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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">ateroskleroz</journal-id><journal-title-group><journal-title xml:lang="ru">Атеросклероз</journal-title><trans-title-group xml:lang="en"><trans-title>Ateroscleroz</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2078-256X</issn><issn pub-type="epub">2949-3633</issn><publisher><publisher-name>НИИТПМ-филиал ИЦиГ СО РАН</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">ateroskleroz-665</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>Липопротеины высокой плотности и аполипопротеин A-I: регуляторная роль и новые терапевтические стратегии лечения атеросклероза</article-title><trans-title-group xml:lang="en"><trans-title>High-density lipoprotein, and apolipoprotein A-I: a regulatory role and novel therapeutic strategies for the treatment atherosclerosis</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>Поляков</surname><given-names>Л. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Polyakov</surname><given-names>L. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лев Михайлович Поляков, д-р мед. наук, проф., зав. лабораторией, зам. директора по научной работе</p><p>СО РАМН</p><p>ФГБУ «НИИ биохимии»</p><p>лаборатория медицинской биотехнологии</p><p>630117</p><p>ул. Тимакова, 2</p><p>Новосибирск</p></bio><bio xml:lang="en"><p>SB RAMS</p><p>Federal state budgetary institution "Research Institute of Biochemistry"</p><p>630117</p><p>st. Timakova, 2</p><p>Novosibirsk</p></bio><email xlink:type="simple">plm@soramn.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>Панин</surname><given-names>Л. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Panin</surname><given-names>L. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лев Евгеньевич Панин, д-р мед. наук, проф., академик, зав. лабораторией, директор</p><p>СО РАМН</p><p>ФГБУ «НИИ биохимии»</p><p>лаборатория молекулярных механизмов межклеточных взаимодействий</p><p>630117</p><p>ул. Тимакова, 2</p><p>Новосибирск</p></bio><bio xml:lang="en"><p>SB RAMS</p><p>Federal state budgetary institution "Research Institute of Biochemistry"</p><p>630117</p><p>st. Timakova, 2</p><p>Novosibirsk</p></bio><email xlink:type="simple">ibch@soramn.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>РАМН</institution></aff><aff xml:lang="en"><institution>RAMS</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2013</year></pub-date><pub-date pub-type="epub"><day>05</day><month>04</month><year>2022</year></pub-date><volume>9</volume><issue>1</issue><fpage>42</fpage><lpage>53</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Поляков Л.М., Панин Л.Е., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Поляков Л.М., Панин Л.Е.</copyright-holder><copyright-holder xml:lang="en">Polyakov L.M., Panin L.E.</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://ateroskleroz.elpub.ru/jour/article/view/665">https://ateroskleroz.elpub.ru/jour/article/view/665</self-uri><abstract><p>   Рассмотрены функции липопротеинов высокой плотности (ЛПВП), не связанные с обменом липидов, входящих в их состав. Представлены результаты собственных исследований, а также литературные данные, свидетельствующие о важной регуляторной роли. Регуляторные эффекты ЛПВП неразрывно связаны с их антиатерогенными свойствами. Однако необходимо учитывать, что механизм антиатерогенного действия ЛПВП не ограничивается только «обратным» транспортом холестерина от периферических тканей в печень, он определяется многими другими факторами, каждый из которых имеет значение не только в контексте защиты организма от атеросклероза, но и в протективной роли ЛПВП в более широком смысле. ЛПВП оказывают важное противовоспалительное действие, обладают антиоксидантными и антиапоптотическими свойствами, регулируют сосудистый тонус и антикоагулянтную активность, действуют как антимикробные и противовирусные агенты. Подчеркнуто, что понимание молекулярных механизмов регуляторных свойств ЛПВП открывает новые перспективы для развития более эффективных методов лечения данной патологии. Новые стратегии лечения должны включать разработку перспективных терапевтических подходов, модулирующих ЛПВП-метаболизм, что позволит повысить их содержание в крови и улучшить «обратный» транспорт холестерина. Рассмотрены два наиболее перспективных направления – создание и использование рекомбинантных или реконструированных ЛПВП, а также пептидов-миметиков аполипопротеина А-I.</p></abstract><trans-abstract xml:lang="en"><p>   In the review show the functions of high-density lipoprotein, is not related to the exchange of lipids within them. The results own research, as well as literary evidenced of the important regula tory role. Regulatory effect of HDL is closely related to their antiatherogenic properties. However, it should be noted that the mechanism of action of antiatherogenic HDL is not limited to a “reverse” transport of cholesterol from peripheral tissues to the liver, it is determined by many other factors, all of which is important not only in the context of defense against athe ro sclerosis, but also in the protective role of HDL in a broader sense. The data show that HDL has an important antiinflammatory effect, have antioxidant and antiapoptotic properties, regulate vascular tone and anticoagulant activity, act as antimicrobial and antiviral agents. Due to the urgency of the problem of atherosclerosis in the emphasis that understanding the molecular mechanisms of the regulatory properties of HDL opens up new prospects for the development of more effective treatments for this disease. New treatment strategies should include the development of promising therapeutic approaches that modulate HDL metabolism, which would increase their levels in the blood and improve the “reverse” cholesterol transport. This review deals with, in our opinion, the two most promising areas – is the creation and use of recombinant HDL or reconstructed, as well as peptide-mimetics of apolipoprotein A-I.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>атеросклероз</kwd><kwd>липопротеины высокой плотности</kwd><kwd>аполипопротеин А-I</kwd><kwd>регуляторная роль</kwd><kwd>апоА-I-пептиды-миметики</kwd><kwd>стратегии лечения</kwd></kwd-group><kwd-group xml:lang="en"><kwd>atherosclerosis</kwd><kwd>high-density lipoprotein</kwd><kwd>apolipoprotein A-I</kwd><kwd>the regulatory role of apoA-I-mimetic peptides</kwd><kwd>treatment strategies</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">Bornstein J. Insulin-reversible inhibition of glucose utilization by serum lipoprotein fractions // J. Biol. Chem. 1953. V. 205. P. 513–519.</mixed-citation><mixed-citation xml:lang="en">Bornstein J. 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