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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Human Physiology</journal-id><journal-title-group><journal-title xml:lang="en">Human Physiology</journal-title><trans-title-group xml:lang="ru"><trans-title>Физиология человека</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0131-1646</issn><issn publication-format="electronic">3034-6150</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">664102</article-id><article-id pub-id-type="doi">10.31857/S0131164624040107</article-id><article-id pub-id-type="edn">BSPZVV</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Adaptive Changes in Human Leukocytes in Response to a Long-Term Stay in Antarctica</article-title><trans-title-group xml:lang="ru"><trans-title>Адаптивные изменения в лейкоцитах человека в ответ на длительное пребывание в Антарктиде</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Veiko</surname><given-names>N. N.</given-names></name><name xml:lang="ru"><surname>Вейко</surname><given-names>Н. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ershova</surname><given-names>E. S.</given-names></name><name xml:lang="ru"><surname>Ершова</surname><given-names>Е. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Malinovskaya</surname><given-names>E. M.</given-names></name><name xml:lang="ru"><surname>Малиновская</surname><given-names>Е М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Savinova</surname><given-names>E. A.</given-names></name><name xml:lang="ru"><surname>Савинова</surname><given-names>Е. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chudakova</surname><given-names>J. M.</given-names></name><name xml:lang="ru"><surname>Чудакова</surname><given-names>Ю. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Eliseeva</surname><given-names>J. I.</given-names></name><name xml:lang="ru"><surname>Елисеева</surname><given-names>Ю. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kostyuk</surname><given-names>S. V.</given-names></name><name xml:lang="ru"><surname>Костюк</surname><given-names>С. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Sadova</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Садова</surname><given-names>А. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shmarov</surname><given-names>V. A.</given-names></name><name xml:lang="ru"><surname>Шмаров</surname><given-names>В. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Rykova</surname><given-names>M. P.</given-names></name><name xml:lang="ru"><surname>Рыкова</surname><given-names>М. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Osetskiy</surname><given-names>N. Yu.</given-names></name><name xml:lang="ru"><surname>Осецкий</surname><given-names>Н. Ю.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ponomarev</surname><given-names>S. A.</given-names></name><name xml:lang="ru"><surname>Пономарёв</surname><given-names>С. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>shmarov.v.a@gmail.com</email><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Medical Genetic Research Center, Russian Academy of Medical Sciences</institution></aff><aff><institution xml:lang="ru">ФГБНУ Медико-генетический научный центр имени академика Н.П. Бочкова</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Institute of Biomedical Problems, RAS</institution></aff><aff><institution xml:lang="ru">ФГБУН ГНЦ РФ – Институт медико-биологических проблем РАН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-10-31" publication-format="electronic"><day>31</day><month>10</month><year>2024</year></pub-date><volume>50</volume><issue>4</issue><fpage>120</fpage><lpage>136</lpage><history><date date-type="received" iso-8601-date="2025-02-25"><day>25</day><month>02</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Russian Academy of Sciences</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Российская академия наук</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Russian Academy of Sciences</copyright-holder><copyright-holder xml:lang="ru">Российская академия наук</copyright-holder></permissions><self-uri xlink:href="https://journals.eco-vector.com/0131-1646/article/view/664102">https://journals.eco-vector.com/0131-1646/article/view/664102</self-uri><abstract xml:lang="en"><p>Oxidative stress and aging are known to alter the copy number (CN) of satellite III repeat (1q12) (SatIII(1q)) and telomeric repeat (TR) in the DNA of human cells. The extreme conditions of Antarctica could potentially affect the CN of these repeats in human blood cells, which may be associated with inhibition of the antioxidant system and activation of apoptosis. In this work, we analyzed the CN of ribosomal DNA (rDNA), SatIII(1q), and TR repeats in the leukocytes of 11 male members of the expedition to Vostok station in 2019–2020. To observe dynamic changes in the number of repeating elements of the genome and the degree of their oxidation, six blood samples were taken: before arrival in Antarctica, after 27, 85, 160, 270, and 315 days of wintering. To analyze adaptive changes, the expression levels of the BAX, BCL2, NOX4, NRF2, SOD1, and HIF1 genes were measured. We detected a decrease in SatIII(1q) CN and an increase in TR CN against the background of a stable rDNA CN in human blood cells during wintering. These changes, along with a decrease in the 8-oxodG in DNA, are associated with an increase in the activity of the <italic>NOX4</italic> gene, a decrease in the activity of the <italic>NRF2</italic> gene, and an increase in the expression of the proapoptotic protein BAX. Thus, wintering in Antarctica stimulates an adaptive response in the human body, which includes increased elimination from the bloodstream of “ballast” cells with a high level of DNA oxidation, a high SatIII(1q) content, and a low TR content. An increase in ROS levels due to chronic activation of the <italic>NOX4</italic> gene along with the blocked <italic>NRF2</italic> gene may play a significant role in the development of the response.</p></abstract><trans-abstract xml:lang="ru"><p>Известно, что окислительный стресс и старение изменяют содержание повтора сателлита III (1q12) (SatIII(1q)) и теломерного повтора (<italic>telomere repeat</italic>,<italic> TR</italic>) в ДНК клеток человека. Экстремальные условия Антарктиды потенциально могут влиять на количество этих повторов в клетках крови человека, что может быть связано с угнетением антиоксидантной системы и активацией апоптоза. В данной работе были проанализированы содержание повтора рибосомной ДНК (рДНК), повторов SatIII(1q) и TR в лейкоцитах 11 мужчин – членов экспедиции на станцию Восток в 2019–2020 гг. Для наблюдения динамических изменений в количестве повторяющихся элементов генома и степени окисления ДНК проводили 6 заборов крови: до прибытия в Антарктиду, через 27, 85, 160, 270 и 315 дней зимовки. Для анализа адаптивных изменений измеряли уровни экспрессии генов белков BAX, BCL2, NOX4, NRF2, SOD1, HIF1. Удалось обнаружить снижение содержания SatIII(1q) и увеличение содержания TR на фоне стабильного содержания рДНК в клетках крови людей в ходе зимовки. Эти изменения наряду со снижением маркера окисления 8-oxodG в ДНК ассоциированы с увеличением активности гена <italic>NOX4</italic>, снижением активности гена <italic>NRF2</italic>, а также увеличением экспрессии гена проапоптотического белка BAX. Таким образом, зимовка в Антарктиде стимулирует в организме человека адаптивный ответ, который включает усиление элиминации из кровотока "балластных" клеток с высоким уровнем окисления ДНК, с высоким содержанием повтора SatIII(1q) и низким содержанием TR. В развитии ответа значительную роль может играть повышение уровня АФК вследствие хронической активации <italic>гена NOX4</italic> на фоне блокирования активности гена антиокислительного транскрипционного фактора NRF2.</p></trans-abstract><kwd-group xml:lang="en"><kwd>rDNA</kwd><kwd>SatIII</kwd><kwd>telomeric repeat</kwd><kwd>NOX4</kwd><kwd>NRF2</kwd><kwd>Antarctica</kwd><kwd>apoptosis</kwd><kwd>oxidative stress</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>рДНК</kwd><kwd>SatIII</kwd><kwd>теломерный повтор</kwd><kwd>NOX4</kwd><kwd>NRF2</kwd><kwd>Антарктида</kwd><kwd>апоптоз</kwd><kwd>окислительный стресс</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>de Koning A.P., Gu W., Castoe T.A. et al. Repetitive elements may comprise over two-thirds of the human genome // PLoS Genet. 2011. V. 7. № 12. P. e1002384.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Monlong J., Cossette P., Meloche C. et al. Human copy number variants are enriched in regions of low mappability // Nucleic Acids Res. 2018. V. 46. № 14. P. 7236.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Brahmachary M., Guilmatre A., Quilez J. et al. Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats // PLoS Genet. 2014. V. 10. № 6. P. e1004418.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Warburton P.E., Hasson D., Guillem F. et al. Analysis of the largest tandemly repeated DNA families in the human genome // BMC Genomics. 2008. V. 9. P. 533.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Black E.M., Giunta S. Repetitive fragile sites: Centromere satellite DNA as a source of genome instability in human diseases // Genes (Basel). 2018. V. 9. № 12. P. 615.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Hannan A.J. Tandem repeats mediating genetic plasticity in health and disease // Nat. Rev. Genet. 2018. V. 19. № 5. P. 286.</mixed-citation></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Veiko N.N., Egolina N.A., Radzivil G.G. et al. Quantitative analysis of repetitive sequences in human genomic DNA and detection of an elevated ribosomal repeat copy number in patients with schizophrenia (the results of molecular and cytogenetic analysis) // Mol. Biol. 2003 V. 37. № 3. P. 409.</mixed-citation><mixed-citation xml:lang="ru">Вейко Н.Н., Еголина Н.А., Радзивил Г.Г. и др. Количественное определение повторяющихся последовательностей в геномной ДНК человека. Обнаружение увеличенного количества рибосомных повторов в геномах больных шизофренией (результаты молекулярного и цитогенетического анализов) // Молекулярная биология. 2003. Т. 37. № 3. С. 409.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><mixed-citation>Korzeneva I.B., Kostuyk S.V., Ershova E.S. et al. Human circulating ribosomal DNA content significantly increases while circulating satellite III (1q12) content decreases under chronic occupational exposure to low-dose gamma- neutron and tritium beta-radiation // Mutat. Res. 2016. V. 791–792. P. 49.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Malinovskaya E.M., Ershova E.S., Golimbet V.E. et al. Copy number of human ribosomal genes with aging: Unchanged mean, but narrowed range and decreased variance in elderly group // Front. Genet. 2018. V. 9. P. 306.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Ershova E.S., Malinovskaya E.M., Konkova M.S. et al. Copy number variation of human Satellite III (1q12) with aging // Front. Genet. 2019. V. 10. P. 704.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Ershova E.S., Agafonova O.N., Zakharova N.V. et al. Copy number variation of Satellite III (1q12) in patients with schizophrenia // Front. Genet. 2019. V. 10. P. 1132.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Ershova E.S., Savinova E.A., Kameneva L.V. et al. Satellite III (1q12) copy number variation in cultured human skin fibroblasts from schizophrenic patients and healthy controls // Front. Biosci. 2023. V. 28. № 8. P. 191.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Konkova M.S., Ershova E.S., Savinova E.A. et al. 1Q12 loci movement in the interphase nucleus under the action of ROS is an important component of the mechanism that determines copy number variation of Satellite III (1q12) in health and schizophrenia // Front. Cell Dev. Biol. 2020. V. 8. P. 386.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Veiko N.N., Ershova E.S., Veiko R.V. et al. Mild cognitive impairment is associated with low copy number of ribosomal genes in the genomes of elderly people // Front. Genet. 2022. V. 13. P. 967448.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Chestkov I.V., Jestkova E.M., Ershova E.S. et al. Abundance of ribosomal RNA gene copies in the genomes of schizophrenia patients // Schizophr. Res. 2018. V. 197. P. 305.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Li S., Otsuka I., Tanifuji T. et al. Ribosomal DNA gene copies are increased in blood and brain of Japanese schizophrenia patients // PLoS One. 2023. V. 18. № 1. P. e0280694.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Porokhovnik L.N., Veiko N.N., Ershova E.S., Kostyuk S.V. The role of human Satellite III (1q12) copy number variation in the adaptive response during aging, stress, and pathology: A pendulum model // Genes (Basel). 2021. V. 12. №10. P. 1524.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Cooke H.J., Hindley J. Cloning of human satellite III DNA: different components are on different chromosomes // Nucleic Acids Res. 1979. V. 6. № 10. P. 3177.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Umriukhin P.E., Ershova E.S., Filev A.D. et al. The psychoemotional stress-induced changes in the abundance of SatIII (1q12) and telomere repeats, but not ribosomal DNA, in human leukocytes // Genes (Basel). 2022. V. 13. № 2. P. 343.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Valgardsdottir R., Chiodi I., Giordano M. et al. Transcription of Satellite III non-coding RNAs is a general stress response in human cells // Nucleic Acids Res. 2008. V. 36. № 2. P. 423.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Bersani F., Lee E., Kharchenko P.V. et al. Pericentromeric satellite repeat expansions through RNA-derived DNA intermediates in cancer // Proc. Natl. Acad. Sci. U.S.A. 2015. V. 112. № 49. P. 15148.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Turner K.J., Vasu V., Griffin D.K. Telomere biology and human phenotype // Cells. 2019. V. 8. № 1. P. 73.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Blackburn E.H., Epel E.S., Lin J. Human telomere biology: A contributory and interactive factor in aging, disease risks, and protection // Science. 2015. V. 350. № 6265. P. 1193.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Shay J.W. Telomeres and aging // Curr. Opin. Cell Biol. 2018. V. 52. P. 1.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Gomes N.M., Ryder O.A., Houck M.L. et al. Comparative biology of mammalian telomeres: hypotheses on ancestral states and the roles of telomeres in longevity determination // Aging Cell. 2011. V. 10. № 5. P. 761.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Barnes R.P., Fouquerel E., Opresko P.L. The impact of oxidative DNA damage and stress on telomere homeostasis // Mech. Ageing Dev. 2019. V. 177. P. 37.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Shigenaga M.K., Ames B.N. Assays for 8-hydroxy-2’-deoxyguanosine: a biomarker of in vivo oxidative DNA damage // Free Radic. Biol. Med. 1991. V. 10. № 3–4. P. 211.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Pilger A., Rüdiger H.W. 8-Hydroxy-2’-deoxyguanosine as a marker of oxidative DNA damage related to occupational and environmental exposures // Int. Arch. Occup. Environ. Health. 2006. V. 80. № 1. P. 1.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Guo S., Chen X. The human Nox4: Gene, structure, physiological function and pathological significance // J. Drug Target. 2015. V. 23. № 10. P. 888.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Kasai S., Shimizu S., Tatara Y. et al. Regulation of Nrf2 by mitochondrial reactive oxygen species in physiology and pathology // Biomolecules. 2020. V. 10. № 2. P. 320.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Mir S., Golden B.D.O., Griess B.J. et al. Upregulation of Nox4 induces a pro-survival Nrf2 response in cancer-associated fibroblasts that promotes tumorigenesis and metastasis, in part via Birc5 induction // Breast Cancer Res. 2022. V. 24. № 1. P. 48.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Milani P., Ambrosi G., Gammoh O. et al. SOD1 and DJ-1 converge at Nrf2 pathway: a clue for antioxidant therapeutic potential in neurodegeneration // Oxid. Med. Cell. Longev. 2013. V. 2013. P. 836760.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Niwa J., Yamada S., Ishigaki S. et al. Disulfide bond mediates aggregation, toxicity, and ubiquitylation of familial amyotrophic lateral sclerosis-linked mutant SOD1 // J. Biol. Chem. 2007. V. 282. № 38. P. 28087.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Bi Z., Zhang Q., Fu Y. et al. Nrf2 and HIF1α converge to arsenic-induced metabolic reprogramming and the formation of the cancer stem-like cells // Theranostics. 2020. V. 10. № 9. P. 4134.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Yu H., Chen B., Ren Q. Baicalin relieves hypoxia-aroused H9c2 cell apoptosis by activating Nrf2/HO-1-mediated HIF1α/BNIP3 pathway // Artif. Cells Nanomed. Biotechnol. 2019. V. 47. № 1. P. 3657.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Di Gregorio J., Cilenti L., Ambivero C.T. et al. UBXN7 cofactor of CRL3KEAP1 and CRL2VHL ubiquitin ligase complexes mediates reciprocal regulation of NRF2 and HIF-1α proteins // Biochim. Biophys. Acta Mol. Cell Res. 2021. V. 1868. № 4. P. 118963.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Oltvai Z.N., Milliman C.L., Korsmeyer S.J. Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death // Cell. 1993. V. 74. № 4. P. 609.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Hardwick J.M, Soane L. Multiple functions of BCL-2 family proteins // Cold Spring Harb. Perspect. Biol. 2013. V. 5. № 2. P. a008722.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Korsmeyer S.J., Shutter J.R., Veis D.J. et al. Bcl-2/Bax: A rheostat that regulates an anti-oxidant pathway and cell death // Semin. Cancer Biol. 1993. V. 4. № 6. P. 327.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Ershova E.S., Savinova E.A., Kameneva L.V. et al. Antipsychotics affect Satellite III (1q12) copy number variations in the cultured human skin fibroblasts // Int. J. Mol. Sci. 2023. V. 24. № 14. P. 11283.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Ershova E.S., Jestkova E.M., Chestkov I.V. et al. Quantification of cell-free DNA in blood plasma and DNA damage degree in lymphocytes to evaluate dysregulation of apoptosis in schizophrenia patients // J. Psychiatr. Res. 2017. V. 87. P. 15.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Kuwabara T., Naruiwa N., Kawabe T. et al. Human change and adaptation in Antarctica: Psychological research on Antarctic wintering-over at Syowa station // Int. J. Circumpolar Health. 2021. V. 80. № 1. P. 1886704.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Yadav A.P., Mishra K.P., Ganju L., Singh S.B. Wintering in Antarctica: Impact on immune response of Indian expeditioners // Neuroimmunomodulation. 2012. V. 19. № 6. P. 327.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Ikeda A., Ohno G., Otani S. et al. Disease and injury statistics of Japanese Antarctic research expeditions during the wintering period: evaluation of 6837 cases in the 1st–56th parties – Antarctic health report in 1956–2016 // Int. J. Circumpolar Health. 2019. V. 78. № 1. P. 1611327.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Van Ombergen A., Rossiter A., Ngo-Anh T.J. “White Mars” – nearly two decades of biomedical research at the Antarctic Concordia station // Exp. Physiol. 2021. V. 106. № 1. P. 6.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Mrakic-Sposta S., Montorsi M., Porcelli S. et al. Effects of prolonged exposure to hypobaric hypoxia on oxidative stress: Overwintering in Antarctic Concordia Station // Oxid. Med. Cell. Longev. 2022. V. 2022. P. 4430032.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>O’Brien K.A., Pollock R.D., Stroud M. et al. Human physiological and metabolic responses to an attempted winter crossing of Antarctica: the effects of prolonged hypobaric hypoxia // Physiol. Rep. 2018. V. 6. № 5. P. e13613.</mixed-citation></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">Morukov B.V., Rykova M.P., Antropova E.N. et al. Immunological aspects of a space flight to Mars // Human Physiology. 2013. V. 39. № 2. P. 126.</mixed-citation><mixed-citation xml:lang="ru">Моруков Б.В., Рыкова М.П., Антропова Е.Н. и др. Иммунологические аспекты пилотируемого марсианского полета // Физиология человека. 2013. Т. 39. № 2. С. 19.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">Ponomarev S., Kutko O., Rykova M. et al. Changes in the cellular component of the human innate immunity system in short-term isolation //Acta Astronautica. 2020. V. 166. P. 89.</mixed-citation><mixed-citation xml:lang="ru">Ponomarev S., Kutko O., Rykova M. et al. Changes in the cellular component of the human innate immunity system in short-term isolation // Acta Astronautica. 2020. V. 166. P. 89.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><mixed-citation>Ponomarev S., Kalinin S., Sadova A. et al. Immunological Aspects of Isolation and Confinement // Front. Immunol. 2021. V. 12. P. 697435.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Junghans P., Schrader G., Faust H. et al. Studies of the protein and the energy metabolism in man during a wintering in Antarctica // Isotopes Environ. Health Stud. 2012. V. 48. № 2. P. 208.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Ershova E.S., Shmarina G.V., Martynov A.V. et al. NADPH-oxidase 4 gene over-expression in peripheral blood lymphocytes of the schizophrenia patients // PLoS One. 2022. V. 17. № 6. P. e0269130.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Enukashvily N.I., Donev R., Waisertreiger I.S., Podgornaya O.I. Human chromosome 1 satellite 3 DNA is decondensed, demethylated and transcribed in senescent cells and in A431 epithelial carcinoma cells // Cytogenet. Genome Res. 2007. V. 118. № 1. P. 42.</mixed-citation></ref></ref-list></back></article>
