Toxicity and teratogenicity effects of valproic acid on zebrafish (Danio rerio) embryos in relation to autism spectrum disorder

丙戊酸 斑马鱼 达尼奥 毒性 畸形学 发育毒性 药理学 胚胎 生物 自闭症 毒理 生理学 怀孕 心理学 内科学 医学 神经科学 癫痫 胎儿 精神科 遗传学 基因
作者
Nur Atikah Saleh Hodin,Siok Geok Chong,Noraini Abu Bakar,Muhammad Syafiq Akmal Mohd Fahmi,Nurul Farhana Ramlan,Nik Nur Aini Zulaikha Zulkifli Hamid,Muhammad Syuqor Iqbal Mohd Fadzar,Abdul Rahman Zulkifli,Anis Irfan Norazhar,Siti Nurulhuda Mastuki,Siti Munirah Mohd Faudzi,Wan Norhamidah Wan Ibrahim,Mohammad Noor Amal Azmai
出处
期刊:Teratology [Wiley]
卷期号:115 (16): 1475-1485 被引量:4
标识
DOI:10.1002/bdr2.2227
摘要

Valproic acid (VPA) is a widely prescribed antiepileptic drug with various medicinal efficacies. Accumulated evidence implied that prenatal exposure to VPA is highly associated with autism spectrum disorder (ASD). In this study, the zebrafish were exposed to a set of VPA concentrations (0, 5, 10, 20, 40, 80, 160, 320, 640, 1280, and 2560 μM) at 5 h post fertilization (hpf) to 120 hpf. The adverse effects of VPA were extensively studied through the evaluations on the mortality, heartbeats, spontaneous tail coiling, and hatching rate. Morphological observations were conducted at 120 hpf, following the exposure termination. Basic locomotor responses and anxiety-like behavioral alterations evaluated for behavioral impairments are the hallmark feature of ASD. The exposure to VPA at teratogenic concentrations reduced the aforementioned parameters in a dose-dependent manner (p ≤ .05). At the selected non-teratogenic concentrations of VPA, the treated larvae demonstrated profound alterations of basic locomotor responses. No significant changes of anxiety and thigmotactic behaviors were observed on the VPA-treated fish compared to the control (p ≥ .005). This study depicted that embryonic zebrafish exposure to VPA produced significant toxicity and teratogenicity effects as well as the alterations of basic behavioral responses. Overall, this study provides a fundamental insight of the toxicity effects at morphological and behavioral levels to facilitate the understanding of ASD mechanisms at different molecular levels.
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