Suppr超能文献

NMDA 受体调节的机制。

Mechanisms of NMDA receptor regulation.

机构信息

Institut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, Université PSL, CNRS, INSERM, F-75005 Paris, France.

出版信息

Curr Opin Neurobiol. 2023 Dec;83:102815. doi: 10.1016/j.conb.2023.102815. Epub 2023 Nov 20.

Abstract

N-methyl-D-aspartate receptors (NMDARs) are glutamate-gated ion channels widely expressed in the central nervous system that play key role in brain development and plasticity. On the downside, NMDAR dysfunction, be it hyperactivity or hypofunction, is harmful to neuronal function and has emerged as a common theme in various neuropsychiatric disorders including autism spectrum disorders, epilepsy, intellectual disability, and schizophrenia. Not surprisingly, NMDAR signaling is under a complex set of regulatory mechanisms that maintain NMDAR-mediated transmission in check. These include an unusual large number of endogenous agents that directly bind NMDARs and tune their activity in a subunit-dependent manner. Here, we review current knowledge on the regulation of NMDAR signaling. We focus on the regulation of the receptor by its microenvironment as well as by external (i.e. pharmacological) factors and their underlying molecular and cellular mechanisms. Recent developments showing how NMDAR dysregulation participate to disease mechanisms are also highlighted.

摘要

N-甲基-D-天冬氨酸受体(NMDARs)是广泛表达于中枢神经系统的谷氨酸门控离子通道,在大脑发育和可塑性中发挥关键作用。不利的一面是,NMDAR 功能障碍,无论是过度活跃还是功能低下,都对神经元功能有害,并已成为各种神经精神疾病的共同主题,包括自闭症谱系障碍、癫痫、智力障碍和精神分裂症。毫不奇怪,NMDAR 信号受到一套复杂的调节机制的控制,这些机制可以控制 NMDAR 介导的传递。其中包括大量直接结合 NMDAR 并以亚基依赖性方式调节其活性的内源性物质。在这里,我们回顾了 NMDAR 信号转导调节的最新知识。我们专注于受体由其微环境以及外部(即药理学)因素调节,以及它们的潜在分子和细胞机制。还强调了最近的研究进展,这些进展表明 NMDAR 失调如何参与疾病机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验