<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">vedomostiregmed</journal-id><journal-title-group><journal-title xml:lang="ru">Регуляторные исследования и экспертиза лекарственных средств</journal-title><trans-title-group xml:lang="en"><trans-title>Regulatory Research and Medicine Evaluation</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">3034-3062</issn><issn pub-type="epub">3034-3453</issn><publisher><publisher-name>Federal State Budgetary Institution ‘Scientific Centre for Expert Evaluation of Medicinal Products’ of the Ministry of Health of the Russian Federation (FSBI ‘SCEEMP’)</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">vedomostiregmed-102</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>ДОКЛИНИЧЕСКОЕ И КЛИНИЧЕСКОЕ ИЗУЧЕНИЕ ЛЕКАРСТВЕННЫХ СРЕДСТВ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PRECLINICAL AND CLINICAL STUDY OF MEDICINES</subject></subj-group></article-categories><title-group><article-title>Определение активности ферментов метаболизма лекарственных средств - перспектива использования в клинической практике</article-title><trans-title-group xml:lang="en"><trans-title>Determination of the activity of drug-metabolizing enzymes - the prospects for their use in clinical practice</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>Смирнов</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Smirnov</surname><given-names>V. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Егоренков</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Egorenkov</surname><given-names>E. 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>Красных</surname><given-names>Л. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Krasnykh</surname><given-names>L. M.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Василенко</surname><given-names>Г. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Vasilenko</surname><given-names>G. F.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Раменская</surname><given-names>Г. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Ramenskaya</surname><given-names>G. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научный центр экспертизы средств медицинского применения; Первый Московский государственный медицинский университет им. И. М. Сеченова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Scientific Centre for Expert Evaluation of Medicinal Products; I. M. Sechenov First Moscow State Medical University</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><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Научный центр экспертизы средств медицинского применения</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Scientific Centre for Expert Evaluation of Medicinal Products</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>13</day><month>02</month><year>2018</year></pub-date><volume>0</volume><issue>4</issue><fpage>28</fpage><lpage>32</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Смирнов В.В., Егоренков Е.А., Красных Л.М., Василенко Г.Ф., Раменская Г.В., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Смирнов В.В., Егоренков Е.А., Красных Л.М., Василенко Г.Ф., Раменская Г.В.</copyright-holder><copyright-holder xml:lang="en">Smirnov V.V., Egorenkov E.A., Krasnykh L.M., Vasilenko G.F., Ramenskaya G.V.</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.vedomostincesmp.ru/jour/article/view/102">https://www.vedomostincesmp.ru/jour/article/view/102</self-uri><abstract><p>Одной из распространенных проблем современной медицины является риск возникновения нежелательных реакций при приеме различных лекарственных средств. Причины развития таких реакций могут быть разными, однако чаще всего они возникают из-за повышенной или пониженной активности системы ферментов метаболизма ксенобиотиков, в основе которой лежит система изоферментов цитохрома P450 (также известная как CYP). В настоящее время разработан ряд различных методик, позволяющих оценить активность данной системы у конкретного пациента. Авторами были изучены основные методы определения активности ферментов метаболизма лекарственных средств, подходы к их внедрению в клиническую практику и перспективы их использования с целью персонализации фармации и рационализации фармакотерапии.</p></abstract><trans-abstract xml:lang="en"><p>One of the common issues of modern medicine is the risk of adverse drug effects when administering certain medicines. The causes of these effects may be various, but they mostly occur because of increased or decreased activity of xenobiotic-metabolizing enzymes, based on cytochrome P450 isoenzyme system (also known as CYP). For the date there is a number of different ways to determine the activity of the mentioned system in specific patient. The authors have studied the basic methods of determining the activity of drug-metabolizing enzymes and the approaches to their introduction into clinical practice, as well as the prospects of using them for the purpose of personalization of pharmacy and pharmacotherapy rationalization.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>цитохром P450</kwd><kwd>CYP</kwd><kwd>фенотипирование</kwd><kwd>персонализированная медицина</kwd><kwd>фармакотерапия</kwd><kwd>cytochrome P450</kwd><kwd>CYP</kwd><kwd>phenotyping</kwd><kwd>personalized therapy</kwd><kwd>pharmacotherapy</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">Кукес ВГ. Метаболизм лекарственных средств: клинико-фармакологические аспекты. М.: Реафарм; 2004.</mixed-citation><mixed-citation xml:lang="en">Kukes VG. The metabolism of medicines: clinical and pharmacological aspects.  Moscow: Reafarm; 2004 (in Russian).</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Кукес ВГ, Бочков НП, ред. Клиническая фармакогенетика. М.: ГЭОТАР; 2007.</mixed-citation><mixed-citation xml:lang="en">Kukes VG, Bochkov NP, eds. Clinical pharmacogenetics. Moscow: GEOTAR; 2007 (in Russian).</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Hedgecoe AM. Terminology and the construction of scientific disciplines: the case of pharmacogenomics. Science, technology and human values 2003; 28: 513-37; Hedgecoe A. The politics of personalized medicine - pharmacogenetics in the clinic. Cambridge University Press; 2004.</mixed-citation><mixed-citation xml:lang="en">Hedgecoe AM. Terminology and the construction of scientific disciplines: the case  of pharmacogenomics. Science, technology and human values 2003; 28: 513–37; Hedgecoe  A. The politics of personalized medicine — pharmacogenetics in the clinic. Cambridge University Press; 2004.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Hocum BT, White JR, Heck JW, Thirumaran RK, Moyer N, Newman R, Ashcraft K. Cytochrome P450 gene and drug interaction analysis in patients referred for pharmacogenetic testing. Am J Health Syst Pharm. 2016; 73(2): 61-7.</mixed-citation><mixed-citation xml:lang="en">Hocum BT, White JR, Heck JW, Thirumaran RK, Moyer N, Newman R, Ashcraft K.  Cytochrome P450 gene and drug interaction analysis in patients referred for  pharmacogenetic testing. Am J Health Syst Pharm. 2016; 73(2): 61–7.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Samer CF, Lorenzini KI, Rollason V, Daali Y, Desmeules JA. Applications of CYP450 testing in the clinical setting. Mol Diagn Ther. 2013; 17(3): 165-84.</mixed-citation><mixed-citation xml:lang="en">Samer CF, Lorenzini KI, Rollason V, Daali Y, Desmeules JA. Applications of CYP450  testing in the clinical setting. Mol Diagn Ther. 2013; 17(3): 165–84.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Khojasteh SC, Prabhu S, Kenny JR, Halladay JS, Lu AY. Chemical inhibitors of cytochrome P450 isoforms in human liver microsomes: a re-evaluation of P450 isoform selectivity. Eur J Drug Metab Pharmacokinet. 2011; 36(1): 1-16.</mixed-citation><mixed-citation xml:lang="en">Khojasteh SC, Prabhu S, Kenny JR, Halladay JS, Lu AY. Chemical inhibitors of  cytochrome P450 isoforms in human liver microsomes: a re-evaluation of P450 isoform  selectivity. Eur J Drug Metab Pharmacokinet. 2011; 36(1): 1–16.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Emoto C, Murayama N, Rostami-Hodjegan A, Yamazaki H. Methodologies for investigating drug metabolism at the early drug discovery stage: prediction of hepatic drug clearance and P450 contribution. Curr Drug Metab. 2010; 11(8): 678-85.</mixed-citation><mixed-citation xml:lang="en">Emoto C, Murayama N, Rostami-Hodjegan A, Yamazaki H. Methodologies for  investigating drug metabolism at the early drug discovery stage: prediction of  hepatic drug clearance and P450 contribution. Curr Drug Metab. 2010; 11(8): 678–85.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Spaggiari D, Geiser L, Daali Y, Rudaz S. A cocktail approach for assessing the in vitro activity of human cytochrome P450s: an overview of current methodologies. J Pharm Biomed Anal. 2014; 101: 221-37.</mixed-citation><mixed-citation xml:lang="en">Spaggiari D, Geiser L, Daali Y, Rudaz S. A cocktail approach for assessing the in  vitro activity of human cytochrome P450s: an overview of current methodologies. J  Pharm Biomed Anal. 2014; 101: 221–37.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Lo MW, Goldberg MR, McCrea JB, Lu H, Furtek CI, Bjornsson TD. Pharmacokinetics of losartan, an angiotensin II receptor antagonist, and its active metabolite EXP3174 in humans. Clin Pharmacol Ther. 1995; 58(6): 641-9.</mixed-citation><mixed-citation xml:lang="en">Lo MW, Goldberg MR, McCrea JB, Lu H, Furtek CI, Bjornsson TD. Pharmacokinetics of  losartan, an angiotensin II receptor antagonist,  and its active metabolite EXP3174  in humans. Clin Pharmacol Ther. 1995; 58(6): 641–9.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Stearns RA, Chakravarty PK, Chen R, Chiu SH. Biotransformation of losartan to its active carboxylic acid metabolite in human liver microsomes. Role of cytochrome P4502C and 3A subfamily members. Drug metabolism and disposition: the biological fate of chemicals. Drug Metab Dispos. 1995; 23(2): 207-15.</mixed-citation><mixed-citation xml:lang="en">Stearns RA, Chakravarty PK, Chen R, Chiu SH. Biotransformation of losartan to  its active carboxylic acid metabolite in human liver microsomes. Role of cytochrome  P4502C and 3A subfamily members.Drug metabolism and disposition: the biological fate  of chemicals. Drug Metab Dispos. 1995; 23(2): 207–15.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Yun CH, Lee HS, Lee H, Rho JK, Jeong HG, Guengerich FP. Oxidation of the angiotensin II receptor antagonist losartan (DuP 753) in human liver microsomes. Role of cytochrome P4503A(4) in formation of the active metabolite EXP3174. Drug Metab Dispos. 1995; 23(2): 207-15.</mixed-citation><mixed-citation xml:lang="en">Yun CH, Lee HS, Lee H, Rho JK, Jeong HG, Guengerich FP. Oxidation of the  angiotensin II receptor antagonist losartan (DuP 753) in human liver microsomes.  Role of cytochrome P4503A(4) in formation of the active metabolite EXP3174. Drug Metab Dispos. 1995; 23(2): 207–15.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Choi JS, Choi I, Choi DH. Effects of nifedipine on the pharmacokinetics of repaglinide in rats: possible role of CYP3A4 and P-glycoprotein inhibition by nifedipine. Pharmacol Rep. 2013; 65(5): 1422-30.</mixed-citation><mixed-citation xml:lang="en">Choi JS, Choi I, Choi DH. Effects of nifedipine on the pharmacokinetics of  repaglinide in rats: possible role of CYP3A4 and P-glycoprotein inhibition by nifedipine. Pharmacol Rep. 2013; 65(5): 1422–30.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Zong H, Zhuge B, Lu X, Huo X, Fang H, Song J, Sun J. Characterization of a novel cytochrome P450 from Amycolatopsis sp. CGMCC1149 for hydroxylation of lovastatin. Biotechnol Appl Biochem. 2015; 62(1): 9-16.</mixed-citation><mixed-citation xml:lang="en">Zong H, Zhuge B, Lu X, Huo X, Fang H, Song J, Sun J. Characterization of a novel  cytochrome P450 from Amycolatopsis sp. CGMCC1149 for hydroxylation of lovastatin.  Biotechnol Appl Biochem. 2015; 62(1): 9–16.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
