<?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">cardiotomsk</journal-id><journal-title-group><journal-title xml:lang="ru">Сибирский журнал клинической и экспериментальной медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Siberian Journal of Clinical and Experimental Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2713-2927</issn><issn pub-type="epub">2713-265X</issn><publisher><publisher-name>TSU publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.29001/2073-8552-2023-38-4-86-96</article-id><article-id custom-type="elpub" pub-id-type="custom">cardiotomsk-2057</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 И ЛЕКЦИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS AND LECTURES</subject></subj-group></article-categories><title-group><article-title>Влияние кишечной микробиоты на устойчивость миокарда к ишемическому-реперфузионному повреждению</article-title><trans-title-group xml:lang="en"><trans-title>Effect of intestinal microbiota on myocardial resistance to ischemia-reperfusion 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/0000-0003-3096-9747</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Борщев</surname><given-names>Ю. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Borshchev</surname><given-names>Yu. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Борщев Юрий Юрьевич, канд. биол. наук, заведующий научно-исследовательским отделом токсикологии, Институт экспериментальной медицины, Национальный медицинский исследовательский центр имени В.А. Алмазова ; научный сотрудник лаборатории химиопрофилактики рака и онкофармакологии, Национальный медицинский исследовательский центр онкологии имени Н.Н. Петрова </p><p>197341, Санкт-Петербург, ул. Аккуратова, 2</p></bio><bio xml:lang="en"><p> Yuriy Yu. Borshchev, Cand. Sci. (Biol.), Head of the Research Department of Toxicology, Institute of Experimental Medicine, V.A. Almazov National Medical Research Center; Research Scientist, Laboratory of Cancer Chemoprevention and Oncopharmacology, NMRC of Oncology named after N.N. Petrov </p><p>2, Akkuratova str., Saint-Petersburg, 197341</p></bio><email xlink:type="simple">niscon@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/0000-0003-1705-7217</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сонин</surname><given-names>Д. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Sonin</surname><given-names>D. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Сонин Дмитрий Леонидович, канд. мед. наук, руководитель и ведущий научный сотрудник научно-исследовательского отдела микроциркуляции и метаболизма миокарда, Институт экспериментальной медицины, Национальный медицинский исследовательский центр имени В.А. Алмазова; заведующий научно-исследовательской лабораторией метаболизма миокарда, Первый Санкт-Петербургский государственный медицинский университет имени академика И.П. Павлова </p><p>197341, Санкт-Петербург, ул. Аккуратова, 2</p></bio><bio xml:lang="en"><p>Dmitry L. Sonin, Cand. Sci. (Med.), Leading Research Scientist, Head of Department of Microcirculation and Myocardial Metabolism, Institute of Experimental Medicine, V.A. Almazov National Medical Research Center of Ministry of Health of the Russian Federation; Head of Myocardial Metabolism Laboratory of Academician I.P. Pavlov First St. Petersburg State Medical University</p><p>2, Akkuratova str., Saint-Petersburg, 197341</p></bio><email xlink:type="simple">sonin_d@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/0000-0001-6382-5286</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Минасян</surname><given-names>С. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Minasyan</surname><given-names>S. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Минасян Саркис Минасович, канд. мед. наук, старший научный сотрудник, научно-исследовательский отдел микроциркуляции и метаболизма миокарда, Институт экспериментальной медицины</p><p>197341, Санкт-Петербург, ул. Аккуратова, 2</p></bio><bio xml:lang="en"><p>Sarkis M. Minasyan, Cand. Sci. (Med.), Senior Research Scientist, Research Department of Microcirculation and Myocardial Metabolism, Institute of Experimental Medicine</p><p>2, Akkuratova str., Saint-Petersburg, 197341</p></bio><email xlink:type="simple">carkis@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Борщева</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Borshcheva</surname><given-names>O. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Борщева Ольга Викторовна, научный сотрудник, научно-исследовательский отдел токсикологии, Институт экспериментальной медицины</p><p>197341, Санкт-Петербург, ул. Аккуратова, 2</p></bio><bio xml:lang="en"><p>Ol’ga V. Borshcheva, Research Scientist, Research Department of Toxicology, Institute of Experimental Medicine</p><p>2, Akkuratova str., Saint-Petersburg, 197341</p></bio><email xlink:type="simple">violga27@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/0000-0001-6637-3633</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Буровенко</surname><given-names>И. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Burovenko</surname><given-names>I. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Буровенко Инесса Юрьевна, младший научный сотрудник, научно-исследовательский отдел токсикологии, Институт экспериментальной медицины</p><p>197341, Санкт-Петербург, ул. Аккуратова, 2</p></bio><bio xml:lang="en"><p>Inessa Yu. Burovenko, Junior Research Scientist, Research Department of Toxicology, Institute of Experimental Medicine</p><p>2, Akkuratova str., Saint-Petersburg, 197341</p></bio><email xlink:type="simple">burovenko.inessa@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5129-9944</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Галагудза</surname><given-names>М. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Galagudza</surname><given-names>M. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Галагудза Михаил Михайлович, д-р мед. наук, профессор, чл.-корр. РАН, директор Института экспериментальной медицины</p><p>197341, Санкт-Петербург, ул. Аккуратова, 2</p></bio><bio xml:lang="en"><p>Michael M. Galagudza, Dr. Sci. (Med.), Professor, Associate Member of Russian Academy of Sciences, Head of Institute of Experimental Medicine</p><p>2, Akkuratova str., Saint-Petersburg, 197341</p></bio><email xlink:type="simple">alagoudza@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Национальный медицинский исследовательский центр имени В.А. Алмазова Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Almazov National Medical Research Centre of the Ministry of Health of Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>30</day><month>12</month><year>2023</year></pub-date><volume>38</volume><issue>4</issue><fpage>86</fpage><lpage>96</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Борщев Ю.Ю., Сонин Д.Л., Минасян С.М., Борщева О.В., Буровенко И.Ю., Галагудза М.М., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Борщев Ю.Ю., Сонин Д.Л., Минасян С.М., Борщева О.В., Буровенко И.Ю., Галагудза М.М.</copyright-holder><copyright-holder xml:lang="en">Borshchev Y.Y., Sonin D.L., Minasyan S.M., Borshcheva O.V., Burovenko I.Y., Galagudza M.M.</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.sibjcem.ru/jour/article/view/2057">https://www.sibjcem.ru/jour/article/view/2057</self-uri><abstract><p>Последние 10–15 лет ознаменованы бурным увеличением объема знаний о роли кишечной микробиоты в регуляции разнообразных физиологических процессов. В частности, отмечены взаимосвязи между нарушениями состава кишечной микрофлоры и увеличением риска развития сердечно-сосудистых заболеваний (ССЗ). Появляются также работы, в которых продемонстрирована возможность уменьшения выраженности ишемического-реперфузионного повреждения (ИРП) миокарда в результате различных воздействий на состав кишечной микробиоты. В настоящем обзоре проанализирована литература последних лет, посвященная влиянию кишечной микробиоты на устойчивость миокарда к ИРП. Показано, что модуляция кишечного микробиома посредством изменения характера питания, введения пробиотиков, антибиотиков, а также трансплантации кишечной микрофлоры приводит к уменьшению размера инфаркта миокарда. В качестве возможных механизмов кардиопротекции, опосредованной изменениями функционального состояния микробиоты, рассматриваются нормализация повышенной проницаемости кишечного эпителиального барьера с уменьшением проявлений системного воспаления, изменения уровня секреции некоторых гормонов, усиление продукции короткоцепочечных жирных кислот и модуляция метаболизма желчных кислот под действием ферментов кишечных бактерий. Концепция повышения устойчивости миокарда к ИРП за счет модуляции состава кишечной микробиоты является совершенно новым научным направлением, требующим детального изучения в эксперименте с возможностью быстрого внедрения полученных результатов в клиническую практику.</p></abstract><trans-abstract xml:lang="en"><p>The last 10–15 years have been marked by a rapid increase in the volume of knowledge about the role of the intestinal microbiota in the regulation of various physiological processes. In particular, the interrelations between disturbances in the composition of the intestinal microflora and an increase in the risk of developing cardiovascular diseases were noted. There are also emerging works that demonstrate the possibility of reducing the severity of myocardial ischemia-reperfusion injury as a result of various effects on the composition of intestinal microbiota. This review analyzes the recent literature on the influence of intestinal microbiota on myocardial resistance to ischemia-reperfusion injury. It has been shown that modulation of the intestinal microbiome by changing the nature of nutrition, probiotics, antibiotics, and intestinal microflora transplantation leads to a reduction in the size of myocardial infarction. Normalization of increased permeability of intestinal epithelial barrier with reduction of manifestations of systemic inflammation, changes in the level of secretion of some hormones, increased production of short-chain fatty acids and modulation of bile acid metabolism under the action of intestinal bacterial enzymes are considered as possible mechanisms of cardioprotection mediated by changes in the functional state of microbiota. The concept of increasing myocardial resistance to ischemia-reperfusion injury by modulating the composition of the intestinal microbiota is a completely new scientific direction that requires detailed study in experiment with the possibility of rapid implementation of the results obtained in clinical practice.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>кишечная микробиота</kwd><kwd>пробиотики</kwd><kwd>антибиотики</kwd><kwd>сердце</kwd><kwd>ишемия</kwd><kwd>реперфузия</kwd><kwd>размер инфаркта</kwd><kwd>кардиопротекция</kwd></kwd-group><kwd-group xml:lang="en"><kwd>gut microbiota</kwd><kwd>probiotics</kwd><kwd>antibiotics</kwd><kwd>heart</kwd><kwd>ischemia</kwd><kwd>reperfusion</kwd><kwd>infarct size</kwd><kwd>cardioprotection</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование выполнено за счет гранта Российского научного фонда (проект № 23-15-00139).</funding-statement><funding-statement xml:lang="en">The study was supported by the Russian Science Foundation grant No. 23-15-00139.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Dai H., Much A.A., Maor E., Asher E., Younis A., Xu Y. et al. Global, regional, and national burden of ischaemic heart disease and its attributable risk factors, 1990–2017: results from the Global Burden of Disease Study 2017. Eur. Heart J. Qual. Care Clin. Outcomes. 2022;8(1):50–60. DOI: 10.1093/ehjqcco/qcaa076.</mixed-citation><mixed-citation xml:lang="en">Dai H., Much A.A., Maor E., Asher E., Younis A., Xu Y. et al. Global, regional, and national burden of ischaemic heart disease and its attributable risk factors, 1990–2017: results from the Global Burden of Disease Study 2017. Eur. Heart J. Qual. Care Clin. Outcomes. 2022;8(1):50–60. DOI: 10.1093/ehjqcco/qcaa076.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Camacho X., Nedkoff L., Wright F.L., Nghiem N., Buajitti E., Goldacre R. et al. Relative contribution of trends in myocardial infarction event rates and case fatality to declines in mortality: an international comparative study of 1.95 million events in 80.4 million people in four countries. Lancet. Public Health. 2022;7(3):e229–e239. DOI: 10.1016/S24682667(22)00006-8.</mixed-citation><mixed-citation xml:lang="en">Camacho X., Nedkoff L., Wright F.L., Nghiem N., Buajitti E., Goldacre R. et al. Relative contribution of trends in myocardial infarction event rates and case fatality to declines in mortality: an international comparative study of 1.95 million events in 80.4 million people in four countries. Lancet. Public Health. 2022;7(3):e229–e239. DOI: 10.1016/S24682667(22)00006-8.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Perrino C., Ferdinandy P., Bøtker H.E., Brundel B.J.J.M., Collins P., Davidson S.M. et al. Improving translational research in sex-specific effects of comorbidities and risk factors in ischaemic heart disease and cardioprotection: position paper and recommendations of the ESC Working Group on Cellular Biology of the Heart. Cardiovasc. Res. 2021;117(2):367–385. DOI: 10.1093/cvr/cvaa155.</mixed-citation><mixed-citation xml:lang="en">Perrino C., Ferdinandy P., Bøtker H.E., Brundel B.J.J.M., Collins P., Davidson S.M. et al. Improving translational research in sex-specific effects of comorbidities and risk factors in ischaemic heart disease and cardioprotection: position paper and recommendations of the ESC Working Group on Cellular Biology of the Heart. Cardiovasc. Res. 2021;117(2):367–385. DOI: 10.1093/cvr/cvaa155.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Postler T.S., Ghosh S. Understanding the holobiont: how microbial metabolites affect human health and shape the immune system. Cell. Metab. 2017;26(1):110–130. DOI: 10.1016/j.cmet.2017.05.008.</mixed-citation><mixed-citation xml:lang="en">Postler T.S., Ghosh S. Understanding the holobiont: how microbial metabolites affect human health and shape the immune system. Cell. Metab. 2017;26(1):110–130. DOI: 10.1016/j.cmet.2017.05.008.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Rahman M.M., Islam F., Or-Rashid M.H., Mamun A.A., Rahaman M.S., Islam M.M. et al. The gut microbiota (microbiome) in cardiovascular disease and its therapeutic regulation. Front. Cell. Infect. Microbiol. 2022;12:903570. DOI: 10.3389/fcimb.2022.903570.</mixed-citation><mixed-citation xml:lang="en">Rahman M.M., Islam F., Or-Rashid M.H., Mamun A.A., Rahaman M.S., Islam M.M. et al. The gut microbiota (microbiome) in cardiovascular disease and its therapeutic regulation. Front. Cell. Infect. Microbiol. 2022;12:903570. DOI: 10.3389/fcimb.2022.903570.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Danilo C.A., Constantopoulos E., McKee L.A., Chen H., Regan J.A., Lipovka Y. et al. Bifidobacterium animalis subsp. Lactis 420 mitigates the pathological impact of myocardial infarction in the mouse. Benef. Microbes. 2017;8(2):257–269. DOI: 10.3920/BM2016.0119.</mixed-citation><mixed-citation xml:lang="en">Danilo C.A., Constantopoulos E., McKee L.A., Chen H., Regan J.A., Lipovka Y. et al. Bifidobacterium animalis subsp. Lactis 420 mitigates the pathological impact of myocardial infarction in the mouse. Benef. Microbes. 2017;8(2):257–269. DOI: 10.3920/BM2016.0119.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Yang T., Santisteban M.M., Rodriguez V., Li E., Ahmari N., Carvajal J.M., Zadeh M. et al. Gut dysbiosis is linked to hypertension. Hypertension. 2015;65(6):1331–1340. DOI: 10.1161/HYPERTENSIONAHA.115.05315.</mixed-citation><mixed-citation xml:lang="en">Yang T., Santisteban M.M., Rodriguez V., Li E., Ahmari N., Carvajal J.M., Zadeh M. et al. Gut dysbiosis is linked to hypertension. Hypertension. 2015;65(6):1331–1340. DOI: 10.1161/HYPERTENSIONAHA.115.05315.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Sun S., Lulla A., Sioda M., Winglee K., Wu M.C., Jacobs D.R.Jr. et al. Gut microbiota composition and blood pressure. Hypertension. 2019;73(5):998–1006. DOI: 10.1161/HYPERTENSIONAHA.118.12109.</mixed-citation><mixed-citation xml:lang="en">Sun S., Lulla A., Sioda M., Winglee K., Wu M.C., Jacobs D.R.Jr. et al. Gut microbiota composition and blood pressure. Hypertension. 2019;73(5):998–1006. DOI: 10.1161/HYPERTENSIONAHA.118.12109.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Yang Z., Wang Q., Liu Y., Wang L., Ge Z., Li Z. et al. Gut microbiota and hypertension: association, mechanisms and treatment. Clin. Exp. Hypertens. 2023;45(1):2195135. DOI: 10.1080/10641963.2023.2195135.</mixed-citation><mixed-citation xml:lang="en">Yang Z., Wang Q., Liu Y., Wang L., Ge Z., Li Z. et al. Gut microbiota and hypertension: association, mechanisms and treatment. Clin. Exp. Hypertens. 2023;45(1):2195135. DOI: 10.1080/10641963.2023.2195135.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Pluznick J. A novel SCFA receptor, the microbiota, and blood pressure regulation. Gut Microbes. 2014;5(2):202–207. DOI: 10.4161/ gmic.27492.</mixed-citation><mixed-citation xml:lang="en">Pluznick J. A novel SCFA receptor, the microbiota, and blood pressure regulation. Gut Microbes. 2014;5(2):202–207. DOI: 10.4161/ gmic.27492.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Shen X., Li L., Sun Z., Zang G., Zhang L., Shao C. et al. Gut microbiota and atherosclerosis-focusing on the plaque stability. Front. Cardiovasc. Med. 2013;8:668532. DOI: 10.3389/fcvm.2021.668532.</mixed-citation><mixed-citation xml:lang="en">Shen X., Li L., Sun Z., Zang G., Zhang L., Shao C. et al. Gut microbiota and atherosclerosis-focusing on the plaque stability. Front. Cardiovasc. Med. 2013;8:668532. DOI: 10.3389/fcvm.2021.668532.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Emoto T., Yamashita T., Sasaki N., Hirota Y., Hayashi T., So A. et al. Analysis of gut microbiota in coronary artery disease patients: a possible link between gut microbiota and coronary artery disease. J. Atheroscler. Thromb. 2016;23(8):908–921. DOI: 10.5551/jat.32672.</mixed-citation><mixed-citation xml:lang="en">Emoto T., Yamashita T., Sasaki N., Hirota Y., Hayashi T., So A. et al. Analysis of gut microbiota in coronary artery disease patients: a possible link between gut microbiota and coronary artery disease. J. Atheroscler. Thromb. 2016;23(8):908–921. DOI: 10.5551/jat.32672.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Tuomisto S., Huhtala H., Martiskainen M., Goebeler S., Lehtimäki T., Karhunen P.J. Age-dependent association of gut bacteria with coronary atherosclerosis: Tampere Sudden Death Study. PLoS One. 2019;14(8):e0221345. DOI: 10.1371/journal.pone.0221345.</mixed-citation><mixed-citation xml:lang="en">Tuomisto S., Huhtala H., Martiskainen M., Goebeler S., Lehtimäki T., Karhunen P.J. Age-dependent association of gut bacteria with coronary atherosclerosis: Tampere Sudden Death Study. PLoS One. 2019;14(8):e0221345. DOI: 10.1371/journal.pone.0221345.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Oktaviono Y.H., Dyah Lamara A., Saputra P.B.T., Arnindita J.N., Pasahari D., Saputra M.E. et al. The roles of trimethylamine-N-oxide in atherosclerosis and its potential therapeutic aspect: A literature review. Biomol. Biomed. 2023;online ahead of print. DOI: 10.17305/bb.2023.8893.</mixed-citation><mixed-citation xml:lang="en">Oktaviono Y.H., Dyah Lamara A., Saputra P.B.T., Arnindita J.N., Pasahari D., Saputra M.E. et al. The roles of trimethylamine-N-oxide in atherosclerosis and its potential therapeutic aspect: A literature review. Biomol. Biomed. 2023;online ahead of print. DOI: 10.17305/bb.2023.8893.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Jia B., Zou Y., Han X., Bae J.W., Jeon C.O. Gut microbiome-mediated mechanisms for reducing cholesterol levels: implications for ameliorating cardiovascular disease. Trends Microbiol. 2023;31(1):76–91. DOI: 10.1016/j.tim.2022.08.003.</mixed-citation><mixed-citation xml:lang="en">Jia B., Zou Y., Han X., Bae J.W., Jeon C.O. Gut microbiome-mediated mechanisms for reducing cholesterol levels: implications for ameliorating cardiovascular disease. Trends Microbiol. 2023;31(1):76–91. DOI: 10.1016/j.tim.2022.08.003.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Jia Q., Li H., Zhou H., Zhang X., Zhang A., Xie Y. et al. Role and effective therapeutic target of gut microbiota in heart failure. Cardiovasc. Ther. 2019;2019:5164298. DOI: 10.1155/2019/5164298.</mixed-citation><mixed-citation xml:lang="en">Jia Q., Li H., Zhou H., Zhang X., Zhang A., Xie Y. et al. Role and effective therapeutic target of gut microbiota in heart failure. Cardiovasc. Ther. 2019;2019:5164298. DOI: 10.1155/2019/5164298.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Mamic P., Chaikijurajai T., Tang W.H.W. Gut microbiome – a potential mediator of pathogenesis in heart failure and its comorbidities: State-ofthe-art review. J. Mol. Cell. Cardiol. 2021;152:105–117. DOI: 10.1016/j.yjmcc.2020.12.001.</mixed-citation><mixed-citation xml:lang="en">Mamic P., Chaikijurajai T., Tang W.H.W. Gut microbiome – a potential mediator of pathogenesis in heart failure and its comorbidities: State-ofthe-art review. J. Mol. Cell. Cardiol. 2021;152:105–117. DOI: 10.1016/j.yjmcc.2020.12.001.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Tang W.H.W., Bäckhed F., Landmesser U., Hazen S.L. Intestinal microbiota in cardiovascular health and disease: JACC State-of-the-Art Review. J. Am. Coll. Cardiol. 2019;73(16):2089–2105. DOI: 10.1016/j.jacc.2019.03.024.</mixed-citation><mixed-citation xml:lang="en">Tang W.H.W., Bäckhed F., Landmesser U., Hazen S.L. Intestinal microbiota in cardiovascular health and disease: JACC State-of-the-Art Review. J. Am. Coll. Cardiol. 2019;73(16):2089–2105. DOI: 10.1016/j.jacc.2019.03.024.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Nesci A., Carnuccio C., Ruggieri V., D’Alessandro A., Di Giorgio A., Santoro L et al. Gut microbiota and cardiovascular disease: evidence on the metabolic and inflammatory background of a complex relationship. Int. J. Mol. Sci. 2023;24(10):9087. DOI: 10.3390/ijms24109087.</mixed-citation><mixed-citation xml:lang="en">Nesci A., Carnuccio C., Ruggieri V., D’Alessandro A., Di Giorgio A., Santoro L et al. Gut microbiota and cardiovascular disease: evidence on the metabolic and inflammatory background of a complex relationship. Int. J. Mol. Sci. 2023;24(10):9087. DOI: 10.3390/ijms24109087.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Cao H., Zhu Y., Hu G., Zhang Q., Zheng L. Gut microbiome and metabolites, the future direction of diagnosis and treatment of atherosclerosis? Pharmacol. Res. 2023;187:106586. DOI: 10.1016/j.phrs.2022.106586.</mixed-citation><mixed-citation xml:lang="en">Cao H., Zhu Y., Hu G., Zhang Q., Zheng L. Gut microbiome and metabolites, the future direction of diagnosis and treatment of atherosclerosis? Pharmacol. Res. 2023;187:106586. DOI: 10.1016/j.phrs.2022.106586.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Шляхто Е.В., Петрищев Н.Н., Галагудза М.М., Власов Т.Д., Нифонтов Е.М. Кардиопротекция: фундаментальные и клинические аспекты. CПб.: НП-Принт; 2013:399.</mixed-citation><mixed-citation xml:lang="en">Shlyakhto E.V., Petrishchev N.N., Galagudza M.M., Vlasov T.D., Nifontov E.M. Cardioprotection: fundamental and clinical aspects. Saint Petersburg: NP-Print; 2013:399. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Lam V., Su J., Koprowski S., Hsu A., Tweddell J.S., Rafiee P. et al. Intestinal microbiota determine severity of myocardial infarction in rats. FASEB J. 2012;26(4):1727–1735. DOI: 10.1096/fj.11-197921.</mixed-citation><mixed-citation xml:lang="en">Lam V., Su J., Koprowski S., Hsu A., Tweddell J.S., Rafiee P. et al. Intestinal microbiota determine severity of myocardial infarction in rats. FASEB J. 2012;26(4):1727–1735. DOI: 10.1096/fj.11-197921.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Gan X.T., Ettinger G., Huang C.X., Burton J.P., Haist J.V. et al. Probiotic administration attenuates myocardial hypertrophy and heart failure after myocardial infarction in the rat. Circ. Heart Fail. 2014;7(3):491–499. DOI: 10.1161/CIRCHEARTFAILURE.113.000978.</mixed-citation><mixed-citation xml:lang="en">Gan X.T., Ettinger G., Huang C.X., Burton J.P., Haist J.V. et al. Probiotic administration attenuates myocardial hypertrophy and heart failure after myocardial infarction in the rat. Circ. Heart Fail. 2014;7(3):491–499. DOI: 10.1161/CIRCHEARTFAILURE.113.000978.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Lam V., Su J., Hsu A., Gross G.J., Salzman N.H., Baker J.E. Intestinal microbial metabolites are linked to severity of myocardial infarction in rats. PLoS One. 2016;11(8):e0160840. DOI: 10.1371/journal.pone.0160840.</mixed-citation><mixed-citation xml:lang="en">Lam V., Su J., Hsu A., Gross G.J., Salzman N.H., Baker J.E. Intestinal microbial metabolites are linked to severity of myocardial infarction in rats. PLoS One. 2016;11(8):e0160840. DOI: 10.1371/journal.pone.0160840.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Liu Z., Liu H.Y., Zhou H., Zhan Q., Lai W., Zeng Q. et al. Moderate-intensity exercise affects gut microbiome composition and influences cardiac function in myocardial infarction mice. Front. Microbiol. 2017;8:1687. DOI: 10.3389/fmicb.2017.01687.</mixed-citation><mixed-citation xml:lang="en">Liu Z., Liu H.Y., Zhou H., Zhan Q., Lai W., Zeng Q. et al. Moderate-intensity exercise affects gut microbiome composition and influences cardiac function in myocardial infarction mice. Front. Microbiol. 2017;8:1687. DOI: 10.3389/fmicb.2017.01687.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Sadeghzadeh J., Vakili A., Sameni H.R., Shadnoush M., Bandegi A.R., Zahedi Khorasani M. The effect of oral consumption of probiotics in prevention of heart injury in a rat myocardial infarction model: a histopathological, hemodynamic and biochemical evaluation. Iran Biomed. J. 2017;21(3):174–181. DOI: 10.18869/acadpub.ibj.21.3.174.</mixed-citation><mixed-citation xml:lang="en">Sadeghzadeh J., Vakili A., Sameni H.R., Shadnoush M., Bandegi A.R., Zahedi Khorasani M. The effect of oral consumption of probiotics in prevention of heart injury in a rat myocardial infarction model: a histopathological, hemodynamic and biochemical evaluation. Iran Biomed. J. 2017;21(3):174–181. DOI: 10.18869/acadpub.ibj.21.3.174.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Borshchev Y.Y., Minasian S.M., Burovenko I.Y., Borshchev V.Y., Protsak E.S., Semenova N.Y. et al. Effects of tetracycline on myocardial infarct size in obese rats with chemically-induced colitis. PLoS One. 2019;14(11):e0225185. DOI: 10.1371/journal.pone.0225185.</mixed-citation><mixed-citation xml:lang="en">Borshchev Y.Y., Minasian S.M., Burovenko I.Y., Borshchev V.Y., Protsak E.S., Semenova N.Y. et al. Effects of tetracycline on myocardial infarct size in obese rats with chemically-induced colitis. PLoS One. 2019;14(11):e0225185. DOI: 10.1371/journal.pone.0225185.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Trinei M., Carpi A., Menabo’ R., Storto M., Fornari M., Marinelli A. et al. Dietary intake of cyanidin-3-glucoside induces a long-lasting cardioprotection from ischemia/reperfusion injury by altering the microbiota. J. Nutr. Biochem. 2022;101:108921. DOI: 10.1016/j.jnutbio.2021.108921.</mixed-citation><mixed-citation xml:lang="en">Trinei M., Carpi A., Menabo’ R., Storto M., Fornari M., Marinelli A. et al. Dietary intake of cyanidin-3-glucoside induces a long-lasting cardioprotection from ischemia/reperfusion injury by altering the microbiota. J. Nutr. Biochem. 2022;101:108921. DOI: 10.1016/j.jnutbio.2021.108921.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Borshchev Y.Y., Burovenko I.Y., Karaseva A.B., Minasian S.M., Protsak E.S., Borshchev V.Y. et al. Probiotic therapy with Lactobacillus acidophilus and Bifidobacterium animalis subsp. lactis results in infarct size limitation in rats with obesity and chemically induced colitis. Microorganisms. 2022;10(11):2293. DOI: 10.3390/microorganisms10112293.</mixed-citation><mixed-citation xml:lang="en">Borshchev Y.Y., Burovenko I.Y., Karaseva A.B., Minasian S.M., Protsak E.S., Borshchev V.Y. et al. Probiotic therapy with Lactobacillus acidophilus and Bifidobacterium animalis subsp. lactis results in infarct size limitation in rats with obesity and chemically induced colitis. Microorganisms. 2022;10(11):2293. DOI: 10.3390/microorganisms10112293.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Borshchev Yu.Yu., Sonin D.L., Burovenko I.Yu., Borshchev V.Yu., Cheburkin Yu.V.,Borshcheva O.V. et al. The effect of probiotic strains on myocardial infarction size, biochemical and immunological parameters in rats with systemic inflammatory response syndrome and polymorbidity. J. Evol. Biochem. Physiol. 2022;58(6):2058–2069. DOI: 10.1134/S0022093022060321.</mixed-citation><mixed-citation xml:lang="en">Borshchev Yu.Yu., Sonin D.L., Burovenko I.Yu., Borshchev V.Yu., Cheburkin Yu.V.,Borshcheva O.V. et al. The effect of probiotic strains on myocardial infarction size, biochemical and immunological parameters in rats with systemic inflammatory response syndrome and polymorbidity. J. Evol. Biochem. Physiol. 2022;58(6):2058–2069. DOI: 10.1134/S0022093022060321.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Gagné M.A., Barbeau C., Frégeau G., Gilbert K., Mathieu O., Auger J. et al. Dysbiotic microbiota contributes to the extent of acute myocardial infarction in rats. Sci. Rep. 2022;12(1):16517. DOI: 10.1038/s41598022-20826-z.</mixed-citation><mixed-citation xml:lang="en">Gagné M.A., Barbeau C., Frégeau G., Gilbert K., Mathieu O., Auger J. et al. Dysbiotic microbiota contributes to the extent of acute myocardial infarction in rats. Sci. Rep. 2022;12(1):16517. DOI: 10.1038/s41598022-20826-z.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao J., Zhang Q., Cheng W., Dai Q., Wei Z., Guo M. et al. Heart-gut microbiota communication determines the severity of cardiac injury after myocardial ischaemia / reperfusion. Cardiovasc. Res. 2023;119(6):1390– 1402. DOI: 10.1093/cvr/cvad023.</mixed-citation><mixed-citation xml:lang="en">Zhao J., Zhang Q., Cheng W., Dai Q., Wei Z., Guo M. et al. Heart-gut microbiota communication determines the severity of cardiac injury after myocardial ischaemia / reperfusion. Cardiovasc. Res. 2023;119(6):1390– 1402. DOI: 10.1093/cvr/cvad023.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Zhong X., Zhao Y., Huang L., Liu J., Wang K., Gao X. et al. Remodeling of the gut microbiome by Lactobacillus johnsonii alleviates the development of acute myocardial infarction. Front. Microbiol. 2023;14:1140498. DOI: 10.3389/fmicb.2023.1140498.</mixed-citation><mixed-citation xml:lang="en">Zhong X., Zhao Y., Huang L., Liu J., Wang K., Gao X. et al. Remodeling of the gut microbiome by Lactobacillus johnsonii alleviates the development of acute myocardial infarction. Front. Microbiol. 2023;14:1140498. DOI: 10.3389/fmicb.2023.1140498.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Wu Z.X., Li S.F., Chen H., Song J.X., Gao Y.F., Zhang F. et al. The changes of gut microbiota after acute myocardial infarction in rats. PLoS One. 2017;12(7):e0180717. DOI: 10.1371/journal.pone.0180717.</mixed-citation><mixed-citation xml:lang="en">Wu Z.X., Li S.F., Chen H., Song J.X., Gao Y.F., Zhang F. et al. The changes of gut microbiota after acute myocardial infarction in rats. PLoS One. 2017;12(7):e0180717. DOI: 10.1371/journal.pone.0180717.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Цибульников С.Ю., Маслов Л.Н., Цепокина А.В., Хуторная М.В., Кутихин А.Г., Цибульникова М.Р. и др. Проблема конечного эффектора ишемического прекондиционирования сердца. Российский физиологический журнал им. И.М. Сеченова. 2016;102(4):421–435.</mixed-citation><mixed-citation xml:lang="en">Tsibulnikov S.Yu., Maslov L.N., Tsepokina A.V., Khutornaya M.V., Kutikhin A.G., Tsibulnikova M.R. et al. Problem of end effector of ischemic preconditioning of the heart. Russian journal of physiology. 2016;102(4):421–235. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Altamirano F., Wang Z.V., Hill J.A. Cardioprotection in ischaemia-reperfusion injury: novel mechanisms and clinical translation. J. Physiol. 2015;593(17):3773–3788. DOI: 10.1113/JP270953.</mixed-citation><mixed-citation xml:lang="en">Altamirano F., Wang Z.V., Hill J.A. Cardioprotection in ischaemia-reperfusion injury: novel mechanisms and clinical translation. J. Physiol. 2015;593(17):3773–3788. DOI: 10.1113/JP270953.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Шляхто Е.В., Нифонтов Е.М., Галагудза М.М. Ограничение ишемического и реперфузионного повреждения миокарда с помощью преи посткондиционирования: молекулярные механизмы и мишени для фармакотерапии. Креативная кардиология. 2007;1(2):75–101.</mixed-citation><mixed-citation xml:lang="en">Shlyakhto E.V., Nifontov E.M., Galagudza M.M. Limitation of ischemic and reperfusion myocardial injury using preand postconditioning: molecular mechanisms and targets for pharmacotherapy. Creative cardiology. 2007;1(2):75–101. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Lama Tamang R., Juritsch A.F., Ahmad R., Salomon J.D., Dhawan P., Ramer-Tait A.E. et al. The diet-microbiota axis: a key regulator of intestinal permeability in human health and disease. Tissue Barriers. 2023;11(2):2077069. DOI: 10.1080/21688370.2022.2077069.</mixed-citation><mixed-citation xml:lang="en">Lama Tamang R., Juritsch A.F., Ahmad R., Salomon J.D., Dhawan P., Ramer-Tait A.E. et al. The diet-microbiota axis: a key regulator of intestinal permeability in human health and disease. Tissue Barriers. 2023;11(2):2077069. DOI: 10.1080/21688370.2022.2077069.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Hanna A., Frangogiannis N.G. Inflammatory cytokines and chemokines as therapeutic targets in heart failure. Cardiovasc. Drugs Ther. 2020;34(6):849–863. DOI: 10.1007/s10557-020-07071-0.</mixed-citation><mixed-citation xml:lang="en">Hanna A., Frangogiannis N.G. Inflammatory cytokines and chemokines as therapeutic targets in heart failure. Cardiovasc. Drugs Ther. 2020;34(6):849–863. DOI: 10.1007/s10557-020-07071-0.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Belosjorow S., Bolle I., Duschin A., Heusch G., Schulz R. TNF-alpha antibodies are as effective as ischemic preconditioning in reducing infarct size in rabbits. Am. J. Physiol. Heart Circ. Physiol. 2003;284(3):H927– H930. DOI: 10.1152/ajpheart.00374.2002.</mixed-citation><mixed-citation xml:lang="en">Belosjorow S., Bolle I., Duschin A., Heusch G., Schulz R. TNF-alpha antibodies are as effective as ischemic preconditioning in reducing infarct size in rabbits. Am. J. Physiol. Heart Circ. Physiol. 2003;284(3):H927– H930. DOI: 10.1152/ajpheart.00374.2002.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Lin J., Li Q., Jin T., Wang J., Gong Y., Lv Q. et al. Cardiomyocyte IL-1R2 protects heart from ischemia/reperfusion injury by attenuating IL-17RA-mediated cardiomyocyte apoptosis. Cell Death Dis. 2022;13(1):90. DOI: 10.1038/s41419-022-04533-1.</mixed-citation><mixed-citation xml:lang="en">Lin J., Li Q., Jin T., Wang J., Gong Y., Lv Q. et al. Cardiomyocyte IL-1R2 protects heart from ischemia/reperfusion injury by attenuating IL-17RA-mediated cardiomyocyte apoptosis. Cell Death Dis. 2022;13(1):90. DOI: 10.1038/s41419-022-04533-1.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Karmazyn M., Gan X.T., Rajapurohitam V. The potential contribution of circulating and locally produced leptin to cardiac hypertrophy and failure. Can. J. Physiol. Pharmacol. 2013;91:883–888. DOI: 10.1139/cjpp-20130057.</mixed-citation><mixed-citation xml:lang="en">Karmazyn M., Gan X.T., Rajapurohitam V. The potential contribution of circulating and locally produced leptin to cardiac hypertrophy and failure. Can. J. Physiol. Pharmacol. 2013;91:883–888. DOI: 10.1139/cjpp-20130057.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Polyakova E.A., Mikhaylov E.N., Galagudza M.M., Shlyakhto E.V. Hyperleptinemia results in systemic inflammation and the exacerbation of ischemia-reperfusion myocardial injury. Heliyon. 2021;7(11):e08491. DOI: 10.1016/j.heliyon.2021.e08491.</mixed-citation><mixed-citation xml:lang="en">Polyakova E.A., Mikhaylov E.N., Galagudza M.M., Shlyakhto E.V. Hyperleptinemia results in systemic inflammation and the exacerbation of ischemia-reperfusion myocardial injury. Heliyon. 2021;7(11):e08491. DOI: 10.1016/j.heliyon.2021.e08491.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Chiang J.Y. Bile acid metabolism and signaling. Compr. Physiol. 2013;3(3):1191–1212. DOI: 10.1002/cphy.c120023.</mixed-citation><mixed-citation xml:lang="en">Chiang J.Y. Bile acid metabolism and signaling. Compr. Physiol. 2013;3(3):1191–1212. DOI: 10.1002/cphy.c120023.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Fiorucci S., Distrutti E. Bile acid-activated receptors, intestinal microbiota, and the treatment of metabolic disorders. Trends Mol. Med. 2015;21(11):702–714. DOI: 10.1016/j.molmed.2015.09.001.</mixed-citation><mixed-citation xml:lang="en">Fiorucci S., Distrutti E. Bile acid-activated receptors, intestinal microbiota, and the treatment of metabolic disorders. Trends Mol. Med. 2015;21(11):702–714. DOI: 10.1016/j.molmed.2015.09.001.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Pu J., Yuan A., Shan P., Gao E., Wang X., Wang Y. et al. Cardiomyocyte-expressed farnesoid-X-receptor is a novel apoptosis mediator and contributes to myocardial ischaemia/reperfusion injury. Eur. Heart J. 2013;34(24):1834–1845. DOI: 10.1093/eurheartj/ehs011.</mixed-citation><mixed-citation xml:lang="en">Pu J., Yuan A., Shan P., Gao E., Wang X., Wang Y. et al. Cardiomyocyte-expressed farnesoid-X-receptor is a novel apoptosis mediator and contributes to myocardial ischaemia/reperfusion injury. Eur. Heart J. 2013;34(24):1834–1845. DOI: 10.1093/eurheartj/ehs011.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Gao J., Liu X., Wang B., Xu H., Xia Q., Lu T. et al. Farnesoid X receptor deletion improves cardiac function, structure and remodeling following myocardial infarction in mice. Mol. Med. Rep. 2017;16(1):673–679. DOI: 10.3892/mmr.2017.6643.</mixed-citation><mixed-citation xml:lang="en">Gao J., Liu X., Wang B., Xu H., Xia Q., Lu T. et al. Farnesoid X receptor deletion improves cardiac function, structure and remodeling following myocardial infarction in mice. Mol. Med. Rep. 2017;16(1):673–679. DOI: 10.3892/mmr.2017.6643.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Gao Y., Zhao Y., Yuan A., Xu L., Huang X., Su Y. et al. Effects of farnesoid-X-receptor SUMOylation mutation on myocardial ischemia / reperfusion injury in mice. Exp. Cell. Res. 2018;371(2):301–310. DOI: 10.1016/j.yexcr.2018.07.004.</mixed-citation><mixed-citation xml:lang="en">Gao Y., Zhao Y., Yuan A., Xu L., Huang X., Su Y. et al. Effects of farnesoid-X-receptor SUMOylation mutation on myocardial ischemia / reperfusion injury in mice. Exp. Cell. Res. 2018;371(2):301–310. DOI: 10.1016/j.yexcr.2018.07.004.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Wang J., Zhang J., Lin X., Wang Y., Wu X., Yang F. et al. DCA-TGR5 signaling activation alleviates inflammatory response and improves cardiac function in myocardial infarction. J. Mol. Cell. Cardiol. 2021;151:3–14. DOI: 10.1016/j.yjmcc.2020.10.014.</mixed-citation><mixed-citation xml:lang="en">Wang J., Zhang J., Lin X., Wang Y., Wu X., Yang F. et al. DCA-TGR5 signaling activation alleviates inflammatory response and improves cardiac function in myocardial infarction. J. Mol. Cell. Cardiol. 2021;151:3–14. DOI: 10.1016/j.yjmcc.2020.10.014.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Thomas C., Gioiello A., Noriega L., Strehle A., Oury J., Rizzo G. et al. TGR5-mediated bile acid sensing controls glucose homeostasis. Cell. Metab. 2009;10(3):167–177. DOI: 10.1016/j.cmet.2009.08.001.</mixed-citation><mixed-citation xml:lang="en">Thomas C., Gioiello A., Noriega L., Strehle A., Oury J., Rizzo G. et al. TGR5-mediated bile acid sensing controls glucose homeostasis. Cell. Metab. 2009;10(3):167–177. DOI: 10.1016/j.cmet.2009.08.001.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Ravassa S., Zudaire A., Díez J. GLP-1 and cardioprotection: from bench to bedside. Cardiovasc. Res. 2012;94(2):316–323. DOI: 10.1093/cvr/cvs123.</mixed-citation><mixed-citation xml:lang="en">Ravassa S., Zudaire A., Díez J. GLP-1 and cardioprotection: from bench to bedside. Cardiovasc. Res. 2012;94(2):316–323. DOI: 10.1093/cvr/cvs123.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Lu Y., Zhang Y., Zhao X., Shang C., Xiang M., Li L., Cui X. Microbiota-derived short-chain fatty acids: Implications for cardiovascular and metabolic disease. Front. Cardiovasc. Med. 2022;9:900381. DOI: 10.3389/fcvm.2022.900381.</mixed-citation><mixed-citation xml:lang="en">Lu Y., Zhang Y., Zhao X., Shang C., Xiang M., Li L., Cui X. Microbiota-derived short-chain fatty acids: Implications for cardiovascular and metabolic disease. Front. Cardiovasc. Med. 2022;9:900381. DOI: 10.3389/fcvm.2022.900381.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Chang P.V., Hao L., Offermanns S., Medzhitov R. The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition. Proc. Natl. Acad. Sci. USA. 2014;111(6):2247– 2252. DOI: 10.1073/pnas.1322269111.</mixed-citation><mixed-citation xml:lang="en">Chang P.V., Hao L., Offermanns S., Medzhitov R. The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition. Proc. Natl. Acad. Sci. USA. 2014;111(6):2247– 2252. DOI: 10.1073/pnas.1322269111.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Lymperopoulos A., Suster M.S., Borges J.I. Short-chain fatty acid receptors and cardiovascular function. Int. J. Mol. Sci. 2022;23(6):3303. DOI: 10.3390/ijms23063303.</mixed-citation><mixed-citation xml:lang="en">Lymperopoulos A., Suster M.S., Borges J.I. Short-chain fatty acid receptors and cardiovascular function. Int. J. Mol. Sci. 2022;23(6):3303. DOI: 10.3390/ijms23063303.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Deng F., Zhang L.Q., Wu H., Chen Y., Yu W.Q., Han R.H. et al. Propionate alleviates myocardial ischemia-reperfusion injury aggravated by Angiotensin II dependent on caveolin-1/ACE2 axis through GPR41. Int. J. Biol. Sci. 2022;18(2):858–872. DOI: 10.7150/ijbs.67724.</mixed-citation><mixed-citation xml:lang="en">Deng F., Zhang L.Q., Wu H., Chen Y., Yu W.Q., Han R.H. et al. Propionate alleviates myocardial ischemia-reperfusion injury aggravated by Angiotensin II dependent on caveolin-1/ACE2 axis through GPR41. Int. J. Biol. Sci. 2022;18(2):858–872. DOI: 10.7150/ijbs.67724.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Tang T.W.H., Chen H.C., Chen C.Y., Yen C.Y.T., Lin C.J., PrajnamitraR.P. et al. Loss of gut microbiota alters immune system composition and cripples postinfarction cardiac repair. Circulation. 2019;139(5):647–659. DOI: 10.1161/CIRCULATIONAHA.118.035235.</mixed-citation><mixed-citation xml:lang="en">Tang T.W.H., Chen H.C., Chen C.Y., Yen C.Y.T., Lin C.J., PrajnamitraR.P. et al. Loss of gut microbiota alters immune system composition and cripples postinfarction cardiac repair. Circulation. 2019;139(5):647–659. DOI: 10.1161/CIRCULATIONAHA.118.035235.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Lin C.J., Cheng Y.C., Chen H.C., Chao Y.K., Nicholson M.W., Yen E.C.L. et al. Commensal gut microbiota-derived acetate and propionate enhance heart adaptation in response to cardiac pressure overload in mice. Theranostics. 2022;12(17):7319–7334. DOI: 10.7150/thno.76002.</mixed-citation><mixed-citation xml:lang="en">Lin C.J., Cheng Y.C., Chen H.C., Chao Y.K., Nicholson M.W., Yen E.C.L. et al. Commensal gut microbiota-derived acetate and propionate enhance heart adaptation in response to cardiac pressure overload in mice. Theranostics. 2022;12(17):7319–7334. DOI: 10.7150/thno.76002.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Sun Y., Zhou C., Chen Y., He X., Gao F., Xue D. Quantitative increase in short-chain fatty acids, especially butyrate protects kidney from ischemia/reperfusion injury. J. Investig. Med. 2022;70(1):29–35. DOI: 10.1136/jim-2020-001715.</mixed-citation><mixed-citation xml:lang="en">Sun Y., Zhou C., Chen Y., He X., Gao F., Xue D. Quantitative increase in short-chain fatty acids, especially butyrate protects kidney from ischemia/reperfusion injury. J. Investig. Med. 2022;70(1):29–35. DOI: 10.1136/jim-2020-001715.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Chen R., Xu Y., Wu P., Zhou H., Lasanajak Y., Fang Y. et al. Transplantation of fecal microbiota rich in short chain fatty acids and butyric acid treat cerebral ischemic stroke by regulating gut microbiota. Pharmacol. Res. 2019;148:104403. DOI: 10.1016/j.phrs.2019.104403.</mixed-citation><mixed-citation xml:lang="en">Chen R., Xu Y., Wu P., Zhou H., Lasanajak Y., Fang Y. et al. Transplantation of fecal microbiota rich in short chain fatty acids and butyric acid treat cerebral ischemic stroke by regulating gut microbiota. Pharmacol. Res. 2019;148:104403. DOI: 10.1016/j.phrs.2019.104403.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Baba A.A., Srinivas M., Shariff A., Nazir T. Role of short chain fatty acids in mesenteric ischemia reperfusion injury in rats. Eur. J. Pediatr. Surg. 2010;20(2):98–101. DOI: 10.1055/s-0029-1241836.</mixed-citation><mixed-citation xml:lang="en">Baba A.A., Srinivas M., Shariff A., Nazir T. Role of short chain fatty acids in mesenteric ischemia reperfusion injury in rats. Eur. J. Pediatr. Surg. 2010;20(2):98–101. DOI: 10.1055/s-0029-1241836.</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>
