<?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">problendo</journal-id><journal-title-group><journal-title xml:lang="ru">Проблемы Эндокринологии</journal-title><trans-title-group xml:lang="en"><trans-title>Problems of Endocrinology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0375-9660</issn><issn pub-type="epub">2308-1430</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/probl13148</article-id><article-id custom-type="elpub" pub-id-type="custom">problendo-13148</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>Репродуктивная эндокринология</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Reproductive Endocrinology</subject></subj-group></article-categories><title-group><article-title>Андрогены и болезнь Паркинсона: роль у человека и в эксперименте</article-title><trans-title-group xml:lang="en"><trans-title>Androgens and Parkinson’s disease: the role in humans and in experiment</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6197-195X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Хамадьянова</surname><given-names>А. У.</given-names></name><name name-style="western" xml:lang="en"><surname>Hamadyanova</surname><given-names>A. U.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Хамадьянова Аида Ульфатовна</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 4425-5371</p></bio><bio xml:lang="en"><p>Aida U. Hamadyanova</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 4425-5371</p></bio><email xlink:type="simple">sagidullin12@bk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2405-1801</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кузнецов</surname><given-names>К. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuznetsov</surname><given-names>K. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кузнецов Кирилл Олегович</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 3053-3773</p></bio><bio xml:lang="en"><p>Kirill O. Kuznetsov</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 3053-3773</p></bio><email xlink:type="simple">kirillkuznetsov@aol.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8719-608X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гайфуллина</surname><given-names>Э. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Gaifullina</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гайфуллина Энже Ильнуровна</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 5232-0354</p></bio><bio xml:lang="en"><p>Enzhe I. Gaifullina</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 5232-0354</p></bio><email xlink:type="simple">enzhegaifullina@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7733-9772</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каландин</surname><given-names>Д. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kalandin</surname><given-names>D. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Каландин Дмитрий Андреевич</p><p>Санкт-Петербург</p><p>SPIN-код: 7153-8561</p></bio><bio xml:lang="en"><p>Dmitriy A. Kalandin</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 7153-8561</p></bio><email xlink:type="simple">dm.keni@yandex.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0345-3489</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Хамидуллина</surname><given-names>Р. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Khamidullina</surname><given-names>R. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Хамидуллина Радмила Рафитовна</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 7327-4655</p></bio><bio xml:lang="en"><p>Radmila R. Khamudillina</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 7327-4655</p></bio><email xlink:type="simple">khamidullina_radmila@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3501-7756</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Халитова</surname><given-names>И. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Khalitova</surname><given-names>I. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Халитова Ильсина Фаргатовна</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 6339-3531</p></bio><bio xml:lang="en"><p>Ilsina F. Khalitova</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 6339-3531</p></bio><email xlink:type="simple">ilsina.khalitova@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3275-5013</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Фаизов</surname><given-names>Р. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Faizov</surname><given-names>R. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Фаизов Радмир Мидхатович</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 6447-2557</p></bio><bio xml:lang="en"><p>Radmir M. Faizov</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 6447-2557</p></bio><email xlink:type="simple">fradmir177@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7440-3943</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Камалетдинова</surname><given-names>Н. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Kamaletdinova</surname><given-names>N. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Камалетдинова Нелли Олеговна</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 7394-6220</p></bio><bio xml:lang="en"><p>Nelli O. Kamaletdinova</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 7394-6220</p></bio><email xlink:type="simple">nelli-kamaletdinova@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8513-2464</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Асланова</surname><given-names>Б. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Aslanova</surname><given-names>B. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Асланова Бикеханум Фикретдиновна</p><p>Ростов-на-Дону</p><p>SPIN-код: 8023-9633</p></bio><bio xml:lang="en"><p>Bikekhanum F. Aslanova</p><p>Rostov-on-Don</p><p>SPIN-код: 8023-9633</p></bio><email xlink:type="simple">bikesha99@gmail.com</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4191-8638</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Накиева</surname><given-names>А. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Nakieva</surname><given-names>A. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Накиева Аделина Гарифовна</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 7722-4354</p></bio><bio xml:lang="en"><p>Adelina G. Nakieva</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 7722-4354</p></bio><email xlink:type="simple">full-house8@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2357-781X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бурангулова</surname><given-names>Л. Э.</given-names></name><name name-style="western" xml:lang="en"><surname>Burangulova</surname><given-names>L. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бурангулова Лиана Эльвировна</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 6832-9521</p></bio><bio xml:lang="en"><p>Liana E. Burangulova</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 6832-9521</p></bio><email xlink:type="simple">liandoklianchuk@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0047-1382</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гайсина</surname><given-names>Г. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Gaisina</surname><given-names>G. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гайсина Гульназ Олеговна</p><p>119021, г. Москва, переулок Хользунова, д. 7</p><p>SPIN-код: 4522-5373</p></bio><bio xml:lang="en"><p>Gulnaz O. Gaisina</p><p>119021, Moscow, pereulok Holzunova 7</p><p>SPIN-код: 4522-5373</p></bio><email xlink:type="simple">alyssiya18pennywise@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Башкирский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Bashkir state medical university</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Первый Санкт-Петербургский государственный медицинский университет им. акад. И.П. Павлова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>First Pavlov state medical university of St. Petersburg</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Ростовский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Rostov state medical university</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>20</day><month>12</month><year>2022</year></pub-date><volume>68</volume><issue>6</issue><fpage>146</fpage><lpage>156</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Хамадьянова А.У., Кузнецов К.О., Гайфуллина Э.И., Каландин Д.А., Хамидуллина Р.Р., Халитова И.Ф., Фаизов Р.М., Камалетдинова Н.О., Асланова Б.Ф., Накиева А.Г., Бурангулова Л.Э., Гайсина Г.О., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Хамадьянова А.У., Кузнецов К.О., Гайфуллина Э.И., Каландин Д.А., Хамидуллина Р.Р., Халитова И.Ф., Фаизов Р.М., Камалетдинова Н.О., Асланова Б.Ф., Накиева А.Г., Бурангулова Л.Э., Гайсина Г.О.</copyright-holder><copyright-holder xml:lang="en">Hamadyanova A.U., Kuznetsov K.O., Gaifullina E.I., Kalandin D.A., Khamidullina R.R., Khalitova I.F., Faizov R.M., Kamaletdinova N.O., Aslanova B.F., Nakieva A.G., Burangulova L.E., Gaisina G.O.</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.probl-endojournals.ru/jour/article/view/13148">https://www.probl-endojournals.ru/jour/article/view/13148</self-uri><abstract><p>Болезнь Паркинсона (БП) является вторым по распространенности нейродегенеративным заболеванием после болезни Альцгеймера. Имеются данные, что БП имеет более широкую распространенность среди мужчин, что свидетельствует об имеющейся роли половых гормонов в патогенезе развития заболевания. В статье представлен обзор исследований, посвященных изучению половых различий в заболеваемости и симптомах БП. Медикаментозная терапия андрогенами, предшественниками андрогенов, антиандрогенами и препаратами, модифицирующими метаболизм андрогенов, доступна для лечения различных эндокринных состояний, имея трансляционное значение для БП, но ни один из этих препаратов еще не показал достаточной эффективности. Хотя в настоящее время доказано, что БП более распространена у мужчин, чем у женщин, андрогены не всегда оказывают какое-либо влияние на симптомы или прогрессирование заболевания. Ингибиторы 5α-редуктазы показали нейропротекторную и антидискинетическую активность и нуждаются в дальнейшем исследовании. Несмотря на то что нейропротекторный эффект дутастерида наблюдался только до повреждения дофаминовых нейронов, отсутствие негативного влияния делает его привлекательным препаратом для применения у пациентов с БП благодаря его антидискинетическим свойствам.</p></abstract><trans-abstract xml:lang="en"><p>Parkinson’s disease (PD) is the second most common neurodegenerative disease after Alzheimer’s disease. There is evidence that PD has a wider prevalence among men, which indicates the existing role of sex hormones in the pathogenesis of the disease. The article presents an overview of studies devoted to the study of sex differences in the incidence and symptoms of PD. Drug therapy with androgens, androgen precursors, antiandrogens and drugs that modify androgen metabolism is available for the treatment of various endocrine conditions, having translational significance for PD, but none of these drugs has yet shown sufficient effectiveness. Although PD has now been proven to be more common in men than in women, androgens do not always have any effect on the symptoms or progression of the disease. 5α-reductase inhibitors have shown neuroprotective and anti-dyskinetic activity and need further investigation. Despite the fact that the neuroprotective effect of dutasteride was observed only before damage to DA neurons, the absence of a negative effect makes it an attractive drug for use in patients with PD due to its anti-dyskinetic properties.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>болезнь Паркинсона</kwd><kwd>тестостерон</kwd><kwd>андрогены</kwd><kwd>дигидротестостерон</kwd><kwd>половые различия</kwd><kwd>эстрогены</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Parkinson’s disease</kwd><kwd>testosterone</kwd><kwd>androgen</kwd><kwd>dihydrotestosterone</kwd><kwd>sex differences</kwd><kwd>estrogens</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">Armstrong MJ, Okun MS. Diagnosis and Treatment of Parkinson Disease: A Review. JAMA. 2020;323(6):548-560. doi: https://doi.org/10.1001/jama.2019.22360</mixed-citation><mixed-citation xml:lang="en">Armstrong MJ, Okun MS. Diagnosis and Treatment of Parkinson Disease: A Review. JAMA. 2020;323(6):548-560. doi: https://doi.org/10.1001/jama.2019.22360</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Катунина Е.А., Бездольный Ю.Н. Эпидемиология болезни Паркинсона // Журнал неврологии и психиатрии им. С.С. Корсакова. — 2013. — Т. 113. — №12. — С. 81-88.</mixed-citation><mixed-citation xml:lang="en">Katunina EA, Bezdolnyj YUN. Epidemiology of Parkinson’s disease. ZHurnal nevrologii i psihiatrii im. S.S. Korsakova. 2013;113(12):81-88. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Park A, Stacy M. Non-motor symptoms in Parkinson’s disease. J Neurol. 2009;256(3):293-298. doi: https://doi.org/10.1007/s00415-009-5240-1</mixed-citation><mixed-citation xml:lang="en">Park A, Stacy M. Non-motor symptoms in Parkinson’s disease. J Neurol. 2009;256(3):293-298. doi: https://doi.org/10.1007/s00415-009-5240-1</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Lesage S, Brice A. Parkinson’s disease: from monogenic forms to genetic susceptibility factors. Hum Mol Genet. 2009;18(1):48-59. doi: https://doi.org/10.1093/hmg/ddp012</mixed-citation><mixed-citation xml:lang="en">Lesage S, Brice A. Parkinson’s disease: from monogenic forms to genetic susceptibility factors. Hum Mol Genet. 2009;18(1):48-59. doi: https://doi.org/10.1093/hmg/ddp012</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Meoni S, Macerollo A, Moro E. Sex differences in movement disorders. Nat Rev Neurol. 2020;16(2):84-96. doi: https://doi.org/10.1038/s41582-019-0294-x</mixed-citation><mixed-citation xml:lang="en">Meoni S, Macerollo A, Moro E. Sex differences in movement disorders. Nat Rev Neurol. 2020;16(2):84-96. doi: https://doi.org/10.1038/s41582-019-0294-x</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Pringsheim T, Jette N, Frolkis A, Steeves TD. The prevalence of Parkinson’s disease: a systematic review and meta-analysis. Mov Disord. 2014;29(13):1583-1590. doi: https://doi.org/10.1002/mds.25945</mixed-citation><mixed-citation xml:lang="en">Pringsheim T, Jette N, Frolkis A, Steeves TD. The prevalence of Parkinson’s disease: a systematic review and meta-analysis. Mov Disord. 2014;29(13):1583-1590. doi: https://doi.org/10.1002/mds.25945</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Аралбаева А.Д., Каменова С.У., Кужыбаева К.К. Болезнь Паркинсона // Вестник Казахского Национального медицинского университета. — 2019. — №1. — С. 199-201.</mixed-citation><mixed-citation xml:lang="en">Aralbaeva AD, Kamenova SU, Kuzhybaeva KK. Parkinson’s disease. Vestnik Kazahskogo Nacional’nogo medicinskogo universiteta. 2019;1:199-201. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Hirsch L, Jette N, Frolkis A, Steeves T, Pringsheim T. The incidence of Parkinson’s disease: A systematic review and meta-analysis. Neuroepidemiology. 2016;46(4):292-300. doi: https://doi.org/10.1159/000445751</mixed-citation><mixed-citation xml:lang="en">Hirsch L, Jette N, Frolkis A, Steeves T, Pringsheim T. The incidence of Parkinson’s disease: A systematic review and meta-analysis. Neuroepidemiology. 2016;46(4):292-300. doi: https://doi.org/10.1159/000445751</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Shulman LM, Bhat V. Gender disparities in Parkinson’s disease. Expert Rev Neurother. 2006;6(3):407-416. doi: https://doi.org/10.1586/14737175.6.3.407</mixed-citation><mixed-citation xml:lang="en">Shulman LM, Bhat V. Gender disparities in Parkinson’s disease. Expert Rev Neurother. 2006;6(3):407-416. doi: https://doi.org/10.1586/14737175.6.3.407</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Swerdlow RH, Parker WD, Currie LJ, et al. Gender ratio differences between Parkinson’s disease patients and their affected relatives. Parkinsonism Relat Disord. 2001;7(2):129-133. doi: https://doi.org/10.1016/s1353-8020(00)00029-8</mixed-citation><mixed-citation xml:lang="en">Swerdlow RH, Parker WD, Currie LJ, et al. Gender ratio differences between Parkinson’s disease patients and their affected relatives. Parkinsonism Relat Disord. 2001;7(2):129-133. doi: https://doi.org/10.1016/s1353-8020(00)00029-8</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Taylor KS, Cook JA, Counsell CE. Heterogeneity in male to female risk for Parkinson’s disease. J Neurol Neurosurg Psychiatry. 2007;78(8):905-906. doi: https://doi.org/10.1136/jnnp.2006.104695</mixed-citation><mixed-citation xml:lang="en">Taylor KS, Cook JA, Counsell CE. Heterogeneity in male to female risk for Parkinson’s disease. J Neurol Neurosurg Psychiatry. 2007;78(8):905-906. doi: https://doi.org/10.1136/jnnp.2006.104695</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Van Den Eeden SK, Tanner CM, Bernstein AL, et al. Incidence of Parkinson’s disease: variation by age, gender, and race/ethnicity. Am J Epidemiol. 2003;157(11):1015-1022. doi: https://doi.org/10.1093/aje/kwg068</mixed-citation><mixed-citation xml:lang="en">Van Den Eeden SK, Tanner CM, Bernstein AL, et al. Incidence of Parkinson’s disease: variation by age, gender, and race/ethnicity. Am J Epidemiol. 2003;157(11):1015-1022. doi: https://doi.org/10.1093/aje/kwg068</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Wooten GF, Currie LJ, Bovbjerg VE, et al. Are men at greater risk for Parkinson’s disease than women? J Neurol Neurosurg Psychiatry. 2004;75(4):637-639. doi: https://doi.org/10.1136/jnnp.2003.020982</mixed-citation><mixed-citation xml:lang="en">Wooten GF, Currie LJ, Bovbjerg VE, et al. Are men at greater risk for Parkinson’s disease than women? J Neurol Neurosurg Psychiatry. 2004;75(4):637-639. doi: https://doi.org/10.1136/jnnp.2003.020982</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Haaxma CA, Bloem BR, Borm GF, et al. Gender differences in Parkinson’s disease. J Neurol Neurosurg Psychiatry. 2007;78(8):819-824. doi: https://doi.org/10.1136/jnnp.2006.103788</mixed-citation><mixed-citation xml:lang="en">Haaxma CA, Bloem BR, Borm GF, et al. Gender differences in Parkinson’s disease. J Neurol Neurosurg Psychiatry. 2007;78(8):819-824. doi: https://doi.org/10.1136/jnnp.2006.103788</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Twelves D, Perkins KS, Counsell C. Systematic review of incidence studies of Parkinson’s disease. Mov Disord. 2003;18(1):19-31. doi: https://doi.org/10.1002/mds.10305</mixed-citation><mixed-citation xml:lang="en">Twelves D, Perkins KS, Counsell C. Systematic review of incidence studies of Parkinson’s disease. Mov Disord. 2003;18(1):19-31. doi: https://doi.org/10.1002/mds.10305</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Frentzel D, Judanin G, Borozdina O, et al. Increase of Reproductive Life Span Delays Age of Onset of Parkinson’s Disease. Front Neurol. 2017;8(2):371-377. doi: https://doi.org/10.3389/fneur.2017.00397</mixed-citation><mixed-citation xml:lang="en">Frentzel D, Judanin G, Borozdina O, et al. Increase of Reproductive Life Span Delays Age of Onset of Parkinson’s Disease. Front Neurol. 2017;8(2):371-377. doi: https://doi.org/10.3389/fneur.2017.00397</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Ragonese P, D’Amelio M, Callari G, et al. Age at menopause predicts age at onset of Parkinson’s disease. Mov Disord. 2006;21(12):2211-2214. doi: https://doi.org/10.1002/mds.21127</mixed-citation><mixed-citation xml:lang="en">Ragonese P, D’Amelio M, Callari G, et al. Age at menopause predicts age at onset of Parkinson’s disease. Mov Disord. 2006;21(12):2211-2214. doi: https://doi.org/10.1002/mds.21127</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Bourque M, Morissette M, Di Paolo T. Repurposing sex steroids and related drugs as potential treatment for Parkinson’s disease. Neuropharmacology. 2019;147(2):37-54. doi: https://doi.org/10.1016/j.neuropharm.2018.04.005</mixed-citation><mixed-citation xml:lang="en">Bourque M, Morissette M, Di Paolo T. Repurposing sex steroids and related drugs as potential treatment for Parkinson’s disease. Neuropharmacology. 2019;147(2):37-54. doi: https://doi.org/10.1016/j.neuropharm.2018.04.005</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Jurado-Coronel JC, Cabezas R, Ávila Rodríguez MF, et al. Sex differences in Parkinson’s disease: Features on clinical symptoms, treatment outcome, sexual hormones and genetics. Front Neuroendocrinol. 2018;50(2):18-30. doi: https://doi.org/10.1016/j.yfrne.2017.09.002</mixed-citation><mixed-citation xml:lang="en">Jurado-Coronel JC, Cabezas R, Ávila Rodríguez MF, et al. Sex differences in Parkinson’s disease: Features on clinical symptoms, treatment outcome, sexual hormones and genetics. Front Neuroendocrinol. 2018;50(2):18-30. doi: https://doi.org/10.1016/j.yfrne.2017.09.002</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Do Rego JL, Seong JY, Burel D, et al. Neurosteroid biosynthesis: enzymatic pathways and neuroendocrine regulation by neurotransmitters and neuropeptides. Front Neuroendocrinol. 2009;30(3):259-301. doi: https://doi.org/10.1016/j.yfrne.2009.05.006</mixed-citation><mixed-citation xml:lang="en">Do Rego JL, Seong JY, Burel D, et al. Neurosteroid biosynthesis: enzymatic pathways and neuroendocrine regulation by neurotransmitters and neuropeptides. Front Neuroendocrinol. 2009;30(3):259-301. doi: https://doi.org/10.1016/j.yfrne.2009.05.006</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">McEwan IJ, Brinkmann AO. Androgen physiology: Receptor and metabolic disorders. In: Endotext. South Dartmouth: MA. MDText.com, Inc; 2000.</mixed-citation><mixed-citation xml:lang="en">McEwan IJ, Brinkmann AO. Androgen physiology: Receptor and metabolic disorders. In: Endotext. South Dartmouth: MA. MDText.com, Inc; 2000.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Thomas P. Membrane androgen receptors unrelated to nuclear steroid receptors. Endocrinology. 2019;160(4):772-781. doi: https://doi.org/10.1210/en.2018-00987</mixed-citation><mixed-citation xml:lang="en">Thomas P. Membrane androgen receptors unrelated to nuclear steroid receptors. Endocrinology. 2019;160(4):772-781. doi: https://doi.org/10.1210/en.2018-00987</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Callewaert L, Christiaens V, Haelens A, et al. Implications of a polyglutamine tract in the function of the human androgen receptor. Biochem Biophys Res Commun. 2003;306(1):46-52. doi: https://doi.org/10.1016/s0006-291x(03)00902-1</mixed-citation><mixed-citation xml:lang="en">Callewaert L, Christiaens V, Haelens A, et al. Implications of a polyglutamine tract in the function of the human androgen receptor. Biochem Biophys Res Commun. 2003;306(1):46-52. doi: https://doi.org/10.1016/s0006-291x(03)00902-1</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Tirabassi G, Cignarelli A, Perrini S, et al. Influence of CAG Repeat Polymorphism on the Targets of Testosterone Action. Int J Endocrinol. 2015;2015(2):1-12. doi: https://doi.org/10.1155/2015/298107</mixed-citation><mixed-citation xml:lang="en">Tirabassi G, Cignarelli A, Perrini S, et al. Influence of CAG Repeat Polymorphism on the Targets of Testosterone Action. Int J Endocrinol. 2015;2015(2):1-12. doi: https://doi.org/10.1155/2015/298107</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Kaufman JM, Lapauw B, Mahmoud A, et al. Aging and the Male Reproductive System. Endocr Rev. 2019;40(4):906-972. doi: https://doi.org/10.1210/er.2018-00178</mixed-citation><mixed-citation xml:lang="en">Kaufman JM, Lapauw B, Mahmoud A, et al. Aging and the Male Reproductive System. Endocr Rev. 2019;40(4):906-972. doi: https://doi.org/10.1210/er.2018-00178</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Harman SM, Metter EJ, Tobin JD, Pearson J, Blackman MR; Baltimore longitudinal study of aging. Longitudinal effects of aging on serum total and free testosterone levels in healthy men. Baltimore Longitudinal Study of Aging. J Clin Endocrinol Metab. 2001;86(2):724-731. doi: https://doi.org/10.1210/jcem.86.2.7219</mixed-citation><mixed-citation xml:lang="en">Harman SM, Metter EJ, Tobin JD, Pearson J, Blackman MR; Baltimore longitudinal study of aging. Longitudinal effects of aging on serum total and free testosterone levels in healthy men. Baltimore Longitudinal Study of Aging. J Clin Endocrinol Metab. 2001;86(2):724-731. doi: https://doi.org/10.1210/jcem.86.2.7219</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Okun MS, McDonald WM, DeLong MR. Refractory nonmotor symptoms in male patients with Parkinson disease due to testosterone deficiency: a common unrecognized comorbidity. Arch Neurol. 2002;59(5):807-811. doi: https://doi.org/10.1001/archneur.59.5.807</mixed-citation><mixed-citation xml:lang="en">Okun MS, McDonald WM, DeLong MR. Refractory nonmotor symptoms in male patients with Parkinson disease due to testosterone deficiency: a common unrecognized comorbidity. Arch Neurol. 2002;59(5):807-811. doi: https://doi.org/10.1001/archneur.59.5.807</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Okun MS, Crucian GP, Fischer L, et al. Testosterone deficiency in a Parkinson’s disease clinic: results of a survey. J Neurol Neurosurg Psychiatry. 2004;75(1):165-166.</mixed-citation><mixed-citation xml:lang="en">Okun MS, Crucian GP, Fischer L, et al. Testosterone deficiency in a Parkinson’s disease clinic: results of a survey. J Neurol Neurosurg Psychiatry. 2004;75(1):165-166.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Luchetti S, Bossers K, Frajese GV, Swaab DF. Neurosteroid biosynthetic pathway changes in substantia nigra and caudate nucleus in Parkinson’s disease. Brain Pathol. 2010;20(5):945-951. doi: https://doi.org/10.1111/j.1750-3639.2010.00396.x</mixed-citation><mixed-citation xml:lang="en">Luchetti S, Bossers K, Frajese GV, Swaab DF. Neurosteroid biosynthetic pathway changes in substantia nigra and caudate nucleus in Parkinson’s disease. Brain Pathol. 2010;20(5):945-951. doi: https://doi.org/10.1111/j.1750-3639.2010.00396.x</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Okun MS, Wu SS, Jennings D, et al. Testosterone level and the effect of levodopa and agonists in early Parkinson disease: results from the INSPECT cohort. J Clin Mov Disord. 2014;1(1):8. doi: https://doi.org/10.1186/2054-7072-1-8</mixed-citation><mixed-citation xml:lang="en">Okun MS, Wu SS, Jennings D, et al. Testosterone level and the effect of levodopa and agonists in early Parkinson disease: results from the INSPECT cohort. J Clin Mov Disord. 2014;1(1):8. doi: https://doi.org/10.1186/2054-7072-1-8</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Chung SD, Lin HC, Tsai MC, et al. Androgen deprivation therapy did not increase the risk of Alzheimer’s and Parkinson’s disease in patients with prostate cancer. Andrology. 2016;4(3):481-485. doi: https://doi.org/10.1111/andr.12187</mixed-citation><mixed-citation xml:lang="en">Chung SD, Lin HC, Tsai MC, et al. Androgen deprivation therapy did not increase the risk of Alzheimer’s and Parkinson’s disease in patients with prostate cancer. Andrology. 2016;4(3):481-485. doi: https://doi.org/10.1111/andr.12187</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Young JWS, Sutradhar R, Rangrej J, et al. Androgen deprivation therapy and the risk of parkinsonism in men with prostate cancer. World J Urol. 2017;35(9):1417-1423. doi: https://doi.org/10.1007/s00345-017-2010-z</mixed-citation><mixed-citation xml:lang="en">Young JWS, Sutradhar R, Rangrej J, et al. Androgen deprivation therapy and the risk of parkinsonism in men with prostate cancer. World J Urol. 2017;35(9):1417-1423. doi: https://doi.org/10.1007/s00345-017-2010-z</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Khasnavis S, Ghosh A, Roy A, Pahan K. Castration induces Parkinson disease pathologies in young male mice via inducible nitric-oxide synthase. J Biol Chem. 2013;288(29):20843-20855. doi: 10.1074/jbc.M112.443556.</mixed-citation><mixed-citation xml:lang="en">Khasnavis S, Ghosh A, Roy A, Pahan K. Castration induces Parkinson disease pathologies in young male mice via inducible nitric-oxide synthase. J Biol Chem. 2013;288(29):20843-20855. doi: 10.1074/jbc.M112.443556.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Murray HE, Pillai AV, McArthur SR, et al. Dose- and sex-dependent effects of the neurotoxin 6-hydroxydopamine on the nigrostriatal dopaminergic pathway of adult rats: differential actions of estrogen in males and females. Neuroscience. 2003;116(1):213-222. doi: https://doi.org/10.1016/s0306-4522(02)00578-x</mixed-citation><mixed-citation xml:lang="en">Murray HE, Pillai AV, McArthur SR, et al. Dose- and sex-dependent effects of the neurotoxin 6-hydroxydopamine on the nigrostriatal dopaminergic pathway of adult rats: differential actions of estrogen in males and females. Neuroscience. 2003;116(1):213-222. doi: https://doi.org/10.1016/s0306-4522(02)00578-x</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Tamás A, Lubics A, Lengvári I, Reglodi D. Effects of age, gender, and gonadectomy on neurochemistry and behavior in animal models of Parkinson’s disease. Endocrine. 2006;29(2):275-287. doi: https://doi.org/10.1385/ENDO:29:2:275</mixed-citation><mixed-citation xml:lang="en">Tamás A, Lubics A, Lengvári I, Reglodi D. Effects of age, gender, and gonadectomy on neurochemistry and behavior in animal models of Parkinson’s disease. Endocrine. 2006;29(2):275-287. doi: https://doi.org/10.1385/ENDO:29:2:275</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Cunningham RL, Macheda T, Watts LT, et al. Androgens exacerbate motor asymmetry in male rats with unilateral 6-hydroxydopamine lesion. Horm Behav. 2011;60(5):617-624. doi: https://doi.org/10.1016/j.yhbeh.2011.08.012</mixed-citation><mixed-citation xml:lang="en">Cunningham RL, Macheda T, Watts LT, et al. Androgens exacerbate motor asymmetry in male rats with unilateral 6-hydroxydopamine lesion. Horm Behav. 2011;60(5):617-624. doi: https://doi.org/10.1016/j.yhbeh.2011.08.012</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Antzoulatos E, Jakowec MW, Petzinger GM, Wood RI. MPTP Neurotoxicity and Testosterone Induce Dendritic Remodeling of Striatal Medium Spiny Neurons in the C57Bl/6 Mouse. Parkinsons Dis. 2011;2011(1):1-10. doi: https://doi.org/10.4061/2011/138471</mixed-citation><mixed-citation xml:lang="en">Antzoulatos E, Jakowec MW, Petzinger GM, Wood RI. MPTP Neurotoxicity and Testosterone Induce Dendritic Remodeling of Striatal Medium Spiny Neurons in the C57Bl/6 Mouse. Parkinsons Dis. 2011;2011(1):1-10. doi: https://doi.org/10.4061/2011/138471</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Dluzen DE. Effects of testosterone upon MPTP-induced neurotoxicity of the nigrostriatal dopaminergic system of C57/B1 mice. Brain Res. 1996;715(1-2):113-118. doi: https://doi.org/10.1016/0006-8993(95)01566-3.</mixed-citation><mixed-citation xml:lang="en">Dluzen DE. Effects of testosterone upon MPTP-induced neurotoxicity of the nigrostriatal dopaminergic system of C57/B1 mice. Brain Res. 1996;715(1-2):113-118. doi: https://doi.org/10.1016/0006-8993(95)01566-3.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Litim N, Bourque M, Al Sweidi S, et al. The 5α-reductase inhibitor Dutasteride but not Finasteride protects dopamine neurons in the MPTP mouse model of Parkinson’s disease. Neuropharmacology. 2015;97(1):86-94. doi: https://doi.org/10.1016/j.neuropharm.2015.05.015</mixed-citation><mixed-citation xml:lang="en">Litim N, Bourque M, Al Sweidi S, et al. The 5α-reductase inhibitor Dutasteride but not Finasteride protects dopamine neurons in the MPTP mouse model of Parkinson’s disease. Neuropharmacology. 2015;97(1):86-94. doi: https://doi.org/10.1016/j.neuropharm.2015.05.015</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Litim N, Morissette M, Caruso D, et al. Effect of the 5α-reductase enzyme inhibitor dutasteride in the brain of intact and parkinsonian mice. J Steroid Biochem Mol Biol. 2017;174:242-256. doi: https://doi.org/10.1016/j.jsbmb.2017.09.021</mixed-citation><mixed-citation xml:lang="en">Litim N, Morissette M, Caruso D, et al. Effect of the 5α-reductase enzyme inhibitor dutasteride in the brain of intact and parkinsonian mice. J Steroid Biochem Mol Biol. 2017;174:242-256. doi: https://doi.org/10.1016/j.jsbmb.2017.09.021</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Ruffoli R, Giambelluca MA, Scavuzzo MC, et al. MPTPinduced Parkinsonism is associated with damage to Leydig cells and testosterone loss. Brain Res. 2008;1229:218-223. doi: https://doi.org/10.1016/j.brainres.2008.06.116</mixed-citation><mixed-citation xml:lang="en">Ruffoli R, Giambelluca MA, Scavuzzo MC, et al. MPTPinduced Parkinsonism is associated with damage to Leydig cells and testosterone loss. Brain Res. 2008;1229:218-223. doi: https://doi.org/10.1016/j.brainres.2008.06.116</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Allen JA, Diemer T, Janus P, et al. Bacterial endotoxin lipopolysaccharide and reactive oxygen species inhibit Leydig cell steroidogenesis via perturbation of mitochondria. Endocrine. 2004;25(3):265-275. doi: https://doi.org/10.1385/ENDO:25:3:265</mixed-citation><mixed-citation xml:lang="en">Allen JA, Diemer T, Janus P, et al. Bacterial endotoxin lipopolysaccharide and reactive oxygen species inhibit Leydig cell steroidogenesis via perturbation of mitochondria. Endocrine. 2004;25(3):265-275. doi: https://doi.org/10.1385/ENDO:25:3:265</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Lee SY, Gong EY, Hong CY, et al. ROS inhibit the expression of testicular steroidogenic enzyme genes via the suppression of Nur77 transactivation. Free Radic Biol Med. 2009;47(11):1591-600. doi: https://doi.org/10.1016/j.freeradbiomed.2009.09.004</mixed-citation><mixed-citation xml:lang="en">Lee SY, Gong EY, Hong CY, et al. ROS inhibit the expression of testicular steroidogenic enzyme genes via the suppression of Nur77 transactivation. Free Radic Biol Med. 2009;47(11):1591-600. doi: https://doi.org/10.1016/j.freeradbiomed.2009.09.004</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Melcangi RC, Caruso D, Levandis G, et al. Modifications of neuroactive steroid levels in an experimental model of nigrostriatal degeneration: potential relevance to the pathophysiology of Parkinson’s disease. J Mol Neurosci. 2012;46(1):177-183. doi: https://doi.org/10.1007/s12031-011-9570-y</mixed-citation><mixed-citation xml:lang="en">Melcangi RC, Caruso D, Levandis G, et al. Modifications of neuroactive steroid levels in an experimental model of nigrostriatal degeneration: potential relevance to the pathophysiology of Parkinson’s disease. J Mol Neurosci. 2012;46(1):177-183. doi: https://doi.org/10.1007/s12031-011-9570-y</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Okun MS, Fernandez HH, Rodriguez RL, et al. Testosterone therapy in men with Parkinson disease: results of the TEST-PD Study. Arch Neurol. 2006;63(5):729-735. doi: https://doi.org/10.1001/archneur.63.5.729</mixed-citation><mixed-citation xml:lang="en">Okun MS, Fernandez HH, Rodriguez RL, et al. Testosterone therapy in men with Parkinson disease: results of the TEST-PD Study. Arch Neurol. 2006;63(5):729-735. doi: https://doi.org/10.1001/archneur.63.5.729</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Okun MS, Walter BL, McDonald WM, et al. Beneficial effects of testosterone replacement for the nonmotor symptoms of Parkinson disease. Arch Neurol. 2002;59(11):1750-1753. doi: https://doi.org/10.1001/archneur.59.11.1750</mixed-citation><mixed-citation xml:lang="en">Okun MS, Walter BL, McDonald WM, et al. Beneficial effects of testosterone replacement for the nonmotor symptoms of Parkinson disease. Arch Neurol. 2002;59(11):1750-1753. doi: https://doi.org/10.1001/archneur.59.11.1750</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Mitchell E, Thomas D, Burnet R. Testosterone improves motor function in Parkinson’s disease. J Clin Neurosci. 2006;13(1):133-136. doi: https://doi.org/10.1016/j.jocn.2005.02.014</mixed-citation><mixed-citation xml:lang="en">Mitchell E, Thomas D, Burnet R. Testosterone improves motor function in Parkinson’s disease. J Clin Neurosci. 2006;13(1):133-136. doi: https://doi.org/10.1016/j.jocn.2005.02.014</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Bhasin S, Brito JP, Cunningham GR, et al. Testosterone therapy in men with hypogonadism: An endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2018;103(5):1715-1744. doi: https://doi.org/10.1210/jc.2018-00229</mixed-citation><mixed-citation xml:lang="en">Bhasin S, Brito JP, Cunningham GR, et al. Testosterone therapy in men with hypogonadism: An endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2018;103(5):1715-1744. doi: https://doi.org/10.1210/jc.2018-00229</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Rodrigues dos Santos M, Bhasin S. Benefits and Risks of Testosterone Treatment in Men with Age-Related Decline in Testosterone. Annu Rev Med. 2021;72(1):75-91. doi: https://doi.org/10.1146/annurev-med-050219-034711</mixed-citation><mixed-citation xml:lang="en">Rodrigues dos Santos M, Bhasin S. Benefits and Risks of Testosterone Treatment in Men with Age-Related Decline in Testosterone. Annu Rev Med. 2021;72(1):75-91. doi: https://doi.org/10.1146/annurev-med-050219-034711</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Ekue A, Boulanger JF, Morissette M, Di Paolo T. Lack of effect of testosterone and dihydrotestosterone compared to 17beta-oestradiol in 1-methyl-4-phenyl-1,2,3,6, tetrahydropyridine-mice. J Neuroendocrinol. 2002;14(9):731-736. doi: https://doi.org/10.1046/j.1365-2826.2002.00833.x</mixed-citation><mixed-citation xml:lang="en">Ekue A, Boulanger JF, Morissette M, Di Paolo T. Lack of effect of testosterone and dihydrotestosterone compared to 17beta-oestradiol in 1-methyl-4-phenyl-1,2,3,6, tetrahydropyridine-mice. J Neuroendocrinol. 2002;14(9):731-736. doi: https://doi.org/10.1046/j.1365-2826.2002.00833.x</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Gillies GE, Murray HE, Dexter D, McArthur S. Sex dimorphisms in the neuroprotective effects of estrogen in an animal model of Parkinson’s disease. Pharmacol Biochem Behav. 2004;78(3):513-522. doi: https://doi.org/10.1016/j.pbb.2004.04.022</mixed-citation><mixed-citation xml:lang="en">Gillies GE, Murray HE, Dexter D, McArthur S. Sex dimorphisms in the neuroprotective effects of estrogen in an animal model of Parkinson’s disease. Pharmacol Biochem Behav. 2004;78(3):513-522. doi: https://doi.org/10.1016/j.pbb.2004.04.022</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Cui R, Kang Y, Wang L, et al. Testosterone Propionate Exacerbates the Deficits of Nigrostriatal Dopaminergic System and Downregulates Nrf2 Expression in Reserpine-Treated Aged Male Rats. Front Aging Neurosci. 2017;9(1):75-91. doi: https://doi.org/10.3389/fnagi.2017.00172</mixed-citation><mixed-citation xml:lang="en">Cui R, Kang Y, Wang L, et al. Testosterone Propionate Exacerbates the Deficits of Nigrostriatal Dopaminergic System and Downregulates Nrf2 Expression in Reserpine-Treated Aged Male Rats. Front Aging Neurosci. 2017;9(1):75-91. doi: https://doi.org/10.3389/fnagi.2017.00172</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Фролова Г.А. Сравнительная характеристика эффектов блокирования рецепторов половых гормонов у самцов и самок белых крыс с разным уровнем активности на некоторые показатели поведения // Вісник проблем біології і медицини. — 2013. — Т. 2. — №3. — С. 235-239.</mixed-citation><mixed-citation xml:lang="en">Frolova GA. Comparative characteristics of the effects of blocking sex hormone receptors in male and female white rats with different levels of activity on some behavior indicators. Vіsnik problem bіologії і medicini. 2013;2(3):235-239. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Kuiper GG, Carlsson B, Grandien K, et al. Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta. Endocrinology. 1997;138(3):863-870. doi: https://doi.org/10.1210/endo.138.3.4979</mixed-citation><mixed-citation xml:lang="en">Kuiper GG, Carlsson B, Grandien K, et al. Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta. Endocrinology. 1997;138(3):863-870. doi: https://doi.org/10.1210/endo.138.3.4979</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Bourque M, Morissette M, Di Paolo T. Raloxifene activates G protein-coupled estrogen receptor 1/Akt signaling to protect dopamine neurons in 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine mice. Neurobiol Aging. 2014;35(10):2347-2356. doi: https://doi.org/10.1016/j.neurobiolaging.2014.03.017</mixed-citation><mixed-citation xml:lang="en">Bourque M, Morissette M, Di Paolo T. Raloxifene activates G protein-coupled estrogen receptor 1/Akt signaling to protect dopamine neurons in 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine mice. Neurobiol Aging. 2014;35(10):2347-2356. doi: https://doi.org/10.1016/j.neurobiolaging.2014.03.017</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Nitkowska M, Tomasiuk R, Czyżyk M, Friedman A. Prolactin and sex hormones levels in males with Parkinson’s disease. Acta Neurol Scand. 2015;131(6):411-416. doi: https://doi.org/10.1111/ane.12334</mixed-citation><mixed-citation xml:lang="en">Nitkowska M, Tomasiuk R, Czyżyk M, Friedman A. Prolactin and sex hormones levels in males with Parkinson’s disease. Acta Neurol Scand. 2015;131(6):411-416. doi: https://doi.org/10.1111/ane.12334</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Georgianos PI, Vaios V, Eleftheriadis T, et al. Mineralocorticoid Antagonists in ESRD: An Overview of Clinical Trial Evidence. Curr Vasc Pharmacol. 2017;15(6):599-606. doi: https://doi.org/10.2174/1570161115666170201113817</mixed-citation><mixed-citation xml:lang="en">Georgianos PI, Vaios V, Eleftheriadis T, et al. Mineralocorticoid Antagonists in ESRD: An Overview of Clinical Trial Evidence. Curr Vasc Pharmacol. 2017;15(6):599-606. doi: https://doi.org/10.2174/1570161115666170201113817</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Hermidorff MM, Faria Gde O, Amâncio Gde C, et al. Nongenomic effects of spironolactone and eplerenone in cardiomyocytes of neonatal Wistar rats: do they evoke cardioprotective pathways? Biochem Cell Biol. 2015;93(1):83-93. doi: https://doi.org/10.1139/bcb-2014-0110</mixed-citation><mixed-citation xml:lang="en">Hermidorff MM, Faria Gde O, Amâncio Gde C, et al. Nongenomic effects of spironolactone and eplerenone in cardiomyocytes of neonatal Wistar rats: do they evoke cardioprotective pathways? Biochem Cell Biol. 2015;93(1):83-93. doi: https://doi.org/10.1139/bcb-2014-0110</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Teive HA, Munhoz RP, Werneck LC. Worsening of motor symptoms and gynecomastia during spironolactone treatment in a patient with Parkinson’s disease and congestive heart failure. Mov Disord. 2007;22(11):1678-1679. doi: https://doi.org/10.1002/mds.21579</mixed-citation><mixed-citation xml:lang="en">Teive HA, Munhoz RP, Werneck LC. Worsening of motor symptoms and gynecomastia during spironolactone treatment in a patient with Parkinson’s disease and congestive heart failure. Mov Disord. 2007;22(11):1678-1679. doi: https://doi.org/10.1002/mds.21579</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Majidi Zolbanin N, Zolali E, Mohajjel Nayebi A. Testosterone replacement attenuates haloperidol-induced catalepsy in male rats. Adv Pharm Bull. 2014;4(3):237-241. doi: https://doi.org/10.5681/apb.2014.034</mixed-citation><mixed-citation xml:lang="en">Majidi Zolbanin N, Zolali E, Mohajjel Nayebi A. Testosterone replacement attenuates haloperidol-induced catalepsy in male rats. Adv Pharm Bull. 2014;4(3):237-241. doi: https://doi.org/10.5681/apb.2014.034</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Cunningham RL, Giuffrida A, Roberts JL. Androgens induce dopaminergic neurotoxicity via caspase-3-dependent activation of protein kinase Cdelta. Endocrinology. 2009;150(12):5539-5548. doi: https://doi.org/10.1210/en.2009-0640</mixed-citation><mixed-citation xml:lang="en">Cunningham RL, Giuffrida A, Roberts JL. Androgens induce dopaminergic neurotoxicity via caspase-3-dependent activation of protein kinase Cdelta. Endocrinology. 2009;150(12):5539-5548. doi: https://doi.org/10.1210/en.2009-0640</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Duong P, Tenkorang MAA, Trieu J, et al. Neuroprotective and neurotoxic outcomes of androgens and estrogens in an oxidative stress environment. Biol Sex Differ. 2020;11(1):12. doi: https://doi.org/10.1186/s13293-020-0283-1</mixed-citation><mixed-citation xml:lang="en">Duong P, Tenkorang MAA, Trieu J, et al. Neuroprotective and neurotoxic outcomes of androgens and estrogens in an oxidative stress environment. Biol Sex Differ. 2020;11(1):12. doi: https://doi.org/10.1186/s13293-020-0283-1</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Haussermann P, Goecker D, Beier K, Schroeder S. Lowdose cyproterone acetate treatment of sexual acting out in men with dementia. Int Psychogeriatr. 2003;15(2):181-186. doi: https://doi.org/10.1017/s104161020300886x</mixed-citation><mixed-citation xml:lang="en">Haussermann P, Goecker D, Beier K, Schroeder S. Lowdose cyproterone acetate treatment of sexual acting out in men with dementia. Int Psychogeriatr. 2003;15(2):181-186. doi: https://doi.org/10.1017/s104161020300886x</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Giatti S, Diviccaro S, Falvo E, et al. Physiopathological role of the enzymatic complex 5α-reductase and 3α/β-hydroxysteroid oxidoreductase in the generation of progesterone and testosterone neuroactive metabolites. Front Neuroendocrinol. 2020;57:100836. doi: https://doi.org/10.1016/j.yfrne.2020.100836</mixed-citation><mixed-citation xml:lang="en">Giatti S, Diviccaro S, Falvo E, et al. Physiopathological role of the enzymatic complex 5α-reductase and 3α/β-hydroxysteroid oxidoreductase in the generation of progesterone and testosterone neuroactive metabolites. Front Neuroendocrinol. 2020;57:100836. doi: https://doi.org/10.1016/j.yfrne.2020.100836</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Melcangi RC, Garcia-Segura LM, Mensah-Nyagan AG. Neuroactive steroids: state of the art and new perspectives. Cell Mol Life Sci. 2008;65(5):777-797. doi: https://doi.org/10.1007/s00018-007-7403-5</mixed-citation><mixed-citation xml:lang="en">Melcangi RC, Garcia-Segura LM, Mensah-Nyagan AG. Neuroactive steroids: state of the art and new perspectives. Cell Mol Life Sci. 2008;65(5):777-797. doi: https://doi.org/10.1007/s00018-007-7403-5</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Castelli MP, Casti A, Casu A, et al. Regional distribution of 5α-reductase type 2 in the adult rat brain: an immunohistochemical analysis. Psychoneuroendocrinology. 2013;38(2):281-293. doi: https://doi.org/10.1016/j.psyneuen.2012.06.008</mixed-citation><mixed-citation xml:lang="en">Castelli MP, Casti A, Casu A, et al. Regional distribution of 5α-reductase type 2 in the adult rat brain: an immunohistochemical analysis. Psychoneuroendocrinology. 2013;38(2):281-293. doi: https://doi.org/10.1016/j.psyneuen.2012.06.008</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Finn DA, Beadles-Bohling AS, Beckley EH, et al. A new look at the 5alpha-reductase inhibitor finasteride. CNS Drug Rev. 2006;12(1):53-76. doi: https://doi.org/10.1111/j.1527-3458.2006.00053.x</mixed-citation><mixed-citation xml:lang="en">Finn DA, Beadles-Bohling AS, Beckley EH, et al. A new look at the 5alpha-reductase inhibitor finasteride. CNS Drug Rev. 2006;12(1):53-76. doi: https://doi.org/10.1111/j.1527-3458.2006.00053.x</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Xu Y, Dalrymple SL, Becker RE, et al. Pharmacologic basis for the enhanced efficacy of dutasteride against prostatic cancers. Clin Cancer Res. 2006;12(13):4072-4079. doi: https://doi.org/10.1158/1078-0432.CCR-06-0184</mixed-citation><mixed-citation xml:lang="en">Xu Y, Dalrymple SL, Becker RE, et al. Pharmacologic basis for the enhanced efficacy of dutasteride against prostatic cancers. Clin Cancer Res. 2006;12(13):4072-4079. doi: https://doi.org/10.1158/1078-0432.CCR-06-0184</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Paba S, Frau R, Godar SC, et al. Steroid 5α-reductase as a novel therapeutic target for schizophrenia and other neuropsychiatric disorders. Curr Pharm Des. 2011;17(2):151-167. doi: https://doi.org/10.2174/138161211795049589</mixed-citation><mixed-citation xml:lang="en">Paba S, Frau R, Godar SC, et al. Steroid 5α-reductase as a novel therapeutic target for schizophrenia and other neuropsychiatric disorders. Curr Pharm Des. 2011;17(2):151-167. doi: https://doi.org/10.2174/138161211795049589</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Bortolato M, Cannas A, Solla P, et al. Finasteride attenuates pathological gambling in patients with Parkinson disease. J Clin Psychopharmacol. 2012;32(3):424-425. doi: https://doi.org/10.1097/JCP.0b013e3182549c2a</mixed-citation><mixed-citation xml:lang="en">Bortolato M, Cannas A, Solla P, et al. Finasteride attenuates pathological gambling in patients with Parkinson disease. J Clin Psychopharmacol. 2012;32(3):424-425. doi: https://doi.org/10.1097/JCP.0b013e3182549c2a</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Frau R, Savoia P, Fanni S, et al. The 5-alpha reductase inhibitor finasteride reduces dyskinesia in a rat model of Parkinson’s disease. Exp Neurol. 2017;291(4):1-7. doi: https://doi.org/10.1016/j.expneurol.2017.01.012</mixed-citation><mixed-citation xml:lang="en">Frau R, Savoia P, Fanni S, et al. The 5-alpha reductase inhibitor finasteride reduces dyskinesia in a rat model of Parkinson’s disease. Exp Neurol. 2017;291(4):1-7. doi: https://doi.org/10.1016/j.expneurol.2017.01.012</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Fanni S, Scheggi S, Rossi F, et al. 5alpha-reductase inhibitors dampen L-DOPA-induced dyskinesia via normalization of dopamine D1-receptor signaling pathway and D1-D3 receptor interaction. Neurobiol Dis. 2019;121(4):120-130. doi: https://doi.org/10.1016/j.nbd.2018.09.018</mixed-citation><mixed-citation xml:lang="en">Fanni S, Scheggi S, Rossi F, et al. 5alpha-reductase inhibitors dampen L-DOPA-induced dyskinesia via normalization of dopamine D1-receptor signaling pathway and D1-D3 receptor interaction. Neurobiol Dis. 2019;121(4):120-130. doi: https://doi.org/10.1016/j.nbd.2018.09.018</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Frau R, Mosher LJ, Bini V, et al. The neurosteroidogenic enzyme 5α-reductase modulates the role of D1 dopamine receptors in rat sensorimotor gating. Psychoneuroendocrinology. 2016;63(4):59-67. doi: https://doi.org/10.1016/j.psyneuen.2015.09.014</mixed-citation><mixed-citation xml:lang="en">Frau R, Mosher LJ, Bini V, et al. The neurosteroidogenic enzyme 5α-reductase modulates the role of D1 dopamine receptors in rat sensorimotor gating. Psychoneuroendocrinology. 2016;63(4):59-67. doi: https://doi.org/10.1016/j.psyneuen.2015.09.014</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Федотова Ю.О. Влияние агониста и антагониста Д2-типа дофаминовых рецепторов на обучение при разном уровне андрогенов у крыс // Орбиталь. — 2017. — №1. — С. 38-48.</mixed-citation><mixed-citation xml:lang="en">Fedotova YuO. The effect of D2-type dopamine receptor agonist and antagonist on learning at different levels of androgens in rats. Orbital. 2017;1:38-48. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Masoud ST, Vecchio LM, Bergeron Y, et al. Increased expression of the dopamine transporter leads to loss of dopamine neurons, oxidative stress and l-DOPA reversible motor deficits. Neurobiol Dis. 2015;74(4):66-75. doi: https://doi.org/10.1016/j.nbd.2014.10.016</mixed-citation><mixed-citation xml:lang="en">Masoud ST, Vecchio LM, Bergeron Y, et al. Increased expression of the dopamine transporter leads to loss of dopamine neurons, oxidative stress and l-DOPA reversible motor deficits. Neurobiol Dis. 2015;74(4):66-75. doi: https://doi.org/10.1016/j.nbd.2014.10.016</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Vallée M. Neurosteroids and potential therapeutics: Focus on pregnenolone. J Steroid Biochem Mol Biol. 2016;160(4):78-87. doi: https://doi.org/10.1016/j.jsbmb.2015.09.030</mixed-citation><mixed-citation xml:lang="en">Vallée M. Neurosteroids and potential therapeutics: Focus on pregnenolone. J Steroid Biochem Mol Biol. 2016;160(4):78-87. doi: https://doi.org/10.1016/j.jsbmb.2015.09.030</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Azuma T, Matsubara T, Shima Y, et al. Neurosteroids in cerebrospinal fluid in neurologic disorders. J Neurol Sci. 1993;120(1):87-92. doi: https://doi.org/10.1016/0022-510x(93)90030-3</mixed-citation><mixed-citation xml:lang="en">Azuma T, Matsubara T, Shima Y, et al. Neurosteroids in cerebrospinal fluid in neurologic disorders. J Neurol Sci. 1993;120(1):87-92. doi: https://doi.org/10.1016/0022-510x(93)90030-3</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Bélanger N, Grégoire L, Bédard P, Di Paolo T. Estradiol and dehydroepiandrosterone potentiate levodopainduced locomotor activity in 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine monkeys. Endocrine. 2003;21(1):97-101. doi: https://doi.org/10.1385/endo:21:1:97</mixed-citation><mixed-citation xml:lang="en">Bélanger N, Grégoire L, Bédard P, Di Paolo T. Estradiol and dehydroepiandrosterone potentiate levodopainduced locomotor activity in 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine monkeys. Endocrine. 2003;21(1):97-101. doi: https://doi.org/10.1385/endo:21:1:97</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Bélanger N, Grégoire L, Bédard PJ, Di Paolo T. DHEA improves symptomatic treatment of moderately and severely impaired MPTP monkeys. Neurobiol Aging. 2006;27(11):1684-1693. doi: https://doi.org/10.1016/j.neurobiolaging.2005.09.028</mixed-citation><mixed-citation xml:lang="en">Bélanger N, Grégoire L, Bédard PJ, Di Paolo T. DHEA improves symptomatic treatment of moderately and severely impaired MPTP monkeys. Neurobiol Aging. 2006;27(11):1684-1693. doi: https://doi.org/10.1016/j.neurobiolaging.2005.09.028</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">D’Astous M, Morissette M, Tanguay B, et al. Dehydroepiandrosterone (DHEA) such as 17beta-estradiol prevents MPTP-induced dopamine depletion in mice. Synapse. 2003;47(1):10-14. doi: https://doi.org/10.1002/syn.10145</mixed-citation><mixed-citation xml:lang="en">D’Astous M, Morissette M, Tanguay B, et al. Dehydroepiandrosterone (DHEA) such as 17beta-estradiol prevents MPTP-induced dopamine depletion in mice. Synapse. 2003;47(1):10-14. doi: https://doi.org/10.1002/syn.10145</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Frau R, Miczán V, Traccis F, et al. Prenatal THC exposure produces a hyperdopaminergic phenotype rescued by pregnenolone. Nat Neurosci. 2019;22(12):1975-1985. doi: https://doi.org/10.1038/s41593-019-0512-2</mixed-citation><mixed-citation xml:lang="en">Frau R, Miczán V, Traccis F, et al. Prenatal THC exposure produces a hyperdopaminergic phenotype rescued by pregnenolone. Nat Neurosci. 2019;22(12):1975-1985. doi: https://doi.org/10.1038/s41593-019-0512-2</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Davison SL, Bell R, Donath S, et al. Androgen levels in adult females: changes with age, menopause, and oophorectomy. J Clin Endocrinol Metab. 2005;90(7):3847-3853. doi: https://doi.org/10.1210/jc.2005-0212</mixed-citation><mixed-citation xml:lang="en">Davison SL, Bell R, Donath S, et al. Androgen levels in adult females: changes with age, menopause, and oophorectomy. J Clin Endocrinol Metab. 2005;90(7):3847-3853. doi: https://doi.org/10.1210/jc.2005-0212</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Collier TJ, Kanaan NM, Kordower JH. Ageing as a primary risk factor for Parkinson’s disease: evidence from studies of non-human primates. Nat Rev Neurosci. 2011;12(6):359-366. doi: https://doi.org/10.1038/nrn3039</mixed-citation><mixed-citation xml:lang="en">Collier TJ, Kanaan NM, Kordower JH. Ageing as a primary risk factor for Parkinson’s disease: evidence from studies of non-human primates. Nat Rev Neurosci. 2011;12(6):359-366. doi: https://doi.org/10.1038/nrn3039</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Collier TJ, Kanaan NM, Kordower JH. Aging and Parkinson’s disease: Different sides of the same coin? Mov Disord. 2017;32(7):983-990. doi: https://doi.org/10.1002/mds.27037</mixed-citation><mixed-citation xml:lang="en">Collier TJ, Kanaan NM, Kordower JH. Aging and Parkinson’s disease: Different sides of the same coin? Mov Disord. 2017;32(7):983-990. doi: https://doi.org/10.1002/mds.27037</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Reeve A, Simcox E, Turnbull D. Ageing and Parkinson’s disease: why is advancing age the biggest risk factor? Ageing Res Rev. 2014;14(100):19-30. doi: https://doi.org/10.1016/j.arr.2014.01.004</mixed-citation><mixed-citation xml:lang="en">Reeve A, Simcox E, Turnbull D. Ageing and Parkinson’s disease: why is advancing age the biggest risk factor? Ageing Res Rev. 2014;14(100):19-30. doi: https://doi.org/10.1016/j.arr.2014.01.004</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Darbin O. The aging striatal dopamine function. Parkinsonism Relat Disord. 2012;18(5):426-432. doi: https://doi.org/10.1016/j.parkreldis.2011.11.025</mixed-citation><mixed-citation xml:lang="en">Darbin O. The aging striatal dopamine function. Parkinsonism Relat Disord. 2012;18(5):426-432. doi: https://doi.org/10.1016/j.parkreldis.2011.11.025</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Rollo CD. Dopamine and aging: intersecting facets. Neurochem Res. 2009;34(4):601-629. doi: https://doi.org/10.1007/s11064-008-9858-7</mixed-citation><mixed-citation xml:lang="en">Rollo CD. Dopamine and aging: intersecting facets. Neurochem Res. 2009;34(4):601-629. doi: https://doi.org/10.1007/s11064-008-9858-7</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Erixon-Lindroth N, Farde L, Wahlin TB, et al. The role of the striatal dopamine transporter in cognitive aging. Psychiatry Res. 2005;138(1):1-12. doi: https://doi.org/10.1016/j.pscychresns.2004.09.005</mixed-citation><mixed-citation xml:lang="en">Erixon-Lindroth N, Farde L, Wahlin TB, et al. The role of the striatal dopamine transporter in cognitive aging. Psychiatry Res. 2005;138(1):1-12. doi: https://doi.org/10.1016/j.pscychresns.2004.09.005</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Volkow ND, Gur RC, Wang GJ, et al. Association between decline in brain dopamine activity with age and cognitive and motor impairment in healthy individuals. Am J Psychiatry. 1998;155(3):344-349. doi: https://doi.org/10.1176/ajp.155.3.344</mixed-citation><mixed-citation xml:lang="en">Volkow ND, Gur RC, Wang GJ, et al. Association between decline in brain dopamine activity with age and cognitive and motor impairment in healthy individuals. Am J Psychiatry. 1998;155(3):344-349. doi: https://doi.org/10.1176/ajp.155.3.344</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Volkow ND, Logan J, Fowler JS, et al. Association between agerelated decline in brain dopamine activity and impairment in frontal and cingulate metabolism. Am J Psychiatry. 2000;157(1):75-80. doi: https://doi.org/10.1176/ajp.157.1.75</mixed-citation><mixed-citation xml:lang="en">Volkow ND, Logan J, Fowler JS, et al. Association between agerelated decline in brain dopamine activity and impairment in frontal and cingulate metabolism. Am J Psychiatry. 2000;157(1):75-80. doi: https://doi.org/10.1176/ajp.157.1.75</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang N, Bo H, Song C, et al. Increased vulnerability with aging to MPTP: the mechanisms underlying mitochondrial dynamics. Neurol Res. 2014;36(8):722-732. doi: https://doi.org/10.1179/1743132813Y.0000000296</mixed-citation><mixed-citation xml:lang="en">Jiang N, Bo H, Song C, et al. Increased vulnerability with aging to MPTP: the mechanisms underlying mitochondrial dynamics. Neurol Res. 2014;36(8):722-732. doi: https://doi.org/10.1179/1743132813Y.0000000296</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">McCormack AL, Di Monte DA, Delfani K, et al. Aging of the nigrostriatal system in the squirrel monkey. J Comp Neurol. 2004;471(4):387-395. doi: https://doi.org/10.1002/cne.20036</mixed-citation><mixed-citation xml:lang="en">McCormack AL, Di Monte DA, Delfani K, et al. Aging of the nigrostriatal system in the squirrel monkey. J Comp Neurol. 2004;471(4):387-395. doi: https://doi.org/10.1002/cne.20036</mixed-citation></citation-alternatives></ref><ref id="cit93"><label>93</label><citation-alternatives><mixed-citation xml:lang="ru">Lang AE. The progression of Parkinson disease: a hypothesis. Neurology. 2007;68(12):948-952. doi: https://doi.org/10.1212/01.wnl.0000257110.91041.5d</mixed-citation><mixed-citation xml:lang="en">Lang AE. The progression of Parkinson disease: a hypothesis. Neurology. 2007;68(12):948-952. doi: https://doi.org/10.1212/01.wnl.0000257110.91041.5d</mixed-citation></citation-alternatives></ref><ref id="cit94"><label>94</label><citation-alternatives><mixed-citation xml:lang="ru">Jenner P. Molecular mechanisms of L-DOPA-induced dyskinesia. Nat Rev Neurosci. 2008;9(9):665-677. doi: https://doi.org/10.1038/nrn2471</mixed-citation><mixed-citation xml:lang="en">Jenner P. Molecular mechanisms of L-DOPA-induced dyskinesia. Nat Rev Neurosci. 2008;9(9):665-677. doi: https://doi.org/10.1038/nrn2471</mixed-citation></citation-alternatives></ref><ref id="cit95"><label>95</label><citation-alternatives><mixed-citation xml:lang="ru">Siderowf A, Stern M. Update on Parkinson disease. Ann Intern Med. 2003;138(8):651-658. doi: https://doi.org/10.7326/0003-4819-138-8-200304150-00013</mixed-citation><mixed-citation xml:lang="en">Siderowf A, Stern M. Update on Parkinson disease. Ann Intern Med. 2003;138(8):651-658. doi: https://doi.org/10.7326/0003-4819-138-8-200304150-00013</mixed-citation></citation-alternatives></ref><ref id="cit96"><label>96</label><citation-alternatives><mixed-citation xml:lang="ru">Gundersen V. Parkinson’s Disease: Can Targeting Inflammation Be an Effective Neuroprotective Strategy? Front Neurosci. 2021;14(4):78-87. doi: https://doi.org/10.3389/fnins.2020.580311</mixed-citation><mixed-citation xml:lang="en">Gundersen V. Parkinson’s Disease: Can Targeting Inflammation Be an Effective Neuroprotective Strategy? Front Neurosci. 2021;14(4):78-87. doi: https://doi.org/10.3389/fnins.2020.580311</mixed-citation></citation-alternatives></ref><ref id="cit97"><label>97</label><citation-alternatives><mixed-citation xml:lang="ru">Smeyne RJ, Noyce AJ, Byrne M, et al. Infection and Risk of Parkinson’s Disease. J Parkinsons Dis. 2021;11(1):31-43. doi: https://doi.org/10.3233/JPD-202279</mixed-citation><mixed-citation xml:lang="en">Smeyne RJ, Noyce AJ, Byrne M, et al. Infection and Risk of Parkinson’s Disease. J Parkinsons Dis. 2021;11(1):31-43. doi: https://doi.org/10.3233/JPD-202279</mixed-citation></citation-alternatives></ref><ref id="cit98"><label>98</label><citation-alternatives><mixed-citation xml:lang="ru">Sadasivan S, Sharp B, Schultz-Cherry S, Smeyne RJ. Synergistic effects of influenza and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) can be eliminated by the use of influenza therapeutics: experimental evidence for the multi-hit hypothesis. NPJ Park Dis. 2017;3(1):18. doi: https://doi.org/10.1038/s41531-017-0019-z</mixed-citation><mixed-citation xml:lang="en">Sadasivan S, Sharp B, Schultz-Cherry S, Smeyne RJ. Synergistic effects of influenza and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) can be eliminated by the use of influenza therapeutics: experimental evidence for the multi-hit hypothesis. NPJ Park Dis. 2017;3(1):18. doi: https://doi.org/10.1038/s41531-017-0019-z</mixed-citation></citation-alternatives></ref><ref id="cit99"><label>99</label><citation-alternatives><mixed-citation xml:lang="ru">Cadegiani FA. Repurposing existing drugs for COVID-19: an endocrinology perspective. BMC Endocr Disord. 2020;20(1):149. doi: https://doi.org/10.1186/s12902-020-00626-0</mixed-citation><mixed-citation xml:lang="en">Cadegiani FA. Repurposing existing drugs for COVID-19: an endocrinology perspective. BMC Endocr Disord. 2020;20(1):149. doi: https://doi.org/10.1186/s12902-020-00626-0</mixed-citation></citation-alternatives></ref><ref id="cit100"><label>100</label><citation-alternatives><mixed-citation xml:lang="ru">Cadegiani FA, McCoy J, Gustavo Wambier C, Goren A. Early Antiandrogen Therapy With Dutasteride Reduces Viral Shedding, Inflammatory Responses, and Time-to-Remission in Males With COVID-19: A Randomized, Double-Blind, Placebo-Controlled Interventional Trial (EAT-DUTA AndroCoV Trial – Biochemical). Cureus. 2021;3(1):18. doi: https://doi.org/10.7759/cureus.13047</mixed-citation><mixed-citation xml:lang="en">Cadegiani FA, McCoy J, Gustavo Wambier C, Goren A. Early Antiandrogen Therapy With Dutasteride Reduces Viral Shedding, Inflammatory Responses, and Time-to-Remission in Males With COVID-19: A Randomized, Double-Blind, Placebo-Controlled Interventional Trial (EAT-DUTA AndroCoV Trial – Biochemical). Cureus. 2021;3(1):18. doi: https://doi.org/10.7759/cureus.13047</mixed-citation></citation-alternatives></ref><ref id="cit101"><label>101</label><citation-alternatives><mixed-citation xml:lang="ru">McCoy J, Cadegiani FA, Wambier CG, et al. 5-alpha-reductase inhibitors are associated with reduced frequency of COVID-19 symptoms in males with androgenetic alopecia. J Eur Acad Dermatol Venereol. 2021;35(4):243-246. doi: https://doi.org/10.1111/jdv.17021.</mixed-citation><mixed-citation xml:lang="en">McCoy J, Cadegiani FA, Wambier CG, et al. 5-alpha-reductase inhibitors are associated with reduced frequency of COVID-19 symptoms in males with androgenetic alopecia. J Eur Acad Dermatol Venereol. 2021;35(4):243-246. doi: https://doi.org/10.1111/jdv.17021.</mixed-citation></citation-alternatives></ref><ref id="cit102"><label>102</label><citation-alternatives><mixed-citation xml:lang="ru">Lazzeri M, Duga S, Azzolini E, et al. Humanitas COVID-19 Task Force, The Humanitas Gavazzeni COVID-19 Task Force. Impact of chronic exposure to 5-alpha reductase inhibitors on the risk of hospitalization for COVID-19: a case-control study in male population from two COVID-19 regional centers of Lombardy, Italy. Minerva Urol Nephrol. 2022;74(1):77-84. doi: https://doi.org/10.23736/S2724-6051.20.04081-3</mixed-citation><mixed-citation xml:lang="en">Lazzeri M, Duga S, Azzolini E, et al. Humanitas COVID-19 Task Force, The Humanitas Gavazzeni COVID-19 Task Force. Impact of chronic exposure to 5-alpha reductase inhibitors on the risk of hospitalization for COVID-19: a case-control study in male population from two COVID-19 regional centers of Lombardy, Italy. Minerva Urol Nephrol. 2022;74(1):77-84. doi: https://doi.org/10.23736/S2724-6051.20.04081-3</mixed-citation></citation-alternatives></ref><ref id="cit103"><label>103</label><citation-alternatives><mixed-citation xml:lang="ru">Tauchen J, Jurášek M, Huml L, Rimpelová S. Medicinal Use of Testosterone and Related Steroids Revisited. Molecules. 2021;26(4):1032. doi: https://doi.org/10.3390/molecules26041032</mixed-citation><mixed-citation xml:lang="en">Tauchen J, Jurášek M, Huml L, Rimpelová S. Medicinal Use of Testosterone and Related Steroids Revisited. Molecules. 2021;26(4):1032. doi: https://doi.org/10.3390/molecules26041032</mixed-citation></citation-alternatives></ref><ref id="cit104"><label>104</label><citation-alternatives><mixed-citation xml:lang="ru">Gorczyca D, Kwiatkowska D. Duality nature of Selective Androgen Receptor Modulators and Specific Steroids Substance. Disaster Emerg Med J. 2019;4(2):60-62. doi: https://doi.org/10.5603/DEMJ.2019.0012</mixed-citation><mixed-citation xml:lang="en">Gorczyca D, Kwiatkowska D. Duality nature of Selective Androgen Receptor Modulators and Specific Steroids Substance. Disaster Emerg Med J. 2019;4(2):60-62. doi: https://doi.org/10.5603/DEMJ.2019.0012</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>
