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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">agx</journal-id><journal-title-group><journal-title xml:lang="ru">Андрология и генитальная хирургия</journal-title><trans-title-group xml:lang="en"><trans-title>Andrology and Genital Surgery</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2070-9781</issn><issn pub-type="epub">2412-8902</issn><publisher><publisher-name></publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17650/2070-9781-2019-20-3-56-65</article-id><article-id custom-type="elpub" pub-id-type="custom">agx-367</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>ОРИГИНАЛЬНАЯ СТАТЬЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL REPORT</subject></subj-group></article-categories><title-group><article-title>Оксидативный статус предстательной железы и его динамика на фоне этиотропной антимикробной химиотерапии у больных хроническим бактериальным простатитом</article-title><trans-title-group xml:lang="en"><trans-title>Oxidative status of prostate and its dynamics against etiotropic antimicrobial chemotherapy in patients with chronic bacterial prostatitis</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0906-9851</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Братчиков</surname><given-names>О. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Bratchikov</surname><given-names>О. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Олег Иванович Братчиков </p><p>305041 Курск, ул. К. Маркса, 3</p></bio><bio xml:lang="en"><p>3 Karla Marksa St., Kursk 305041</p></bio><email xlink:type="simple">bratov45@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/0000-0001-9265-9467</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Дубонос</surname><given-names>П. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Dubonos</surname><given-names>Р. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>305041 Курск, ул. К. Маркса, 3</p></bio><bio xml:lang="en"><p>3 Karla Marksa St., Kursk 305041</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6316-9020</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тюзиков</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tyuzikov</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>150000 Ярославль, Первомайский пер., 3в </p></bio><bio xml:lang="en"><p>3v Pervomaysky Lane, Yaroslavl 150000</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБОУ ВО «Курский государственный медицинский университет» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Kursk State Medical University, Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Медицинский центр «Тандем-Плюс»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Medical Center “Tandem-Plus”</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>30</day><month>09</month><year>2019</year></pub-date><volume>20</volume><issue>3</issue><fpage>56</fpage><lpage>65</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Братчиков О.И., Дубонос П.А., Тюзиков И.А., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Братчиков О.И., Дубонос П.А., Тюзиков И.А.</copyright-holder><copyright-holder xml:lang="en">Bratchikov О.I., Dubonos Р.A., Tyuzikov I.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://agx.elpub.ru/jour/article/view/367">https://agx.elpub.ru/jour/article/view/367</self-uri><abstract><p>Цель исследования – изучить некоторые исходные характеристики оксидативного статуса предстательной железы и их динамику на фоне этиотропной антимикробной монохимиотерапии у больных хроническим бактериальным простатитом (ХБП).</p><sec><title>Материалы и методы</title><p>Материалы и методы. В исследование включены 90 мужчин в возрасте 24–46 лет (средний возраст 38,2 ± 1,4 года) с ХБП, составивших основную группу, и 30 клинически здоровых мужчин в возрасте 20–45 лет (средний возраст 35,5 ± 1,5 года), вошедших в контрольную группу. Все мужчины в ходе исследования подвергались однотипному комплексному обследованию, а результаты обследования мужчин контрольной группы принимались в качестве референсных значений условной нормы. Проводили сбор жалоб и анамнеза, общефизикальное, специальное урологическое, микробиологическое, лабораторное, сонографическое исследование. Этиотропную антимикробную монохимиотерапию назначали индивидуально по результатам микробиологических исследований секрета предстательной железы; в качестве базового препарата в подгруппе лечения (n = 15), выделенной из основной группы на 2‑м этапе исследования, в «слепом» исследовании использовали левофлоксацин в дозе 500 мг 1 раз в сутки в течение 28 дней. Для оценки характеристик оксидативного статуса предстательной железы выполняли биохимические исследования секрета предстательной железы (определяли уровень активных форм кислорода (АФК), продуктов перекисного окисления липидов (диеновых конъюгат, малонового диальдегида), активность супероксиддисмутазы).</p></sec><sec><title>Результаты</title><p>Результаты. У больных ХБП в секрете предстательной железы выявлены лабораторные признаки выраженного окислительного стресса – усиленное образование АФК, повышение их функциональной активности (свободнорадикальная агрессия), усиление перекисного окисления липидов и повышение функциональной нагрузки на простатическую супероксиддисмутазу. Микробиологическая эффективность монохимиотерапии ХБП составила 86,7 %. Наблюдалась положительная динамика ряда клиниколабораторных параметров на фоне терапии, однако она не приводила к полной ликвидации болевого синдрома и оксидативных нарушений в секрете предстательной железы, а также статистически значимо не улучшала качество жизни пациентов и секреторную функцию предстательной железы. У больных ХБП установлена статистически значимая положительная корреляция между количеством АФК и активностью супероксиддисмутазы в секрете предстательной железы (n = 90; r = 0,413; р = 0,001), а также между количеством АФК в секрете предстательной железы и клиническим индексом боли (n = 90; r = 0,304; р = 0,001), что отражало существенную роль свободнорадикальной агрессии как неинфекционного компонента многофакторного патогенеза болевого синдрома при ХБП.</p></sec><sec><title>Заключение</title><p>Заключение. Устойчивость резидуальных оксидативных нарушений и функционального дефицита в предстательной железе после стандартного курса антимикробной монохимиотерапии является основанием для дополнительного назначения антиоксидантов и антигипоксантов при ХБП.</p></sec></abstract><trans-abstract xml:lang="en"><p>The study objective is to investigate some initial characteristics of prostate oxidative status and their dynamics during the course of etiotropic antimicrobial monochemotherapy in patients with chronic bacterial prostatitis (CBP).</p><sec><title>Materials and methods</title><p>Materials and methods. The work is based on treatment of 90 men aged 24–46 years (mean age 38.2 ± 1.4 years) with CBP (the treatment group), and 30 clinically healthy men aged 20–45 years (mean age 35.5 ± 1.5 years) (control group). All men underwent the same type of comprehensive examination during the study, and the results of the examination of the men of the control group were taken as reference values of the conditional norm. Complaints and anamnesis were collected. General physical, special urological, microbiological, laboratory, sonographic studies were performed. The etiotropic antimicrobial monochemotherapy was selected according to the results of microbiological studies of the secretion of the prostate gland, and levofloxacin (500 mg within 28 days) was chosen as a base drug for the subgroup of treatment (n = 15) isolated from the treatment group in the 2nd stage of the study. To assess the characteristics of the prostate oxidative status and its dynamics during etiotropic antimicrobial monochemotherapy, various modifications of biochemical studies of the secretion of the prostate were performed (reactive oxygen species (ROS), lipid peroxidation products (diol conjugates, malonic dialdehyde), activity of superoxide dismutase).</p></sec><sec><title>Results</title><p>Results. In patients with CBP in the secretion of the prostate due to increased ROS formation, increased functional activity (free radical aggression), increased reactions of lipid peroxidation and increased functional load on prostatic superoxide dismutase. Antimicrobial monochemotherapy of CBP was characterized by a microbiological efficacy of 86.7 % and was accompanied by a positive dynamics of a number of clinical and laboratory parameters of chronic bacterial prostatitis, however, this did not lead to the complete elimination of pain syndrome and oxidative disorders in the secretion of the prostate, and also did not significantly improve the quality life of patients and prostate secretory function. In patients with CBP a significant positive relationship was found between the amount of ROS and superoxide dismutase activity in the secretion of the prostate (n = 90; r = 0.413; p = 0.001); and the positive relationship between the amount of ROS in the secretion of the prostate and the clinical pain index (n = 90, r = 0.304, p = 0.001), which reflected the essential role of free radical prostatic aggression as an non-infectious component of the multifactorial pathogenesis of the pain syndrome in CBP.</p></sec><sec><title>Conclusion</title><p>Conclusion. The persistence of residual oxidative disorders and functional deficits in the prostate after a standard course of microbial monochemotherapy justifies the advisability of the additional administration of antioxidants and antihypoxic agents in CBP.</p></sec><sec><title> </title><p> </p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>хронический бактериальный простатит</kwd><kwd>окислительный стресс</kwd><kwd>перекисное окисление липидов</kwd><kwd>супероксиддисмутаза</kwd><kwd>антимикробная монохимиотерапия</kwd><kwd>антиоксиданты</kwd><kwd>антигипоксанты</kwd></kwd-group><kwd-group xml:lang="en"><kwd>chronic bacterial prostatitis</kwd><kwd>oxidative stress</kwd><kwd>lipid peroxidation</kwd><kwd>superoxide dismutase</kwd><kwd>antimicrobial monochemotherapy</kwd><kwd>antioxidants</kwd><kwd>Antihypoxants</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">Harman D. 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