Bhandari Ranjana, Paliwal Jyoti K, Kuhad Anurag
Pharmacology Research Laboratory, University Institute of Pharmaceutical Sciences, UGC-Centre of Advanced Study, Panjab University, Chandigarh, India.
Adv Neurobiol. 2020;24:97-141. doi: 10.1007/978-3-030-30402-7_4.
Autism spectrum disorder (ASD) is a complex heterogeneous consortium of pervasive development disorders (PDD) which ranges from atypical autism, autism, and Asperger syndrome affecting brain in the developmental stage. This debilitating neurodevelopmental disorder results in both core as well as associated symptoms. Core symptoms observed in autistic patients are lack of social interaction, pervasive, stereotyped, and restricted behavior while the associated symptoms include irritability, anxiety, aggression, and several comorbid disorders.ASD is a polygenic disorder and is multifactorial in origin. Copy number variations (CNVs) of several genes that regulate the synaptogenesis and signaling pathways are one of the major factors responsible for the pathogenesis of autism. The complex integration of various CNVs cause mutations in the genes which code for molecules involved in cell adhesion, voltage-gated ion-channels, scaffolding proteins as well as signaling pathways (PTEN and mTOR pathways). These mutated genes are responsible for affecting synaptic transmission by causing plasticity dysfunction responsible, in turn, for the expression of ASD.Epigenetic modifications affecting DNA transcription and various pre-natal and post-natal exposure to a variety of environmental factors are also precipitating factors for the occurrence of ASD. All of these together cause dysregulation of glutamatergic signaling as well as imbalance in excitatory: inhibitory pathways resulting in glial cell activation and release of inflammatory mediators responsible for the aberrant social behavior which is observed in autistic patients.In this chapter we review and provide insight into the intricate integration of various genetic, epigenetic, and environmental factors which play a major role in the pathogenesis of this disorder and the mechanistic approach behind this integration.
自闭症谱系障碍(ASD)是一组复杂的异质性广泛性发育障碍(PDD),包括非典型自闭症、自闭症和阿斯伯格综合征,会影响发育阶段的大脑。这种使人衰弱的神经发育障碍会导致核心症状以及相关症状。自闭症患者观察到的核心症状是社交互动缺乏、普遍存在的刻板和受限行为,而相关症状包括易怒、焦虑、攻击行为以及几种共病。ASD是一种多基因疾病,其病因是多因素的。几个调节突触形成和信号通路的基因的拷贝数变异(CNV)是自闭症发病机制的主要因素之一。各种CNV的复杂整合导致编码参与细胞粘附、电压门控离子通道、支架蛋白以及信号通路(PTEN和mTOR通路)的分子的基因突变。这些突变基因通过导致可塑性功能障碍来影响突触传递,进而导致ASD的表现。影响DNA转录的表观遗传修饰以及各种产前和产后暴露于多种环境因素也是ASD发生的诱发因素。所有这些共同导致谷氨酸能信号失调以及兴奋与抑制通路失衡,从而导致胶质细胞激活和释放炎症介质,这些炎症介质导致自闭症患者出现异常的社交行为。在本章中,我们回顾并深入探讨各种遗传、表观遗传和环境因素的复杂整合,这些因素在该疾病的发病机制中起主要作用以及这种整合背后的机制。