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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">scbmt</journal-id><journal-title-group><journal-title xml:lang="ru">БИОМЕДИЦИНА</journal-title><trans-title-group xml:lang="en"><trans-title>Journal Biomed</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2074-5982</issn><issn pub-type="epub">2713-0428</issn><publisher><publisher-name>Scientific center of biomedical technologies of Federal Medical and Biological Agency</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">scbmt-103</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>НОВЫЕ БИОМЕДИЦИНСКИЕ ИТЕХНОЛОГИИ</subject></subj-group></article-categories><title-group><article-title>Инсулиновый рецептор в мозге: новая мишень в лечении центральной инсулиновой резистентности</article-title><trans-title-group xml:lang="en"><trans-title>Insulin signaling system in the brain: new target in the treatment of central insulin resistance</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>Помыткин</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Pomytkin</surname><given-names>I. A.</given-names></name></name-alternatives><email xlink:type="simple">ipomytkin@gmail.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>Красильникова</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Krasil’Nikova</surname><given-names>I. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пинелис</surname><given-names>В. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Pinelis</surname><given-names>V. G.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каркищенко</surname><given-names>Н. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Karkischenko</surname><given-names>N. N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>ФГАОУ ВО Первый Московский государственный медицинский университет им. И.М. Сеченова Минздрава России (Сеченовский Университет)</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-2"><institution>ФГАУ «Национальный медицинский исследовательский центр здоровья детей» Минздрава России</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-3"><institution>ФГБУН «Научный центр биомедицинских технологий ФМБА России»</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>26</day><month>02</month><year>2019</year></pub-date><volume>0</volume><issue>3</issue><fpage>17</fpage><lpage>34</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Помыткин И.А., Красильникова И.А., Пинелис В.Г., Каркищенко Н.Н., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Помыткин И.А., Красильникова И.А., Пинелис В.Г., Каркищенко Н.Н.</copyright-holder><copyright-holder xml:lang="en">Pomytkin I.A., Krasil’Nikova I.A., Pinelis V.G., Karkischenko N.N.</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://journal.scbmt.ru/jour/article/view/103">https://journal.scbmt.ru/jour/article/view/103</self-uri><abstract><p>Настоящий обзор посвящен сигнальной системе инсулинового рецептора в мозге, которая имеет ряд существенных отличий от периферической системы. В клетках мозга преобладает, а в нейронах - экспрессируется исключительно высокоафинная короткая изоформа А рецептора (IR-A), которая способна связывать не только инсулин, но и инсулиноподобный фактор 2 (IGF-2). IR-A участвует в регуляции синаптической пластичности, росте дендритов и аксонов, в регуляции взрослого нейрогенеза. Инсулиновая система в мозге играет роль в процессах формирования памяти и регуляции пищевого поведения. Нарушения инсулиновой сигнализации приводят к развитию центральной инсулиновой резистентности, наиболее известным проявлением которой является болезнь Альцгеймера. Разработка средств лечения центральной инсулиновой резистентности с учетом специфики инсулиновой сигнализации в мозге является новым многообещающим подходом в терапии заболеваний центральной нервной системы.</p></abstract><trans-abstract xml:lang="en"><p>This review relates to insulin signaling system in the brain, which differs from those in peripheral tissues. Brain cells express predominantly, and neurons exclusively, the high affinity short isoform A of the insulin receptor (IR-A). IR-A binds insulin and insulin-like growth factor 2 (IGF-2) with physiologically relevant affinity, in contrast to isoform B (IR-B), major isoform in adult peripheral tissues. IR-A is involved in the regulation of synaptic plasticity, the growth of dendrites and axons, and the regulation of adult neurogenesis. The insulin system in the brain plays a role in the processes of memory formation and the regulation of eating behavior. Impairments of insulin signaling in the brain lead to the development of central insulin resistance, the most prominent manifestation of which is Alzheimer's disease. The development of drugs specifically targeting central insulin resistance represents a new promising approach in the treatment of diseases of the central nervous system.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>инсулин</kwd><kwd>инсулиновый рецептор</kwd><kwd>центральная нервная система</kwd><kwd>мозг</kwd></kwd-group><kwd-group xml:lang="en"><kwd>insulin</kwd><kwd>insulin receptor</kwd><kwd>central nervous system</kwd><kwd>brain</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">Abbott M.A., Wells D.G., Fallon J.R. The insulin receptor tyrosine kinase substrate p58/53 and the insulin receptor are components of CNS synapses // J. Neurosci. 1999. V. 19. Pp. 7300-7308.</mixed-citation><mixed-citation xml:lang="en">Abbott M.A., Wells D.G., Fallon J.R. The insulin receptor tyrosine kinase substrate p58/53 and the insulin receptor are components of CNS synapses // J. 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