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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="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">phkinetica</journal-id><journal-title-group><journal-title xml:lang="ru">Фармакокинетика и Фармакодинамика</journal-title><trans-title-group xml:lang="en"><trans-title>Pharmacokinetics and Pharmacodynamics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2587-7836</issn><issn pub-type="epub">2686-8830</issn><publisher><publisher-name>ООО «Издательство ОКИ»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.37489/2587-7836-2026-2-73-78</article-id><article-id custom-type="edn" pub-id-type="custom">TJPLHK</article-id><article-id custom-type="elpub" pub-id-type="custom">phkinetica-532</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>ДОКЛИНИЧЕСКИЕ ИССЛЕДОВАНИЯ ФАРМАКОДИНАМИКИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PRECLINICAL PHARMACODYNAMICS STUDIES</subject></subj-group></article-categories><title-group><article-title>Нефропротективное действие ресвератрола при цисплатин-индуцированном остром повреждении почек</article-title><trans-title-group xml:lang="en"><trans-title>Nephroprotective activity of resveratrol in cisplatin-induced acute kidney injury</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2212-0508</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нетребенко</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Netrebenko</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Нетребенко Александр Сергеевич – к. м. н., ассистент кафедры фармакологии и клинической фармакологии</p><p>Белгород</p></bio><bio xml:lang="en"><p>Aleksandr S. Netrebenko – PhD, Cand. Sci. (Med.), assistant of Department of Pharmacology and Clinical Pharmacology</p><p>Belgorod</p></bio><email xlink:type="simple">AlexNetrebenko@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/0000-0002-1493-3376</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Покровский</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Pokrovsky</surname><given-names>M. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Покровский Михаил Владимирович – д. м. н., профессор, профессор кафедры фармакологии и клинической фармакологии, руководитель Научно-исследовательского института фармакологии живых систем</p><p>Белгород</p></bio><bio xml:lang="en"><p>Mikhail V. Pokrovsky – PhD, Dr. Sci. (Med.), Professor, Professor of the Department of Pharmacology and Clinical Pharmacology, Head of Research Institute of Pharmacology of Living Systems</p><p>Belgorod</p></bio><email xlink:type="simple">mpokrovsky@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Белгородский государственный национальный исследовательский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Belgorod National Research University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>30</day><month>06</month><year>2026</year></pub-date><volume>0</volume><issue>2</issue><fpage>73</fpage><lpage>78</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Нетребенко А.С., Покровский М.В., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Нетребенко А.С., Покровский М.В.</copyright-holder><copyright-holder xml:lang="en">Netrebenko A.S., Pokrovsky M.V.</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.pharmacokinetica.ru/jour/article/view/532">https://www.pharmacokinetica.ru/jour/article/view/532</self-uri><abstract><sec><title>Актуальность</title><p>Актуальность. В России ежегодно выявляется более 600 000 случаев заболеваний онкологией, в 18,9 % процесс диагностируется на IV стадии. Химиотерапия является основным методом лечения пациентов с метастатическими формами рака. Цисплатин – широко используемый химиотерапевтический препарат, однако он обладает значительной нефротоксичностью, которая часто приводит к редукции дозы или даже полному прекращению его приёма. Учитывая данный факт, профилактика развития цисплатин-индуцированного острого повреждения почек является крайне важной задачей.</p></sec><sec><title>Цель исследования</title><p>Цель исследования: изучить нефропротективные свойства ресвератрола при цисплатин-индуцированном остром повреждении почек.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. Исследование проведено в НИИ фармакологии живых систем Белгородского национального исследовательского университета на 40 белых лабораторных крысах-самцах линии Wistar массой 250–300 г. Для моделирования острого почечного повреждения животным вводили цисплатин в дозе 5 мг/кг внутрибрюшинно в 1-й и 8-й день эксперимента. С целью нефропротекции ежедневно перорально давали ресвератрол в дозе 4 мг/кг или 12 мг/кг в течение 2 недель. Спустя 14 суток после первого введения цисплатина выполняли функциональные пробы и лабораторные исследования.</p></sec><sec><title>Результаты</title><p>Результаты. Использование ресвератрола при цисплатин-индуцированном остром повреждении почек сопровождалось выраженными дозозависимыми нефропротективными эффектами, проявившимися в снижении уровня креатинина и мочевины плазмы крови, росте скорости клубочковой фильтрации, нормализации фракционной экскреции натрия и улучшении показателя уровня микроциркуляции в паренхиме почек.</p></sec><sec><title>Выводы</title><p>Выводы. Результаты исследования демонстрируют перспективность использования ресвератрола с целью профилактики развития цисплатин-индуцированного острого повреждения почек.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Background</title><p>Background. In Russia, more than 600,000 cases of cancer are diagnosed annually, with 18.9 % of cases diagnosed at stage IV. Chemotherapy is the primary treatment for patients with metastatic cancer. Cisplatin is a widely used chemotherapeutic agent; however, it exhibits significant nephrotoxicity, often leading to dose reduction or even complete discontinuation of treatment. Given this, preventing the development of cisplatin-induced acute kidney injury is crucial.</p><p>The aim of the study was to investigate the nephroprotective properties of resveratrol in cisplatin-induced acute kidney injury.</p></sec><sec><title>Materials and methods</title><p>Materials and methods. The study was conducted at the Research Institute of Pharmacology of Living Systems, Belgorod National Research University, using 40 male Wistar laboratory rats weighing 250–300g. To simulate acute kidney injury, animals were administered cisplatin at a dose of 5 mg/kg intraperitoneally on days 1 and 8 of the experiment. For nephroprotection, resveratrol was administered orally daily at a dose of 4 mg/kg or 12 mg/kg for 2 weeks. Functional tests and laboratory studies were performed 14 days after the first cisplatin administration.</p></sec><sec><title>Results</title><p>Results. The use of resveratrol in cisplatin-induced acute kidney injury was accompanied by pronounced dose-dependent nephroprotective effects, manifested by a decrease in plasma creatinine and urea levels, an increase in glomerular filtration rate, normalization of fractional sodium excretion, and an improvement in renal parenchymal microcirculation.</p></sec><sec><title>Conclusions</title><p>Conclusions. The results of the study demonstrate the potential of using resveratrol to prevent the development of cisplatin-induced acute kidney injury.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>ресвератрол</kwd><kwd>цисплатин-индуцированное острое повреждение почек</kwd><kwd>микроциркуляция</kwd></kwd-group><kwd-group xml:lang="en"><kwd>resveratrol</kwd><kwd>cisplatin-induced acute kidney injury</kwd><kwd>microcirculation</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">Окладников С.М., Никитина С.Ю. Здравоохранение в России. 2023: Стат.сб./Росстат. М., 3-46 2023. 179 с.</mixed-citation><mixed-citation xml:lang="en">[Okladnikov SM, Nikitina SY. Healthcare in Russia. 2023: Stat.sb./Rosstat. Moscow, 3-46 2023. 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