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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">pmj</journal-id><journal-title-group><journal-title xml:lang="ru">Тихоокеанский медицинский журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Pacific Medical Journal</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1609-1175</issn><publisher><publisher-name>TGMU</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">pmj-681</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>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL RESEARCHES</subject></subj-group></article-categories><title-group><article-title>ВЛИЯНИЕ ПЕРИФЕРИЧЕСКИ-ИНДУЦИРОВАННОГО НЕЙРОВОСПАЛЕНИЯ НА КОГНИТИВНЫЕ ФУНКЦИИ У МОЛОДЫХ И СТАРЫХ МЫШЕЙ</article-title><trans-title-group xml:lang="en"><trans-title>EFFECT OF PERIPHERICALLY-INDUCED NEUROINFLAMMATION ON COGNITIVE FUNCTION IN YOUNG AND OLD MICE</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>Тыртышная</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tyrtyshnaya</surname><given-names>A. A.</given-names></name></name-alternatives><email xlink:type="simple">dr.anna.kelvin@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>Зозуля</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Zozulya</surname><given-names>A. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт биологии моря им. А.В. Жирмунского ДВО РАН; Дальневосточный федеральный университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Marine Biology named after A.V. Zhirmunskiy FEB RAS; Far Eastern Federal University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Институт биологии моря им. А.В. Жирмунского ДВО РАН</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Marine Biology named after A.V. Zhirmunskiy FEB RAS</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>28</day><month>06</month><year>2014</year></pub-date><volume>0</volume><issue>2</issue><fpage>23</fpage><lpage>26</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Тыртышная А.А., Зозуля А.А., 2014</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="ru">Тыртышная А.А., Зозуля А.А.</copyright-holder><copyright-holder xml:lang="en">Tyrtyshnaya A.A., Zozulya A.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://www.tmj-vgmu.ru/jour/article/view/681">https://www.tmj-vgmu.ru/jour/article/view/681</self-uri><abstract><p>Оценивали влияние периферически индуцированного нейровоспаления на выраженности когнитивных нарушений в зависимости от возраста у мышей. Нейровоспаление индуцировали путем внутрибрюшинного введения 3- и 18-месячным животным бактериальных липополисахаридов Escherichia coli 0111:B4 (Sigma Aldrich) в дозировке 5 мг/кг. У 18-месячных мышей выявлены более выраженные когнитивный дефицит и снижение локомоторной активности по сравнению с группой «молодых» животных. Иммуногистохимическими методами в гиппокампе у 18-месячных мышей показаны более выраженные активация микроглии и астроглиоз.</p></abstract><trans-abstract xml:lang="en"><p>The article is devoted to experimental evaluation of the impact of peripherically-induced neuroinflammation on the severity of cognitive impairment, depending on age. Methods. Neuroinflammation has been induced in the 3- and 18-month-old white male mice with an intraperitoneal injection of bacterial lipopolysaccharides Escherichia coli 0111: B4 (Sigma Aldrich) 5 mg/kg. After 24 hours, the researchers determined locomotor activity and a working memory in Y-maze. Then the test animals were taken out of the experience and assessed the expression of the proteins GFAP and OX-42 on transverse hippocampal sections. Results. In 18-month-old mice there have been revealed more severe cognitive deficit and decreased locomotor activity compared with the group of “young” test animals. Immunohistochemical methods in hippocampus of 18-month-old mice showed more pronounced activation of microglia and astrogliosis. Conclusions. Aging is accompanied by increased tendency to neuroinflammation. Stimulation of the immune system by bacterial endotoxin increases the severity of inflammatory reactions in the brain of aged mice compared to young animals, regularly provoking neurodegeneration and cognitive deficit.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>липополисахарид</kwd><kwd>нейровоспаление</kwd><kwd>двигательная активность</kwd><kwd>спонтанные альтерации</kwd></kwd-group><kwd-group xml:lang="en"><kwd>lipopolysaccharide</kwd><kwd>neuroinflammation</kwd><kwd>motor activity</kwd><kwd>spontaneous alterations</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">Фоменко С.Е., Кушнерова Н.Ф., Спрыгин В.Г., Момот Т.В. Нарушение обменных процессов в печени крыс под действием стресса // Тихоокеанский мед. журнал. 2013. № 2. С. 67-70.</mixed-citation><mixed-citation xml:lang="en">Фоменко С.Е., Кушнерова Н.Ф., Спрыгин В.Г., Момот Т.В. Нарушение обменных процессов в печени крыс под действием стресса // Тихоокеанский мед. журнал. 2013. № 2. С. 67-70.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Benarroch E. Neuron-astrocyte interactions: partnership for normal function and disease in the central nervous system // Mayo Clinic Proceedings. 2005. Vol. 80, No. 10. P. 1326-1338.</mixed-citation><mixed-citation xml:lang="en">Benarroch E. Neuron-astrocyte interactions: partnership for normal function and disease in the central nervous system // Mayo Clinic Proceedings. 2005. Vol. 80, No. 10. P. 1326-1338.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Godbout J.P., Glaser R. Stress-induced immune dysregulation: implications for wound healing, infectious disease and cancer // J. Neuroimmune Pharmacology. 2006. Vol. 1, No. 4, P. 421-427.</mixed-citation><mixed-citation xml:lang="en">Godbout J.P., Glaser R. Stress-induced immune dysregulation: implications for wound healing, infectious disease and cancer // J. Neuroimmune Pharmacology. 2006. Vol. 1, No. 4, P. 421-427.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Guzmana J.N., Sanchez-Padillaa J., Schumackerb P.T. The role of calcium and mitochondrial oxidant stress in the loss of substantia nigra pars compacta dopaminergic neurons in Parkinson’s disease // Neuroscience. 2011. Vol. 198. P. 221-231</mixed-citation><mixed-citation xml:lang="en">Guzmana J.N., Sanchez-Padillaa J., Schumackerb P.T. The role of calcium and mitochondrial oxidant stress in the loss of substantia nigra pars compacta dopaminergic neurons in Parkinson’s disease // Neuroscience. 2011. Vol. 198. P. 221-231</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Johnson, R.W., Godbout, J.P. Aging, neuroinflammation and behavior // Psychoneuroimmunology. 2006. Vol. 1. P. 379-391.</mixed-citation><mixed-citation xml:lang="en">Johnson, R.W., Godbout, J.P. Aging, neuroinflammation and behavior // Psychoneuroimmunology. 2006. Vol. 1. P. 379-391.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Knowles J., Danielle S., Thuy-Vi N. [et al.] A small molecule p75NTR ligand prevents cognitive deficits and neurite degeneration in an Alzheimer's mouse model // Neurobiology of Aging. 2013. Vol. 34. P. 2052-2063.</mixed-citation><mixed-citation xml:lang="en">Knowles J., Danielle S., Thuy-Vi N. [et al.] A small molecule p75NTR ligand prevents cognitive deficits and neurite degeneration in an Alzheimer's mouse model // Neurobiology of Aging. 2013. Vol. 34. P. 2052-2063.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Richwine A., Parkin A., Buchanan J. [et al.] Architectural changes to CA1 pyramidal neurons in adult and aged mice after peripheral immune stimulation // Psychoneuroendocrinology. 2008. Vol. 33, No. 10. P. 1369-1377.</mixed-citation><mixed-citation xml:lang="en">Richwine A., Parkin A., Buchanan J. [et al.] Architectural changes to CA1 pyramidal neurons in adult and aged mice after peripheral immune stimulation // Psychoneuroendocrinology. 2008. Vol. 33, No. 10. P. 1369-1377.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Sas K., Robotkab H., Toldib J. [et al.] Mitochondria, metabolic disturbances, oxidative stress and the kynurenine system, with focus on neurodegenerative disorders // Journal of the Neurological Sciences. 2007. Vol. 257, No. 1-2. P. 221-239.</mixed-citation><mixed-citation xml:lang="en">Sas K., Robotkab H., Toldib J. [et al.] Mitochondria, metabolic disturbances, oxidative stress and the kynurenine system, with focus on neurodegenerative disorders // Journal of the Neurological Sciences. 2007. Vol. 257, No. 1-2. P. 221-239.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Sutherland G.T., Chami B., Youssef P., Witting P.K. Oxidative stress in Alzheimer's disease: Primary villain or physiological byproduct? // Redox Report. 2013. Vol. 18, No. 4 P. 134-141.</mixed-citation><mixed-citation xml:lang="en">Sutherland G.T., Chami B., Youssef P., Witting P.K. Oxidative stress in Alzheimer's disease: Primary villain or physiological byproduct? // Redox Report. 2013. Vol. 18, No. 4 P. 134-141.</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>
