丙戊酸暴露作为研究ASD形态分子特征的体外模型:系统综述。

Quezia Damaris Jones Severino Vasconcelos, Michele Aramburu Serafini, Jaqueline Vieira Carletti, Gislei Frota Aragão, Carmem Gottfried, Victorio Bambini-Junior
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引用次数: 0

摘要

背景:自闭症谱系障碍(ASD)是一种复杂的神经发育障碍,具有很强的遗传和环境基础。它经常导致社交和沟通障碍,以及重复行为。丙戊酸(VPA)已被证明在动物模型中,当在关键发育时期给药时,会诱发自闭症样特征。然而,它对细胞在体外复制ASD特征的影响尚不清楚。目的:通过对体外VPA模型的研究,阐明ASD的分子和形态学特征,强调其潜力并提出未来的研究方向。方法:检索PubMed、SciELO、Embase、Web of Science、Scopus等数据库,经筛选纳入11篇研究。结果:研究探讨了VPA对各种细胞培养的影响,包括人类神经细胞系、初级成人神经元和初级胚胎神经元。发现VPA具有剂量和时间依赖性的神经毒性,对未成熟和未分化的细胞具有更大的毒性。在体外,VPA可以影响基因表达,增加氧化应激,破坏神经发生和突触发生,影响gaba能系统,并改变脑发育和细胞分化的关键信号通路,如Wnt/β-catenin。结论:体外模型为VPA诱导的形态分子改变及其与ASD的关系提供了有价值的见解。这些发现强调需要进一步研究VPA的细胞效应,以加深我们对其在ASD病理中的作用的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Valproate Exposure as an In vitro Model for Studying Morpho-Molecular Features of ASD: A Systematic Review.

Background: Autism Spectrum Disorder (ASD) is a complex neurodevelopmental disorder with a strong genetic and environmental basis. It frequently causes social and communication deficits, as well as repetitive behaviours. Valproic acid (VPA) has been shown to induce autisticlike features in animal models when administered during critical development periods. However, not much is known about its effect on cells to replicate ASD characteristics in vitro.

Objective: This review explores in vitro VPA models to elucidate the molecular and morphological characteristics of ASD, emphasizing their potential and proposing directions for future research.

Methods: PubMed, SciELO, Embase, Web of Science, and Scopus databases were searched, and 11 studies were included after screening.

Results: The studies explored VPA's effects on various cell cultures, including human neural cell lines, primary adult neurons, and primary embryonic neurons. VPA was found to be neurotoxic in a dose- and time-dependent manner, with greater toxicity in immature and undifferentiated cells. In vitro, VPA can influence gene expression, increase oxidative stress, disrupt neurogenesis and synaptogenesis, affect the GABAergic system, and alter critical signaling pathways for brain development and cell differentiation, such as Wnt/β-catenin.

Conclusion: In vitro models provide valuable insights into the morpho-molecular alterations induced by VPA and their connection to ASD. These findings highlight the need for further research into VPA's cellular effects to deepen our understanding of its role in ASD pathology.

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