<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Annals of Clinical and Experimental Neurology</journal-id><journal-title-group><journal-title xml:lang="en">Annals of Clinical and Experimental Neurology</journal-title><trans-title-group xml:lang="ru"><trans-title>Анналы клинической и экспериментальной неврологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-5473</issn><issn publication-format="electronic">2409-2533</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1152</article-id><article-id pub-id-type="doi">10.17816/ACEN.1152</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Cellular and Molecular Mechanisms Underlying Transcranial Magnetic Stimulation: Experimental Data for Evaluating Changes in Nervous Tissue</article-title><trans-title-group xml:lang="ru"><trans-title>Клеточные и молекулярные механизмы транскраниальной магнитной стимуляции: экспериментальные данные в оценке изменений нервной ткани</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0006-2258-6155</contrib-id><name-alternatives><name xml:lang="en"><surname>Krasilnikova</surname><given-names>Anna P.</given-names></name><name xml:lang="ru"><surname>Красильникова</surname><given-names>Анна Павловна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>student</p></bio><bio xml:lang="ru"><p>студент</p></bio><email>av_egorova@bk.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7112-2556</contrib-id><name-alternatives><name xml:lang="en"><surname>Egorova</surname><given-names>Anna V.</given-names></name><name xml:lang="ru"><surname>Егорова</surname><given-names>Анна Валериевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.), Assistant professor, researcher, Laboratory of neuromorphology, Brain Institute, Assistant professor, Department of histology, embryology and cytology</p></bio><bio xml:lang="ru"><p>канд. мед. наук, доцент, н. с. лаб. нейроморфологии Института мозга, доцент каф. гистологии, эмбриологии и цитологии</p></bio><email>av_egorova@bk.ru</email><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5222-5322</contrib-id><name-alternatives><name xml:lang="en"><surname>Voronkov</surname><given-names>Dmitry N.</given-names></name><name xml:lang="ru"><surname>Воронков</surname><given-names>Дмитрий Николаевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.), senior researcher, Laboratory of neuromorphology, Brain Institute</p></bio><bio xml:lang="ru"><p>канд. мед. наук, с. н. с. лаб. нейроморфологии Института мозга</p></bio><email>av_egorova@bk.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1841-1177</contrib-id><name-alternatives><name xml:lang="en"><surname>Poydasheva</surname><given-names>Alexandra G.</given-names></name><name xml:lang="ru"><surname>Пойдашева</surname><given-names>Александра Георгиевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.), researcher, Non-invasive neuromodulation group, Institute of Neurorehabilitation and Rehabilitation Technologies</p></bio><bio xml:lang="ru"><p>канд. мед. наук, н. с. группы неинвазивной нейромодуляции Института нейрореабилитации и восстановительных технологий</p></bio><email>av_egorova@bk.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8708-6940</contrib-id><name-alternatives><name xml:lang="en"><surname>Glinkina</surname><given-names>Valeria V.</given-names></name><name xml:lang="ru"><surname>Глинкина</surname><given-names>Валерия Владимировна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Dr. Sci. (Med.), Professor, Head, Department of histology, embryology and cytology</p></bio><bio xml:lang="ru"><p>д-р мед. наук, профессор, зав. каф. гистологии, эмбриологии и цитологии</p></bio><email>av_egorova@bk.ru</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0552-6939</contrib-id><name-alternatives><name xml:lang="en"><surname>Sukhorukov</surname><given-names>Vladimir S.</given-names></name><name xml:lang="ru"><surname>Сухоруков</surname><given-names>Владимир Сергеевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Dr. Sci. (Med.), Professor, Head, Laboratory of neuromorphology, Brain Institute, Professor, Department of histology, embryology and cytology</p></bio><bio xml:lang="ru"><p>д-р мед. наук, профессор, зав. лаб. нейроморфологии Института мозга, профессор каф. гистологии, эмбриологии и цитологии </p></bio><email>av_egorova@bk.ru</email><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Lomonosov Moscow State University</institution></aff><aff><institution xml:lang="ru">Московский государственный университет имени М.В. Ломоносова</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Research Center of Neurology</institution></aff><aff><institution xml:lang="ru">Научный центр неврологии</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Pirogov Russian National Research Medical University</institution></aff><aff><institution xml:lang="ru">Российский научно-исследовательский медицинский университет имени Н.И. Пирогова</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-12-06" publication-format="electronic"><day>06</day><month>12</month><year>2024</year></pub-date><volume>18</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>96</fpage><lpage>109</lpage><history><date date-type="received" iso-8601-date="2024-06-20"><day>20</day><month>06</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-09-09"><day>09</day><month>09</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Krasilnikova A.P., Egorova A.V., Voronkov D.N., Poydasheva A.G., Glinkina V.V., Sukhorukov V.S.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Красильникова А.П., Егорова А.В., Воронков Д.Н., Пойдашева А.Г., Глинкина В.В., Сухоруков В.С.</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Krasilnikova A.P., Egorova A.V., Voronkov D.N., Poydasheva A.G., Glinkina V.V., Sukhorukov V.S.</copyright-holder><copyright-holder xml:lang="ru">Красильникова А.П., Егорова А.В., Воронков Д.Н., Пойдашева А.Г., Глинкина В.В., Сухоруков В.С.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://annaly-nevrologii.com/pathID/article/view/1152">https://annaly-nevrologii.com/pathID/article/view/1152</self-uri><abstract xml:lang="en"><p>Transcranial magnetic stimulation (TMS) is a non-invasive method for targeted modulation of the electrical activity of brain neurons with a magnetic field. Although TMS efficacy was demonstrated in the treatment of several neurological and mental disorders, changes in nervous tissue at the cellular and molecular levels with different duration and intensity of stimulation have been relatively understudied by cellular neurobiology methods. Aim. The aim of this review was to evaluate and summarize new experimental data on the fundamental mechanisms underlying the action of TMS and its potential in modulating structural and functional changes in nervous tissue. This article summarizes recent data on the effects of different TMS protocols on the mechanisms underlying synaptic plasticity, neurogenesis, and neuronal differentiation. Separate sections summarize the neuroprotective effects of this method and glial microenvironment response. Studies to investigate the mechanisms of TMS will contribute to the development of more effective and reliable treatment protocols.</p></abstract><trans-abstract xml:lang="ru"><p>Транскраниальная магнитная стимуляция (ТМС) — неинвазивный метод направленного воздействия на электрическую активность нейронов головного мозга магнитным полем. Несмотря на доказанную эффективность в лечении ряда неврологических и психических заболеваний, изменения в нервной ткани на клеточном и молекулярном уровнях при разной длительности и интенсивности стимуляции мало изучены методами клеточной нейробиологии. Целью работы явился анализ и обобщение новых экспериментальных данных о фундаментальных механизмах действия ТМС и потенциальных возможностях данного метода в модуляции структурно-функциональных изменений в нервной ткани. В работе систематизированы современные сведения о влиянии разных протоколов ТМС на механизмы синаптической пластичности, нейрогенез и дифференцировку нейронов. Отдельные разделы посвящены нейропротективным эффектам данного метода, а также ответной реакции глиального микроокружения. Исследования механизмов ТМС будут способствовать разработке более результативных и надёжных протоколов лечения.</p></trans-abstract><kwd-group xml:lang="en"><kwd>transcranial magnetic stimulation</kwd><kwd>neuroplasticity</kwd><kwd>glia</kwd><kwd>neurogenesis</kwd><kwd>neuroprotection</kwd><kwd>synaptogenesis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>транскраниальная магнитная стимуляция</kwd><kwd>нейропластичность</kwd><kwd>глия</kwd><kwd>нейрогенез</kwd><kwd>нейропротекция</kwd><kwd>синаптогенез</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="en">Government of the Russian Federation</institution></institution-wrap><institution-wrap><institution xml:lang="ru">Правительство РФ</institution></institution-wrap></funding-source></award-group></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Zhong G., Yang Z., Jiang T. Precise modulation strategies for transcranial magnetic stimulation: advances and future directions. Neurosci. Bull. 2021;37(12):1718–1734. DOI: 10.1007/s12264-021-00781-x</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Hallett M. Transcranial magnetic stimulation: a primer. Neuron. 2007;55(2):187–199. DOI: 10.1016/j.neuron.2007.06.026</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Burke M.J., Fried P.J., Pascual-Leone A. Transcranial magnetic stimulation: neurophysiological and clinical applications. Handb. Clin. Neurol. 2019;163:73–92. DOI: 10.1016/B978-0-12-804281-6.00005-7</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Lefaucheur J.P., Aleman A., Baeken C. et al. Evidence-based guidelines on the therapeutic use of repetitive transcranial magnetic stimulation (rTMS): an update (2014–2018). Clin. Neurophysiol. 2020;131(2):474–528. DOI: 10.1016/j.clinph.2019.11.002</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>De Risio L., Borgi M., Pettorruso M. et al. Recovering from depression with repetitive transcranial magnetic stimulation (rTMS): a systematic review and meta-analysis of preclinical studies. Transl. Psychiatry. 2020;10(1):393. DOI: 10.1038/s41398-020-01055-2</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Croarkin P.E., Elmaadawi A.Z., Aaronson S.T. et al. Left prefrontal transcranial magnetic stimulation for treatment-resistant depression in adolescents: a double-blind, randomized, sham-controlled trial. Neuropsychopharmacology. 2021;46(2):462–469. DOI: 10.1038/s41386-020-00829-y</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Blumberger D.M., Mulsant B.H., Thorpe K.E. et al. Effectiveness of standard sequential bilateral repetitive transcranial magnetic stimulation vs bilateral theta burst stimulation in older adults with depression: the FOUR-D randomized noninferiority clinical trial. JAMA Psychiatry. 2022;79(11):1065–1073. DOI: 10.1001/jamapsychiatry.2022.2862</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Yang S., Chang M.C. Effect of repetitive transcranial magnetic stimulation on pain management: a systematic narrative review. Front. Neurol. 2020;11:114. DOI: 10.3389/fneur.2020.00114</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Pei Q., Wu B., Tang Y. et al. Repetitive transcranial magnetic stimulation at different frequencies for postherpetic neuralgia: a double-blind, sham-controlled, randomized trial. Pain Physician. 2019;22(4):E303–E313.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Фоменко О.Ю., Шелыгин Ю.А., Аполихина И.А. и др. Междисциплинарный консенсус по использованию высокоинтенсивной импульсной магнитной терапии для лечения нейрогенной тазовой боли при пудендальной нейропатии. Акушерство и гинекология. 2023;(10):160–176. Fomenko O.Yu., Shelygin Yu.A., Apolihina I.A. et al. Interdisciplinary consensus on the use of high-intensity pulsed electromagnetic field therapy in the treatment of neurogenic pelvic pain. Obstetrics and Gynecology. 2023;(10):160–176. DOI: 10.18565/aig.2023.117</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Khedr E.M., Etraby A.E., Hemeda M. et al. Long-term effect of repetitive transcranial magnetic stimulation on motor function recovery after acute ischemic stroke: rTMS in acute ischemic stroke. Acta. Neurol. Scand. 2010;121(1):30–37. DOI: 10.1111/j.1600-0404.2009.01195.x</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Бакулин И.С., Пойдашева А.Г., Супонева Н.А., Пирадов М.А. Транскраниальная магнитная стимуляция в прогнозировании восстановления двигательной функции руки при инсульте. Нервные болезни. 2023;(3):3–8. Bakulin I.S., Poydasheva A.G., Suponeva N.A., Piradov M.A. Transcranial magnetic stimulation in the prognosis of recovery for hand motor function after stroke. Nervnye bolezni. 2023;(3):3–8. DOI: 10.24412/2226-0757-2023-13000</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Mi T.M., Garg S., Ba F. et al. High-frequency rTMS over the supplementary motor area improves freezing of gait in Parkinson’s disease: a randomized controlled trial. Parkinsonism. Relat. Disord. 2019;68:85–90. DOI: 10.1016/j.parkreldis.2019.10.009</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Khedr E.M., Mohamed K.O., Soliman R.K. et al. The effect of high-frequency repetitive transcranial magnetic stimulation on advancing Parkinson’s disease with dysphagia: double blind randomized clinical trial. Neurorehabil. Neural. Repair. 2019;33(6):442–452. DOI: 10.1177/1545968319847968</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Korzhova J., Bakulin I., Sinitsyn D. et al. High‐frequency repetitive transcranial magnetic stimulation and intermittent theta‐burst stimulation for spasticity management in secondary progressive multiple sclerosis. Eur. J. Neurol. 2019;26(4):680-e44. DOI: 10.1111/ene.13877</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Starling A.J., Tepper S.J., Marmura M.J. et al. A multicenter, prospective, single arm, open label, observational study of sTMS for migraine prevention (ESPOUSE Study). Cephalalgia. 2018;38(6):1038–1048. DOI: 10.1177/0333102418762525</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Zhong J., Lan W., Feng Y. et al. Efficacy of repetitive transcranial magnetic stimulation on chronic migraine: a meta-analysis. Front. Neurol. 2022;13:1050090. DOI: 10.3389/fneur.2022.1050090</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Lerner A.J., Wassermann E.M., Tamir D.I. Seizures from transcranial magnetic stimulation 2012–2016: Results of a survey of active laboratories and clinics. Clin. Neurophysiol. 2019;130(8):1409–1416. DOI: 10.1016/j.clinph.2019.03.016</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Rossi S., Hallett M., Rossini P.M. et al. Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research. Clin. Neurophysiol. 2009;120(12):2008–2039. DOI: 10.1016/j.clinph.2009.08.016</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Cruciani A., Mancuso M., Sveva V. et al. Using TMS-EEG to assess the effects of neuromodulation techniques: a narrative review. Front. Hum. Neurosci. 2023;17:1247104. DOI: 10.3389/fnhum.2023.1247104</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Bergmann T.O., Karabanov A., Hartwigsen G. et al. Combining non-invasive transcranial brain stimulation with neuroimaging and electrophysiology: current approaches and future perspectives. Neuroimage. 2016;140:4–19. DOI: 10.1016/j.neuroimage.2016.02.012</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Boonzaier J., Petrov P.I., Otte W.M. et al. Design and evaluation of a rodent-specific transcranial magnetic stimulation coil: an in silico and in vivo validation study. Neuromodulation. 2020;23(3):324–334. DOI: 10.1111/ner.13025</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Jiang W., Isenhart R., Liu C.Y. et al. A C-shaped miniaturized coil for transcranial magnetic stimulation in rodents. J. Neural. Eng. 2023;20(2):026022. DOI: 10.1088/1741-2552/acc097</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Liu L., Ding M., Wu J. et al. Design and evaluation of a rodent-specific focal transcranial magnetic stimulation coil with the custom shielding application in rats. Front. Neurosci. 2023;17:1129590. DOI: 10.3389/fnins.2023.1129590</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Bolland S.J., Goryachev M., Opitz A. et al. Translational modelling of low and medium intensity transcranial magnetic stimulation from rodents to humans. 2024. (Pre-print). DOI: 10.1101/2024.04.27.591424</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Shirinpour S., Hananeia N., Rosado J. et al. Multi-scale modeling toolbox for single neuron and subcellular activity under Transcranial Magnetic Stimulation. Brain Stimul. 2021;14(6):1470–1482. DOI: 10.1016/j.brs.2021.09.004</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Huang Y.Z., Edwards M.J., Rounis E. et al. Theta burst stimulation of the human motor cortex. Neuron. 2005;45(2):201–206. DOI: 10.1016/j.neuron.2004.12.033</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Li C., Huang Y., Bai Y. et al. Critical role of glutamatergic and GABAergic neurotransmission in the central mechanisms of theta‐burst stimulation. Hum. Brain Mapp. 2019;40(6):2001–2009. DOI: 10.1002/hbm.24485</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Siebner H.R., Funke K., Aberra A.S. et al. Transcranial magnetic stimulation of the brain: what is stimulated? — A consensus and critical position paper. Clin. Neurophysiol. 2022;140:59–97. DOI: 10.1016/j.clinph.2022.04.022</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Romero M.C., Davare M., Armendariz M., Janssen P. Neural effects of transcranial magnetic stimulation at the single-cell level. Nat. Commun. 2019;10(1):2642. DOI: 10.1038/s41467-019-10638-7</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Sasaki R., Liao W., Opie G.M., Semmler J.G. Effect of current direction and muscle activation on motor cortex neuroplasticity induced by repetitive paired‐pulse transcranial magnetic stimulation. Eur. J. Neurosci. 2023;58(5):3270–3285. DOI: 10.1111/ejn.16099</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Gomez-Feria J., Fernandez-Corazza M., Martin-Rodriguez J.F., Mir P. TMS intensity and focality correlation with coil orientation at three non-motor regions. Phys. Med. Biol. 2022;67(5):055002. DOI: 10.1088/1361-6560/ac4ef9</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Chervyakov A.V., Chernyavsky A.Yu., Sinitsyn D.O., Piradov M.A. Possible mechanisms underlying the therapeutic effects of transcranial magnetic stimulation. Front. Hum. Neurosci. 2015;9:303. DOI: 10.3389/fnhum.2015.00303</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Xing Y., Zhang Y., Li C. et al. Repetitive transcranial magnetic stimulation of the brain after ischemic stroke: mechanisms from animal models. Cell. Mol. Neurobiol. 2023;43(4):1487–1497. DOI: 10.1007/s10571-022-01264-x</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Deng X., Chen X., Li Y. et al. Online and offline effects of parietal 10 Hz repetitive transcranial magnetic stimulation on working memory in healthy controls. Hum. Brain Mapp. 2024;45:e26636. DOI: 10.1002/hbm.26636</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Valero-Cabré A., Amengual J.L., Stengel C. et al. Transcranial magnetic stimulation in basic and clinical neuroscience: a comprehensive review of fundamental principles and novel insights. Neurosci. Biobehav. Rev. 2017;83:381–404. DOI: 10.1016/j.neubiorev.2017.10.006</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Chan J.H.L., Lin C.S.‐Y., Pierrot‐Deseilligny E., Burke D. Excitability changes in human peripheral nerve axons in a paradigm mimicking paired‐pulse transcranial magnetic stimulation. J. Physiol. 2002;542(Pt 3):951–961. DOI: 10.1113/jphysiol.2002.018937</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Pell G.S., Roth Y., Zangen A. Modulation of cortical excitability induced by repetitive transcranial magnetic stimulation: Influence of timing and geometrical parameters and underlying mechanisms. Prog. Neurobiol. 2011;93(1):59–98. DOI: 10.1016/j.pneurobio.2010.10.003</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Бакулин И.С., Пойдашева А.Г., Медынцев А.А. и др. Транскраниальная магнитная стимуляция в когнитивной нейронауке: методологические основы и безопасность. Российский журнал когнитивной науки. 2020;7(3):25–44. Bakulin I.S., Poydasheva A.G., Medyntsev A.A. et al. Transcranial magnetic stimulation in cognitive neuroscience: methodological basis and safety. Russ. J. Cogn. Sci. 2020;7(3):25–44. DOI: 10.47010/20.3.2</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Hoogendam J.M., Ramakers G.M.J., Di Lazzaro V. Physiology of repetitive transcranial magnetic stimulation of the human brain. Brain Stimul. 2010;3(2):95–118. DOI: 10.1016/j.brs.2009.10.005</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Belardinelli P., König F., Liang C. et al. TMS-EEG signatures of glutamatergic neurotransmission in human cortex. Sci. Rep. 2021;11(1):8159. DOI: 10.1038/s41598-021-87533-z</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Vlachos A., Müller-Dahlhaus F., Rosskopp J. et al. Repetitive magnetic stimulation induces functional and structural plasticity of excitatory postsynapses in mouse organotypic hippocampal slice cultures. J. Neurosci. 2012;32(48):17514–17523. DOI: 10.1523/JNEUROSCI.0409-12.2012</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Bonilla-Quintana M., Wörgötter F. Exploring new roles for actin upon LTP induction in dendritic spines. Sci. Rep. 2021;11(1):7072. DOI: 10.1038/s41598-021-86367-z</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Tang A.D., Bennett W., Bindoff A.D. et al. Subthreshold repetitive transcranial magnetic stimulation drives structural synaptic plasticity in the young and aged motor cortex. Brain. Stimul. 2021;14(6):1498–1507. DOI: 10.1016/j.brs.2021.10.001</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Cambiaghi M., Cherchi L., Masin L. et al. High-frequency repetitive transcranial magnetic stimulation enhances layer II/III morphological dendritic plasticity in mouse primary motor cortex. Behav. Brain Res. 2021;410:113352. DOI: 10.1016/j.bbr.2021.113352</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Lenz M., Platschek S., Priesemann V. et al. Repetitive magnetic stimulation induces plasticity of excitatory postsynapses on proximal dendrites of cultured mouse CA1 pyramidal neurons. Brain Struct. Funct. 2015;220(6):3323–3337. DOI: 10.1007/s00429-014-0859-9</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Rogasch N.C., Zipser C., Darmani G. et al. The effects of NMDA receptor blockade on TMS-evoked EEG potentials from prefrontal and parietal cortex. Sci. Rep. 2020;10(1):3168. DOI: 10.1038/s41598-020-59911-6</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Lenz M., Galanis C., Müller-Dahlhaus F. et al. Repetitive magnetic stimulation induces plasticity of inhibitory synapses. Nat. Commun. 2016;7:10020. DOI: 10.1038/ncomms10020</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Contreras A., Hines D.J., Hines R.M. Molecular specialization of GABAergic synapses on the soma and axon in cortical and hippocampal circuit function and dysfunction. Front. Mol. Neurosci. 2019;12:154. DOI: 10.3389/fnmol.2019.00154</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Bannai H., Lévi S., Schweizer C. et al. Activity-dependent tuning of inhibitory neurotransmission based on GABAAR diffusion dynamics. Neuron. 2009;62(5):670–682. DOI: 10.1016/j.neuron.2009.04.023</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Thomson A.C., De Graaf T.A., Schuhmann T. et al. Transcranial Magnetic stimulation (TMS) modulates functional activity of SH-SY5Y cells: an in vitro model provides support for assumed excitability changes. bioRxiv. 2020. DOI: 10.1101/2020.08.19.257295</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Panja D., Dagyte G., Bidinosti M. et al. Novel translational control in arc-dependent long term potentiation consolidation in vivo. J. Biol. Chem. 2009;284(46):31498–31511. DOI: 10.1074/jbc.M109.056077</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Fujiki M., Yee K.M., Steward O. Non-invasive high frequency repetitive transcranial magnetic stimulation (hfrTMS) robustly activates molecular pathways implicated in neuronal growth and synaptic plasticity in select populations of neurons. Front. Neurosci. 2020;14:558. DOI: 10.3389/fnins.2020.00558</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Puighermanal E., Biever A., Pascoli V. et al. Ribosomal protein S6 phosphorylation is involved in novelty-induced locomotion, synaptic plasticity and mRNA translation. Front. Mol. Neurosci. 2017;10:419. DOI: 10.3389/fnmol.2017.00419</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Ma J., Zhang Z., Su Y. et al. Magnetic stimulation modulates structural synaptic plasticity and regulates BDNF–TrkB signal pathway in cultured hippocampal neurons. Neurochem. Int. 2013;62(1):84–91. DOI: 10.1016/j.neuint.2012.11.010</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Ma S.M., Ni J.X., Li X.Y. et al. High-frequency repetitive transcranial magnetic stimulation reduces pain in postherpetic neuralgia. Pain. Med. 2015;16(11):2162–2170. DOI: 10.1111/pme.12832</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Liu G., Li X.M., Tian S. et al. The effect of magnetic stimulation on differentiation of human induced pluripotent stem cells into neuron. J. Cell. Biochem. 2020;121(10):4130–4141. DOI: 10.1002/jcb.29647</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Rodger J., Mo C., Wilks T. et al. Transcranial pulsed magnetic field stimulation facilitates reorganization of abnormal neural circuits and corrects behavioral deficits without disrupting normal connectivity. FASEB J. 2012;26(4):1593–1606. DOI: 10.1096/fj.11-194878</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Makowiecki K., Harvey A.R., Sherrard R.M., Rodger J. Low-intensity repetitive transcranial magnetic stimulation improves abnormal visual cortical circuit topography and upregulates BDNF in mice. J. Neurosci. 2014;34(32):10780–10792. DOI: 10.1523/JNEUROSCI.0723-14.2014</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Hong I., Garrett A., Maker G. et al. Repetitive low intensity magnetic field stimulation in a neuronal cell line: a metabolomics study. PeerJ. 2018;6:e4501. DOI: 10.7717/peerj.4501</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Funke K. Transcranial magnetic stimulation of rodents. In: Handbook of Behavioral Neuroscience. Elsevier; 2019:365–387. DOI: 10.1016/B978-0-12-812028-6.00020-3</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Chalfouh C., Guillou C., Hardouin J. et al. The regenerative effect of trans-spinal magnetic stimulation after spinal cord injury: mechanisms and pathways underlying the effect. Neurotherapeutics. 2020;17(4):2069–2088. DOI: 10.1007/s13311-020-00915-5</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Guo F., Lou J., Han X. et al. Repetitive transcranial magnetic stimulation ameliorates cognitive impairment by enhancing neurogenesis and suppressing apoptosis in the hippocampus in rats with ischemic stroke. Front. Physiol. 2017;8:559. DOI: 10.3389/fphys.2017.00559</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Cao H., Zuo C., Gu Z. et al. High frequency repetitive transcranial magnetic stimulation alleviates cognitive deficits in 3xTg-AD mice by modulating the PI3K/Akt/GLT-1 axis. Redox. Biol. 2022;54:102354. DOI: 10.1016/j.redox.2022.102354</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Grehl S., Viola H.M., Fuller-Carter P.I. et al. Cellular and molecular changes to cortical neurons following low intensity repetitive magnetic stimulation at different frequencies. Brain Stimul. 2015;8(1):114–123. DOI: 10.1016/j.brs.2014.09.012</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Wang Y., Fang K., He S. et al. Effects of repetitive magnetic stimulation on the growth of primarily cultured hippocampus neurons in vitro and their expression of iron-containing enzymes. Neuropsychiatr. Dis. Treat. 2019;15:927–934. DOI: 10.2147/NDT.S199328</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Ueyama E., Ukai S., Ogawa A. et al. Chronic repetitive transcranial magnetic stimulation increases hippocampal neurogenesis in rats. Psychiatry Clin. Neurosci. 2011;65(1):77–81. DOI: 10.1111/j.1440-1819.2010.02170.x</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Sabelström H., Stenudd M., Réu P. et al. Resident neural stem cells restrict tissue damage and neuronal loss after spinal cord injury in mice. Science. 2013;342(6158):637–640. DOI: 10.1126/science.1242576</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Robac A., Neveu P., Hugede A. et al. Repetitive trans spinal magnetic stimulation improves functional recovery and tissue repair in contusive and penetrating spinal cord injury models in rats. Biomedicines. 2021;9(12):1827. DOI: 10.3390/biomedicines9121827</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Wu C.H., Chen C.C., Hung T.H. et al. Activation of TrkB/Akt signaling by a TrkB receptor agonist improves long-term histological and functional outcomes in experimental intracerebral hemorrhage. J. Biomed. Sci. 2019;26(1):53. DOI: 10.1186/s12929-019-0543-8</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Guo F., Han X., Zhang J. et al. Repetitive transcranial magnetic stimulation promotes neural stem cell proliferation via the regulation of MiR-25 in a rat model of focal cerebral ischemia. PLoS One. 2014;9(10):e109267. DOI: 10.1371/journal.pone.0109267</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Müller M.B., Toschi N., Kresse A.E. et al. Long-term repetitive transcranial magnetic stimulation increases the expression of brain-derived neurotrophic factor and cholecystokinin mRNA, but not neuropeptide tyrosine mRNA in specific areas of rat brain. Neuropsychopharmacology. 2000;23(2):205–215. DOI: 10.1016/S0893-133X(00)00099-3</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Chen Y., Zhang R., Xue F. et al. Quetiapine and repetitive transcranial magnetic stimulation ameliorate depression-like behaviors and up-regulate the proliferation of hippocampal-derived neural stem cells in a rat model of depression: the involvement of the BDNF/ERK signal pathway. Pharmacol. Biochem. Behav. 2015;136:39–46. DOI: 10.1016/j.pbb.2015.07.005</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Chen C., Ahn E.H., Liu X. et al. Optimized TrkB agonist ameliorates Alzheimer’s disease pathologies and improves cognitive functions via inhibiting delta-secretase. ACS Chem. Neurosci. 2021;12(13):2448–2461. DOI: 10.1021/acschemneuro.1c00181</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Liao J., Chen C., Ahn E.H. et al. Targeting both BDNF/TrkB pathway and delta-secretase for treating Alzheimer’s disease. Neuropharmacology. 2021;197:108737. DOI: 10.1016/j.neuropharm.2021.108737</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Liu H., Han X., Chen H. et al. Repetitive magnetic stimulation promotes neural stem cells proliferation by upregulating MiR-106b in vitro. J. Huazhong. Univ. Sci. Technolog. Med. Sci. 2015;35(5):766–772. DOI: 10.1007/s11596-015-1505-3</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Cui M., Ge H., Zeng H. et al. Repetitive transcranial magnetic stimulation promotes neural stem cell proliferation and differentiation after intracerebral hemorrhage in mice. Cell Transplant. 2019;28(5):568–584. DOI: 10.1177/0963689719834870</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Deng Y., Guo F., Han X., Huang X. Repetitive transcranial magnetic stimulation increases neurological function and endogenous neural stem cell migration via the SDF-1α/CXCR4 axis after cerebral infarction in rats. Exp. Ther. Med. 2021;22(3):1037. DOI: 10.3892/etm.2021.10469</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Zong X., Gu J., Zhou S. et al. Continuous theta-burst stimulation enhances and sustains neurogenesis following ischemic stroke. Theranostics. 2022;12(13):5710–5726. DOI: 10.7150/thno.71832</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Peng J.-J., Sha R., Li M.-X. et al. Repetitive transcranial magnetic stimulation promotes functional recovery and differentiation of human neural stem cells in rats after ischemic stroke. Exp. Neurol. 2019;313:1–9. DOI: 10.1016/j.expneurol.2018.12.002</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Ferreira S.A., Pinto N., Serrenho I. et al. Contribution of glial cells to the neuroprotective effects triggered by repetitive magnetic stimulation: a systematic review. Neural. Regen. Res. 2024;19(1):116–123. DOI: 10.4103/1673-5374.374140</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>Ullian E.M., Sapperstein S.K., Christopherson K.S., Barres B.A. Control of synapse number by glia. Science. 2001;291(5504):657–661. DOI: 10.1126/science.291.5504.657</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Tucker R.P., Adams J.C. Molecular evolution of the Thrombospondin superfamily. Semin. Cell. Dev. Biol. 2024;155(Pt B):12–21. DOI: 10.1016/j.semcdb.2023.05.004</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Nagai J., Rajbhandari A.K., Gangwani M.R. et al. Hyperactivity with disrupted attention by activation of an astrocyte synaptogenic cue. Cell. 2019;177(5):1280–1292.e20. DOI: 10.1016/j.cell.2019.03.019</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Zhuang Y., Xu X., Li H. et al. Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury. CNS Neurosci. Ther. 2023;29(10):2873–2883. DOI: 10.1111/cns.14223</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>Chung W.-S., Clarke L.E., Wang G.X. et al. Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways. Nature. 2013;504(7480):394–400. DOI: 10.1038/nature12776</mixed-citation></ref><ref id="B87"><label>87.</label><mixed-citation>Lee J.-H., Kim .J, Noh S. et al. Astrocytes phagocytose adult hippocampal synapses for circuit homeostasis. Nature. 2021;590(7847):612–617. DOI: 10.1038/s41586-020-03060-3.</mixed-citation></ref><ref id="B88"><label>88.</label><mixed-citation>Murai K.K., Nguyen L.N., Irie F. et al. Control of hippocampal dendritic spine morphology through ephrin-A3/EphA4 signaling. Nat. Neurosci. 2003;6(2):153–160. DOI: 10.1038/nn994</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Filosa A., Paixão S., Honsek S.D. et al. Neuron-glia communication via EphA4/ephrin-A3 modulates LTP through glial glutamate transport. Nat. Neurosci. 2009;12(10):1285–1292. DOI: 10.1038/nn.2394</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>Monai H., Hirase H. Astrocytes as a target of transcranial direct current stimulation (tDCS) to treat depression. Neurosci. Res. 2018;126:15–21. DOI: 10.1016/j.neures.2017.08.012</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>Clarke D., Beros J., Bates K.A. et al. Low intensity repetitive magnetic stimulation reduces expression of genes related to inflammation and calcium signalling in cultured mouse cortical astrocytes. Brain Stimul. 2021;14(1):183–191. DOI: 10.1016/j.brs.2020.12.007</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>Roque C., Pinto N., Vaz Patto M., Baltazar G. Astrocytes contribute to the neuronal recovery promoted by high‐frequency repetitive magnetic stimulation in in vitro models of ischemia. J. Neurosci. Res. 2021;99:1414–1432. DOI: 10.1002/jnr.24792</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>Raus S., Selakovic V., Manojlovic-Stojanoski M. et al. Response of hippocampal neurons and glial cells to alternating magnetic field in gerbils submitted to global cerebral ischemia. Neurotox. Res. 2013;23(1):79–91. DOI: 10.1007/s12640-012-9333-8</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Fang Z.-Y., Li Z., Xiong L. et al. Magnetic stimulation influences injury-induced migration of white matter astrocytes. Electromagn. Biol. Med. 2010;29(3):113–121. DOI: 10.3109/15368378.2010.500568</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Eichler A., Kleidonas D., Turi Z. et al. Microglial cytokines mediate plasticity induced by 10 Hz repetitive magnetic stimulation. J. Neurosci. 2023;43(17):3042–3060. DOI: 10.1523/JNEUROSCI.2226-22.2023</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Chen J., Zeng Y., Hong J. et al. Effects of HF-rTMS on microglial polarization and white matter integrity in rats with poststroke cognitive impairment. Behav. Brain Res. 2023;439:114242. DOI: 10.1016/j.bbr.2022.114242.</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Cullen C.L., Senesi M., Tang A.D. et al. Low‐intensity transcranial magnetic stimulation promotes the survival and maturation of newborn oligodendrocytes in the adult mouse brain. Glia. 2019;67(8):1462–1477. DOI: 10.1002/glia.23620</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>Cullen C.L., Pepper R.E., Clutterbuck M.T. et al. Periaxonal and nodal plasticities modulate action potential conduction in the adult mouse brain. Cell. Rep. 2021;34(3):108641. DOI: 10.1016/j.celrep.2020.108641</mixed-citation></ref></ref-list></back></article>
