自闭症谱系障碍
丙戊酸
神经科学
神经发育障碍
自闭症
诱导多能干细胞
医学
表观遗传学
病因学
精神科
生物信息学
心理学
癫痫
胚胎干细胞
生物
生物化学
基因
作者
David Zárate-López,Ana Laura Torres-Chávez,Alma Y. Gálvez‐Contreras,Óscar González-Pérez
出处
期刊:Current Neuropharmacology
[Bentham Science]
日期:2024-02-01
卷期号:22 (2): 260-289
被引量:8
标识
DOI:10.2174/1570159x22666231003121513
摘要
Abstract: Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder with increased prevalence and incidence in recent decades. Its etiology remains largely unclear, but it seems to involve a strong genetic component and environmental factors that, in turn, induce epigenetic changes during embryonic and postnatal brain development. In recent decades, clinical studies have shown that inutero exposure to valproic acid (VPA), a commonly prescribed antiepileptic drug, is an environmental factor associated with an increased risk of ASD. Subsequently, prenatal VPA exposure in rodents has been established as a reliable translational model to study the pathophysiology of ASD, which has helped demonstrate neurobiological changes in rodents, non-human primates, and brain organoids from human pluripotent stem cells. This evidence supports the notion that prenatal VPA exposure is a valid and current model to replicate an idiopathic ASD-like disorder in experimental animals. This review summarizes and describes the current features reported with this animal model of autism and the main neurobiological findings and correlates that help elucidate the pathophysiology of ASD. Finally, we discuss the general framework of the VPA model in comparison to other environmental and genetic ASD models.
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