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<article article-type="research-article" dtd-version="1.2" xml:lang="ru" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2658-6533</journal-id><journal-title-group><journal-title>Research Results in Biomedicine</journal-title></journal-title-group><issn pub-type="epub">2658-6533</issn></journal-meta><article-meta><article-id pub-id-type="doi">10.18413/2313-8955-2015-1-4-66-68</article-id><article-id pub-id-type="publisher-id">499</article-id><article-categories><subj-group subj-group-type="heading"><subject>Pharmacology</subject></subj-group></article-categories><title-group><article-title>CORRECTION OF ADMA-INDUCED PREECLAMPSIA WITH THE USE OF PHOSPHODIESTERASE 5 AND SELECTIVE INHIBITOR OF ARGINASE II ZB49-0010</article-title><trans-title-group xml:lang="en"><trans-title>CORRECTION OF ADMA-INDUCED PREECLAMPSIA WITH THE USE OF PHOSPHODIESTERASE 5 AND SELECTIVE INHIBITOR OF ARGINASE II ZB49-0010</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Gureev</surname><given-names>Vladimir V.</given-names></name><name xml:lang="en"><surname>Gureev</surname><given-names>Vladimir V.</given-names></name></name-alternatives><email>produmen@yandex.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Martynova</surname><given-names>Olga V.</given-names></name><name xml:lang="en"><surname>Martynova</surname><given-names>Olga V.</given-names></name></name-alternatives><email>m.olga91@mail.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Antsiferova</surname><given-names>Oksana E.</given-names></name><name xml:lang="en"><surname>Antsiferova</surname><given-names>Oksana E.</given-names></name></name-alternatives><email>AnciferovaO@ya.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Martynov</surname><given-names>Mikhail A.</given-names></name><name xml:lang="en"><surname>Martynov</surname><given-names>Mikhail A.</given-names></name></name-alternatives><email>ma.martynov@rambler.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Pokrovskaia</surname><given-names>Tatyana G.</given-names></name><name xml:lang="en"><surname>Pokrovskaia</surname><given-names>Tatyana G.</given-names></name></name-alternatives></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Lokteva</surname><given-names>Tatyana I.</given-names></name><name xml:lang="en"><surname>Lokteva</surname><given-names>Tatyana I.</given-names></name></name-alternatives><email>1161779@bsu.edu.ru</email></contrib></contrib-group><pub-date pub-type="epub"><year>2015</year></pub-date><volume>1</volume><issue>4</issue><fpage>0</fpage><lpage>0</lpage><self-uri content-type="pdf" xlink:href="/media/medicine/2015/4/med13.pdf" /><abstract xml:lang="ru"><p>Simulation experimental ADMA-like preeclampsia was carried out by administering the rats with L-NAME during 14-20 days of pregnancy. In animals, there was an increase in blood pressure, proteinuria, impaired microcirculation in the placenta, the violation of the regulation of vascular tone and destructive changes in the ischemic placenta. The use of phosphodiesterase 5 and selective inhibitor of arginase II ZB49-0010 leads to the expression of morphological and functional correction of violations occurring in modeling of experimental preeclampsia</p></abstract><trans-abstract xml:lang="en"><p>Simulation experimental ADMA-like preeclampsia was carried out by administering the rats with L-NAME during 14-20 days of pregnancy. In animals, there was an increase in blood pressure, proteinuria, impaired microcirculation in the placenta, the violation of the regulation of vascular tone and destructive changes in the ischemic placenta. The use of phosphodiesterase 5 and selective inhibitor of arginase II ZB49-0010 leads to the expression of morphological and functional correction of violations occurring in modeling of experimental preeclampsia</p></trans-abstract><kwd-group xml:lang="ru"><kwd>rats</kwd><kwd>N-nitro-L-arginine methyl ester</kwd><kwd>endothelial dysfunction</kwd><kwd>preeclampsia</kwd><kwd>phosphodiesterase 5</kwd><kwd>a selective inhibitor of arginase II</kwd></kwd-group><kwd-group xml:lang="en"><kwd>rats</kwd><kwd>N-nitro-L-arginine methyl ester</kwd><kwd>endothelial dysfunction</kwd><kwd>preeclampsia</kwd><kwd>phosphodiesterase 5</kwd><kwd>a selective inhibitor of arginase II</kwd></kwd-group></article-meta></front><back><ref-list><title>Список литературы</title><ref id="B1"><mixed-citation>Adu-Bonsaffoh. Nitric oxide dysregulation in the pathogenesis of preeclampsia among Ghanaian women. / Adu-Bonsaffoh [et al.] &amp;nbsp;Integr Blood Press Control. . &amp;ndash; 2015.&amp;nbsp; Vol. 19;8. 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