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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">Scientific Notes of V.I. Vernadsky Crimean Federal University. Biology. Chemistry</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">Scientific Notes of V.I. Vernadsky Crimean Federal University. Biology. Chemistry</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Ученые записки Крымского федерального университета имени В.И. Вернадского. Биология. Химия.</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="print">2413-1725</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">91817</article-id>
   <article-id pub-id-type="doi">10.29039/2413-1725-2024-10-3-106-127</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>БИОЛОГИЧЕСКИЕ НАУКИ</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>BIOLOGICAL SCIENCES</subject>
    </subj-group>
    <subj-group>
     <subject>БИОЛОГИЧЕСКИЕ НАУКИ</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">OXIDATIVE STRESS AS A MOLECULAR BASIS FOR NEURODEGENERATIVE DISEASES AND ANTIOXIDANT THERAPY PATHWAYS</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>ОКИСЛИТЕЛЬНЫЙ СТРЕСС КАК МОЛЕКУЛЯРНАЯ ОСНОВА НЕЙРОДЕГЕНЕРАТИВНЫХ ЗАБОЛЕВАНИЙ И ПУТИ АНТИОКСИДАНТНОЙ ТЕРАПИИ</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Микашинович</surname>
       <given-names>З. И.</given-names>
      </name>
      <name xml:lang="en">
       <surname>Mikashinovich</surname>
       <given-names>Z. I.</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Телесманич</surname>
       <given-names>Н. Р.</given-names>
      </name>
      <name xml:lang="en">
       <surname>Telesmanich</surname>
       <given-names>N. R.</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Смирнова</surname>
       <given-names>О. Б.</given-names>
      </name>
      <name xml:lang="en">
       <surname>Smirnova</surname>
       <given-names>O. B.</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">Ростовский государственный медицинский университет</institution>
    </aff>
    <aff>
     <institution xml:lang="en">Rostov State Medical University</institution>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2024-12-12T13:33:56+03:00">
    <day>12</day>
    <month>12</month>
    <year>2024</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2024-12-12T13:33:56+03:00">
    <day>12</day>
    <month>12</month>
    <year>2024</year>
   </pub-date>
   <volume>10</volume>
   <issue>3</issue>
   <fpage>106</fpage>
   <lpage>127</lpage>
   <history>
    <date date-type="received" iso-8601-date="2024-12-11T00:00:00+03:00">
     <day>11</day>
     <month>12</month>
     <year>2024</year>
    </date>
   </history>
   <self-uri xlink:href="https://sn-biolchem.cfuv.ru/okislitelnyj-stress-kak-molekulyarnaya-osnova-nejrodegenerativnyh-zabolevanij-i-puti-antioksidantnoj-terapii/">https://sn-biolchem.cfuv.ru/okislitelnyj-stress-kak-molekulyarnaya-osnova-nejrodegenerativnyh-zabolevanij-i-puti-antioksidantnoj-terapii/</self-uri>
   <abstract xml:lang="ru">
    <p>В  обзоре  представлены  результаты  клинических  и  экспериментальных  исследований, демонстрирующие  патогенетическую  роль  окислительного  стресса  в  генезе  нейродегенеративных &#13;
заболеваний  (НДЗ).  Различные  по  этиологии  и  клинической  симптоматике  заболевания  нервной системы  имеют  общие  механизмы,  связанные  с  повреждением  биомолекул:  неправильной  укладкой белков, их агрегацией, нарушением про- и антиоксидантного баланса. Усиление образования активных форм  кислорода  (АФК)  индуцирует  митоптоз,  апоптоз,  ферроптоз  –  факторов,  приводящих  к нарушению функциональной активности структурных единиц нейрона как главного элемента нервной системы.  Несмотря  на  то,  что  однозначного  признания  эффективности  антиоксидантной  терапии  в настоящее время нет, тем не менее, применение антиоксидантов можно рассматривать как важнейшее звено нейропротекции, имеющей патогенетическое обоснование</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The review presents the results of clinical and experimental studies demonstrating the pathogenetic role of oxidative stress in the genesis of neurodegenerative diseases (NDD), obtained using a complex of clinical, laboratory and instrumental methods that reveal the role of oxidative stress and antioxidants in NDD. In the process of preparing the materials, sources from international and domestic databases were used: Scopus, Web of Science, Pub Medline, RSCI, mainly over the past 15 years (2010–2024).&#13;
Diseases of the nervous system that differ in etiology and clinical symptoms have common mechanisms associated with damage to biomolecules: improper protein stacking, their aggregation, and violation of the pro- and antioxidant balance. Increased formation of reactive oxygen species (ROS) induces mitoptosis, apoptosis, and ferroptosis, factors that lead to impaired functional activity of neuron structural units as the main element of the nervous system. Given the complexity of the pathogenesis of NDZ, a promising methodological approach is to calculate the leading factors of pathogenesis. Undoubtedly, this makes it possible to standardize diagnosis and therapy, and subsequently create clinical recommendations. The purpose of this work was to analyze the role of participants in oxidative stress in key stages of the inflammatory process underlying NDZ. Despite the fact that there is currently no unambiguous recognition of the effectiveness of antioxidant therapy, nevertheless, the use of antioxidants can be considered as the most important link in neuroprotection, which has a pathogenetic justification.&#13;
Metabolic correction in NDH can be divided into 3 groups: natural antioxidants, then endogenous oxidants coming from food, the 3rd group includes drugs of combination therapy and immunotherapy. Mexidol and selenoproteins have antihypoxic and antioxidant effects, which are realized at both the neuronal and vascular levels. Prospects for the development of effective metabolic drugs are associated with the restoration of mitochondrial dysfunction. Synchronization of the metabolic processes underlying the functioning of neuron structures will ensure neurogeneration, slow down neurodegenerative processes and increase life expectancy.&#13;
FDA-approved drugs such as acetylcholinesterase inhibitors (donepezil, rivastigmine), as well as levodopa for the treatment of PD, which cross the blood-brain barrier and restore dopamine levels in the substantia nigra, only alleviate symptoms and slow the progression of diseases for several years. New therapeutic approaches aimed at neuroregeneration, i.e. structural and functional restoration of the damaged nervous system through immunomodulation, inhibition of the formation of protein aggregates, disaggregation of improperly folded proteins and induction of autophagy, give hope that the process of degeneration of affected neurons may slow down, and the recovery rate and life expectancy will increase. Due to the complex nature of NDT, a multi-purpose treatment approach is recommended, as it can have additional positive effects.</p>
   </trans-abstract>
   <kwd-group xml:lang="ru">
    <kwd>окислительный  стресс</kwd>
    <kwd>активные  формы  кислорода</kwd>
    <kwd>болезнь  Паркинсона</kwd>
    <kwd>болезнь  Альцгеймера</kwd>
    <kwd>аутоиммунные нарушения</kwd>
    <kwd>ранняя диагностика</kwd>
    <kwd>антиокидантная терапия</kwd>
   </kwd-group>
   <kwd-group xml:lang="en">
    <kwd>oxidative stress</kwd>
    <kwd>reactive oxygen species</kwd>
    <kwd>antioxidants</kwd>
    <kwd>Parkinson’s disease</kwd>
    <kwd>Alzheimer’s disease</kwd>
    <kwd>autoimmune disorders</kwd>
    <kwd>early diagnosis</kwd>
    <kwd>stabilometry</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
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