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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">cardiovascular</journal-id><journal-title-group><journal-title xml:lang="ru">Кардиоваскулярная терапия и профилактика</journal-title><trans-title-group xml:lang="en"><trans-title>Cardiovascular Therapy and Prevention</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1728-8800</issn><issn pub-type="epub">2619-0125</issn><publisher><publisher-name>«SILICEA-POLIGRAF» LLC</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">cardiovascular-1550</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>ИНФАРКТ МИОКАРДА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>MYOCARDIAL INFARCTION</subject></subj-group></article-categories><title-group><article-title>Состояние системы цитохрома Р-450 3А4 у больных острым инфарктом миокарда</article-title><trans-title-group xml:lang="en"><trans-title>Cytochrome P-450 3A4 system in patients with acute myocardial infarction</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>Владимиров</surname><given-names>А. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Vladimirov</surname><given-names>A. G.</given-names></name></name-alternatives><email xlink:type="simple">drvl@mail.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>Кукес</surname><given-names>В. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Kukes</surname><given-names>V. G.</given-names></name></name-alternatives><email xlink:type="simple">drvl@mail.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>Андреев</surname><given-names>Д. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Andreev</surname><given-names>D. A.</given-names></name></name-alternatives><email xlink:type="simple">drvl@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГУЗ Госпиталь для ветеранов войн №3</institution><country>Россия</country></aff><aff xml:lang="en"><institution>ГУЗ Госпиталь для ветеранов войн №3</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Институт клинической фармакологии ФГУ “НЦ ЭСМП” Росздравнадзора</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Clinical Pharmacology Institute, Research Center for Medical Substances Expertise</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Московская медицинская академия им. И.М. Сеченова, г. Москва</institution><country>Россия</country></aff><aff xml:lang="en"><institution>I.M. Sechenov Moscow Medical Academy. Moscow</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2008</year></pub-date><pub-date pub-type="epub"><day>20</day><month>08</month><year>2008</year></pub-date><volume>7</volume><issue>4</issue><fpage>35</fpage><lpage>40</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Владимиров А.Г., Кукес В.Г., Андреев Д.А., 2008</copyright-statement><copyright-year>2008</copyright-year><copyright-holder xml:lang="ru">Владимиров А.Г., Кукес В.Г., Андреев Д.А.</copyright-holder><copyright-holder xml:lang="en">Vladimirov A.G., Kukes V.G., Andreev D.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://cardiovascular.elpub.ru/jour/article/view/1550">https://cardiovascular.elpub.ru/jour/article/view/1550</self-uri><abstract><sec><title>Цель</title><p>Цель. Определить особенности функционирования системы CYP3A4 в остром периоде инфаркта миокарда (ИМ), ее связь с клинико-лабораторными показателями.</p></sec><sec><title>Материал и методы</title><p>Материал и методы. В исследование были включены 50 пациентов, госпитализированных в первые 24 часа острого инфаркта миокарда с подъемом сегмента ST (HMnST). (MEGX) - Тест моноэтилглици-нэксилидида проводили сразу после поступления пациента, до назначения терапии, на 4-5 и 14 сутки заболевания.</p></sec><sec><title>Результаты</title><p>Результаты. Исходный уровень MEGX оказался достоверно выше в группе неосложненного течения ИМ (132,1+16,85 нг/мл), чем в группе пациентов с симптомами сердечной недостаточности (СИ) (31,9+2,02 нг/мл; р&lt;0,001) и группе здоровых добровольцев (63,6+14,01 нг/мл; р&lt;0,001). Прием фенобарбитала достоверно повышает активность CYP 3A4 в обеих группах пациентов с ИМ.</p></sec><sec><title>Заключение</title><p>Заключение. Активность системы CYP 3A4 в остром периоде HMnST угнетена у пациентов при наличии признаков острой СИ. Это связано с развитием у пациентов этой группы признаков повреждения печени (ишемического и застойного характера). При HMnST возможно проведение фармакологической стимуляции CYP 3A4.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Aim</title><p>Aim. To investigate CYP 3A4 system functioning and its clinico-laboratory correlations in acute myocardial infarction (AMI).</p></sec><sec><title>Material and methods</title><p>Material and methods. The study included 50 patients hospitalized in the first 24 hours of AMI with ST segment elevation (STE-AMI). Monoethylglycinexylidide (MEGX) test was performed at the hospital admission, at Day 4-5 and Day 14.</p></sec><sec><title>Results</title><p>Results. Baseline MEGX level was significantly higher in non-complicated AMI group (132,1+16,85 ng/ml) than in patients with heart failure (HF) symptoms (31,9+2,02 ng/ml; p&lt;0,001) or healthy volunteers (63,6+14,01 ng/ ml; p&lt;0,001). Phenobarbital administration significantly enhanced CYP 3A4 activity in both AMI groups.</p></sec><sec><title>Conclusion</title><p>Conclusion. In AMI, CYP 3A4 system activity was suppressed among patients with acute HF symptoms. This could be explained by ischemic and congestive liver disturbances. In STE-AMI, pharmacological CYP 3A4 stimulation is possible.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>моноэтилглицинэксилидид</kwd><kwd>CYP 3A4</kwd><kwd>инфаркт миокарда</kwd><kwd>сердечная недостаточность</kwd><kwd>фенобарбитал</kwd></kwd-group><kwd-group xml:lang="en"><kwd>monoethylglycinexylidide</kwd><kwd>CYP 3A4</kwd><kwd>myocardial infarction</kwd><kwd>heart failure</kwd><kwd>phenobarbital</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">Применение MEGX-теста для оценки активности изо-фермента цитохрома 3-450 ЗА4. Методические рекомендации. Москва 2004.</mixed-citation><mixed-citation xml:lang="en">Применение MEGX-теста для оценки активности изо-фермента цитохрома 3-450 ЗА4. Методические рекомендации. 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