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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">systhiper</journal-id><journal-title-group><journal-title xml:lang="ru">Системные гипертензии</journal-title><trans-title-group xml:lang="en"><trans-title>Systemic Hypertension</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2075-082X</issn><issn pub-type="epub">2542-2189</issn><publisher><publisher-name>LLC «ИнтерМедсервис»</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">systhiper-372</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></article-categories><title-group><article-title>Плейотропные свойства дигидропиридиновых антагонистов кальциевых каналов‌‌</article-title><trans-title-group xml:lang="en"><trans-title>Pleiotropic features of dihydropyridine calcium channel antagonists</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>Аникин</surname><given-names>Г. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Anikin</surname><given-names>G. S.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>ГБОУ ВПО Первый Московский государственный медицинский университет им. И.М.Сеченова Минздрава России; ФГБУ Поликлиника №3 Управления делами Президента Российской Федерации</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>23</day><month>12</month><year>2022</year></pub-date><volume>11</volume><issue>3</issue><fpage>81</fpage><lpage>83</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Аникин Г.С., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Аникин Г.С.</copyright-holder><copyright-holder xml:lang="en">Anikin G.S.</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.syst-hypertension.ru/jour/article/view/372">https://www.syst-hypertension.ru/jour/article/view/372</self-uri><abstract><p>Современную медицину трудно представить без надежных и безопасных лекарственных средств. Зачастую нежелательные лекарственные реакции являются поводом для отмены средства, которое в целом эффективно. Так, у дигидропиридиновых блокаторов кальциевых каналов основными нежелательными лекарственными реакциями, служащими поводом для отмены данных препаратов, являются отеки голеней и тахикардия. Лерканидипин - относительно новый представитель данного класса, представляет собой высоколипофильное соединение, которое долго ингибирует кальциевые каналы L-типа благодаря сохранению высокой внутримембранной концентрации. В обзоре представлены данные об эффективности и безопасности лерканидипина,а также о его плейотропных свойствах.</p></abstract><trans-abstract xml:lang="en"><p>It is hard to imagine modern medicine without safe drugs (D). Often, adverse drug reactions (ADR) are the reason for drug with drawal, which is quite effective as a whole. The main dihydropyridine calcium channel antagonists (DCCA) ADR are the edema of shin and tachycardia, causing this drug with drawal. Lercanidipine is aquite new member of this class; it is a highly lipophilic compound, which blocking the influx of calcium ions through L-type calcium channels, by maintaining the high intramembrane concentration. This review provides the data on the efficacy and safety of lercanidipine and its pleiotropic features.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>артериальная гипертензия</kwd><kwd>дигидропиридиновые блокаторы кальциевых каналов</kwd><kwd>нежелательные лекарственные реакции</kwd><kwd>лерканидипин</kwd></kwd-group><kwd-group xml:lang="en"><kwd>arterial hypertension</kwd><kwd>dihydropyridine calcium channel antagonists</kwd><kwd>adverse drug reactions</kwd><kwd>lercanidipine</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">Grundy J.S, Foster R.T. The nifedipine gastrointestinal therapeutic system (GITS). 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