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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">smjournal</journal-id><journal-title-group><journal-title xml:lang="ru">Спортивная медицина: наука и практика</journal-title><trans-title-group xml:lang="en"><trans-title>Sports medicine: research and practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2223-2524</issn><issn pub-type="epub">2587-9014</issn><publisher><publisher-name>NEICON</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17238/ISSN2223-2524.2018.3.65</article-id><article-id custom-type="elpub" pub-id-type="custom">smjournal-114</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>ФАРМАКОЛОГИЧЕСКАЯ ПОДДЕРЖКА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>SPORTS PHARMACOLOGY</subject></subj-group></article-categories><title-group><article-title>Некоторые аспекты безопасности и фармакологической эффективности (влияние на мышечную дисфункцию) новых производных хромон-3-альдегида</article-title><trans-title-group xml:lang="en"><trans-title>Safety and pharmacological efficiency (influence on muscular dysfunction) of new derivatives of chromon-3-aldehyde</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>Воронков</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Voronkov</surname><given-names>A. 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>Поздняков</surname><given-names>Д. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Pozdnyakov</surname><given-names>D. I.</given-names></name></name-alternatives><email xlink:type="simple">pozdniackow.dmitry@yandex.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>Руковицина</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Rukovitsyna</surname><given-names>V. M.</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>Оганесян</surname><given-names>Э. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Oganesyan</surname><given-names>E. T.</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>Пятигорский медико-фармацевтический институт, филиал ФГБОУ ВО Волгоградский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Pyatigorsk Medical Pharmaceutical Institute, Branch of the Volgograd State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>21</day><month>08</month><year>2020</year></pub-date><volume>8</volume><issue>3</issue><fpage>65</fpage><lpage>71</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Воронков А.В., Поздняков Д.И., Руковицина В.М., Оганесян Э.Т., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Воронков А.В., Поздняков Д.И., Руковицина В.М., Оганесян Э.Т.</copyright-holder><copyright-holder xml:lang="en">Voronkov A.V., Pozdnyakov D.I., Rukovitsyna V.M., Oganesyan E.T.</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.smjournal.ru/jour/article/view/114">https://www.smjournal.ru/jour/article/view/114</self-uri><abstract><p>Цель исследования: в эксперименте оценить безопасность применения новых производных хромон-3-альдегида и возможность их применения для коррекции мышечного утомления. Материалы и методы: работа выполнена на 120 мышах-самцах линии Balb/c. Объектами для исследования послужили галоген-замещенные производные хромон-3-альдегида под шифрами X3AF и X3ACl. Для оценки безопасности применения исследуемых соединений определяли их острую токсичность с расчетом LD50 по методу Финни. Далее изучали влияние исследуемых объектов при профилактическом введении на развитие мышечного утомления в условиях электромиостимуляционного теста. Результаты: проведенное исследование показало, что новые галоген-замещенные производные хромон-3-альдегида под шифрами X3AF и X3ACl обладают оптимальным профилем безопасности применения и способны смягчать проявления мышечной дисфункции. При этом соединение Х3АF превосходило по величине фармакологического эффекта вещество X3ACl и референтный препарат «Милдронат». Выводы: низкая токсичность и высокая фармакологическая эффективность новых галоген-замещенных производных хромон-3-альдегида делает данные соединения перспективными объектами для дальнейшего изучения с целью создания средствa для коррекции мышечной дисфункции.</p></abstract><trans-abstract xml:lang="en"><p>Objective: to estimate the safety of application of new derivatives of chromon-3-aldehyde and the possibility of its application for correction of muscular dysfunction. Materials and methods: the experiment was performed on 120 mice-males of the Balb/c line. Research objects - halogenated derivatives of chromon-3-aldehyde under codes of X3AF and X3ACl. The safety assessment of its application included the determination ofits single dose toxicity with calculation of LD50 using the Finni method. Further, the influence of derivatives on the development of muscular dysfunction using the myostimmulation test after its preventive introduction was studied. Results: the conducted research showed that new halogenated derivatives of chromon-3-aldehyde under codes of X3AF and X3ACl possessed an optimum profile of safety and wereable to alleviate the manifestations of muscle dysfunction. At the same time the substanceX3AF surpassed the substance X3ACl and comparison drug «Mildronat» in the size of pharmacological action. Conclusions: the low toxicity and high pharmacological efficiency of new halogenated derivatives of chromon-3-aldehyde makes these compounds the perspective ob</p></trans-abstract><kwd-group xml:lang="ru"><kwd>мышечное утомление</kwd><kwd>фармакология</kwd><kwd>токсичность лекарственных средств</kwd></kwd-group><kwd-group xml:lang="en"><kwd>muscule fatigue</kwd><kwd>pharmacology</kwd><kwd>drugs toxicity</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">Gea J, Pascual S, Casadevall C, Orozco-Levi M, Barreiro E. 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