James David M, Davidson Elizabeth A, Yanes Julio, Moshiree Baharak, Dallman Julia E
Department of Biology, University of Miami, Coral Gables, FL, United States.
Department of Gastroenterology and Hepatology, Atrium Health, Charlotte, NC, United States.
Front Cell Dev Biol. 2021 Apr 15;9:662916. doi: 10.3389/fcell.2021.662916. eCollection 2021.
Research involving autism spectrum disorder (ASD) most frequently focuses on its key diagnostic criteria: restricted interests and repetitive behaviors, altered sensory perception, and communication impairments. These core criteria, however, are often accompanied by numerous comorbidities, many of which result in severe negative impacts on quality of life, including seizures, epilepsy, sleep disturbance, hypotonia, and GI distress. While ASD is a clinically heterogeneous disorder, gastrointestinal (GI) distress is among the most prevalent co-occurring symptom complex, manifesting in upward of 70% of all individuals with ASD. Consistent with this high prevalence, over a dozen family foundations that represent genetically distinct, molecularly defined forms of ASD have identified GI symptoms as an understudied area with significant negative impacts on quality of life for both individuals and their caregivers. Moreover, GI symptoms are also correlated with more pronounced irritability, social withdrawal, stereotypy, hyperactivity, and sleep disturbances, suggesting that they may exacerbate the defining behavioral symptoms of ASD. Despite these facts (and to the detriment of the community), GI distress remains largely unaddressed by ASD research and is frequently regarded as a symptomatic outcome rather than a potential contributory factor to the behavioral symptoms. Allowing for examination of both ASD's impact on the central nervous system (CNS) as well as its impact on the GI tract and the associated microbiome, the zebrafish has recently emerged as a powerful tool to study ASD. This is in no small part due to the advantages zebrafish present as a model system: their precocious development, their small transparent larval form, and their parallels with humans in genetics and physiology. While ASD research centered on the CNS has leveraged these advantages, there has been a critical lack of GI-centric ASD research in zebrafish models, making a holistic view of the gut-brain-microbiome axis incomplete. Similarly, high-throughput ASD drug screens have recently been developed but primarily focus on CNS and behavioral impacts while potential GI impacts have not been investigated. In this review, we aim to explore the great promise of the zebrafish model for elucidating the roles of the gut-brain-microbiome axis in ASD.
涉及自闭症谱系障碍(ASD)的研究大多聚焦于其关键诊断标准:兴趣受限和重复行为、感觉知觉改变以及沟通障碍。然而,这些核心标准常常伴有众多共病,其中许多对生活质量造成严重负面影响,包括癫痫发作、癫痫、睡眠障碍、肌张力减退和胃肠道不适。虽然ASD是一种临床异质性疾病,但胃肠道(GI)不适是最常见的并发症状群之一,在所有ASD个体中出现率超过70%。与此高患病率相一致的是,代表基因不同、分子定义形式的ASD的十几个家族基金会已将胃肠道症状确定为一个研究不足的领域,对个体及其照顾者的生活质量有重大负面影响。此外,胃肠道症状还与更明显的易怒、社交退缩、刻板行为、多动和睡眠障碍相关,表明它们可能会加剧ASD的典型行为症状。尽管存在这些事实(且对该群体不利),但胃肠道不适在ASD研究中基本未得到解决,并且常常被视为一种症状性结果,而非行为症状的潜在促成因素。斑马鱼能够同时研究ASD对中枢神经系统(CNS)的影响以及对胃肠道和相关微生物群的影响,最近已成为研究ASD的有力工具。这在很大程度上得益于斑马鱼作为模型系统所具有的优势:它们发育早熟、幼体形态小且透明,以及在遗传学和生理学方面与人类的相似性。虽然以中枢神经系统为中心的ASD研究利用了这些优势,但在斑马鱼模型中严重缺乏以胃肠道为中心的ASD研究,使得对肠-脑-微生物群轴的整体认识不完整。同样,最近已开发出高通量ASD药物筛选方法,但主要关注中枢神经系统和行为影响,而潜在的胃肠道影响尚未得到研究。在本综述中,我们旨在探讨斑马鱼模型在阐明肠-脑-微生物群轴在ASD中的作用方面的巨大前景。