Yeh Mason L, Levine Eric S
Department of Neuroscience, University of Connecticut School of Medicine, 263 Farmington Avenue, Farmington, CT 06032, USA.
OBM Neurobiol. 2017;1(2). doi: 10.21926/obm.neurobiol.1702005. Epub 2017 Apr 27.
Autism spectrum disorders (ASDs) are diagnosed on the basis of three behavioral features, namely, (1) deficits in social communication, (2) absence or delay in language and (3) stereotypy. The consensus regarding the neurological pathogenesis of ASDs is aberrant synaptogenesis and synapse function. Further, it is now widely accepted that ASD is neurodevelopmental in nature, placing emphasis on derangements occurring at the level of intra- and intercellular signaling during corticogenesis. At present, there is an ever-growing list of mutations in putative susceptibility genes in affected individuals, preventing effective transformation of knowledge gathered from basic science research to the clinic. In response, the focus of ASD biology has shifted toward the identification of cellular signaling pathways that are common to various ASD-related mutations in hopes that these shared pathways may serve as more promising treatment targets than targeting individual genes or proteins. To this end, the endogenous cannabinoid (endocannabinoid, eCB) system has recently emerged as a promising therapeutic target in the field of ASD research. The eCB system is altered in several neurological disorders, but the role of these bioactive lipids in ASD etiology remains poorly understood. In this perspective, we review current evidence linking eCB signaling to ASDs and put forth the notion that continued focus on eCBs in autism research may provide valuable insight into pathophysiology and treatment strategies. In addition to its role in modulating transmitter release at mature synapses, the eCB signaling system plays important roles in many aspects of cortical development, and disruption of these effects of eCBs may also be related to ASD pathophysiology.
自闭症谱系障碍(ASD)是根据三种行为特征进行诊断的,即:(1)社交沟通缺陷;(2)语言缺失或延迟;(3)刻板行为。关于ASD神经发病机制的共识是异常的突触发生和突触功能。此外,现在人们普遍认为ASD本质上是神经发育性的,强调在皮质发生过程中细胞内和细胞间信号传导水平出现的紊乱。目前,受影响个体中假定的易感基因的突变列表不断增加,阻碍了从基础科学研究中获取的知识有效地转化到临床。作为回应,ASD生物学的重点已转向识别各种与ASD相关突变共有的细胞信号通路,希望这些共享通路可能比针对单个基因或蛋白质成为更有前景的治疗靶点。为此,内源性大麻素(eCB)系统最近已成为ASD研究领域中一个有前景的治疗靶点。eCB系统在几种神经疾病中发生改变,但这些生物活性脂质在ASD病因中的作用仍知之甚少。从这个角度来看,我们综述了目前将eCB信号与ASD联系起来的证据,并提出在自闭症研究中持续关注eCB可能为病理生理学和治疗策略提供有价值的见解。除了在调节成熟突触处的递质释放方面的作用外,eCB信号系统在皮质发育的许多方面也发挥着重要作用,而eCBs这些作用的破坏也可能与ASD病理生理学有关。