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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">scbmt</journal-id><journal-title-group><journal-title xml:lang="ru">БИОМЕДИЦИНА</journal-title><trans-title-group xml:lang="en"><trans-title>Journal Biomed</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2074-5982</issn><issn pub-type="epub">2713-0428</issn><publisher><publisher-name>Scientific center of biomedical technologies of Federal Medical and Biological Agency</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">scbmt-95</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>МЕТОДЫ БИОМЕДИЦИНСКИХ ИССЛЕДОВАНИЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>METHODS OF BIOMEDICAL RESEARCHES</subject></subj-group></article-categories><title-group><article-title>Локализация общего и фосфорилированного α-синуклеина в периферической нервной системе интактных крыс (тестирование антител разных клонов)</article-title><trans-title-group xml:lang="en"><trans-title>Localization of total and Ser 129 phosphorylated α-synuclein in the rat peripheral nervous system (testing of different antibodies)</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>Д. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Voronkov</surname><given-names>D. N.</given-names></name></name-alternatives><email xlink:type="simple">voronkovdm@gmail.com</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>Сальникова</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Salnikova</surname><given-names>O. 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>Худоерков</surname><given-names>Р. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Khudoerkov</surname><given-names>R. M.</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>ФГБНУ «Научный центр неврологии»</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>26</day><month>02</month><year>2019</year></pub-date><volume>0</volume><issue>2</issue><fpage>22</fpage><lpage>32</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Воронков Д.Н., Сальникова О.В., Худоерков Р.М., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Воронков Д.Н., Сальникова О.В., Худоерков Р.М.</copyright-holder><copyright-holder xml:lang="en">Voronkov D.N., Salnikova O.V., Khudoerkov R.M.</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://journal.scbmt.ru/jour/article/view/95">https://journal.scbmt.ru/jour/article/view/95</self-uri><abstract><p>Развитию двигательных симптомов при болезни Паркинсона предшествует накопление α-синуклеина в периферической нервной системе, что позволяет рассматривать α-синуклеин как биомаркер этой патологии. Вместе с тем, для совершенствования экспериментальных моделей и разработки эффективных диагностических тестов требуются более точные знания о локализации α-синуклеина в норме. Иммуногистохимически в периферической нервной системе интактных крыс исследовали локализацию α-синуклеина и вариант его формы, фосфорилированной по остатку серина 129, с помощью панели антител разных производителей и обнаружили его локализацию в пресинаптических нервных окончаниях дорсальных рогов спинного мозга, в телах нейронов превертебральных ганглиев, сплетениях стенок сосудов и GFAP-негативных глиальных клетках. Разные антитела к фосфорилированному α-синуклеину давали неоднозначную реакцию: у отдельных нейронов спинального ганглия окрашивались тела клеток, их отростки и ядра, но ни одно из изучаемых антител не давало реакцию связывания в мелких ноцицептивных непепетидергических нейронах. Неоднозначность результатов может быть обусловлена как разной доступностью эпитопов, выявляемых антителами при взаимодействий α-синуклеина с другими белками, так и в результате неспецифического связывания антител с неидентифицированными мишенями.</p></abstract><trans-abstract xml:lang="en"><p>The deposition of α-synuclein (α-Syn) in the peripheral nervous system precedes the motor symptoms of Parkinson's disease and is considered as a pathological sign and biomarker. However, data on the localization of α-Syn in the intact nervous system require clarification for the future development of experimental models and diagnostic tests. Localization of α-Syn and its the remainder of serine 129 phosphorylated form in peripheral nervous system of intact rats were studied by immunohistochemistry with use of different commercially available antibodies. α-Syn were found in presynaptic terminals of spinal dorsal horn, neuronal somata of prevertebral ganglia, nerve plexuses of vascular wall and GFAP-negative glial cells. Different antibodies to phosphorylated α-Syn shown uneven binding. Staining of processes, somata or nuclei of certain dorsal root ganglia neurons were found. No one of used antibodies detected small nociceptive IB4-positive neurons. The ambiguity of the obtained results can be related both to the different availability of epitopes detected by antibodies as a result of α-Syn interactions with other proteins, and with non-specific binding of antibodies to unidentified targets.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>периферическая нервная система</kwd><kwd>спинальный ганглий</kwd><kwd>крыса</kwd><kwd>иммуногистохимия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>α-синуклеин</kwd><kwd>α-synuclein</kwd><kwd>peripheral nervous system</kwd><kwd>dorsal root ganglion</kwd><kwd>rat</kwd><kwd>immunohistochemistry</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">Пчелина С.Н. Альфа-синуклеин как биомаркер болезни Паркинсона // Анналы клинической и экспериментальной неврологии. 2011. Т. 5. № 4. С. 46-51.</mixed-citation><mixed-citation xml:lang="en">Пчелина С.Н. 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