<?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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">I.P. Pavlov Journal of Higher Nervous Activity</journal-id><journal-title-group><journal-title xml:lang="en">I.P. Pavlov Journal of Higher Nervous Activity</journal-title><trans-title-group xml:lang="ru"><trans-title>Журнал высшей нервной деятельности им. И.П. Павлова</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0044-4677</issn><issn publication-format="electronic">3034-5316</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">652008</article-id><article-id pub-id-type="doi">10.31857/S0044467723060047</article-id><article-id pub-id-type="edn">SLNBWY</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>ЭКСПЕРИМЕНТАЛЬНАЯ ПАТОЛОГИЯ ВЫСШЕЙ &#13;
НЕРВНОЙ ДЕЯТЕЛЬНОСТИ</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ЭКСПЕРИМЕНТАЛЬНАЯ ПАТОЛОГИЯ ВЫСШЕЙ НЕРВНОЙ ДЕЯТЕЛЬНОСТИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">DISORDERS OF MOTOR ACTIVITY ON THE MODEL OF AUTISM SPECTRUM DISORDERS</article-title><trans-title-group xml:lang="ru"><trans-title>Нарушения двигательной активности на модели расстройств аутистического спектра</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Khairullin</surname><given-names>A. E.</given-names></name><name xml:lang="ru"><surname>Хайруллин</surname><given-names>А. Е.</given-names></name></name-alternatives><email>khajrulli@yandex.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Efimova</surname><given-names>D. V.</given-names></name><name xml:lang="ru"><surname>Ефимова</surname><given-names>Д. В.</given-names></name></name-alternatives><email>khajrulli@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ivanova</surname><given-names>D. V.</given-names></name><name xml:lang="ru"><surname>Иванова</surname><given-names>Д. В.</given-names></name></name-alternatives><email>khajrulli@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Baltina</surname><given-names>T. V.</given-names></name><name xml:lang="ru"><surname>Балтина</surname><given-names>Т. В.</given-names></name></name-alternatives><email>khajrulli@yandex.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Baltin</surname><given-names>M. E.</given-names></name><name xml:lang="ru"><surname>Балтин</surname><given-names>М. Э.</given-names></name></name-alternatives><email>khajrulli@yandex.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Grishin</surname><given-names>S. N.</given-names></name><name xml:lang="ru"><surname>Гришин</surname><given-names>С. Н.</given-names></name></name-alternatives><email>khajrulli@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ziganshin</surname><given-names>A. U.</given-names></name><name xml:lang="ru"><surname>Зиганшин</surname><given-names>А. У.</given-names></name></name-alternatives><email>khajrulli@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Kazan State Medical University</institution></aff><aff><institution xml:lang="ru">Казанский государственный медицинский университет</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Kazan Federal University</institution></aff><aff><institution xml:lang="ru">Казанский Федеральный Университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-11-01" publication-format="electronic"><day>01</day><month>11</month><year>2023</year></pub-date><volume>73</volume><issue>6</issue><fpage>819</fpage><lpage>832</lpage><history><date date-type="received" iso-8601-date="2025-02-02"><day>02</day><month>02</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2023, А.Е. Хайруллин, Д.В. Ефимова, Д.В. Иванова, Т.В. Балтина, М.Э. Балтин, С.Н. Гришин, А.У. Зиганшин</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, А.Е. Хайруллин, Д.В. Ефимова, Д.В. Иванова, Т.В. Балтина, М.Э. Балтин, С.Н. Гришин, А.У. Зиганшин</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="en">А.Е. Хайруллин, Д.В. Ефимова, Д.В. Иванова, Т.В. Балтина, М.Э. Балтин, С.Н. Гришин, А.У. Зиганшин</copyright-holder><copyright-holder xml:lang="ru">А.Е. Хайруллин, Д.В. Ефимова, Д.В. Иванова, Т.В. Балтина, М.Э. Балтин, С.Н. Гришин, А.У. Зиганшин</copyright-holder></permissions><self-uri xlink:href="https://innoscience.ru/0044-4677/article/view/652008">https://innoscience.ru/0044-4677/article/view/652008</self-uri><abstract xml:lang="en"><p id="idm45257550744736">Autism, or autism spectrum disorder (ASD), is a multifactorial disease that is characterized not only by disorders of the psycho-emotional state and social interaction, but also by somatic dysfunctions. A number of studies have also reported changes in the musculoskeletal system in patients with ASD. In this work, by the method of video analysis of movements, we demonstrated a decrease in horizontal and vertical motor activity, in addition, deviant movements were recorded, which indicates a violation in locomotor activity and increased anxiety in rats with a valproate model of autism. However, a mechano-myographic study did not reveal significant changes in the contractility parameters of isolated skeletal muscles of rats with the ASD model. Thus, it can be concluded that general differences in movement may be an independent factor in the diagnosis of autism. A more thorough study using a larger sample and detailed kinematic analysis can help in further assessing the variability of motor functions as a potential diagnostic and prognostic marker of ASD.</p></abstract><trans-abstract xml:lang="ru"><p id="idm45257550742624">Аутизм, или расстройство аутистического спектра (РАС), является многофакторным заболеванием, которое характеризуется не только нарушениями психоэмоционального состояния и социального взаимодействия, но и соматическими дисфункциями. В ряде исследований также сообщалось об изменениях со стороны опорно-двигательной системы у пациентов с РАС. В данной работе методом видеоанализа движений мы продемонстрировали снижение горизонтальной и вертикальной двигательной активности, кроме этого, были зарегистрированы девиантные движения, что говорит о нарушении в локомоторной активности и повышенной тревожности крыс с вальпроатной моделью аутизма. Однако механо-миографическое исследование не выявило достоверных изменений в параметрах сократимости изолированных скелетных мышц крыс с моделью РАС. Таким образом, можно заключить, что общие различия в движении могут быть независимым фактором диагностики аутизма. Более тщательное исследование с использованием большей выборки и подробного кинематического анализа может помочь в дальнейшей оценке вариабельности двигательных функций, как потенциального диагностического и прогностического маркера РАС.</p></trans-abstract><kwd-group xml:lang="en"><kwd>autism</kwd><kwd>autism spectrum disorders</kwd><kwd>ATP</kwd><kwd>P2 receptors</kwd><kwd>skeletal muscles</kwd><kwd>neuromuscular synapse</kwd><kwd>neurotransmission</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>аутизм</kwd><kwd>расстройства аутистического спектра</kwd><kwd>АТФ</kwd><kwd>Р2-рецепторы</kwd><kwd>скелетные мышцы</kwd><kwd>нервно-мышечный синапс</kwd><kwd>нейротрансмиссия</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Архипов А.Ю., Самигуллин Д.В., Семина И.И., Маломуж А.И. Функциональная оценка периферической холинергической нейротрансмиссии у крыс с фетальным вальпроатным синдромом. Российский физиологический журнал им. И.М. Сеченова, 2021. 107 (4–5): 605–615.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Гедзун В.Р., Свинов М.М., Сарычева Н.Ю., Шлапакова П.С., Довбнюк К.О., Дубынин В.А. Влияние пренатального и раннего постнатального введения вальпроата на поведение и цитологические характеристики крыс линии Wistar. Журн. высш. нерв. деят. им. И.П. Павлова. 2020. 70 (5): 682–695.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Зиганшин А.У., Иванова Д.В. Вызванные карбахолном сокращения изолированной тонкой кишки возрастают у крыс с экспериментальным аутизмом, вызванным вальпроевой кислотой. Экспериментальная и клиническая фармакология, 2021. 84 (2): 99–103.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Козловский В.Л., Кенунен О.Г. Структура двигательного поведения лабораторных животных – новые возможности методики “открытого поля”. Физиологический журн. им. И.М. Сеченова, 1992. 78 (1): 120–123.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Патент на полезную модель № 216564 U1 Российская Федерация, МПК A61N 1/04, G09B 23/28. Всасывающий культю нерва электрод для электрической стимуляции: № 2022131919: заявл. 07.12.2022: опубл. 14.02.2023 / С.Н. Гришин, А.Е. Хайруллин, А.У. Зиганшин, Д.В. Ефимова; заявитель Федеральное государственное бюджетное образовательное учреждение высшего образования “Казанский государственный медицинский университет” Министерства здравоохранения Российской Федерации. – EDN GPHYYZ.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Abbracchio M.P., Ceruti S. Roles of P2 receptors in glial cells: Focus on astrocytes. Purinergic Signal, 2006. 2: 595–604. https://doi.org/10.1007/s11302-006-9016-0</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Amiet C., Gourfinkel-An I., Bouzamondo A., Tordjman S., Baulac M., Lechat P., Mottron L., Cohen D. Epilepsy in autism is associated with intellectual disability and gender: evidence from a meta-analysis. Biol Psychiatry, 2008. 64: 577–582.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Arutiunian V., Davydova E., Pereverzeva D., Sorokin A., Tyushkevich S., Mamokhina U., Danilina K., Dragoy O. Reduced grey matter volume of amygdala and hippocampus is associated with the severity of autistic symptoms and language abilities in school-aged children with Autism Spectrum Disorder: an exploratory study. Brain structure &amp; function. 2023. 228 (6): 1573–1579.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Bachevalier J., Loveland K.A. The orbitofrontal-amygdala circuit and self-regulation of social-emotional behavior in autism. Neuroscience and biobehavioral reviews. 2006. 30 (1): 97–117.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Banerjee A., García-Oscos F., Roychowdhury S., Galindo L.C., Hall S., Kilgard M.P., Atzori M. Impairment of cortical GABAergic synaptic transmission in an environmental rat model of autism. The international journal of neuropsychopharmacology. 2013. 16 (6): 1309–1318.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Besag F.M. Epilepsy in patients with autism: links, risks and treatment challenges. Neuropsychiatr Dis. Treat., 2018. 14: 1–10.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Bhat A.N. Motor impairment increases in children with autism spectrum disorder as a function of social communication, cognitive and functional impairment, repetitive behavior severity, and comorbid diagnoses: a SPARK study report. Autism Res. 2021. 14: 202–219.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Blume S.R., Nam H., Luz S., Bangasser D.A., Bhatnagar S. Sex- and Age-dependent Effects of Orexin 1 Receptor Blockade on Open-Field Behavior and Neuronal Activity. Neuroscience, 2018. 381: 11–21. https://doi.org/10.1016/j.neuroscience.2018.04.005</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Burnstock G. Purine and pyrimidine receptors. Cell Mol Life Sci., 2007 64 (12):1471–83. https://doi.org/10.1007/s00018-007-6497-0</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Burnstock G., Krugel U., Abbracchio M.P., Illes P. Purinergic signalling: From normal behaviour to pathological brain function. Prog. Neurobiol., 2011. 95: 229–274. https://doi.org/10.1016/j.pneurobio.2011.08.006</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Cartocci V., Catallo M., Tempestilli M., Segatto M., Pfrieger F.W., Bronzuoli M.R., Scuderi C., Servadio M., Trezza V., Pallottini V. Altered brain cholesterol/isoprenoid metabolism in a rat model of autism spectrum disorders. Neuroscience. 2018. 372: 27–37.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Chaliha D., Albrecht M., Vaccarezza M., Takechi R., Lam V., Al-Salami H., Mamo J. A Systematic Review of the Valproic-Acid-Induced Rodent Model of Autism. Developmental neuroscience. 2020. 42 (1): 12–48.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Cheffer A., Castillo A., Corrêa-Velloso J., Gonçal-ves M.C.B., Naaldijk Y., Nascimento I.C., Burnstock G., Ulrich H. Purinergic system in psychiatric diseases. Mol. Psychiatry, 2018. 23: 94–106.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Christensen J., Pedersen L., Sun Y., Dreier J.W., Brikell I., Dalsgaard S. Association of Prenatal Exposure to Valproate and Other Antiepileptic Drugs With Risk for Attention-Deficit/Hyperactivity Disorder in Offspring. JAMA network open. 2019. 2 (1): e186606. https://doi.org/10.1001/jamanetworkopen.2018. 6606</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Cieslak M., Czarnecka J., Roszek K. The roles of purinergic signaling in psychiatric disorders. Acta Biochim. Pol., 2016. 63 (1): 1–9.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Citrigno L., Muglia M., Qualtieri A., Spadafora P., Cavalcanti F., Pioggia G., Cerasa A. The mitochondrial dysfunction hypothesis in autism spectrum disorders: Current status and future perspectives. Int. J. Mol. Sci., 21: 5785. https://doi.org/10.3390/ijms21165785</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Courchesne E., Pramparo T., Gazestani V.H., Lombardo M.V., Pierce K., Lewis N.E. The ASD living Biology: from cell proliferation to clinical phenotype. Mol. Psychiatry, 2019. 24 (1): 88–107. https://doi.org/10.1038/s41380-018-0056-y</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Doi M., Li M., Usui N., Shimada S. Genomic Strategies for Understanding the Pathophysiology of Autism Spectrum Disorder. Frontiers in molecular neuroscience. 2022. 15: 930941. https://doi.org/10.3389/fnmol.2022.930941</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Elandaloussi Y., Floris D.L., Coupé P., Duchesnay E., Mihailov A., Grigis A., Bègue I., Victor J., Frouin V., Leboyer M., Houenou J., Laidi C. Understanding the relationship between cerebellar structure and social abilities. Molecular autism. 2023. 14 (1): 18. https://doi.org/10.1186/s13229-023-00551-8</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Esposito G., Venuti P. Analysis of toddlers' gait after six months of independent walking to identify autism: a preliminary study. Perceptual and motor skills. 2008. 106 (1): 259–269.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Fatemi S.H., Aldinger K.A., Ashwood P., Bauman M.L., Blaha C.D., Blatt G.J., Chauhan A., Chauhan V., Dager S.R., Dickson P.E., Estes A.M., Goldowitz D., Heck D.H., Kemper T.L., King B.H., Martin L.A., Millen K.J., Mittleman G., Mosconi M.W., Persico A.M., Welsh J.P. Consensus paper: pathological role of the cerebellum in autism. Cerebellum (London, England). 2012. 11 (3): 777–807.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Fournier K.A., Hass C.J., Naik S.K., Lodha N., Cauraugh J.H. Motor coordination in autism spectrum disorders: a synthesis and meta-analysis. Journal of autism and developmental disorders 2010. 40 (10): 1227–1240.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Fumagalli M., Lecca D., Abbracchio M.P., Ceruti S. Pathophysiological role of purines and pyrimidines in neurodevelopment: unveiling new pharmacological approaches to congenital brain diseases. Front. Pharmacol., 2017. 8: 941.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Gandhi T., Lee C.C. Neural Mechanisms Underlying Repetitive Behaviors in Rodent Models of Autism Spectrum Disorders. Frontiers in cellular neuroscience. 2021. 14: 592710. https://doi.org/10.3389/fncel.2020.592710</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Ghaziuddin M., Butler E. Clumsiness in autism and Asperger syndrome: A further report. J. Intellect Disabil. Res., 1988. 42: 43–48.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Gillberg C., Schaumann H., Gillberg I.C. Autism in immigrants: children born in Sweden to mothers born in Uganda. J Intellect Disabil Res., 1995. 39 (2): 141–144. https://doi.org/10.1111/j.1365-2788.1995.tb00482.x</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Green D., Charman T., Pickles A., Chandler S., Loucas T., Simonoff E., Baird G. Impairment in movement skills of children with autistic spectrum disorders. Developmental Medicine &amp; Child Neurology, 2009. 51: 311–316.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Hardan A.Y., Kilpatrick M., Keshavan M.S., Minshew N.J. Motor performance and anatomic magnetic resonance imaging (MRI) of the basal ganglia in autism. Journal of Child Neurology, 2003. 18: 317–324.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Hirsch M.M., Deckmann I., Santos-Terra J., Staevie G.Z., Fontes-Dutra M., Carello-Collar G., Körbes-Rockenbach M., Brum Schwingel G., Bauer-Negrini G., Rabelo B., Gonçalves M.C.B., Corrêa-Velloso J., Naaldijk Y., Castillo A.R.G., Schneider T., Bambini-Junior V., Ulrich H., Gottfried C. Effects of single-dose antipurinergic therapy on behavioral and molecular alterations in the valproic acid-induced animal model of autism. Neuropharmacology. 2020 167: 107930. https://doi.org/10.1016/j.neuropharm.2019.107930</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Huang L., Otrokocsi L., Sperlagh B. Role of P2 receptors in normal brain development and in neurodevelopmental psychiatric disorders. Brain Res. Bull., 2019. 151: 55–64. https://doi.org/10.1016/j.brainresbull.2019.01.030</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Inoue K. Purinergic systems in microglia. Cell. Mol. Life Sci., 2008. 65: 3074–3080. https://doi.org/10.1007/s00018-008-8210-3</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Jiang S., He M., Xiao L., Sun Y., Ding J., Li W., Guo B., Wang L., Wang Y., Gao C., Sun T., Wang F. Prenatal GABAB Receptor Agonist Administration Corrects the Inheritance of Autism-Like Core Behaviors in Offspring of Mice Prenatally Exposed to Valproic Acid. Frontiers in psychiatry. 2022. 13: 835993. https://doi.org/10.3389/fpsyt.2022.835993</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Kataoka S., Takuma K., Hara Y., Maeda Y., Ago Y., Matsuda T. Autism-like behaviours with transient histone hyperacetylation in mice treated prenatally with valproic acid. The international journal of neuropsychopharmacology. 2013. 16 (1): 91–103.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Kern J.K., Trivedi M.H., Garver C.R., Grannemann B.D., Andrews A.A., Savla J.S., Johnson D.G., Mehta J.A., Schroeder J.L. The pattern of sensory processing abnormalities in autism. Autism, 2006. 10: 480–494.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Khairullin A.E., Grishin S.N., Ziganshin A.U. P2 Receptor Signaling in Motor Units in Muscular Dystrophy. International Journal of Molecular Sciences. 2023b. 24 (2): 1587.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Khairullin A.E., Mukhamedyarov M.A., Grishin S.N., Teplov A.Yu., Nagiev K.K., Ziganshin A.U. Synaptic Aspects of the Pathogenesis of Autism, Amyotrophic Lateral Sclerosis, and Alzheimer’s Disease. Biophysics, 2023a. 68 (1): 137–145.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Kingsley R.E. Motor systems, in Kingsley RE (ed): Concise Text of Neuroscience. Baltimore, Lippincott Williams &amp; Wilkins, 2000. 209–336.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Lamb G.V., Green R.J., Olorunju S. Tracking epilepsy and autism. Egypt J. Neurol. Psychiatry Neurosurg., 2019. 55: 55. https://doi.org/10.1186/s41983-019-0103-x</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Lee B.H., Smith T., Paciorkowski A.R. Autism spectrum disorder and epilepsy: Disorders with a shared biology. Epilepsy Behav., 2015. 47: 191–201.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Lee E., Lee J., Kim E. Excitation/Inhibition Imbalance in Animal Models of Autism Spectrum Disorders. Biological psychiatry. 2017. 81 (10): 838–847.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Lister M.F., Sharkey J., Sawatzky D.A., Hodgkiss J.P., Davidson D.J., Rossi A.G., Finlayson K. The role of the purinergic P2X7 receptor in inflammation. J. Inflamm. (Lond), 2007. 4: 5. https://doi.org/10.1186/1476-9255-4-5</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Mabunga D.F., Gonzales E.L., Kim J.W., Kim K.C., Shin C.Y. Exploring the Validity of Valproic Acid Animal Model of Autism. Experimental neurobiology. 2015. 24 (4): 285–300.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Maenner M.J., Warren Z., Williams A.R., Amoakohene E., Bakian A.V., Bilder D.A., Durkin M.S., Fitzgerald R.T., Furnier S.M., Hughes M.M., Ladd-Acosta C.M., McArthur D., Pas E.T., Salinas A., Vehorn A., Williams S., Esler A., Grzybowski A., Hall-Lande J., Nguyen R.H.N., Pierce K., Zahorodny W., Hudson A., Hallas L., Mancilla K.C., Patrick M., Shenouda J., Sidwell K., DiRienzo M., Gutierrez J., Spivey M.H., Lopez M., Pettygrove S., Schwenk Y.D., Washington A., Shaw K.A. Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years – Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2020. Morbidity and mortality weekly report. Surveillance summaries (Washington, D.C: 2002), 2023. 72 (2): 1–14.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Main S.L., Kulesza R.J. Repeated prenatal exposure to valproic acid results in cerebellar hypoplasia and ataxia. Neuroscience. 2017. 6 (340): 34–47.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Ming X., Brimacombe M., Wagner G.C. Prevalence of motor impairment in autism spectrum disorders. Brain &amp; Development, 2007. 29: 565–570.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Minshew N.J., Sung K., Jones B.L., Furman J.M. Underdevelopment of the postural control system in autism. Neurology, 2004. 63: 2056–2061.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Mitchell R., Barton S., Harvey A.S., Williams K. Risk factors for the development of autism spectrum disorder in children with tuberous sclerosis complex: protocol for a systematic review. Systematic reviews. 2017. 6: 49. https://doi.org/10.1186/s13643-017-0448-0</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Naviaux R.K., Zolkipli Z., Wang L., Nakayama T., Naviaux J.C., Le T.P., Schuchbauer M.A., Rogac M., Tang Q., Dugan L.L., Powell S.B. Antipurinergic therapy corrects the autism-like features in the poly (IC) mouse model. PLoS One, 2013. 8: 57380. https://doi.org/10.1371/journal.pone.0057380</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Nimmo-Smith V., Heuvelman H., Dalman C., Lundberg M., Idring S., Carpenter P., Magnusson C., Rai D. Anxiety Disorders in Adults with Autism Spectrum Disorder: A Population-Based Study. Journal of autism and developmental disorders. 2020. 50 (1): 308–318.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Oliveira Á., Illes P., Ulrich H. Purinergic receptors in embryonic and adult neurogenesis. Neuropharmacology, 2016. 104: 272–281.</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Ozonoff S., Young G.S., Goldring S., Greiss-Hess L., Herrera A.M., Steele J., Macari S., Hepburn S., Rogers S.J. Gross motor development, movement abnormalities, and early identification of autism. Journal of autism and developmental disorders. 2008. 38 (4): 644–656.</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Pan P.Y., Bölte S., Kaur P., Jamil S., Jonsson U. Neurological disorders in autism: A systematic review and meta-analysis. Autism. 2021. 25 (3): 812–830.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Pardo C.A., Meffert M.K. Animal models in autism research: The legacy of Paul H. Patterson. Experimental neurology. 2018. 299 (Pt A): 197–198.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Piek J.P., Dyck M.J. Sensory-motor deficits in children with developmental coordination disorder, attention deficit hyperactivity disorder and autistic disorder. Hum. Mov. Sci., 2004. 23 (3–4): 475–488.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Pierce K., Courchesne E. Evidence for a cerebellar role in reduced exploration and stereotyped behavior in autism. Biological psychiatry. 2001. 49 (8): 655–664.</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Provost B., Heimerl S., Lopez B.R. Levels of gross and fine motor development in young children with autism spectrum disorder. Physical &amp; Occupational Therapy in Pediatrics, 2007. 27: 21–36.</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Qi Z., Lyu M., Yang L., Yuan H., Cao Y., Zhai L., Dang W., Liu J., Yang F., Li Y. A Novel and Reliable Rat Model of Autism. Front Psychiatry. 2021. 12: 549810. https://doi.org/10.3389/fpsyt.2021.549810</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Rodier P.M., Ingram J.L., Tisdale B., Nelson S., Romano J. Embryological origin for autism: Developmental anomalies of the cranial nerve motor nuclei. Journal of Comparative Neurology. 1996. 370 (2): 247–261.</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Ren J., Zhao T., Xu Y., Ye H. Interaction between DISC1 and CHL1 in regulation of neurite outgrowth. Brain Res., 2016. 1648 (Pt A): 290–297.</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Saffari A., Arno M., Nasser E., Ronald A., Wong C.C.Y., Schalkwyk L.C., Mill J., Dudbridge F., Meaburn E.L. RNA sequencing of identical twins discordant for autismreveals blood-based signatures implicating immune and transcriptional dysregulation. Mol. Autism, 2019. 10: 38. https://doi.org/10.1186/s13229-019-0285-1</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Schneider T., Przewłocki R. Behavioral alterations in rats prenatally exposed to valproic acid: animal model of autism. Neuropsychopharmacology: official publication of the American College of Neuropsychopharmacology. 2005. 30 (1): 80–89.</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Servadio M., Manduca A., Melancia F., Leboffe L., Schiavi S., Campolongo P., Palmery M., Ascenzi P., di Masi A., Trezza V. Impaired repair of DNA damage is associated with autistic-like traits in rats prenatally exposed to valproic acid. European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology. 2018. 28 (1): 85–96.</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Singh R., Kisku A., Kungumaraj H., Nagaraj V., Pal A., Kuma S., Sulakhiya K. Autism Spectrum Disorders: A Recent Update on Targeting Inflammatory Pathways with Natural Anti-Inflammatory Agents. Biomedicines. 2023. 11 (1): 115. https://doi.org/10.3390/biomedicines11010115</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Smirnova V., Yaikova E., Baltin M., Kharin N., Baltina T., Sachenkov O. Movement estimation methods based on the motion capture system. 2022 Fourth International Conference Neurotechnologies and Neurointerfaces (CNN), 2022. 158–161. https://doi.org/10.1109/CNN56452.2022.9912543</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Smith S.E.P., Li J., Garbett K., Mirnics K., Patterson P.H. Maternal immune activation alters fetal brain development through interleukin-6. J. Neurosci. 2007. 27 (40): 10695–10702.</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Sui L., Chen M. Prenatal exposure to valproic acid enhances synaptic plasticity in the medial prefrontal cortex and fear memories. Brain research bulletin. 2012. 87 (6): 556–563.</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Talos D.M., Sun H., Zhou X., Fitzgerald E.C., Jackson M.C., Klein P.M., Lan V.J., Joseph A., Jensen F.E. The interaction between early life epilepsy and autistic-like behavioral consequences: a role for the mammalian target of rapamycin (mtor) pathway. Plos One, 2012. 7: 35885.</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Taylor M.J., Rosenqvist M.A., Larsson H., Gillberg C., D’Onofrio B.M., Lichtenstein P., Lundström S. Etiology of autism spectrum disorders and autistic traits over time. JAMA Psychiatry, 2020. 77: 936–943. https://doi.org/10.1001/jamapsychiatry.2020.0680</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Watson L.R., Baranek G.T., DiLavore P.C. Toddlers with autism: Developmental perspectives. Infants and Young Children, 2003. 16: 201–214.</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Widiger T.A., Hines A. The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition alternative model of personality disorder. Personality disorders. 2022. 13 (4): 347–355.</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Williams M., Prem S., Zhou X., Matteson P., Yeung P.L., Lu C.W., Pang Z., Brzustowicz L., Millonig J.H., Dicicco-Bloom E. Rapid detection of neuro-developmental phenotypes in human neural precursor cells (NPCs). J. Vis. Exp., 2018. 133: 56628.</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Wood A. Prenatal exposure to sodium valproate is associated with increased risk of childhood autism and autistic spectrum disorder. Evidence-based nursing. 2014. 17 (3): 84. https://doi.org/10.1136/eb-2013-101422</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Zheng W., Hu Y., Chen D., Li Y., Wang S. Improvement of a mouse model of valproic acid-induced autism. Nan Fang Yi Ke Da Xue Xue Bao, 2019. 39 (6): 718–723. https://doi.org/10.12122/j.issn.1673-4254.2019.06.14</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Ziganshin A.U., Khairullin A.E., Hoyle C.H.V., Grishin S.N. Modulatory roles of ATP and adenosine in cholinergic neuromuscular transmission. International Journal of Molecular Sciences, 2020. 21 (17): 1–15.</mixed-citation></ref></ref-list></back></article>
