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迈向自闭症的发育神经生物学

Toward a developmental neurobiology of autism.

作者信息

Polleux Franck, Lauder Jean M

机构信息

Department of Pharmacology-Neuroscience Center, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, USA.

出版信息

Ment Retard Dev Disabil Res Rev. 2004;10(4):303-17. doi: 10.1002/mrdd.20044.

Abstract

Autism is a complex, behaviorally defined, developmental brain disorder with an estimated prevalence of 1 in 1,000. It is now clear that autism is not a disease, but a syndrome with a strong genetic component. The etiology of autism is poorly defined both at the cellular and the molecular levels. Based on the fact that seizure activity is frequently associated with autism and that abnormal evoked potentials have been observed in autistic individuals in response to tasks that require attention, several investigators have recently proposed that autism might be caused by an imbalance between excitation and inhibition in key neural systems including the cortex. Despite considerable ongoing effort toward the identification of chromosome regions affected in autism and the characterization of many potential gene candidates, only a few genes have been reproducibly shown to display specific mutations that segregate with autism, likely because of the complex polygenic nature of this syndrome. Among those, several candidate genes have been shown to control the early patterning and/or the late synaptic maturation of specific neuronal subpopulations controlling the balance between excitation and inhibition in the developing cortex and cerebellum. In the present article, we review our current understanding of the developmental mechanisms patterning the balance between excitation and inhibition in the context of the neurobiology of autism.

摘要

自闭症是一种复杂的、行为学定义的发育性脑疾病,估计患病率为千分之一。现在很清楚,自闭症不是一种疾病,而是一种具有强大遗传成分的综合征。自闭症的病因在细胞和分子水平上都定义不清。基于癫痫活动经常与自闭症相关,并且在自闭症个体中观察到对需要注意力的任务的异常诱发电位这一事实,几位研究人员最近提出,自闭症可能是由包括皮层在内的关键神经系统中兴奋与抑制之间的失衡引起的。尽管目前在确定自闭症中受影响的染色体区域以及表征许多潜在的候选基因方面付出了巨大努力,但只有少数基因被反复证明显示出与自闭症相关的特定突变,这可能是由于该综合征复杂的多基因性质。其中,几个候选基因已被证明可控制特定神经元亚群的早期模式形成和/或晚期突触成熟,这些亚群控制着发育中的皮层和小脑中兴奋与抑制之间的平衡。在本文中,我们回顾了我们目前对自闭症神经生物学背景下兴奋与抑制平衡模式形成的发育机制的理解。

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