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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">vestnik-bio-msu</journal-id><journal-title-group><journal-title xml:lang="ru">Вестник Московского университета. Серия 16. Биология</journal-title><trans-title-group xml:lang="en"><trans-title>Vestnik Moskovskogo universiteta. Seriya 16. Biologiya</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0137-0952</issn><publisher><publisher-name>Lomonosov Moscow State University,  School of Biology</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.55959/MSU0137-0952-16-79-2S-11</article-id><article-id custom-type="elpub" pub-id-type="custom">vestnik-bio-msu-1387</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>ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Регуляция сокращения гладкомышечных клеток сосудов в раннем постнатальном онтогенезе</article-title><trans-title-group xml:lang="en"><trans-title>Regulation of vascular smooth muscle cell contraction during early postnatal ontogenesis</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5104-2399</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гайнуллина</surname><given-names>Д. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Gaynullina</surname><given-names>D. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гайнуллина Дина Камилевна – докт. биол. наук, вед. науч. cотр. кафедры физиологии человека и животных биологического факультета,</p><p>119234, г. Москва, Ленинские горы, д. 1, стр. 12</p></bio><bio xml:lang="en"><p>Department of Human and Animal Physiology, School of Biology, </p><p>Leninskie gory 1–12, Moscow, 119234</p></bio><email xlink:type="simple">dina.gaynullina@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/0000-0002-4230-3849</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тарасова</surname><given-names>О. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Tarasova</surname><given-names>O. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тарасова Ольга Сергеевна – докт. биол. наук, доц., проф. кафедры физиологии человека и животных биологического факультета;</p><p>зав. кафедрой физиологии и патологии факультета фундаментальной медицины,</p><p>119234, г. Москва, Ленинские горы, д. 1, стр. 12</p></bio><bio xml:lang="en"><p>Department of Human and Animal Physiology, School of Biology,  Leninskie gory 1–12, Moscow, 119234;</p><p>Lomonosovsky pr. 27–1, Moscow, 119991</p></bio><email xlink:type="simple">tarasovaos@my.msu.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/0000-0001-8859-7689</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Швецова</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shvetsova</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Швецова Анастасия Алексеевна – канд. биол. наук, ст. науч. сотр. кафедры физиологиичеловека и животных биологического факультета,</p><p>119234, г. Москва, Ленинские горы, д. 1, стр. 12</p></bio><bio xml:lang="en"><p>Department of Human and Animal Physiology, School of Biology, </p><p>Leninskie gory 1–12, Moscow, 119234</p></bio><email xlink:type="simple">anastasiashvetsova92@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Московский государственный университет имени М.В. Ломоносова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Lomonosov Moscow State University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Московский государственный университет имени М.В. Ломоносова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Lomonosov Moscow State University;&#13;
Department of Physiology and Pathology, School of Basic Medicine</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>27</day><month>08</month><year>2024</year></pub-date><volume>79</volume><issue>2S</issue><fpage>55</fpage><lpage>64</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Гайнуллина Д.К., Тарасова О.С., Швецова А.А., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Гайнуллина Д.К., Тарасова О.С., Швецова А.А.</copyright-holder><copyright-holder xml:lang="en">Gaynullina D.K., Tarasova O.S., Shvetsova A.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://vestnik-bio-msu.elpub.ru/jour/article/view/1387">https://vestnik-bio-msu.elpub.ru/jour/article/view/1387</self-uri><abstract><p>Рост организма в раннем постнатальном онтогенезе связан с изменением функционирования многих систем, в том числе сердечно-сосудистой. Для кровеносной системы новорожденных характерны многочисленные структурные и функциональные особенности, что на системном уровне проявляется в существенно более низком артериальном давлении. В этом обзоре рассмотрены различия механизмов регуляции сокращения гладкомышечных клеток сосудов в раннем постнатальном онтогенезе и во взрослом возрасте, включая возрастные изменения функционирования ионных каналов, активность которых влияет на уровень мембранного потенциала и внутриклеточную концентрацию ионов кальция, а также изменения кальциевой чувствительности сократительного аппарата. Заключительный раздел обзора посвящен обсуждению вопроса о связи механизмов регуляции сокращения и дифференцировки гладкомышечных клеток сосудов во время их созревания.</p></abstract><trans-abstract xml:lang="en"><p>Growth of the body in early postnatal ontogenesis is associated with changes in the functioning of many organ systems, including the cardiovascular system. The circulatory system of newborns is characterized by numerous structural and functional features, which at the systemic level is manifested in a significantly lower level of blood pressure. This review describes the differences in the mechanisms of regulation of vascular smooth muscle cell contraction in early postnatal ontogenesis and in adulthood, including age-related changes in the functioning of ion channels, which activity affects membrane potential level and intracellular concentration of calcium ions, as well as changes in calcium sensitivity of the contractile apparatus. The final section of the review discusses the connection between the mechanisms regulating contraction and differentiation of vascular smooth muscle cells during maturation.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>тонус сосудов</kwd><kwd>ионные каналы</kwd><kwd>чувствительность сократительного аппарата к ионам кальция</kwd><kwd>активные формы кислорода</kwd><kwd>дифференцировка</kwd></kwd-group><kwd-group xml:lang="en"><kwd>vascular tone</kwd><kwd>ion channels</kwd><kwd>calcium sensitivity of the contractile apparatus</kwd><kwd>reactive oxygen species</kwd><kwd>differentiation</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Обзор написан в рамках выполнения Научного проекта государственного задания Правительства Российской Федерации Московскому государственному университету имени М.В. Ломоносова № 121032300071-8.</funding-statement><funding-statement xml:lang="en">The research was supported by the Scientific Project of the State Order of the Government of Russian Federation to Lomonosov Moscow State University No. 121032300071-8.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Kent A.L., Kecskes Z., Shadbolt B., Falk M.C. Normative blood pressure data in the early neonatal period. Pediatr Nephrol. 2007;22(9):1335–1341.</mixed-citation><mixed-citation xml:lang="en">Kent A.L., Kecskes Z., Shadbolt B., Falk M.C. Normative blood pressure data in the early neonatal period. Pediatr Nephrol. 2007;22(9):1335–1341.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Noori S., Drabu B., Soleymani S., Seri I. Continuous non-invasive cardiac output measurements in the neonate by electrical velocimetry: A comparison with echocardiography. Arch. Dis. Child. Fetal Neonatal Ed. 2012;97(5):340–344.</mixed-citation><mixed-citation xml:lang="en">Noori S., Drabu B., Soleymani S., Seri I. Continuous non-invasive cardiac output measurements in the neonate by electrical velocimetry: A comparison with echocardiography. Arch. Dis. Child. Fetal Neonatal Ed. 2012;97(5):340–344.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Stulcová B. Postnatal development of cardiac output distribution measured by radioactive microspheres in rats. Biol. Neonate. 1977;32(3–4):119–124.</mixed-citation><mixed-citation xml:lang="en">Stulcová B. Postnatal development of cardiac output distribution measured by radioactive microspheres in rats. Biol. Neonate. 1977;32(3–4):119–124.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Mochalov S. V., Tarasova N. V., Kudryashova T.V., Gaynullina D.K., Kalenchuk V.U., Borovik A.S., Vorotnikov A.V., Tarasova O.S., Schubert R. Higher Ca2+ -sensitivity of arterial contraction in 1-week-old rats is due to a greater Rho-kinase activity. Acta Physiol. 2018;223(3):e13044.</mixed-citation><mixed-citation xml:lang="en">Mochalov S. V., Tarasova N. V., Kudryashova T.V., Gaynullina D.K., Kalenchuk V.U., Borovik A.S., Vorotnikov A.V., Tarasova O.S., Schubert R. Higher Ca2+ -sensitivity of arterial contraction in 1-week-old rats is due to a greater Rho-kinase activity. Acta Physiol. 2018;223(3):e13044.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Puzdrova V.A., Kudryashova T. V., Gaynullina D.K., Mochalov S. V., Aalkjaer C., Nilsson H,, Vorotnikov A.V., Schubert R., Tarasova O.S. Trophic action of sympathetic nerves reduces arterial smooth muscle Ca2+ sensitivity during early post-natal development in rats. Acta Physiol. 2014;212(2):128–141.</mixed-citation><mixed-citation xml:lang="en">Puzdrova V.A., Kudryashova T. V., Gaynullina D.K., Mochalov S. V., Aalkjaer C., Nilsson H,, Vorotnikov A.V., Schubert R., Tarasova O.S. Trophic action of sympathetic nerves reduces arterial smooth muscle Ca2+ sensitivity during early post-natal development in rats. Acta Physiol. 2014;212(2):128–141.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Sofronova S.I., Borzykh A.A., Gaynullina D.K., Kuzmin I. V., Shvetsova A.A., Lukoshkova E.V., Tarasova O.S. Endothelial nitric oxide weakens arterial contractile responses and reduces blood pressure during early postnatal development in rats. Nitric Oxide. 2016;55–56:1–9.</mixed-citation><mixed-citation xml:lang="en">Sofronova S.I., Borzykh A.A., Gaynullina D.K., Kuzmin I. V., Shvetsova A.A., Lukoshkova E.V., Tarasova O.S. Endothelial nitric oxide weakens arterial contractile responses and reduces blood pressure during early postnatal development in rats. Nitric Oxide. 2016;55–56:1–9.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Gaynullina D., Lubomirov L.T., Sofronova S.I., Kalenchuk V.U., Gloe T., Pfitzer G., Tarasova O.S., Schubert R. Functional remodelling of arterial endothelium during early postnatal development in rats. Cardiovasc. Res. 2013;99(4):612–621.</mixed-citation><mixed-citation xml:lang="en">Gaynullina D., Lubomirov L.T., Sofronova S.I., Kalenchuk V.U., Gloe T., Pfitzer G., Tarasova O.S., Schubert R. Functional remodelling of arterial endothelium during early postnatal development in rats. Cardiovasc. Res. 2013;99(4):612–621.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Gaynullina D.K., Schubert R., Tarasova O.S. Changes in endothelial nitric oxide production in systemic vessels during early ontogenesis-a key mechanism for the perinatal adaptation of the circulatory system. Int. J. Mol. Sci. 2019;20(6):1421.</mixed-citation><mixed-citation xml:lang="en">Gaynullina D.K., Schubert R., Tarasova O.S. Changes in endothelial nitric oxide production in systemic vessels during early ontogenesis-a key mechanism for the perinatal adaptation of the circulatory system. Int. J. Mol. Sci. 2019;20(6):1421.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Somlyo A.P., Somlyo A.V. Ca2+ sensitivity of smooth muscle and nonmuscle myosin II: Modulated by G proteins, kinases, and myosin phosphatase. Physiol. Rev. 2003;83(4):1325–1358.</mixed-citation><mixed-citation xml:lang="en">Somlyo A.P., Somlyo A.V. Ca2+ sensitivity of smooth muscle and nonmuscle myosin II: Modulated by G proteins, kinases, and myosin phosphatase. Physiol. Rev. 2003;83(4):1325–1358.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Dimopoulos G.J., Semba S., Kitazawa K., Eto M., Kitazawa T. Ca2+-dependent rapid Ca2+ sensitization of contraction in arterial smooth muscle. Circ. Res. 2007;100(1):121–129.</mixed-citation><mixed-citation xml:lang="en">Dimopoulos G.J., Semba S., Kitazawa K., Eto M., Kitazawa T. Ca2+-dependent rapid Ca2+ sensitization of contraction in arterial smooth muscle. Circ. Res. 2007;100(1):121–129.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Tykocki N.R., Boerman E.M., Jackson W.F. Smooth muscle ion channels and regulation of vascular tone in resistance arteries and arterioles. Compr. Physiol. 2017;7(2):485–581.</mixed-citation><mixed-citation xml:lang="en">Tykocki N.R., Boerman E.M., Jackson W.F. Smooth muscle ion channels and regulation of vascular tone in resistance arteries and arterioles. Compr. Physiol. 2017;7(2):485–581.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Kitazawa T., Kitazawa K. Size-dependent heterogeneity of contractile Ca2+ sensitization in rat arterial smooth muscle. J. Physiol. 2012;590(2):5401–5423.</mixed-citation><mixed-citation xml:lang="en">Kitazawa T., Kitazawa K. Size-dependent heterogeneity of contractile Ca2+ sensitization in rat arterial smooth muscle. J. Physiol. 2012;590(2):5401–5423.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Hansen P.B.L. New role of P/Q-type voltagegated calcium channels. J. Cardiovasc. Pharmacol. 2015;65(5):406–411.</mixed-citation><mixed-citation xml:lang="en">Hansen P.B.L. New role of P/Q-type voltagegated calcium channels. J. Cardiovasc. Pharmacol. 2015;65(5):406–411.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Gollasch M., Haase H., Ried C., Lindschau C., Morano I., Luft F.C., Haller H. L-type calcium channel expression depends on the differentiated state of vascular smooth muscle cells. FASEB J. 1998;12(7):593–601.</mixed-citation><mixed-citation xml:lang="en">Gollasch M., Haase H., Ried C., Lindschau C., Morano I., Luft F.C., Haller H. L-type calcium channel expression depends on the differentiated state of vascular smooth muscle cells. FASEB J. 1998;12(7):593–601.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Quignard J.F., Grazzini E., Guillon G., Harricane M.C., Nargeot J., Richard S. Absence of calcium channels in neonatal rat aortic myocytes. Pflugers Arch. Eur. J. Physiol. 1996;431(5):791–793.</mixed-citation><mixed-citation xml:lang="en">Quignard J.F., Grazzini E., Guillon G., Harricane M.C., Nargeot J., Richard S. Absence of calcium channels in neonatal rat aortic myocytes. Pflugers Arch. Eur. J. Physiol. 1996;431(5):791–793.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Nakanishi T., Gu H., Abe K., Momma K. Developmental changes in the contractile system of the mesenteric small artery of rabbit. Pediatr. Res. 1997;41(1):65–71.</mixed-citation><mixed-citation xml:lang="en">Nakanishi T., Gu H., Abe K., Momma K. Developmental changes in the contractile system of the mesenteric small artery of rabbit. Pediatr. Res. 1997;41(1):65–71.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Lozinskaya I.M., Cox R.H. Effects of age on Ca2+ currents in small mesenteric artery myocytes from WistarKyoto and spontaneously hypertensive rats. Hypertens. 1997;29(6):1329–1336.</mixed-citation><mixed-citation xml:lang="en">Lozinskaya I.M., Cox R.H. Effects of age on Ca2+ currents in small mesenteric artery myocytes from WistarKyoto and spontaneously hypertensive rats. Hypertens. 1997;29(6):1329–1336.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Blood A.B., Zhao Y., Long W., Zhang L., Longo L.D. L-type Ca2+ channels in fetal and adult ovine cerebral arteries. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2002;282(1):51–51.</mixed-citation><mixed-citation xml:lang="en">Blood A.B., Zhao Y., Long W., Zhang L., Longo L.D. L-type Ca2+ channels in fetal and adult ovine cerebral arteries. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2002;282(1):51–51.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Ahmed A., Waters C.M., Leffler C.W., Jaggar J.H. Ionic mechanisms mediating the myogenic response in newborn porcine cerebral arteries. Am. J. Physiol. Heart Circ. Physiol. 2004;287 (5):H2061–H2069.</mixed-citation><mixed-citation xml:lang="en">Ahmed A., Waters C.M., Leffler C.W., Jaggar J.H. Ionic mechanisms mediating the myogenic response in newborn porcine cerebral arteries. Am. J. Physiol. Heart Circ. Physiol. 2004;287 (5):H2061–H2069.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Long W., Zhao Y., Zhang L., Longo L.D. Role of Ca2+ channels in NE-induced increase in [Ca2+]i and tension in fetal and adult cerebral arteries. Am. J. Physiol. Regul. Integr. Comp. Physiol. 1999;277(1):R286–R294.</mixed-citation><mixed-citation xml:lang="en">Long W., Zhao Y., Zhang L., Longo L.D. Role of Ca2+ channels in NE-induced increase in [Ca2+]i and tension in fetal and adult cerebral arteries. Am. J. Physiol. Regul. Integr. Comp. Physiol. 1999;277(1):R286–R294.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Cogolludo A., Moreno L., Lodi F., Tamargo J., Perez-Vizcaino F. Postnatal maturational shift from PKCζ and voltage-gated K+ channels to RhoA/Rho kinase in pulmonary vasoconstriction. Cardiovasc. Res. 2005;66(1):84–93.</mixed-citation><mixed-citation xml:lang="en">Cogolludo A., Moreno L., Lodi F., Tamargo J., Perez-Vizcaino F. Postnatal maturational shift from PKCζ and voltage-gated K+ channels to RhoA/Rho kinase in pulmonary vasoconstriction. Cardiovasc. Res. 2005;66(1):84–93.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Shen C.P., Romero M., Brunelle A., Wolfe C., Dobyns A., Francis M, Taylor M.S., Puglisi J.L., Loggo L.D., Zhang L., Wilson C.G., Wilson S.M. Longterm high-altitude hypoxia influences pulmonary arterial L-type calcium channel-mediated Ca2+ signals and contraction in fetal and adult sheep. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2018;314(3):R433–R446.</mixed-citation><mixed-citation xml:lang="en">Shen C.P., Romero M., Brunelle A., Wolfe C., Dobyns A., Francis M, Taylor M.S., Puglisi J.L., Loggo L.D., Zhang L., Wilson C.G., Wilson S.M. Longterm high-altitude hypoxia influences pulmonary arterial L-type calcium channel-mediated Ca2+ signals and contraction in fetal and adult sheep. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2018;314(3):R433–R446.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Ricci A., Bronzetti E., El-Assouad D., Felici L., Greco S., Mariotta S., Sabbatini M., Amenta F. Influence of age on L-type Ca2+ channels in the pulmonary artery and vein of spontaneously hypertensive rats. Mech. Ageing Dev. 2000;120(1–3):33–44.</mixed-citation><mixed-citation xml:lang="en">Ricci A., Bronzetti E., El-Assouad D., Felici L., Greco S., Mariotta S., Sabbatini M., Amenta F. Influence of age on L-type Ca2+ channels in the pulmonary artery and vein of spontaneously hypertensive rats. Mech. Ageing Dev. 2000;120(1–3):33–44.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">House S.J., Potier M., Bisaillon J., Singer H.A., Trebak M. The non-excitable smooth muscle: Calcium signaling and phenotypic switching during vascular disease. Pflugers Arch. Eur. J. Physiol. 2008;456(5):769–785.</mixed-citation><mixed-citation xml:lang="en">House S.J., Potier M., Bisaillon J., Singer H.A., Trebak M. The non-excitable smooth muscle: Calcium signaling and phenotypic switching during vascular disease. Pflugers Arch. Eur. J. Physiol. 2008;456(5):769–785.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Soni H., Peixoto-Neves D., Buddington R.K., Adebiyi A. Adenosine A1 receptor-operated calcium entry in renal afferent arterioles is dependent on postnatal maturation of TRPC3 channels. Am. J. Physiol. Ren. Physiol. 2017;313(6):F1216–F1222.</mixed-citation><mixed-citation xml:lang="en">Soni H., Peixoto-Neves D., Buddington R.K., Adebiyi A. Adenosine A1 receptor-operated calcium entry in renal afferent arterioles is dependent on postnatal maturation of TRPC3 channels. Am. J. Physiol. Ren. Physiol. 2017;313(6):F1216–F1222.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Chipperfield A.R., Harper A.A. Chloride in smooth muscle. Prog. Biophys. Mol. Biol. 2000;74(3–5):175–221.</mixed-citation><mixed-citation xml:lang="en">Chipperfield A.R., Harper A.A. Chloride in smooth muscle. Prog. Biophys. Mol. Biol. 2000;74(3–5):175–221.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Hübner C.A., Schroeder B.C., Ehmke H. Regulation of vascular tone and arterial blood pressure: role of chloride transport in vascular smooth muscle. Pflugers Arch. Eur. J. Physiol. 2015;467(3):605–614.</mixed-citation><mixed-citation xml:lang="en">Hübner C.A., Schroeder B.C., Ehmke H. Regulation of vascular tone and arterial blood pressure: role of chloride transport in vascular smooth muscle. Pflugers Arch. Eur. J. Physiol. 2015;467(3):605–614.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Nilsson H., Videbæk L.M., Toma C., Mulvany M.J. Role of intracellular calcium for depolarization in rat mesenteric small arteries. J. Vasc. Res. 1998;35:36–44.</mixed-citation><mixed-citation xml:lang="en">Nilsson H., Videbæk L.M., Toma C., Mulvany M.J. Role of intracellular calcium for depolarization in rat mesenteric small arteries. J. Vasc. Res. 1998;35:36–44.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Boedtkjer D.M.B., Kim S., Jensen A.B., Matchkov V.M., Andersson K.E. New selective inhibitors of calcium-activated chloride channels – T16Ainh-A01, CaCCinh-A01 and MONNA – what do they inhibit? Br. J. Pharmacol. 2015;172(16):4158–4171.</mixed-citation><mixed-citation xml:lang="en">Boedtkjer D.M.B., Kim S., Jensen A.B., Matchkov V.M., Andersson K.E. New selective inhibitors of calcium-activated chloride channels – T16Ainh-A01, CaCCinh-A01 and MONNA – what do they inhibit? Br. J. Pharmacol. 2015;172(16):4158–4171.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Nelson M.T., Conway M.A., Knot H.J., Brayden J.E. Chloride channel blockers inhibit myogenic tone in rat cerebral arteries. J. Physiol. 1997;502(2):259–264.</mixed-citation><mixed-citation xml:lang="en">Nelson M.T., Conway M.A., Knot H.J., Brayden J.E. Chloride channel blockers inhibit myogenic tone in rat cerebral arteries. J. Physiol. 1997;502(2):259–264.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Lamb F.S., Barna T.J. Chloride ion currents contribute functionally to norepinephrine-induced vascular contraction. Am. J. Physiol. Heart Circ. Physiol. 1998;275(1):151–160.</mixed-citation><mixed-citation xml:lang="en">Lamb F.S., Barna T.J. Chloride ion currents contribute functionally to norepinephrine-induced vascular contraction. Am. J. Physiol. Heart Circ. Physiol. 1998;275(1):151–160.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Kostyunina D.S., Zhang L., Shvetsova A.A., Selivanova E.K., Tarasova O.S., Matchkov VV., Gaynullina D.K. Trophic sympathetic influence weakens pro-contractile role of Cl− channels in rat arteries during postnatal maturation. Sci. Rep. 2020;10(1):20002.</mixed-citation><mixed-citation xml:lang="en">Kostyunina D.S., Zhang L., Shvetsova A.A., Selivanova E.K., Tarasova O.S., Matchkov VV., Gaynullina D.K. Trophic sympathetic influence weakens pro-contractile role of Cl− channels in rat arteries during postnatal maturation. Sci. Rep. 2020;10(1):20002.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Heinze C., Seniuk A., Sokolov M.V., Huebner A.K., Klementowicz A.E., Szijártó I.A., Schleifenbaum J., Vitzthum H., Gollasch M., Ehmke H., Schroeder B.C., Hübner C.A. Disruption of vascular Ca2+-activated chloride currents lowers blood pressure. J. Clin. Invest. 2014;124(2):675–686.</mixed-citation><mixed-citation xml:lang="en">Heinze C., Seniuk A., Sokolov M.V., Huebner A.K., Klementowicz A.E., Szijártó I.A., Schleifenbaum J., Vitzthum H., Gollasch M., Ehmke H., Schroeder B.C., Hübner C.A. Disruption of vascular Ca2+-activated chloride currents lowers blood pressure. J. Clin. Invest. 2014;124(2):675–686.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Jensen A.B., Joergensen H.B., Dam V.S., Kamaev D., Boedtkjer D., Füchtbauer E.-M., Aalkjaer C., Matchkov V.V. Variable contribution of TMEM16A to tone in murine arterial vasculature. Basic Clin. Pharmacol. Toxicol. 2018;123(1):30–41.</mixed-citation><mixed-citation xml:lang="en">Jensen A.B., Joergensen H.B., Dam V.S., Kamaev D., Boedtkjer D., Füchtbauer E.-M., Aalkjaer C., Matchkov V.V. Variable contribution of TMEM16A to tone in murine arterial vasculature. Basic Clin. Pharmacol. Toxicol. 2018;123(1):30–41.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Broegger T., Jacobsen J.C.B., Secher Dam V., Boedtkjer D.M.B., Kold-Petersen H., Pedersen F.S, Pedersen F.S., Aalkjaer C., Matchkov V.V. Bestrophin is important for the rhythmic but not the tonic contraction in rat mesenteric small arteries. Cardiovasc. Res. 2011;91(4):685–693.</mixed-citation><mixed-citation xml:lang="en">Broegger T., Jacobsen J.C.B., Secher Dam V., Boedtkjer D.M.B., Kold-Petersen H., Pedersen F.S, Pedersen F.S., Aalkjaer C., Matchkov V.V. Bestrophin is important for the rhythmic but not the tonic contraction in rat mesenteric small arteries. Cardiovasc. Res. 2011;91(4):685–693.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Kostyunina D.S., Tarasova O.S., Gaynullina D.K., Matchkov V.V. Pro-contractile role of chloride in arterial smooth muscle: Postnatal decline potentially governed by sympathetic nerves. Exp. Physiol. 2019;104(7):1018–1022.</mixed-citation><mixed-citation xml:lang="en">Kostyunina D.S., Tarasova O.S., Gaynullina D.K., Matchkov V.V. Pro-contractile role of chloride in arterial smooth muscle: Postnatal decline potentially governed by sympathetic nerves. Exp. Physiol. 2019;104(7):1018–1022.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Belevych A.E., Beck R., Tammaro P., Poston L., Smirnov S.V. Developmental changes in the functional characteristics and expression of voltage-gated K+ channel currents in rat aortic myocytes. Cardiovasc. Res. 2002;54(1):152–161.</mixed-citation><mixed-citation xml:lang="en">Belevych A.E., Beck R., Tammaro P., Poston L., Smirnov S.V. Developmental changes in the functional characteristics and expression of voltage-gated K+ channel currents in rat aortic myocytes. Cardiovasc. Res. 2002;54(1):152–161.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Shvetsova A.A., Gaynullina D.K., Tarasova O.S., Schubert R. Negative feedback regulation of vasocontraction by potassium channels in 10- to 15-day-old rats: Dominating role of Kv 7 channels. Acta Physiol. 2019;225(2):e13176.</mixed-citation><mixed-citation xml:lang="en">Shvetsova A.A., Gaynullina D.K., Tarasova O.S., Schubert R. Negative feedback regulation of vasocontraction by potassium channels in 10- to 15-day-old rats: Dominating role of Kv 7 channels. Acta Physiol. 2019;225(2):e13176.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Long W., Zhang L., Longo L.D. Cerebral artery KATP- and KCa-channel activity and contractility: changes with development. Am. J. Physiol. Integr. Comp. Physiol. 2000;279(6):R2004–R2014.</mixed-citation><mixed-citation xml:lang="en">Long W., Zhang L., Longo L.D. Cerebral artery KATP- and KCa-channel activity and contractility: changes with development. Am. J. Physiol. Integr. Comp. Physiol. 2000;279(6):R2004–R2014.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Shvetsova A.A., Gaynullina D.K., Schmidt N., Bugert P., Lukoshkova E. V., Tarasova O.S, Schubert R. TASK-1 channel blockade by AVE1231 increases vasocontractile responses and BP in 1- to 2-week-old but not adult rats. Br. J. Pharmacol. 2020;177(22):5148–5162.</mixed-citation><mixed-citation xml:lang="en">Shvetsova A.A., Gaynullina D.K., Schmidt N., Bugert P., Lukoshkova E. V., Tarasova O.S, Schubert R. TASK-1 channel blockade by AVE1231 increases vasocontractile responses and BP in 1- to 2-week-old but not adult rats. Br. J. Pharmacol. 2020;177(22):5148–5162.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Gomez J.P., Ghisdal P., Morel N. Changes of the potassium currents in rat aortic smooth muscle cells during postnatal development. Pflugers Arch. Eur. J. Physiol. 2000;441(2–3):388–397.</mixed-citation><mixed-citation xml:lang="en">Gomez J.P., Ghisdal P., Morel N. Changes of the potassium currents in rat aortic smooth muscle cells during postnatal development. Pflugers Arch. Eur. J. Physiol. 2000;441(2–3):388–397.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Bregestovski P.D., Printseva O.Yu., Serebryakov V., Stinnakre J., Turmin A., Zamoyski V. Comparison of Ca2+-dependent K+ channels in the membrane of smooth muscle cells isolated from adult and foetal human aorta. Pflugers Arch. 1988;413(1):8–13.</mixed-citation><mixed-citation xml:lang="en">Bregestovski P.D., Printseva O.Yu., Serebryakov V., Stinnakre J., Turmin A., Zamoyski V. Comparison of Ca2+-dependent K+ channels in the membrane of smooth muscle cells isolated from adult and foetal human aorta. Pflugers Arch. 1988;413(1):8–13.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Gollasch M., Wellman G.C., Knot H.J., Jaggar J.H., Damon D.H., Bonev A.D., Nelson M.T. Ontogeny of local sarcoplasmic reticulum Ca2+ signals in cerebral arteries: Ca2+ sparks as elementary physiological events. Circ. Res. 1998;83(11):1104–1114.</mixed-citation><mixed-citation xml:lang="en">Gollasch M., Wellman G.C., Knot H.J., Jaggar J.H., Damon D.H., Bonev A.D., Nelson M.T. Ontogeny of local sarcoplasmic reticulum Ca2+ signals in cerebral arteries: Ca2+ sparks as elementary physiological events. Circ. Res. 1998;83(11):1104–1114.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Ma D., Gaynullina D., Schmidt N., Mladenov M., Schubert R. The functional availability of arterial Kv 7 channels is suppressed considerably by large-conductance calcium-activated potassium channels in 2- to 3-month old but not in 10- to 15-day old rats. Front. Physiol. 2020;11:597395.</mixed-citation><mixed-citation xml:lang="en">Ma D., Gaynullina D., Schmidt N., Mladenov M., Schubert R. The functional availability of arterial Kv 7 channels is suppressed considerably by large-conductance calcium-activated potassium channels in 2- to 3-month old but not in 10- to 15-day old rats. Front. Physiol. 2020;11:597395.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Teng G.Q., Nauli S.M., Brayden J.E., Pearce W.J. Maturation alters the contribution of potassium channels to resting and 5HT-induced tone in small cerebral arteries of the sheep. Dev. Brain Res. 2002;133(2):81–91.</mixed-citation><mixed-citation xml:lang="en">Teng G.Q., Nauli S.M., Brayden J.E., Pearce W.J. Maturation alters the contribution of potassium channels to resting and 5HT-induced tone in small cerebral arteries of the sheep. Dev. Brain Res. 2002;133(2):81–91.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Thorpe R.B., Stockman S.L., Williams J.M., Lincoln T.M., Pearce W.J. Hypoxic depression of PKGmediated inhibition of serotonergic contraction in ovine carotid arteries. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2013;304(9):R734–R743.</mixed-citation><mixed-citation xml:lang="en">Thorpe R.B., Stockman S.L., Williams J.M., Lincoln T.M., Pearce W.J. Hypoxic depression of PKGmediated inhibition of serotonergic contraction in ovine carotid arteries. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2013;304(9):R734–R743.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Bao L., Cox D.H. Gating and ionic currents reveal how the BKCa channel’s Ca2+ sensitivity is enhanced by its β1 subunit. J. Gen. Physiol. 2005;126(4):393–412.</mixed-citation><mixed-citation xml:lang="en">Bao L., Cox D.H. Gating and ionic currents reveal how the BKCa channel’s Ca2+ sensitivity is enhanced by its β1 subunit. J. Gen. Physiol. 2005;126(4):393–412.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Shvetsova A.A., Gaynullina D.K., Tarasova O.S., Schubert R. Remodeling of arterial tone regulation in postnatal development: Focus on smooth muscle cell potassium channels. Int. J. Mol. Sci. 2021;22(11):5413.</mixed-citation><mixed-citation xml:lang="en">Shvetsova A.A., Gaynullina D.K., Tarasova O.S., Schubert R. Remodeling of arterial tone regulation in postnatal development: Focus on smooth muscle cell potassium channels. Int. J. Mol. Sci. 2021;22(11):5413.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Rhodes M.T., Porter V.A., Saqueton C.B., Herron J.M., Resnik E.R., Cornfield D.N. Pulmonary vascular response to normoxia and KCa channel activity is developmentally regulated. Am. J. Physiol. Lung Cell. Mol. Physiol. 2001;280(6):L1250–1257.</mixed-citation><mixed-citation xml:lang="en">Rhodes M.T., Porter V.A., Saqueton C.B., Herron J.M., Resnik E.R., Cornfield D.N. Pulmonary vascular response to normoxia and KCa channel activity is developmentally regulated. Am. J. Physiol. Lung Cell. Mol. Physiol. 2001;280(6):L1250–1257.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Cornfield D.N., Saqueton C.B., Porter V.A, Herron J., Resnik E., Haddad I.Y., Reeve H.L. Voltage-gated K(+)-channel activity in ovine pulmonary vasculature is developmentally regulated. Am. J. Physiol. Lung Cell. Mol. Physiol. 2000;278(6):L1297–L1304.</mixed-citation><mixed-citation xml:lang="en">Cornfield D.N., Saqueton C.B., Porter V.A, Herron J., Resnik E., Haddad I.Y., Reeve H.L. Voltage-gated K(+)-channel activity in ovine pulmonary vasculature is developmentally regulated. Am. J. Physiol. Lung Cell. Mol. Physiol. 2000;278(6):L1297–L1304.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Reeve H.L., Weir E.K., Archer S.L., Cornfield D.N. A maturational shift in pulmonary K+ channels, from Ca2+ sensitive to voltage dependent. Am. J. Physiol. 1998;27596):L1019–1025.</mixed-citation><mixed-citation xml:lang="en">Reeve H.L., Weir E.K., Archer S.L., Cornfield D.N. A maturational shift in pulmonary K+ channels, from Ca2+ sensitive to voltage dependent. Am. J. Physiol. 1998;27596):L1019–1025.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Pearce W.J., Elliott S.R. Maturation enhances the sensitivity of ovine cerebral arteries to the ATP-sensitive potassium channel activator lemakalim. Pediatr. Res. 1994;35(6):729–732.</mixed-citation><mixed-citation xml:lang="en">Pearce W.J., Elliott S.R. Maturation enhances the sensitivity of ovine cerebral arteries to the ATP-sensitive potassium channel activator lemakalim. Pediatr. Res. 1994;35(6):729–732.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Akopov S.E., Zhang L., Pearce W.J. Developmental changes in the calcium sensitivity of rabbit cranial arteries. Biol. Neonate. 1998;74(1):60–71. 54. Akopov S.E., Zhang L., Pearce W.J. Physiological variations in ovine cerebrovascular calcium sensitivity. Am. J. Physiol. Heart Circ. Physiol. 1997;272(5):41–45.</mixed-citation><mixed-citation xml:lang="en">Akopov S.E., Zhang L., Pearce W.J. Developmental changes in the calcium sensitivity of rabbit cranial arteries. Biol. Neonate. 1998;74(1):60–71. 54. Akopov S.E., Zhang L., Pearce W.J. Physiological variations in ovine cerebrovascular calcium sensitivity. Am. J. Physiol. Heart Circ. Physiol. 1997;272(5):41–45.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Sandoval R.J., Injeti E.R., Williams J.M., Georthoffer W.T., Pearce W.J. Myogenic contractility is more dependent on myofilament calcium sensitization in term fetal than adult ovine cerebral arteries. Am. J. Physiol. Heart Circ. Physiol. 2007;293(1):H548–H556.</mixed-citation><mixed-citation xml:lang="en">Sandoval R.J., Injeti E.R., Williams J.M., Georthoffer W.T., Pearce W.J. Myogenic contractility is more dependent on myofilament calcium sensitization in term fetal than adult ovine cerebral arteries. Am. J. Physiol. Heart Circ. Physiol. 2007;293(1):H548–H556.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Воротников А.В., Щербакова О.В., Кудряшова Т.В., Тарасова О.С., Ширинский В.П., Пфитцер Г., Ткачук В.А. Фосфорилирование миозина как основной путь регуляции сокращения гладких мышц. Росс. физиол. журн. им. И.М. Сеченова. 2009;95(10):1058–1073.</mixed-citation><mixed-citation xml:lang="en">Воротников А.В., Щербакова О.В., Кудряшова Т.В., Тарасова О.С., Ширинский В.П., Пфитцер Г., Ткачук В.А. Фосфорилирование миозина как основной путь регуляции сокращения гладких мышц. Росс. физиол. журн. им. И.М. Сеченова. 2009;95(10):1058–1073.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Pearce W.J., Williams J.M., Chang M.M., Gerthoffer W.T. ERK inhibition attenuates 5-HT-induced contractions in fetal and adult ovine carotid arteries. Arch. Physiol. Biochem. 2003;111(1):36–44.</mixed-citation><mixed-citation xml:lang="en">Pearce W.J., Williams J.M., Chang M.M., Gerthoffer W.T. ERK inhibition attenuates 5-HT-induced contractions in fetal and adult ovine carotid arteries. Arch. Physiol. Biochem. 2003;111(1):36–44.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Gaynullina D.K., Kudryashova T.V., Vorotnikov A.V., Schubert R., Tarasova O.S. MAPKs are highly abundant but do not contribute to α1-adrenergic contraction of rat saphenous arteries in the early postnatal period. Int. J. Mol. Sci. 2021;22(11):6037.</mixed-citation><mixed-citation xml:lang="en">Gaynullina D.K., Kudryashova T.V., Vorotnikov A.V., Schubert R., Tarasova O.S. MAPKs are highly abundant but do not contribute to α1-adrenergic contraction of rat saphenous arteries in the early postnatal period. Int. J. Mol. Sci. 2021;22(11):6037.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Akopov S.E., Zhang L., Pearce W.J. Regulation of Ca2+ sensitization by PKC and rho proteins in ovine cerebral arteries: Effects of artery size and age. Am. J. Physiol. Heart Circ. Physiol. 1998;275(3):930–939.</mixed-citation><mixed-citation xml:lang="en">Akopov S.E., Zhang L., Pearce W.J. Regulation of Ca2+ sensitization by PKC and rho proteins in ovine cerebral arteries: Effects of artery size and age. Am. J. Physiol. Heart Circ. Physiol. 1998;275(3):930–939.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Mochalov S.V., Kalenchuk V.U., Gainullina D.K., Vorotnikov A.V., Tarasova O.S. The contribution of protein kinase C and Rho-kinase to the regulation of receptordependent contraction of arteries decreases with age independently of sympathetic innervation. Biophysics (Mosc.). 2008;53(6):626–631.</mixed-citation><mixed-citation xml:lang="en">Mochalov S.V., Kalenchuk V.U., Gainullina D.K., Vorotnikov A.V., Tarasova O.S. The contribution of protein kinase C and Rho-kinase to the regulation of receptordependent contraction of arteries decreases with age independently of sympathetic innervation. Biophysics (Mosc.). 2008;53(6):626–631.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Knock G.A. NADPH oxidase in the vasculature: Expression, regulation and signalling pathways; role in normal cardiovascular physiology and its dysregulation in hypertension. Free Radic. Biol. Med. 2019;145:385–427.</mixed-citation><mixed-citation xml:lang="en">Knock G.A. NADPH oxidase in the vasculature: Expression, regulation and signalling pathways; role in normal cardiovascular physiology and its dysregulation in hypertension. Free Radic. Biol. Med. 2019;145:385–427.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Shvetsova A.A., Gaynullina D.K., Tarasova O.S. The role of reactive oxygen species in the regulation of blood vessel tone in perinatal and early postnatal ontogenesis. J. Evolutionary Biochem. Physiol. 2023;59(6):2210–2227.</mixed-citation><mixed-citation xml:lang="en">Shvetsova A.A., Gaynullina D.K., Tarasova O.S. The role of reactive oxygen species in the regulation of blood vessel tone in perinatal and early postnatal ontogenesis. J. Evolutionary Biochem. Physiol. 2023;59(6):2210–2227.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Brinks L., Moonen R.M.J., Moral-Sanz J., Barreira B., Kessels L., Perez-Vizcaino F., Collogudo A., Villamor E. Hypoxia-induced contraction of chicken embryo mesenteric arteries: Mechanisms and developmental changes. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2016;311(5):R858–R869.</mixed-citation><mixed-citation xml:lang="en">Brinks L., Moonen R.M.J., Moral-Sanz J., Barreira B., Kessels L., Perez-Vizcaino F., Collogudo A., Villamor E. Hypoxia-induced contraction of chicken embryo mesenteric arteries: Mechanisms and developmental changes. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2016;311(5):R858–R869.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Thakor A.S., Richter H.G., Kane A.D., Dunster C., Kelly F.J., Poston L., Giussani D.A. Redox modulation of the fetal cardiovascular defence to hypoxaemia. J. Physiol. 2010;588(21):4235–4247.</mixed-citation><mixed-citation xml:lang="en">Thakor A.S., Richter H.G., Kane A.D., Dunster C., Kelly F.J., Poston L., Giussani D.A. Redox modulation of the fetal cardiovascular defence to hypoxaemia. J. Physiol. 2010;588(21):4235–4247.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Kane A.D., Hansell J.A., Herrera E.A., Allison B.J., Niu Y., Brain K.L., Kaandorp J.J., Derks J.B., Giussani D.A. Xanthine oxidase and the fetal cardiovascular defence to hypoxia in late gestation ovine pregnancy. J. Physiol. 2014;592(3):475–489.</mixed-citation><mixed-citation xml:lang="en">Kane A.D., Hansell J.A., Herrera E.A., Allison B.J., Niu Y., Brain K.L., Kaandorp J.J., Derks J.B., Giussani D.A. Xanthine oxidase and the fetal cardiovascular defence to hypoxia in late gestation ovine pregnancy. J. Physiol. 2014;592(3):475–489.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Michelakis E.D., Rebeyka I., Wu X.C., Nsair A., Thébaud B., Hashimoto K., Dyck J.R., Haromy A., Harry G., Barr A., Archer S.L. O2 sensing in the human ductus arteriosus: Regulation of voltage-gated K+ channels in smooth muscle cells by a mitochondrial redox sensor. Circ. Res. 2002;91(6):478–486.</mixed-citation><mixed-citation xml:lang="en">Michelakis E.D., Rebeyka I., Wu X.C., Nsair A., Thébaud B., Hashimoto K., Dyck J.R., Haromy A., Harry G., Barr A., Archer S.L. O2 sensing in the human ductus arteriosus: Regulation of voltage-gated K+ channels in smooth muscle cells by a mitochondrial redox sensor. Circ. Res. 2002;91(6):478–486.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Cogolludo A.L., Moral-Sanz J., Van Der Sterren S., Frazziano G., Van Cleef A.N.H. Maturation of O2 sensing and signaling in the chicken ductus arteriosus. Am. J. Physiol. Lung Cell. Mol. Physiol. 2009;297(4):619–630.</mixed-citation><mixed-citation xml:lang="en">Cogolludo A.L., Moral-Sanz J., Van Der Sterren S., Frazziano G., Van Cleef A.N.H. Maturation of O2 sensing and signaling in the chicken ductus arteriosus. Am. J. Physiol. Lung Cell. Mol. Physiol. 2009;297(4):619–630.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Reeve H.L., Tolarova S., Nelson D.P., Archer S., Kenneth Weir E. Redox control of oxygen sensing in the rabbit ductus arteriosus. J. Physiol. 2001;533(1):253–261.</mixed-citation><mixed-citation xml:lang="en">Reeve H.L., Tolarova S., Nelson D.P., Archer S., Kenneth Weir E. Redox control of oxygen sensing in the rabbit ductus arteriosus. J. Physiol. 2001;533(1):253–261.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Kajimoto H., Hashimoto K., Bonnet S.N., Haromy A., Harry G., Moudgil R., Nakanishi T., Rebeyka I., Thébaud B., Michelakis E.D., Archer S.I. Oxygen activates the Rho/Rho-kinase pathway and induces RhoB and ROCK-1 expression in human and rabbit ductus arteriosus by increasing mitochondria-derived reactive oxygen species: A newly recognized mechanism for sustaining ductal constriction. Circulation. 2007;115(13):1777–1788.</mixed-citation><mixed-citation xml:lang="en">Kajimoto H., Hashimoto K., Bonnet S.N., Haromy A., Harry G., Moudgil R., Nakanishi T., Rebeyka I., Thébaud B., Michelakis E.D., Archer S.I. Oxygen activates the Rho/Rho-kinase pathway and induces RhoB and ROCK-1 expression in human and rabbit ductus arteriosus by increasing mitochondria-derived reactive oxygen species: A newly recognized mechanism for sustaining ductal constriction. Circulation. 2007;115(13):1777–1788.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Shvetsova A.A., Khlystova M.A., Makukha Y.A., Shateeva V.S., Borzykh A.A., Gaynullina D.K., Tarasova O.S. Reactive oxygen species augment contractile responses of saphenous artery in 10-15-day-old but not adult rats: Substantial role of NADPH oxidases. Free Radic. Biol. Med. 2024;216:24–32.</mixed-citation><mixed-citation xml:lang="en">Shvetsova A.A., Khlystova M.A., Makukha Y.A., Shateeva V.S., Borzykh A.A., Gaynullina D.K., Tarasova O.S. Reactive oxygen species augment contractile responses of saphenous artery in 10-15-day-old but not adult rats: Substantial role of NADPH oxidases. Free Radic. Biol. Med. 2024;216:24–32.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Vogel P.A., Yang X., Moss N.G., Arendshorst W.J. Superoxide enhances Ca2+ entry through L-type channels in the renal afferent arteriole. Hypertension. 2015:66(2):374–381.</mixed-citation><mixed-citation xml:lang="en">Vogel P.A., Yang X., Moss N.G., Arendshorst W.J. Superoxide enhances Ca2+ entry through L-type channels in the renal afferent arteriole. Hypertension. 2015:66(2):374–381.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Ding Y., Winters A., Ding M., Graham S., Akopova I., Muallem S., Wang Y., Hee Hong J., Gryczynski Z., Yang S.-H., Birnbaumer L., Ma R. Reactive oxygen species-mediated TRPC6 protein activation in vascular myocytes, a mechanism for vasoconstrictor-regulated vascular tone. J. Biol. Chem. 2011;286(36):31799–31809.</mixed-citation><mixed-citation xml:lang="en">Ding Y., Winters A., Ding M., Graham S., Akopova I., Muallem S., Wang Y., Hee Hong J., Gryczynski Z., Yang S.-H., Birnbaumer L., Ma R. Reactive oxygen species-mediated TRPC6 protein activation in vascular myocytes, a mechanism for vasoconstrictor-regulated vascular tone. J. Biol. Chem. 2011;286(36):31799–31809.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Snetkov V.A., Smirnov S.V., Kua J., Aaronson P.I., Ward J.P., Knock G.A. Superoxide differentially controls pulmonary and systemic vascular tone through multiple signalling pathways. Cardiovasc. Res. 2011;89(1):214–224.</mixed-citation><mixed-citation xml:lang="en">Snetkov V.A., Smirnov S.V., Kua J., Aaronson P.I., Ward J.P., Knock G.A. Superoxide differentially controls pulmonary and systemic vascular tone through multiple signalling pathways. Cardiovasc. Res. 2011;89(1):214–224.</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Knock G.A., Snetkov V.A., Shaifta Y., Aaronson P.I., Ward J.P.T., Knock G.A. Superoxide constricts rat pulmonary arteries via Rho-kinase-mediated Ca2+ sensitization. Free Radic. Biol. Med. 2009;46(5):633–642.</mixed-citation><mixed-citation xml:lang="en">Knock G.A., Snetkov V.A., Shaifta Y., Aaronson P.I., Ward J.P.T., Knock G.A. Superoxide constricts rat pulmonary arteries via Rho-kinase-mediated Ca2+ sensitization. Free Radic. Biol. Med. 2009;46(5):633–642.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Bruckner M., Binder-Heschl C., Schwaberger B., Mileder L.P., Baik-Schneditz N., Koestenberger M., Avian A., Urlesberger B., Pichler G. Cerebral and peripheral tissue oxygenation in stable neonates: Absent influence of cardiac function. Acta Paediatr. 2020;109(8):1560–1569.</mixed-citation><mixed-citation xml:lang="en">Bruckner M., Binder-Heschl C., Schwaberger B., Mileder L.P., Baik-Schneditz N., Koestenberger M., Avian A., Urlesberger B., Pichler G. Cerebral and peripheral tissue oxygenation in stable neonates: Absent influence of cardiac function. Acta Paediatr. 2020;109(8):1560–1569.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Rudolph A.M. Distribution and regulation of blood flow in the fetal and neonatal lamb. Circ. Res. 1985;57(6):811–821.</mixed-citation><mixed-citation xml:lang="en">Rudolph A.M. Distribution and regulation of blood flow in the fetal and neonatal lamb. Circ. Res. 1985;57(6):811–821.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Charles S.M., Zhang L., Cipolla M.J., Buchholz J.N., Pearce W.J. Roles of cytosolic Ca2+ concentration and myofilament Ca2+ sensitization in age-dependent cerebrovascular myogenic tone. Am. J. Physiol. Heart Circ. Physiol. 2010;299(4):H1034– H1044.</mixed-citation><mixed-citation xml:lang="en">Charles S.M., Zhang L., Cipolla M.J., Buchholz J.N., Pearce W.J. Roles of cytosolic Ca2+ concentration and myofilament Ca2+ sensitization in age-dependent cerebrovascular myogenic tone. Am. J. Physiol. Heart Circ. Physiol. 2010;299(4):H1034– H1044.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Reho J.J., Zheng X., Benjamin J.E., Fisher S.A. Neural programming of mesenteric and renal arteries. Am. J. Physiol. Heart Circ. Physiol. 2014;307(4):H563–H573.</mixed-citation><mixed-citation xml:lang="en">Reho J.J., Zheng X., Benjamin J.E., Fisher S.A. Neural programming of mesenteric and renal arteries. Am. J. Physiol. Heart Circ. Physiol. 2014;307(4):H563–H573.</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Badran A., Nasser S.A., Mesmar J., El-Yazbi A.F., Bitto A, Fardoun M.M., Baydoun E., Eid A.H. Reactive oxygen species: Modulators of phenotypic switch of vascular smooth muscle cells. Int. J. Mol. Sci. 2020;21(22):8764.</mixed-citation><mixed-citation xml:lang="en">Badran A., Nasser S.A., Mesmar J., El-Yazbi A.F., Bitto A, Fardoun M.M., Baydoun E., Eid A.H. Reactive oxygen species: Modulators of phenotypic switch of vascular smooth muscle cells. Int. J. Mol. Sci. 2020;21(22):8764.</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Sawma T., Shaito A., Najm N., Sidani M., Orekhov A., El-Yazbi A.F., Iratni R., Eid A.H. Role of RhoA and Rho-associated kinase in phenotypic switching of vascular smooth muscle cells: Implications for vascular function. Atherosclerosis. 2022;358:12–28.</mixed-citation><mixed-citation xml:lang="en">Sawma T., Shaito A., Najm N., Sidani M., Orekhov A., El-Yazbi A.F., Iratni R., Eid A.H. Role of RhoA and Rho-associated kinase in phenotypic switching of vascular smooth muscle cells: Implications for vascular function. Atherosclerosis. 2022;358:12–28.</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Wamhoff B.R., Bowles D.K., McDonald O.G., Sinha S., Somlyo A.P., Somlyo A.V., Owens G.K. L-type voltage-gated Ca2+ channels modulate expression of smooth muscle differentiation marker genes via a Rho kinase/myocardin/SRF-dependent mechanism. Circ. Res. 2004;95(4):406–414.</mixed-citation><mixed-citation xml:lang="en">Wamhoff B.R., Bowles D.K., McDonald O.G., Sinha S., Somlyo A.P., Somlyo A.V., Owens G.K. L-type voltage-gated Ca2+ channels modulate expression of smooth muscle differentiation marker genes via a Rho kinase/myocardin/SRF-dependent mechanism. Circ. Res. 2004;95(4):406–414.</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Hellstrand P., Albinsson S. Stretch-dependent growth and differentiation in vascular smooth muscle: role of the actin cytoskeleton. Can. J. Physiol. Pharmacol. 2005;83(10):869–875.</mixed-citation><mixed-citation xml:lang="en">Hellstrand P., Albinsson S. Stretch-dependent growth and differentiation in vascular smooth muscle: role of the actin cytoskeleton. Can. J. Physiol. Pharmacol. 2005;83(10):869–875.</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Mack C.P., Somlyo A.V, Hautmann M., Somlyo A.P., Owens G.K. Smooth muscle differentiation marker gene expression is regulated by RhoA-mediated actin polymerization. J. Biol. Chem. 2001;276(1):341–347.</mixed-citation><mixed-citation xml:lang="en">Mack C.P., Somlyo A.V, Hautmann M., Somlyo A.P., Owens G.K. Smooth muscle differentiation marker gene expression is regulated by RhoA-mediated actin polymerization. J. Biol. Chem. 2001;276(1):341–347.</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Clempus R.E., Sorescu D., Dikalova A.E., Pounkova L., Jo P., Sorescu G.P., Schmidt H.H.H., Lassègue B., Griendling K.K. Nox4 is required for maintenance of the differentiated vascular smooth muscle cell phenotype. Arterioscler. Thromb. Vasc. Biol. 2007;27(1):42–48.</mixed-citation><mixed-citation xml:lang="en">Clempus R.E., Sorescu D., Dikalova A.E., Pounkova L., Jo P., Sorescu G.P., Schmidt H.H.H., Lassègue B., Griendling K.K. Nox4 is required for maintenance of the differentiated vascular smooth muscle cell phenotype. Arterioscler. Thromb. Vasc. Biol. 2007;27(1):42–48.</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Xiao Q., Luo Z., Pepe A.E., Margariti A., Zeng L., Xu Q. Embryonic stem cell differentiation into smooth muscle cells is mediated by Nox4-produced H2O2. Am. J. Physiol. Cell Physiol. 2009;296(4):711–723.</mixed-citation><mixed-citation xml:lang="en">Xiao Q., Luo Z., Pepe A.E., Margariti A., Zeng L., Xu Q. Embryonic stem cell differentiation into smooth muscle cells is mediated by Nox4-produced H2O2. Am. J. Physiol. Cell Physiol. 2009;296(4):711–723.</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Shvetsova A.A., Borzykh A.A., Selivanova E.K., Kiryukhina O.O., Gaynullina D.K., Tarasova O.S. Intrauterine nitric oxide deficiency weakens differentiation of vascular smooth muscle in newborn rats. Int. J. Mol. Sci. 2021;22(15):8003.</mixed-citation><mixed-citation xml:lang="en">Shvetsova A.A., Borzykh A.A., Selivanova E.K., Kiryukhina O.O., Gaynullina D.K., Tarasova O.S. Intrauterine nitric oxide deficiency weakens differentiation of vascular smooth muscle in newborn rats. Int. J. Mol. Sci. 2021;22(15):8003.</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Sauzeau V., Rolli-Derkinderen M., Marionneau C., Loirand G., Pacaud P. RhoA expression is controlled by nitric oxide through cGMP-dependent protein kinase activation. J. Biol. Chem. 2003;278(11):9472–9480.</mixed-citation><mixed-citation xml:lang="en">Sauzeau V., Rolli-Derkinderen M., Marionneau C., Loirand G., Pacaud P. RhoA expression is controlled by nitric oxide through cGMP-dependent protein kinase activation. J. Biol. Chem. 2003;278(11):9472–9480.</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Pilz R.B., Casteel D.E. Regulation of gene expression by cyclic GMP. Circ. Res. 2003;93(11):1034–1046.</mixed-citation><mixed-citation xml:lang="en">Pilz R.B., Casteel D.E. Regulation of gene expression by cyclic GMP. Circ. Res. 2003;93(11):1034–1046.</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>
