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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">10.37489/2587-7836-2021-1-30-37</article-id><article-id custom-type="elpub" pub-id-type="custom">phkinetica-269</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>ИССЛЕДОВАНИЯ МЕХАНИЗМА ДЕЙСТВИЯ ЛЕКАРСТВЕННЫХ СРЕДСТВ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>STUDIES OF THE MECHANISM OF ACTION OF DRUGS</subject></subj-group></article-categories><title-group><article-title>К механизму антиаритмического действия фабомотизола дигидрохлорида при алкогольной кардиомиопатии</article-title><trans-title-group xml:lang="en"><trans-title>On the mechanism of the antiarrhythmic action of fabomotizole hydrochloride in alcoholic cardiomyopathy</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3208-198X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мирошкина</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Miroshkina</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мирошкина Ирина Александровна, н. с. лаборатории лекарственной токсикологии</p><p>SPIN-код: 4697-7938</p><p>Москва </p></bio><bio xml:lang="en"><p>Miroshkina Irina A., Research scientist of the laboratory of drug toxicology</p><p>SPIN code: 4697-7938</p><p>Moscow </p></bio><email xlink:type="simple">iris10.81@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/0000-0002-1323-6472</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кожевникова</surname><given-names>Л. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Kozhevnikova</surname><given-names>L. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кожевникова Любовь Михайловна, д. м. н., в. н. с. лаборатории фармакологического; зав. лабораторией хронического воспаления и микроциркуляции</p><p>SPIN-код: 6882-6933</p><p>Москва </p></bio><bio xml:lang="en"><p>Kozhevnikova Lubove M., Dr. Sci. (Med.), Leading Researcher of laboratory of pharmacological screening; Head of laboratory of laboratory of chronic inflammation and microcirculation</p><p>SPIN code: 6882-6933</p><p>Moscow </p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3988-7724</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Цорин</surname><given-names>И. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Tsorin</surname><given-names>I. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Цорин Иосиф Борисович, д. б. н., в. н. с. лаборатории фармакологического скрининга</p><p>SPIN-код: 4015-3025</p><p>Москва </p></bio><bio xml:lang="en"><p>Tsorin Iosif B., Dr. Sci. Biological, Leading researcher of laboratory of pharmacological screening</p><p>SPIN code: 4015-3025</p><p>Moscow </p></bio><email xlink:type="simple">tsorin@yandex.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/0000-0002-4779-427X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Столярук</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Stolyaruk</surname><given-names>V. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Столярук Валерий Николаевич, к. м. н., с. н. с. лаборатории фармакологического скрининга</p><p>SPIN-код: 3405-8229</p><p>Москва </p></bio><bio xml:lang="en"><p>Stolyaruk Valeriy N., PhD Med. Sci., Senior Researcher Scientist of laboratory of pharmacological screening</p><p>SPIN code: 3405-8229</p><p>Moscow </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7407-7516</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Вититнова</surname><given-names>М. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Vititnova</surname><given-names>M. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Вититнова Марина Борисовна, к. б. н., с. н. с. лаборатории фармакологического скрининга</p><p>SPIN-код: 1901-8919</p><p>Москва </p></bio><bio xml:lang="en"><p>Vititnova Marina B., PhD Biological Sci., Senior researcher scientist of laboratory of pharmacological screening</p><p>SPIN code: 1901-8919</p><p>Moscow </p></bio><email xlink:type="simple">MB-Vit@yandex.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/0000-0003-2832-4739</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Крыжановский</surname><given-names>С. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kryzhanovskii</surname><given-names>S. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Крыжановский Сергей Александрович, д. м. н., зав. лабораторией фармакологического скрининга</p><p>SPIN-код: 6596-4865</p><p>Москва </p></bio><bio xml:lang="en"><p>Kryzhanovskiy Sergey A., Dr. Sci. (Med.), Head of laboratory of pharmacological screening</p><p>SPIN code: 6596-4865</p><p>Moscow </p></bio><email xlink:type="simple">SAK-538@yandex.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/0000-0003-0218-8580</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Дурнев</surname><given-names>А. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Durnev</surname><given-names>A. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дурнев Андрей Дмитриевич, д. м. н., профессор, член-корр. РАН, зав. лабораторией лекарственной токсикологии</p><p>SPIN-код: 8426-0380</p><p>Москва </p></bio><bio xml:lang="en"><p>Durnev Andrei Dmitrievich, Dr. Sci. (Med.), professor, corresponding member RAS, Head of the department of drug toxicology</p><p>SPIN code: 8426-0380</p><p>Moscow </p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «НИИ фармакологии имени В.В. Закусова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>FSBI “Zakusov Institute of Pharmacology”</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБНУ «НИИ фармакологии имени В.В. Закусова»; ФГБНУ «НИИ общей патологии и патофизиологии»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>FSBI “Zakusov Institute of Pharmacology”; FSBI ««Institute of General Pathology and Pathophysiology»</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>27</day><month>09</month><year>2021</year></pub-date><volume>0</volume><issue>1</issue><fpage>30</fpage><lpage>37</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Мирошкина И.А., Кожевникова Л.М., Цорин И.Б., Столярук В.Н., Вититнова М.Б., Крыжановский С.А., Дурнев А.Д., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Мирошкина И.А., Кожевникова Л.М., Цорин И.Б., Столярук В.Н., Вититнова М.Б., Крыжановский С.А., Дурнев А.Д.</copyright-holder><copyright-holder xml:lang="en">Miroshkina I.A., Kozhevnikova L.M., Tsorin I.B., Stolyaruk V.N., Vititnova M.B., Kryzhanovskii S.A., Durnev A.D.</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/269">https://www.pharmacokinetica.ru/jour/article/view/269</self-uri><abstract><p>Известно, что основной причиной летальности от хронического алкоголизма является алкогольная кардиомиопатия (АКМП). Для АКМП крайне высок риск развития злокачественных нарушений сердечного ритма, исходом которых приблизительно у 40 % такого рода больных является внезапная сердечная смерть. Материалы и методы. Эксперименты проводили на разработанной нами трансляционной модели АКМП, которая формируется у крыс к концу 24-й недели принудительного приёма 10 % раствора этанола. Для изучения механизмов, лежащих в основе антиаритмического действия фабомотизола дигидрохлорида, использовали комплекс морфогистологических, электрофизиологических и молекулярных исследований. Результаты. Показано, что на фоне систематической терапии фабомотизола дигидрохлоридом (15 мг/кг, в/б) ежедневно в течение 28 дней, начатой по окончании 24-й недели алкоголизации, по сравнению с алкоголизированным контролем значимо уменьшается жировая дистрофия миокарда и восстанавливается порог электрической фибрилляции желудочков сердца. Согласно результатам молекулярных исследований, фабомотизола дигидрохлорид значимо подавляет выявленную у контрольных алкоголизированных животных аномальную экспрессию мРНК генов ключевых рецепторов и белков, ответственных за поддержание в кардиомиоцитах гомеостаза ионов Са++ и регуляцию их ритмической активности: регуляторных белков Ерас1 (p=0,021), Ерас2 (р = 0,018), СаМ (р = 0,00001), а также RyR2 (р = 0,031), IP3R2 (р = 0,006) рецепторов. Заключение. Полученные результаты позволяют высказать предположение о том, что антиаритмическое действие фабомотизола дигидрохлорида в условиях АКМП связано с его способностью подавлять аномальную активность регуляторных белков Ерас2 и RyR2, IP3R2 рецепторов.</p></abstract><trans-abstract xml:lang="en"><p>It is known that the alcoholic cardiomyopathy (ACMP) is the main reason for lethality from chronic alcoholism. For ACMP the risk of development of malignant violations of a heart rhythm which result approximately at 40% of such patients is sudden heart death is extremely high. Materials and methods. Experiments were made on the ACMP translational model developed by us which is formed at rats by the end of the 24th week of compulsory reception of 10 % of ethanol solution. For studying the mechanisms which are the responsible of antiarrhythmic action of a fabomotizole dihydrochloride used a complex of morphohistological, electrophysiological and molecular researches. Results. It is shown that against the background of systematic therapy fabomotizole dihydrochloride (15 mg/kg, i.p.) daily within 28 days after 24 weeks of alcoholization, in comparison with alcoholized control the fat dystrophy of a myocardium significantly decreases and the threshold of electric fibrillation of heart ventricles is restored. According to results of molecular researches, a fabomotizole dihydrochloride significantly suppresses revealed in control alkoholized animals the abnormal mRNA expression of key receptor genes and proteins responsible for maintenance in cardiomyocytes of a homeostasis of ions of Ca++ and regulation of their rhythmic activity: regulatory proteins Epac1 (p = 0.021), Epac2 (p = 0.018), CaM (p = 0.00001) and also RyR2 (p = 0.031), IP3R2 (p = 0.006) receptors. Conclusion. The obtained results suggest that antiarrhythmic action of a fabomotizole dihydrochloride in the conditions of ACMP is connected with its ability to suppress abnormal activity of regulatory proteins Epac2 and RyR2, IP3R2 receptors.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>фабомотизола дигидрохлорид</kwd><kwd>алкогольная кардиомиопатия</kwd><kwd>жировая дистрофия миокарда</kwd><kwd>электрическая стабильность кардиомиоцитов</kwd><kwd>Ерас1</kwd><kwd>Ерас2</kwd><kwd>СаМ</kwd><kwd>RyR2</kwd><kwd>IP3R2</kwd></kwd-group><kwd-group xml:lang="en"><kwd>fabomotizole dihydrochloride</kwd><kwd>alcoholic cardiomyopathy</kwd><kwd>fat dystrophy of a myocardium</kwd><kwd>electric stability of cardiomyocytes</kwd><kwd>Epac1</kwd><kwd>Epac2</kwd><kwd>RyR2</kwd><kwd>IP3R2</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">Guzzo-Merello G, Cobo-Marcos M, Gallego-Delgado M, GarciaPavia P. 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