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The neurobiology of autism.

机译:自闭症的神经生物学。

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Improving clinical tests are allowing us to more precisely classify autism spectrum disorders and diagnose them at earlier ages. This raises the possibility of earlier and potentially more effective therapeutic interventions. To fully capitalize on this opportunity, however, will require better understanding of the neurobiological changes underlying this devastating group of developmental disorders. It is becoming clear that the normal trajectory of neurodevelopment is altered in autism, with aberrations in brain growth, neuronal patterning and cortical connectivity. Changes to the structure and function of synapses and dendrites have also been strongly implicated in the pathology of autism by morphological, genetic and animal modeling studies. Finally, environmental factors are likely to interact with the underlying genetic profile, and foster the clinical heterogeneity seen in autism spectrum disorders. In this review we attempt to link the molecular pathways altered in autism to the neurodevelopmental and clinical changes that characterize the disease. We focus on signaling molecules such as neurotrophin, Reelin, PTEN and hepatocyte growth factor, neurotransmitters such as serotonin and glutamate, and synaptic proteins such as neurexin, SHANK and neuroligin. We also discuss evidence implicating oxidative stress, neuroglial activation and neuroimmunity in autism.
机译:不断改进的临床测试使我们能够更精确地对自闭症谱系障碍进行分类,并在较早的年龄进行诊断。这增加了更早且可能更有效的治疗干预的可能性。然而,要充分利用这一机会,将需要更好地了解这一破坏性发育障碍人群的神经生物学变化。显而易见的是,自闭症会改变神经发育的正常轨迹,导致脑部发育,神经元模式和皮层连通性异常。通过形态,遗传和动物模型研究,突触和树突的结构和功能的变化也与自闭症的病理学密切相关。最后,环境因素可能与潜在的遗传特征相互作用,并促进自闭症谱系障碍中所见的临床异质性。在这篇综述中,我们试图将自闭症中改变的分子途径与表征该疾病的神经发育和临床变化联系起来。我们专注于信号分子,如神经营养蛋白,Reelin,PTEN和肝细胞生长因子,神经递质,如血清素和谷氨酸,以及突触蛋白,如神经毒素,SHANK和Neuroligin。我们还讨论了在自闭症中涉及氧化应激,神经胶质激活和神经免疫的证据。

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