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谷氨酸介导的信号在自闭症谱系障碍的病理生理学中的作用。

Glutamate mediated signaling in the pathophysiology of autism spectrum disorders.

机构信息

Manovikas Biomedical Research & Diagnostic Centre, Manovikas Kendra Rehabilitation & Research Institute for the Handicapped, 482 Madudah, Plot I-24, Sector J, EM Bypass, Kolkata 700107, India.

出版信息

Pharmacol Biochem Behav. 2012 Feb;100(4):841-9. doi: 10.1016/j.pbb.2011.06.023. Epub 2011 Jul 5.

Abstract

Autism spectrum disorder (ASD) is a childhood neurodevelopmental disorder. During fetal and neonatal brain development, the cues for neurodevelopment are regulated in a well orchestrated manner. Generally, neurotransmitters play a major role in the formation of central nervous system (CNS) and peripheral nervous system (PNS). Glutamate, the excitatory neurotransmitter actively participates in various neurodevelopmental processes through complex regulatory events. Excitatory neurotransmitter signaling via glutamate receptors modulates cognitive functions such as memory and learning, which are usually impaired in ASD. Therefore, glutamate and its regulatory molecules are considered as potential targets for these disorders. Pharmacological, biochemical and behavioral studies reveal possible involvement of glutamatergic system in ASD pathology. An abnormal increase in electrical activity resulting from excessive glutamate signaling causes prolonged alterations in behavior, as commonly seen in ASDs. On the contrary, reports on animal models of hypoglutamatergia demonstrate phenotypes that overlap with features seen in autism. So controversies prevail whether to regard autism as hyper- or hypo-glutamatergic disorder. This paper reviews the role of glutamate and its regulatory proteins such as different receptors, transporters and metabolizing enzymes in the pathophysiology of ASD based on evidences gathered through multidisciplinary approaches. All these information raise the possibility of exploiting glutamatergic neurotransmitter system for future therapeutic interventions for ASD.

摘要

自闭症谱系障碍(ASD)是一种儿童神经发育障碍。在胎儿和新生儿大脑发育过程中,神经发育的线索以协调的方式进行调节。一般来说,神经递质在中枢神经系统(CNS)和周围神经系统(PNS)的形成中起主要作用。谷氨酸作为兴奋性神经递质,通过复杂的调节事件积极参与各种神经发育过程。通过谷氨酸受体的兴奋性神经递质信号转导调节认知功能,如记忆和学习,而这些功能在 ASD 中通常受损。因此,谷氨酸及其调节分子被认为是这些疾病的潜在靶点。药理学、生化和行为研究揭示了谷氨酸能系统可能参与 ASD 病理学。由于谷氨酸信号过度引起的电活动异常增加会导致行为的持久改变,这在 ASD 中很常见。相反,关于谷氨酸能低下的动物模型的报道表明,表型与自闭症中所见的特征重叠。因此,对于自闭症是高谷氨酸能障碍还是低谷氨酸能障碍,存在争议。本文综述了谷氨酸及其调节蛋白(如不同的受体、转运体和代谢酶)在 ASD 病理生理学中的作用,这些证据是通过多学科方法收集的。所有这些信息都提高了利用谷氨酸能神经递质系统治疗 ASD 的可能性。

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