osteoblasts of young female piglets. J. Cell. Physiol. 2004;200(2):253–262. doi: 10,1002/jcp.20008</mixed-citation></citation-alternatives></ref><ref id="cit95"><label>95</label><citation-alternatives><mixed-citation xml:lang="ru">Huh J.E., Lee W.I., Kang J.W., Nam D., Choi D.Y., Park D.S., Lee S.H., Lee J.D. Formononetin attenuates osteoclastogenesis via suppressing the RANKL-induced activation of NF-κB, c-Fos, and nuclear factor of activated T-cells cytoplasmic 1 signaling pathway. J. Nat. Prod. 2014;77(11):2423–2431. doi: 10.1021/np500417d</mixed-citation><mixed-citation xml:lang="en">Huh J.E., Lee W.I., Kang J.W., Nam D., Choi D.Y., Park D.S., Lee S.H., Lee J.D. Formononetin attenuates osteoclastogenesis via suppressing the RANKL-induced activation of NF-κB, c-Fos, and nuclear factor of activated T-cells cytoplasmic 1 signaling pathway. J. Nat. Prod. 2014;77(11):2423–2431. doi: 10.1021/np500417d</mixed-citation></citation-alternatives></ref><ref id="cit96"><label>96</label><citation-alternatives><mixed-citation xml:lang="ru">Zverev Ya.F., Rykunova A.Ya. Modern nanocarriers as a factor in increasing the bioavailability and pharmacological activity of flavonoids. Appl. Biochem. Microbiol. 2022;58(9):1002–1020. doi: 10.1134/s0003683822090149</mixed-citation><mixed-citation xml:lang="en">Zverev Ya.F., Rykunova A.Ya. Modern nanocarriers as a factor in increasing the bioavailability and pharmacological activity of flavonoids. Appl. Biochem. Microbiol. 2022;58(9):1002–1020. doi: 10.1134/s0003683822090149</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>
