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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">ometendo</journal-id><journal-title-group><journal-title xml:lang="ru">Ожирение и метаболизм</journal-title><trans-title-group xml:lang="en"><trans-title>Obesity and metabolism</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2071-8713</issn><issn pub-type="epub">2306-5524</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/omet13097</article-id><article-id custom-type="elpub" pub-id-type="custom">ometendo-13097</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>Патофизиологические взаимосвязи метаболического синдрома и микробиоты кишечника</article-title><trans-title-group xml:lang="en"><trans-title>Pathophysiologic interrelationships of metabolic syndrome and gut microbiota</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1577-7077</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Климчук</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Klimchuk</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Климчук Анастасия Васильевна, к.м.н., доцент кафедры внутренней медицины №2</p><p>Симферополь</p></bio><bio xml:lang="en"><p>Anastasia V. Klimchuk, Associate Professor, Department of Internal Medicine No. 2</p><p>Simferopol</p></bio><email xlink:type="simple">anastasiya-klim@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/0009-0007-1828-5496</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Крицкая</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kritskaya</surname><given-names>D. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Крицкая Дарья Владимировна, студентка кафедры внутренней медицины №2</p><p>Scopus Author ID: 1233361</p><p>Симферополь</p></bio><bio xml:lang="en"><p>Daria V. Kritskaya, Student, Department of Internal Medicine No. 2</p><p>Scopus Author ID: 1233361</p><p>Simferopol</p></bio><email xlink:type="simple">dari.kritccc@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/0009-0001-8235-7315</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ивашкова</surname><given-names>Е. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivashkova</surname><given-names>E. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ивашкова Екатерина Олеговна, студентка кафедры внутренней медицины №2</p><p>Симферополь</p></bio><bio xml:lang="en"><p>Ekaterina O. Ivashkova, Student, Department of Internal Medicine No. 2</p><p>Simferopol</p></bio><email xlink:type="simple">ivashkova.catya@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/0000-0001-5175-4468</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коновалова</surname><given-names>П. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Konovalova</surname><given-names>P. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Коновалова Полина Сергеевна, ординатор кафедры терапии</p><p>Москва</p><p> </p></bio><bio xml:lang="en"><p>Polina S. Konovalova, Resident of the Department of Internal Medicine</p><p>Moscow</p></bio><email xlink:type="simple">ponyllin@bk.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5486-7262</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Яцков</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Yatskov</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Яцков Игорь Анатольевич, к.м.н., доцент кафедры внутренней медицины №2</p><p>Scopus Author ID:  57218873902</p><p>295051, Симферополь, бульвар Ленина 5/7 </p></bio><bio xml:lang="en"><p>Igor A. Yatskov, PhD, Associate Professor, Department of Internal Medicine No. 2</p><p>295051, Lenin boulevard 5/7, Simferopol</p></bio><email xlink:type="simple">egermd@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Ордена Трудового Красного Знамени Медицинский Институт имени С. И. Георгиевского ФГАОУ ВО «Крымский федеральный университет имени В. И. Вернадского»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Order of the Red Banner of Labor S. I. Georgievsky Medical Institute V. I. Vernadsky Crimean Federal University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБУ «ГНЦ РФ ФМБЦ им. А.И. Бурназяна»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>FGBU "State Research Center RF FMBC named after A.I. Burnazyan"</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>09</day><month>12</month><year>2025</year></pub-date><volume>22</volume><issue>3</issue><fpage>222</fpage><lpage>228</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Климчук А.В., Крицкая Д.В., Ивашкова Е.О., Коновалова П.С., Яцков И.А., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Климчук А.В., Крицкая Д.В., Ивашкова Е.О., Коновалова П.С., Яцков И.А.</copyright-holder><copyright-holder xml:lang="en">Klimchuk A.V., Kritskaya D.V., Ivashkova E.O., Konovalova P.S., Yatskov I.A.</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.omet-endojournals.ru/jour/article/view/13097">https://www.omet-endojournals.ru/jour/article/view/13097</self-uri><abstract><p>В условиях современного мира все глобальнее становится проблема ожирения и метаболического синдрома. Социальные и экологические факторы, играющие роль в развитии этих состояний, еще не до конца изучены, однако уже сейчас накапливаются данные, свидетельствующие о том, что развитию ожирения и метаболического синдрома способствуют неблагоприятные условия раннего периода жизни, например, заболевания матери в периоды беременности и лактации, использование различных химических и лекарственных агентов, низкая масса плода при рождении, неблагоприятные режим и качество питания. Все эти факторы оказывают воздействие на состояние желудочно-кишечного тракта, в частности приводят к дисбалансу кишечной микрофлоры. Накапливаются данные о том, что микробиом кишечника людей с ожирением структурно и функционально отличен от микрофлоры кишечника здорового человека. Выявление прочной корреляционной связи между этими параметрами может открыть перспективы для профилактики метаболического синдрома и всех ассоциированных с ним состояний путем поддержания здоровья кишечной микрофлоры. Целью данной статьи является освещение данных исследований, проводимых на животных и людях, которые подтверждают наличие патофизиологических механизмов влияния кишечной микрофлоры на развитие ожирения и сопутствующего метаболического синдрома, а также поиск возможностей профилактики данных состояний посредством добавления пре- и пробиотиков к пище.</p></abstract><trans-abstract xml:lang="en"><p>The problem of obesity and metabolic syndrome is becoming increasingly global in the modern world. The social and environmental factors that play a role in the development of these conditions are not yet fully understood, but there is already accumulating evidence that the development of obesity and metabolic syndrome is promoted by unfavorable conditions in early life, such as maternal diseases during pregnancy and lactation, the use of various chemical and medicinal agents, low birth weight of the fetus, and unfavorable dietary patterns and quality of nutrition. All these factors have their impact on the gastrointestinal tract, particularly leading to an imbalance of the intestinal microflora. Evidence is accumulating that the gut microbiome of obese people is structurally and functionally different from the gut microflora of healthy people. The identification of a strong correlation between these parameters may offer prospects for the prevention of metabolic syndrome and all associated conditions by maintaining the health of the gut microflora. The aim of this article is to highlight the data from animal and human studies that confirm the presence of pathophysiological mechanisms of the influence of the intestinal microflora on the development of obesity and the associated metabolic syndrome, and to search for opportunities to prevent these conditions through the addition of pre- and probiotics to food.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>микробиом кишечника</kwd><kwd>микробиота</kwd><kwd>ожирение</kwd><kwd>метаболический синдром</kwd></kwd-group><kwd-group xml:lang="en"><kwd>intestinal microbiome</kwd><kwd>microbiota</kwd><kwd>obesity</kwd><kwd>metabolic syndrome</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена по инициативе авторов без привлечения финансирования.</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">Dinan TG, Cryan JF. Brain–gut–microbiota axis—Mood, metabolism and behaviour. Nat. Rev. Gastroenterol. Hepatol. 2017;14:69–70. doi: https://doi.org/10.1111/spc3.12309</mixed-citation><mixed-citation xml:lang="en">Dinan TG, Cryan JF. Brain–gut–microbiota axis—Mood, metabolism and behaviour. Nat. Rev. Gastroenterol. Hepatol. 2017;14:69–70. doi: https://doi.org/10.1111/spc3.12309</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Bäckhed F, Ley RE, Sonnenburg JL, et al. Host-Bacterial Mutualism in the Human Intestine. Science. 2005;307:1915. doi: https://doi.org/10.1126/science.1104816</mixed-citation><mixed-citation xml:lang="en">Bäckhed F, Ley RE, Sonnenburg JL, et al. Host-Bacterial Mutualism in the Human Intestine. Science. 2005;307:1915. doi: https://doi.org/10.1126/science.1104816</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Bäckhed F, Ding H, Wang T, et al. The gutmicrobiota as an environmental factor that regulates fat storage. Proc. Natl. Acad. Sci. USA. 2004;101:15718. doi: https://doi.org/10.1073/pnas.0407076101</mixed-citation><mixed-citation xml:lang="en">Bäckhed F, Ding H, Wang T, et al. The gutmicrobiota as an environmental factor that regulates fat storage. Proc. Natl. Acad. Sci. USA. 2004;101:15718. doi: https://doi.org/10.1073/pnas.0407076101</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Белоглазов В.А., Яцков И.А., Кумельский Е.Д., Половинкина В.В. Метаболическая эндотоксинемия: возможные причины и последствия // Ожирение и метаболизм. — 2021. — Т.18. — №3 — С.320-326. doi: https://doi.org/10.14341/omet12750</mixed-citation><mixed-citation xml:lang="en">Beloglazov VA, Yatskov IA, Kumelsky ED, Polovinkina VV. Metabolic endotoxemia: possible causes and consequences. Obesity and metabolism. 2021;18(3):320-326. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Thaiss CA, Itav S, Rothschild D, et al. Persistent microbiome alterations modulate the rate of post-dieting weight regain. Nature. 2016;540:544–551. doi: https://doi.org/10.1038/nature20796</mixed-citation><mixed-citation xml:lang="en">Thaiss CA, Itav S, Rothschild D, et al. Persistent microbiome alterations modulate the rate of post-dieting weight regain. Nature. 2016;540:544–551. doi: https://doi.org/10.1038/nature20796</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Sonnenburg ED, Smits SA, Tikhonov M, et al. Diet-induced extinctions in the gut microbiota compound over generations. Nature. 2016;529:212–215. doi: https://doi.org/10.1038/nature16504</mixed-citation><mixed-citation xml:lang="en">Sonnenburg ED, Smits SA, Tikhonov M, et al. Diet-induced extinctions in the gut microbiota compound over generations. Nature. 2016;529:212–215. doi: https://doi.org/10.1038/nature16504</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Lecerf J-M, Dépeint F, Clerc E, et al. Xylo-oligosaccharide (XOS) in combination with inulin modulates both the intestinal environment and immune status in healthy subjects, while XOS alone only shows prebiotic properties. Br. J. Nutr. 2012;108:1847–1858. doi: https://doi.org/10.1017/S0007114511007252</mixed-citation><mixed-citation xml:lang="en">Lecerf J-M, Dépeint F, Clerc E, et al. Xylo-oligosaccharide (XOS) in combination with inulin modulates both the intestinal environment and immune status in healthy subjects, while XOS alone only shows prebiotic properties. Br. J. Nutr. 2012;108:1847–1858. doi: https://doi.org/10.1017/S0007114511007252</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Turnbaugh PJ, Ley RE, Mahowald MA, et al. An obesity-associated gut microbiome with increased capacity for energy harvest. Nature. 2006;444:1027–1031. doi: https://doi.org/10.1038/nature05414</mixed-citation><mixed-citation xml:lang="en">Turnbaugh PJ, Ley RE, Mahowald MA, et al. An obesity-associated gut microbiome with increased capacity for energy harvest. Nature. 2006;444:1027–1031. doi: https://doi.org/10.1038/nature05414</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Ridaura VK, Faith JJ, Rey FE, et al. Gut microbiota from twins discordant for obesity modulate metabolism in mice. Science (80- ). 2013. doi: https://doi.org/10.1126/science.1241214</mixed-citation><mixed-citation xml:lang="en">Ridaura VK, Faith JJ, Rey FE, et al. Gut microbiota from twins discordant for obesity modulate metabolism in mice. Science (80- ). 2013. doi: https://doi.org/10.1126/science.1241214</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Ley RE, Turnbaugh PJ, Klein S, Gordon JI. Human gut microbes associated with obesity. Nature. 2006;444:1022–1023. doi: https://doi.org/10.1038/4441022a</mixed-citation><mixed-citation xml:lang="en">Ley RE, Turnbaugh PJ, Klein S, Gordon JI. Human gut microbes associated with obesity. Nature. 2006;444:1022–1023. doi: https://doi.org/10.1038/4441022a</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Ley RE, Bäckhed F, Turnbaugh P, et al. Obesity alters gut microbialecology. Proc. Natl. Acad. Sci. USA. 2005;102:11070. doi: https://doi.org/10.1073/pnas.0504978102</mixed-citation><mixed-citation xml:lang="en">Ley RE, Bäckhed F, Turnbaugh P, et al. Obesity alters gut microbialecology. Proc. Natl. Acad. Sci. USA. 2005;102:11070. doi: https://doi.org/10.1073/pnas.0504978102</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Nadal I, Santacruz A, Marcos A, et al. Shifts in clostridia, bacteroides and immunoglobulin-coating fecalbacteria associated with weight loss in obese adolescents. Int. J. Obes. 2009;33:758–767. doi: https://doi.org/10.1038/ijo.2008.260</mixed-citation><mixed-citation xml:lang="en">Nadal I, Santacruz A, Marcos A, et al. Shifts in clostridia, bacteroides and immunoglobulin-coating fecalbacteria associated with weight loss in obese adolescents. Int. J. Obes. 2009;33:758–767. doi: https://doi.org/10.1038/ijo.2008.260</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Remely M, Tesar I, Hippe B, et al. Gut microbiota composition correlateswith changes in body fat content due to weight loss. Benef. Microbes. 2015;6:431–439. doi: https://doi.org/10.3920/BM2014.0104</mixed-citation><mixed-citation xml:lang="en">Remely M, Tesar I, Hippe B, et al. Gut microbiota composition correlateswith changes in body fat content due to weight loss. Benef. Microbes. 2015;6:431–439. doi: https://doi.org/10.3920/BM2014.0104</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Sze MA, Schloss PD. Looking for a Signal in the Noise: Revisiting Obesity and the Microbiome. MBio. 2016;7:e01018-16. doi: https://doi.org/10.1128/mbio.01018-16</mixed-citation><mixed-citation xml:lang="en">Sze MA, Schloss PD. Looking for a Signal in the Noise: Revisiting Obesity and the Microbiome. MBio. 2016;7:e01018-16. doi: https://doi.org/10.1128/mbio.01018-16</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Le Chatelier E, Nielsen T, Qin J, et al. Richness of human gut microbiome correlates with metabolic markers. Nature. 2013;500:541–546. doi: https://doi.org/10.1038/nature12506</mixed-citation><mixed-citation xml:lang="en">Le Chatelier E, Nielsen T, Qin J, et al. Richness of human gut microbiome correlates with metabolic markers. Nature. 2013;500:541–546. doi: https://doi.org/10.1038/nature12506</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Turnbaugh PJ, Hamady M, Yatsunenko T, et al. A core gut microbiome in obese and lean twins. Nature. 2009;457:480–484. doi: https://doi.org/10.1038/nature07540</mixed-citation><mixed-citation xml:lang="en">Turnbaugh PJ, Hamady M, Yatsunenko T, et al. A core gut microbiome in obese and lean twins. Nature. 2009;457:480–484. doi: https://doi.org/10.1038/nature07540</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Canfora EE, Meex RCR, Venema K, Blaak EE. Gut microbial metabolites in obesity, NAFLD and T2DM. Nat. Rev. Endocrinol. 2019;15:261–273. doi: https://doi.org/10.1038/s41574-019-0156-z</mixed-citation><mixed-citation xml:lang="en">Canfora EE, Meex RCR, Venema K, Blaak EE. Gut microbial metabolites in obesity, NAFLD and T2DM. Nat. Rev. Endocrinol. 2019;15:261–273. doi: https://doi.org/10.1038/s41574-019-0156-z</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Nehra V, Allen JM, Mailing LJ, et al. Gut Microbiota: Modulation of Host Physiology in Obesity. Physiology. 2016.31:327–335. doi: https://doi.org/10.1152/physiol.00005.2016</mixed-citation><mixed-citation xml:lang="en">Nehra V, Allen JM, Mailing LJ, et al. Gut Microbiota: Modulation of Host Physiology in Obesity. Physiology. 2016.31:327–335. doi: https://doi.org/10.1152/physiol.00005.2016</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Roediger WEW. Utilization of Nutrients by Isolated Epithelial Cells of the Rat Colon. Gastroenterology. 1982;83:424–429</mixed-citation><mixed-citation xml:lang="en">Roediger WEW. Utilization of Nutrients by Isolated Epithelial Cells of the Rat Colon. Gastroenterology. 1982;83:424–429</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Bergman EN. Energy contributions of volatile fatty acids from the gastrointestinal tract in various species. Physiol. Rev. 1990;70:567–590. doi: https://doi.org/10.1152/physrev.1990.70.2.567</mixed-citation><mixed-citation xml:lang="en">Bergman EN. Energy contributions of volatile fatty acids from the gastrointestinal tract in various species. Physiol. Rev. 1990;70:567–590. doi: https://doi.org/10.1152/physrev.1990.70.2.567</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Den Besten G, Lange K, Havinga R, et al. Gut-derived short-chain fatty acids are vividly assimilated into hostcarbohydrates and lipids. Am. J. Physiol. Gastrointest. Liver Physiol. 2013; 305:G900–G910. doi: https://doi.org/10.1152/ajpgi.00265.2013</mixed-citation><mixed-citation xml:lang="en">Den Besten G, Lange K, Havinga R, et al. Gut-derived short-chain fatty acids are vividly assimilated into hostcarbohydrates and lipids. Am. J. Physiol. Gastrointest. Liver Physiol. 2013; 305:G900–G910. doi: https://doi.org/10.1152/ajpgi.00265.2013</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Høverstad T, Midtvedt T. Short-Chain Fatty Acids in Germfree Mice and Rats. J. Nutr. 1986;116:1772–1776. doi: https://doi.org/10.1093/jn/116.9.1772</mixed-citation><mixed-citation xml:lang="en">Høverstad T, Midtvedt T. Short-Chain Fatty Acids in Germfree Mice and Rats. J. Nutr. 1986;116:1772–1776. doi: https://doi.org/10.1093/jn/116.9.1772</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Agustí A, García-Pardo MP, López-Almela I, et al. Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function. Front. Neurosci. 2018;12:155. doi: https://doi.org/10.3389/fnins.2018.00155</mixed-citation><mixed-citation xml:lang="en">Agustí A, García-Pardo MP, López-Almela I, et al. Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function. Front. Neurosci. 2018;12:155. doi: https://doi.org/10.3389/fnins.2018.00155</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Fernandes J, Su W, Rahat-Rozenbloom S, et al. Adiposity, gut microbiota andfaecal short chain fatty acids are linked in adult humans. Nutr. Diabetes. 2014;4:e121. doi: https://doi.org/10.1038/nutd.2014.23</mixed-citation><mixed-citation xml:lang="en">Fernandes J, Su W, Rahat-Rozenbloom S, et al. Adiposity, gut microbiota andfaecal short chain fatty acids are linked in adult humans. Nutr. Diabetes. 2014;4:e121. doi: https://doi.org/10.1038/nutd.2014.23</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Schwiertz A, Taras D, Schäfer K, et al. Microbiota and SCFA in Lean and Overweight Healthy Subjects. Obesity. 2010;18:190–195. doi: https://doi.org/10.1038/oby.2009.167</mixed-citation><mixed-citation xml:lang="en">Schwiertz A, Taras D, Schäfer K, et al. Microbiota and SCFA in Lean and Overweight Healthy Subjects. Obesity. 2010;18:190–195. doi: https://doi.org/10.1038/oby.2009.167</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Gogineni V, Morrow L, Malesker M, Gregory P. Probiotics: History and Evolution. J. Anc. Dis. Prev. Remedies. 2013;1:1–7. doi: https://doi.org/10.3920/BM2014.0103</mixed-citation><mixed-citation xml:lang="en">Gogineni V, Morrow L, Malesker M, Gregory P. Probiotics: History and Evolution. J. Anc. Dis. Prev. Remedies. 2013;1:1–7. doi: https://doi.org/10.3920/BM2014.0103</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Belobrajdi DP, King RA, Christophersen CT, Bird AR. Dietary resistant starch dose-dependently reduces adiposity in obesityprone and obesity-resistant male rats. Nutr. Metab. 2012;9:93. doi: https://doi.org/10.1186/1743-7075-9-93</mixed-citation><mixed-citation xml:lang="en">Belobrajdi DP, King RA, Christophersen CT, Bird AR. Dietary resistant starch dose-dependently reduces adiposity in obesityprone and obesity-resistant male rats. Nutr. Metab. 2012;9:93. doi: https://doi.org/10.1186/1743-7075-9-93</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Samuel BS, Shaito A, Motoike T, et al. Effects of the gut microbiota on host adiposity are modulated by the short-chain fatty-acid binding G protein-coupled receptor, Gpr41. Proc. Natl. Acad. Sci. USA. 2008;105:16767. doi: https://doi.org/10.1073/pnas.0808567105</mixed-citation><mixed-citation xml:lang="en">Samuel BS, Shaito A, Motoike T, et al. Effects of the gut microbiota on host adiposity are modulated by the short-chain fatty-acid binding G protein-coupled receptor, Gpr41. Proc. Natl. Acad. Sci. USA. 2008;105:16767. doi: https://doi.org/10.1073/pnas.0808567105</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">De Vadder F, Kovatcheva-Datchary P, Goncalves D, et al. Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits. Cell. 2014;156:84–96. doi: https://doi.org/10.1016/j.cell.2013.12.016</mixed-citation><mixed-citation xml:lang="en">De Vadder F, Kovatcheva-Datchary P, Goncalves D, et al. Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits. Cell. 2014;156:84–96. doi: https://doi.org/10.1016/j.cell.2013.12.016</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Tolhurst G, Heffron H, Lam YS, et al. Short-Chain Fatty Acids Stimulate Glucagon-Like Peptide-1 Secretion via the G-Protein–Coupled Receptor FFAR2. Diabetes. 2012;61:364. doi: https://doi.org/10.2337/db11-1019</mixed-citation><mixed-citation xml:lang="en">Tolhurst G, Heffron H, Lam YS, et al. Short-Chain Fatty Acids Stimulate Glucagon-Like Peptide-1 Secretion via the G-Protein–Coupled Receptor FFAR2. Diabetes. 2012;61:364. doi: https://doi.org/10.2337/db11-1019</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Zaibi MS, Stocker CJ, O’Dowd J, et al. Roles of GPR41 and GPR43 in leptin secretory responses of murine adipocytes to short chainfatty acids. FEBS Lett. 2010;584:2381–2386. doi: https://doi.org/10.1016/j.febslet.2010.04.027</mixed-citation><mixed-citation xml:lang="en">Zaibi MS, Stocker CJ, O’Dowd J, et al. Roles of GPR41 and GPR43 in leptin secretory responses of murine adipocytes to short chainfatty acids. FEBS Lett. 2010;584:2381–2386. doi: https://doi.org/10.1016/j.febslet.2010.04.027</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Forbes S, Stafford S, Coope G, et al. Selective FFA2 Agonism Appears to Act via Intestinal PYY to Reduce Transit and Food Intake but Does Not Improve Glucose Tolerance in Mouse Models. Diabetes. 2015;64:3763. doi: https://doi.org/10.2337/db15-0481</mixed-citation><mixed-citation xml:lang="en">Forbes S, Stafford S, Coope G, et al. Selective FFA2 Agonism Appears to Act via Intestinal PYY to Reduce Transit and Food Intake but Does Not Improve Glucose Tolerance in Mouse Models. Diabetes. 2015;64:3763. doi: https://doi.org/10.2337/db15-0481</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou J, Martin RJ, Tulley RT, et al. Dietary resistant starch upregulates total GLP-1 and PYY in a sustained daylongmanner through fermentation in rodents. Am. J. Physiol. Endocrinol. Metab. 2008;295:E1160–E1166. doi: https://doi.org/10.1152/ajpendo.90637.2008</mixed-citation><mixed-citation xml:lang="en">Zhou J, Martin RJ, Tulley RT, et al. Dietary resistant starch upregulates total GLP-1 and PYY in a sustained daylongmanner through fermentation in rodents. Am. J. Physiol. Endocrinol. Metab. 2008;295:E1160–E1166. doi: https://doi.org/10.1152/ajpendo.90637.2008</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Chambers ES, Viardot A, Psichas A, et al. Effects of targeted delivery of propionate to the human colonon appetite regulation, body weight maintenance and adiposity in overweight adults. Gut. 2015;64:1744. doi: https://doi.org/10.1136/gutjnl-2014-307913</mixed-citation><mixed-citation xml:lang="en">Chambers ES, Viardot A, Psichas A, et al. Effects of targeted delivery of propionate to the human colonon appetite regulation, body weight maintenance and adiposity in overweight adults. Gut. 2015;64:1744. doi: https://doi.org/10.1136/gutjnl-2014-307913</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Frost G, Sleeth ML, Sahuri-Arisoylu M, et al. The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism. Nat. Commun. 2014;5:3611. doi: https://doi.org/10.1038/ncomms4611</mixed-citation><mixed-citation xml:lang="en">Frost G, Sleeth ML, Sahuri-Arisoylu M, et al. The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism. Nat. Commun. 2014;5:3611. doi: https://doi.org/10.1038/ncomms4611</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Li Z, Yi C-X, Katiraei S, et al. Butyrate reduces appetite and activates brown adipose tissue via the gut-brain neural circuit. Gut. 2018;67:1269. doi: https://doi.org/10.1136/gutjnl-2017-314050</mixed-citation><mixed-citation xml:lang="en">Li Z, Yi C-X, Katiraei S, et al. Butyrate reduces appetite and activates brown adipose tissue via the gut-brain neural circuit. Gut. 2018;67:1269. doi: https://doi.org/10.1136/gutjnl-2017-314050</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Goswami C, Iwasaki Y, Yada T. Short-chain fatty acids suppress food intake by activating vagal afferent neurons. J. Nutr. Biochem. 2018;57:130–135. doi: https://doi.org/10.1016/j.jnutbio.2018.03.009</mixed-citation><mixed-citation xml:lang="en">Goswami C, Iwasaki Y, Yada T. Short-chain fatty acids suppress food intake by activating vagal afferent neurons. J. Nutr. Biochem. 2018;57:130–135. doi: https://doi.org/10.1016/j.jnutbio.2018.03.009</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Gao Z, Yin J, Zhang J, et al. Butyrate Improves Insulin Sensitivity and Increases Energy Expenditure in Mice. Diabetes. 2009;58:1509. doi: https://doi.org/10.2337/db08-1637</mixed-citation><mixed-citation xml:lang="en">Gao Z, Yin J, Zhang J, et al. Butyrate Improves Insulin Sensitivity and Increases Energy Expenditure in Mice. Diabetes. 2009;58:1509. doi: https://doi.org/10.2337/db08-1637</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Sahuri-Arisoylu M, Brody LP, Parkinson JR, et al. Reprogramming of hepatic fat accumulation and ‘browning’ of adipose tissue by theshort-chain fatty acid acetate. Int. J. Obes. 2016;40:955–963. doi: https://doi.org/10.1038/ijo.2016.23</mixed-citation><mixed-citation xml:lang="en">Sahuri-Arisoylu M, Brody LP, Parkinson JR, et al. Reprogramming of hepatic fat accumulation and ‘browning’ of adipose tissue by theshort-chain fatty acid acetate. Int. J. Obes. 2016;40:955–963. doi: https://doi.org/10.1038/ijo.2016.23</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Kondo T, Kishi M, Fushimi T, Kaga T. Acetic Acid Upregulates the Expression of Genes for Fatty Acid Oxidation Enzymes in Liver To Suppress Body Fat Accumulation. J. Agric. Food Chem. 2009;57:5982–5986. doi: https://doi.org/10.1021/jf900470c</mixed-citation><mixed-citation xml:lang="en">Kondo T, Kishi M, Fushimi T, Kaga T. Acetic Acid Upregulates the Expression of Genes for Fatty Acid Oxidation Enzymes in Liver To Suppress Body Fat Accumulation. J. Agric. Food Chem. 2009;57:5982–5986. doi: https://doi.org/10.1021/jf900470c</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Den Besten G, Bleeker A, Gerding A, et al. Short-Chain Fatty Acids Protect Against High-Fat Diet–Induced Obesity via a PPARγ-Dependent Switch From Lipogenesis to Fat Oxidation. Diabetes.2015;64:2398. doi: https://doi.org/10.1194/jlr.R036012</mixed-citation><mixed-citation xml:lang="en">Den Besten G, Bleeker A, Gerding A, et al. Short-Chain Fatty Acids Protect Against High-Fat Diet–Induced Obesity via a PPARγ-Dependent Switch From Lipogenesis to Fat Oxidation. Diabetes.2015;64:2398. doi: https://doi.org/10.1194/jlr.R036012</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Canfora EE, van der Beek CM, Jocken JWE, et al. Colonic infusions of short-chain fatty acid mixtures promote energymetabolism in overweight/obese men: A randomized crossover trial. Sci. Rep. 2017;7:2360. doi: https://doi.org/10.1038/s41598-017-02546-x</mixed-citation><mixed-citation xml:lang="en">Canfora EE, van der Beek CM, Jocken JWE, et al. Colonic infusions of short-chain fatty acid mixtures promote energymetabolism in overweight/obese men: A randomized crossover trial. Sci. Rep. 2017;7:2360. doi: https://doi.org/10.1038/s41598-017-02546-x</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Chambers ES, Byrne CS, Aspey K, et al. Acute oral sodium propionate supplementation raises resting energy expenditure and lipid oxidation in fasted humans. Diabetes Obes. Metab. 2018;20:1034–1039. doi: https://doi.org/10.1111/dom.13159</mixed-citation><mixed-citation xml:lang="en">Chambers ES, Byrne CS, Aspey K, et al. Acute oral sodium propionate supplementation raises resting energy expenditure and lipid oxidation in fasted humans. Diabetes Obes. Metab. 2018;20:1034–1039. doi: https://doi.org/10.1111/dom.13159</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Choi J, Joseph L, Pilote L. Obesity and C-reactive protein in various populations: A systematic review and meta-analysis. Obes. Rev. 2013;14:232–244. doi: https://doi.org/10.1111/obr.12003</mixed-citation><mixed-citation xml:lang="en">Choi J, Joseph L, Pilote L. Obesity and C-reactive protein in various populations: A systematic review and meta-analysis. Obes. Rev. 2013;14:232–244. doi: https://doi.org/10.1111/obr.12003</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Bahceci M, Gokalp D, Bahceci S, et al. The correlation between adiposity and adiponectin, tumor necrosis factor α, interleukin-6 and high sensitivity C-reactive protein levels. Is adipocyte size associated with inflammation in adults? J. Endocrinol. Investig. 2007;30:210–214. doi: https://doi.org/10.1007/BF03347427</mixed-citation><mixed-citation xml:lang="en">Bahceci M, Gokalp D, Bahceci S, et al. The correlation between adiposity and adiponectin, tumor necrosis factor α, interleukin-6 and high sensitivity C-reactive protein levels. Is adipocyte size associated with inflammation in adults? J. Endocrinol. Investig. 2007;30:210–214. doi: https://doi.org/10.1007/BF03347427</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Hotamisligil GS. Inflammation and metabolic disorders. Nature. 2006;444:860–867. doi: https://doi.org/10.1038/nature05485</mixed-citation><mixed-citation xml:lang="en">Hotamisligil GS. Inflammation and metabolic disorders. Nature. 2006;444:860–867. doi: https://doi.org/10.1038/nature05485</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Yuan M, Konstantopoulos N, Lee J, et al. Reversal of Obesity and Diet-Induced Insulin Resistance with Salicylates or Targeted Disruption of Ikkβ. Science. 2001;293:1673. doi: https://doi.org/10.1126/science.1061620</mixed-citation><mixed-citation xml:lang="en">Yuan M, Konstantopoulos N, Lee J, et al. Reversal of Obesity and Diet-Induced Insulin Resistance with Salicylates or Targeted Disruption of Ikkβ. Science. 2001;293:1673. doi: https://doi.org/10.1126/science.1061620</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Osborn O, Olefsky JM. The cellular and signaling networks linking the immune system and metabolism in disease. Nat. Med. 2012;18:363–374. doi: https://doi.org/10.1038/nm.2627</mixed-citation><mixed-citation xml:lang="en">Osborn O, Olefsky JM. The cellular and signaling networks linking the immune system and metabolism in disease. Nat. Med. 2012;18:363–374. doi: https://doi.org/10.1038/nm.2627</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Ukena SN, Singh A, Dringenberg U, et al. Probiotic Escherichia coli Nissle 1917 inhibits leaky gut by enhancing mucosal integrity. PLoS ONE. 2007;2:e1308. doi: https://doi.org/10.1371/journal.pone.0001308</mixed-citation><mixed-citation xml:lang="en">Ukena SN, Singh A, Dringenberg U, et al. Probiotic Escherichia coli Nissle 1917 inhibits leaky gut by enhancing mucosal integrity. PLoS ONE. 2007;2:e1308. doi: https://doi.org/10.1371/journal.pone.0001308</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Cani PD, Amar J, Iglesias MA, et al. Metabolic Endotoxemia Initiates Obesity and Insulin Resistance. Diabetes. 2007;56:1761. doi: https://doi.org/10.2337/db06-1491</mixed-citation><mixed-citation xml:lang="en">Cani PD, Amar J, Iglesias MA, et al. Metabolic Endotoxemia Initiates Obesity and Insulin Resistance. Diabetes. 2007;56:1761. doi: https://doi.org/10.2337/db06-1491</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Guarner F, Malagelada J-R. Gut flora in health and disease. Lancet. 2003;361:512–519. doi: https://doi.org/10.1016/S0140-6736(03)12489-0</mixed-citation><mixed-citation xml:lang="en">Guarner F, Malagelada J-R. Gut flora in health and disease. Lancet. 2003;361:512–519. doi: https://doi.org/10.1016/S0140-6736(03)12489-0</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Everard A, Belzer C, Geurts L, et al. Cross-talk between Akkermansia muciniphila and intestinal epithelium controls dietinduced obesity. Proc. Natl. Acad. Sci. USA. 2013;110:9066–9071. doi: https://doi.org/10.1073/pnas.1219451110</mixed-citation><mixed-citation xml:lang="en">Everard A, Belzer C, Geurts L, et al. Cross-talk between Akkermansia muciniphila and intestinal epithelium controls dietinduced obesity. Proc. Natl. Acad. Sci. USA. 2013;110:9066–9071. doi: https://doi.org/10.1073/pnas.1219451110</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Ewaschuk JB, Diaz H, Meddings L, et al. Secreted bioactive factors from Bifidobacterium infantis enhance epithelial cell barrier function. Am. J. Physiol. Gastrointest. Liver Physiol. 2008;295:G1025–G1034. doi: https://doi.org/10.1152/ajpgi.90227.2008</mixed-citation><mixed-citation xml:lang="en">Ewaschuk JB, Diaz H, Meddings L, et al. Secreted bioactive factors from Bifidobacterium infantis enhance epithelial cell barrier function. Am. J. Physiol. Gastrointest. Liver Physiol. 2008;295:G1025–G1034. doi: https://doi.org/10.1152/ajpgi.90227.2008</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Shen TY, Qin HL, Gao ZG, et al. Influences of enteral nutrition combined with probiotics on gut microflora and barrier function of rats with abdominal infection. World J. Gastroenterol. 2006;12:4352. doi: https://doi.org/10.3748/wjg.v12.i27.4352</mixed-citation><mixed-citation xml:lang="en">Shen TY, Qin HL, Gao ZG, et al. Influences of enteral nutrition combined with probiotics on gut microflora and barrier function of rats with abdominal infection. World J. Gastroenterol. 2006;12:4352. doi: https://doi.org/10.3748/wjg.v12.i27.4352</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Hamer HM, Jonkers D, Venema K, et al. Review article: The role of butyrate on colonic function. Aliment. Pharmacol. Ther. 2008;27:104–119. doi: https://doi.org/10.1111/j.1365-2036.2007.03562.x</mixed-citation><mixed-citation xml:lang="en">Hamer HM, Jonkers D, Venema K, et al. Review article: The role of butyrate on colonic function. Aliment. Pharmacol. Ther. 2008;27:104–119. doi: https://doi.org/10.1111/j.1365-2036.2007.03562.x</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Topping DL, Clifton PM. Short-Chain Fatty Acids and Human Colonic Function: Roles of Resistant Starch and Nonstarch Polysaccharides. Physiol. Rev. 2001;81:1031–1064. doi: https://doi.org/10.1152/physrev.2001.81.3.1031</mixed-citation><mixed-citation xml:lang="en">Topping DL, Clifton PM. Short-Chain Fatty Acids and Human Colonic Function: Roles of Resistant Starch and Nonstarch Polysaccharides. Physiol. Rev. 2001;81:1031–1064. doi: https://doi.org/10.1152/physrev.2001.81.3.1031</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Vinolo MA, Rodrigues HG, Nachbar RT, Curi R. Regulation of inflammation by short chain fatty acids. Nutrients. 2011;3:858–876. doi: https://doi.org/10.3390/nu3100858</mixed-citation><mixed-citation xml:lang="en">Vinolo MA, Rodrigues HG, Nachbar RT, Curi R. Regulation of inflammation by short chain fatty acids. Nutrients. 2011;3:858–876. doi: https://doi.org/10.3390/nu3100858</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Khan MJ, Gerasimidis K, Edwards CA, Shaikh MG. Role of Gut Microbiota in the Aetiology of Obesity:Proposed Mechanisms and Review of the Literature. J. Obes. 2016; 2016:7353642. doi: https://doi.org/10.1155/2016/7353642</mixed-citation><mixed-citation xml:lang="en">Khan MJ, Gerasimidis K, Edwards CA, Shaikh MG. Role of Gut Microbiota in the Aetiology of Obesity:Proposed Mechanisms and Review of the Literature. J. Obes. 2016; 2016:7353642. doi: https://doi.org/10.1155/2016/7353642</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Cani PD, Bibiloni R, Knauf C, et al. Changes in Gut Microbiota Control Metabolic Endotoxemia-Induced Inflammation in High-Fat Diet– Induced Obesity and Diabetes in Mice. Diabetes. 2008;57:1470. doi: https://doi.org/10.2337/db07-1403</mixed-citation><mixed-citation xml:lang="en">Cani PD, Bibiloni R, Knauf C, et al. Changes in Gut Microbiota Control Metabolic Endotoxemia-Induced Inflammation in High-Fat Diet– Induced Obesity and Diabetes in Mice. Diabetes. 2008;57:1470. doi: https://doi.org/10.2337/db07-1403</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Creely SJ, McTernan PG, Kusminski CM, et al. Lipopolysaccharide activates an innate immune system response in human adipose tissue in obesity and type 2 diabetes. Am. J. Physiol. Endocrinol. Metab. 2007;292:E740–E747. doi: https://doi.org/10.1152/ajpendo.00302.2006</mixed-citation><mixed-citation xml:lang="en">Creely SJ, McTernan PG, Kusminski CM, et al. Lipopolysaccharide activates an innate immune system response in human adipose tissue in obesity and type 2 diabetes. Am. J. Physiol. Endocrinol. Metab. 2007;292:E740–E747. doi: https://doi.org/10.1152/ajpendo.00302.2006</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Pearson J, Brownlee I. The Interaction of Large Bowel Microflora with the Colonic Mucus Barrier. Int. J.Inflamm. 2010;2010:321426. doi: https://doi.org/10.4061/2010/321426</mixed-citation><mixed-citation xml:lang="en">Pearson J, Brownlee I. The Interaction of Large Bowel Microflora with the Colonic Mucus Barrier. Int. J.Inflamm. 2010;2010:321426. doi: https://doi.org/10.4061/2010/321426</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Clemente-Postigo M, Oliva-Olivera W, Coin-Aragüez L, et al. Metabolic endotoxemia promotes adipose dysfunction and inflammation in human obesity. Am. J. Physiol. Endocrinol. Metab. 2018;316:E319–E332. doi: https://doi.org/10.1152/ajpendo.00277.2018</mixed-citation><mixed-citation xml:lang="en">Clemente-Postigo M, Oliva-Olivera W, Coin-Aragüez L, et al. Metabolic endotoxemia promotes adipose dysfunction and inflammation in human obesity. Am. J. Physiol. Endocrinol. Metab. 2018;316:E319–E332. doi: https://doi.org/10.1152/ajpendo.00277.2018</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Harte AL, Varma MC, Tripathi G, et al. High fat intake leads to acute postprandial exposure to circulating endotoxin in type 2 diabetic subjects. Diabetes Care. 2012;35:375–382. doi: https://doi.org/10.2337/dc11-1593</mixed-citation><mixed-citation xml:lang="en">Harte AL, Varma MC, Tripathi G, et al. High fat intake leads to acute postprandial exposure to circulating endotoxin in type 2 diabetic subjects. Diabetes Care. 2012;35:375–382. doi: https://doi.org/10.2337/dc11-1593</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Botao W, Qingmin K, Xiu L, et al. A High-Fat Diet Increases Gut Microbiota Biodiversity and Energy Expenditure Due to Nutrient Difference. Nutrients. 2020;20:12. doi: https://doi.org/10.3390/nu12103197</mixed-citation><mixed-citation xml:lang="en">Botao W, Qingmin K, Xiu L, et al. A High-Fat Diet Increases Gut Microbiota Biodiversity and Energy Expenditure Due to Nutrient Difference. Nutrients. 2020;20:12. doi: https://doi.org/10.3390/nu12103197</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Гапонов А.М., Волкова Н.И., Ганенко Л.А., и др. Особенности микробиома толстой кишки у пациентов с ожирением при его различных фенотипах. // Журнал микробиологии, эпидемиологии и иммунобиологии. — 2021. — Т.98. — №2 — С.144-155. doi: https://doi.org/10.36233/0372-9311-66</mixed-citation><mixed-citation xml:lang="en">Gaponov AM, Volkova NI, Ganenkо LA, et al. Characteristics of the colonic microbiome in patients with different obesity phenotypes. Journal of microbiology, epidemiology and immunobiology. 2021;98(2):144-155 (In Russ).</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Dewulf EM, Cani PD, Claus SP, et al. Insight into the prebiotic concept: Lessons from an exploratory, double blind intervention study with inulin-type fructans in obese women. Gut. 2013;62:1112. doi: https://doi.org/10.1136/gutjnl-2012-303304</mixed-citation><mixed-citation xml:lang="en">Dewulf EM, Cani PD, Claus SP, et al. Insight into the prebiotic concept: Lessons from an exploratory, double blind intervention study with inulin-type fructans in obese women. Gut. 2013;62:1112. doi: https://doi.org/10.1136/gutjnl-2012-303304</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Peterson CT, Sharma V, Elmén L, Peterson SN. Immune homeostasis, dysbiosis and the rapeutic modulation of the gut microbiota. Clin. Exp. Immunol. 2015;179:363–377. doi: https://doi.org/10.1111/cei.12474</mixed-citation><mixed-citation xml:lang="en">Peterson CT, Sharma V, Elmén L, Peterson SN. Immune homeostasis, dysbiosis and the rapeutic modulation of the gut microbiota. Clin. Exp. Immunol. 2015;179:363–377. doi: https://doi.org/10.1111/cei.12474</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Cani PD, Possemiers S, Van de Wiele T, et al. Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2- driven improvement of gut permeability. Gut. 2009;58:1091. doi: https://doi.org/10.1136/gut.2008.165886</mixed-citation><mixed-citation xml:lang="en">Cani PD, Possemiers S, Van de Wiele T, et al. Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2- driven improvement of gut permeability. Gut. 2009;58:1091. doi: https://doi.org/10.1136/gut.2008.165886</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Posovszky C, Wabitsch M. Regulation of Appetite, Satiation, and Body Weight by Enteroendocrine Cells. Part 2: Therapeutic Potential of Enteroendocrine Cells in the Treatment of Obesity. Horm. Res. Paediatr. 2015;83:11–18. doi: https://doi.org/10.1159/000369555</mixed-citation><mixed-citation xml:lang="en">Posovszky C, Wabitsch M. Regulation of Appetite, Satiation, and Body Weight by Enteroendocrine Cells. Part 2: Therapeutic Potential of Enteroendocrine Cells in the Treatment of Obesity. Horm. Res. Paediatr. 2015;83:11–18. doi: https://doi.org/10.1159/000369555</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Cani PD, Hoste S, Guiot Y, Delzenne NM. Dietary nondigestible carbohydrates promote L-cell differentiation in the proximal colon of rats. Br. J. Nutr. 2007;98:32–37. doi: https://doi.org/10.1017/S0007114507691648</mixed-citation><mixed-citation xml:lang="en">Cani PD, Hoste S, Guiot Y, Delzenne NM. Dietary nondigestible carbohydrates promote L-cell differentiation in the proximal colon of rats. Br. J. Nutr. 2007;98:32–37. doi: https://doi.org/10.1017/S0007114507691648</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Cani PD, Lecourt E, Dewulf EM, et al. Gut microbiota fermentation of prebiotics increases satietogenic and incretin gut peptide production with consequences for appetite sensation and glucose response after a meal. Am. J. Clin. Nutr. 2009;90:1236–1243. doi: https://doi.org/10.3945/ajcn.2009.28095</mixed-citation><mixed-citation xml:lang="en">Cani PD, Lecourt E, Dewulf EM, et al. Gut microbiota fermentation of prebiotics increases satietogenic and incretin gut peptide production with consequences for appetite sensation and glucose response after a meal. Am. J. Clin. Nutr. 2009;90:1236–1243. doi: https://doi.org/10.3945/ajcn.2009.28095</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Parnell JA, Reimer RA. Weight loss during oligofructose supplementation is associated with decreased ghrelin and increased peptide YY in overweight and obese adults. Am. J. Clin. Nutr. 2009;89:1751–1759. doi: https://doi.org/10.3945/ajcn.2009.27465</mixed-citation><mixed-citation xml:lang="en">Parnell JA, Reimer RA. Weight loss during oligofructose supplementation is associated with decreased ghrelin and increased peptide YY in overweight and obese adults. Am. J. Clin. Nutr. 2009;89:1751–1759. doi: https://doi.org/10.3945/ajcn.2009.27465</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Chambers ES, Byrne CS, Morrison DJ, et al. Dietary supplementation with inulin-propionate ester or inulin improves insulin sensitivity in adults with overweight and obesity with distinct effects on the gut microbiota, plasma metabolome and systemic inflammatory responses: A randomised cross-over trial. Gut. 2019;68:1430. doi: https://doi.org/10.1136/gutjnl-2019-318424</mixed-citation><mixed-citation xml:lang="en">Chambers ES, Byrne CS, Morrison DJ, et al. Dietary supplementation with inulin-propionate ester or inulin improves insulin sensitivity in adults with overweight and obesity with distinct effects on the gut microbiota, plasma metabolome and systemic inflammatory responses: A randomised cross-over trial. Gut. 2019;68:1430. doi: https://doi.org/10.1136/gutjnl-2019-318424</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Tschritter O, Fritsche A, Thamer C, et al. Plasma Adiponectin Concentrations Predict Insulin Sensitivity of Both Glucose and Lipid Metabolism. Diabetes. 2003;52:239. doi: https://doi.org/10.2337/diabetes.52.2.239</mixed-citation><mixed-citation xml:lang="en">Tschritter O, Fritsche A, Thamer C, et al. Plasma Adiponectin Concentrations Predict Insulin Sensitivity of Both Glucose and Lipid Metabolism. Diabetes. 2003;52:239. doi: https://doi.org/10.2337/diabetes.52.2.239</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Alligier M, Dewulf EM, Salazar N, et al. Positive interaction between prebiotics and thiazolidinedione treatment on adiposity in diet-induced obese mice. Obesity. 2014;22:1653–1661. doi: https://doi.org/10.1002/oby.20733</mixed-citation><mixed-citation xml:lang="en">Alligier M, Dewulf EM, Salazar N, et al. Positive interaction between prebiotics and thiazolidinedione treatment on adiposity in diet-induced obese mice. Obesity. 2014;22:1653–1661. doi: https://doi.org/10.1002/oby.20733</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Thorburn A, Muir J, Proietto J. Carbohydrate fermentation decreases hepatic glucose output in healthy subjects. Metabolism. 1993;42:780–785. doi: https://doi.org/10.1016/0026-0495(93)90249-N</mixed-citation><mixed-citation xml:lang="en">Thorburn A, Muir J, Proietto J. Carbohydrate fermentation decreases hepatic glucose output in healthy subjects. Metabolism. 1993;42:780–785. doi: https://doi.org/10.1016/0026-0495(93)90249-N</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Berggren AM, Nyman EMGL, Lundquist I, Björck IME. Influence of orally and rectally administered propionate on cholesterol and glucose metabolism in obese rats. Br. J. Nutr. 1996;76: 287–294. doi: https://doi.org/10.1079/BJN19960032</mixed-citation><mixed-citation xml:lang="en">Berggren AM, Nyman EMGL, Lundquist I, Björck IME. Influence of orally and rectally administered propionate on cholesterol and glucose metabolism in obese rats. Br. J. Nutr. 1996;76: 287–294. doi: https://doi.org/10.1079/BJN19960032</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>
