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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">mrj</journal-id><journal-title-group><journal-title xml:lang="ru">Современная ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Modern Rheumatology Journal</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1996-7012</issn><issn pub-type="epub">2310-158X</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14412/1996-7012-2016-4-73-86</article-id><article-id custom-type="elpub" pub-id-type="custom">mrj-723</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>ЭЙКОЗАНОИДЫ И ВОСПАЛЕНИЕ</article-title><trans-title-group xml:lang="en"><trans-title>EICOSANOIDS AND INFLAMMATION</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каратеев</surname><given-names>А. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Karateev</surname><given-names>A. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Контакты: Андрей Евгеньевич Каратеев; ФБГНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой», 115522, Москва, Каширское шоссе, 34А</p></bio><bio xml:lang="en"><p>Contact: Andrei Evgenyevich Karateev; V.A. Nasonova Research Institute of Rheumatology, 34A, Kashirskoe Shosse, Moscow 115522</p></bio><email xlink:type="simple">aekarat@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>Алейникова</surname><given-names>Т. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Aleinikova</surname><given-names>T. L.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт ревматологии им. В.А. Насоновой</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Первый Московский государственный медицинский университет им. И.М. Сеченова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>I.M. Sechenov First Moscow State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>16</day><month>12</month><year>2016</year></pub-date><volume>10</volume><issue>4</issue><fpage>73</fpage><lpage>86</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Каратеев А.Е., Алейникова Т.Л., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Каратеев А.Е., Алейникова Т.Л.</copyright-holder><copyright-holder xml:lang="en">Karateev A.E., Aleinikova T.L.</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://mrj.ima-press.net/mrj/article/view/723">https://mrj.ima-press.net/mrj/article/view/723</self-uri><abstract><p>Воспаление является важнейшим элементом патогенеза основных заболеваний человека. Это определяет принципиальное значение противовоспалительной терапии в современной концепции целенаправленного патогенетического лечения. Рациональный выбор противовоспалительных средств и разработка новых, перспективных препаратов немыслимы без четких знаний особенностей развития воспалительной реакции. Ключевую роль в процессе воспаления играют метаболиты полиненасыщенных жирных кислот – эйкозаноиды. Эти субстанции оказывают разнообразные и часто антагонистические биологические эффекты, что определяется их химической природой и особенностями рецепторов, с которыми они взаимодействуют. Одни из них (простагландины, лейкотриены, эоксины и гепоксилины) являются мощными медиаторами воспаления и боли, другие (липоксины, производные эпоксиэйкозатриеновой кислоты, резолвины, протектины, марезин и эндоканнабиноиды) оказывают противовоспалительное и цитопротективное действие, способствуя разрешению воспалительной реакции. В настоящем обзоре рассмотрены основные классы эйкозаноидов, их метаболизм, эффекты и клиническое значение, а также возможности фармакологического вмешательства в их синтез или взаимодействие с рецепторами. </p></abstract><trans-abstract xml:lang="en"><p>Inflammation is the most important element in the pathogenesis of major human diseases. It determines the fundamental value of anti-inflammatory therapy in the modern concept of targeted pathogenetic treatment. The rational choice of anti-inflammatory drugs and the design of new promising agents are inconceivable without clear knowledge of the characteristics of development of an inflammatory response. Eicosanoids, the metabolites of polyunsaturated fatty acids, play a key role in the process of inflammation. These substances have diverse and frequently antagonistic biological effects, which is determined by their chemical structure and specific features of receptors with which they interact. Some of them (prostaglandins, leukotrienes, auxins, and hepoxilins) are potential mediators of inflammation and pain; others (lipoxins, epoxyeicosatrienoic acid derivatives, resolvins, protectins, maresins, and endocannabinoids) have anti-inflammatory and cytoprotective activities, contributing to the resolution of the inflammatory response. This review describes considers the main classes of eicosanoids, their metabolism, effects, and clinical significance, as well as the possibilities of pharmacological interventions in their synthesis or interaction with receptors. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>воспаление</kwd><kwd>эйкозаноиды</kwd><kwd>циклооксигеназа 2</kwd><kwd>липооксигеназа 5</kwd><kwd>микросомальная ПГЕ2-синтетаза</kwd><kwd>простагландины</kwd><kwd>лейкотриены</kwd><kwd>эоксины</kwd><kwd>гепоксилины</kwd><kwd>липоксины</kwd><kwd>эпоксиэйкозатриеновая кислота</kwd><kwd>резолвины</kwd><kwd>протектины</kwd><kwd>марезин</kwd><kwd>эндоканнабиноиды</kwd><kwd>нестероидные противовоспалительные препараты</kwd><kwd>оксикамы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>inflammation</kwd><kwd>eicosanoids</kwd><kwd>cyclooxygenase 2</kwd><kwd>5-lipoxygenase</kwd><kwd>microsomal PGE2-synthase</kwd><kwd>prostaglandins</kwd><kwd>leukotrienes</kwd><kwd>auxins</kwd><kwd>hepoxilins</kwd><kwd>lipoxins</kwd><kwd>epoxyeicosatrienoic acid</kwd><kwd>resolvins</kwd><kwd>protectins</kwd><kwd>maresin</kwd><kwd>endocannabinoids</kwd><kwd>nonsteroidal anti-inflammatory drugs</kwd><kwd>oxicams</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Tabas I, Glass CK. 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