Spooren Will, Lesage Anne, Lavreysen Hilde, Gasparini Fabrizio, Steckler Thomas
CNS Disease Biology Area, pRED, Building 74/3W308, Basel CH-4070, Switzerland.
Curr Top Behav Neurosci. 2010;2:391-413. doi: 10.1007/7854_2010_36.
Psychiatric and neurological disorders are linked to changes in synaptic excitatory processes with a key role for glutamate, that is, the most abundant excitatory amino-acid. Molecular cloning of the metabotropic glutamate (mGlu) receptors has led to the identification of eight mGlu receptors, which, in contrast to ligand-gated ion channels (responsible for fast excitatory transmission), modulate and fine-tune the efficacy of synaptic transmission. mGlu receptors are G protein-coupled and constitute a new group of "drugable" targets for the treatment of various CNS disorders. The recent discovery of small molecules that selectively bind to receptors of Groups I (mGlu1 and mGlu5) and II (mGlu2 and mGlu3) allowed significant advances in our understanding of the roles of these receptors in brain function and dysfunction including anxiety. Although investigation of the role of the Group III (mGlu4, 6, 7, and 8) receptors is less advanced, the generation of genetically manipulated animals and recent advances in the identification of subtype-selective compounds have revealed some first insights into the therapeutic potential of this group of receptors.
精神疾病和神经疾病与突触兴奋性过程的变化有关,谷氨酸起关键作用,谷氨酸是最丰富的兴奋性氨基酸。代谢型谷氨酸(mGlu)受体的分子克隆已鉴定出8种mGlu受体,与配体门控离子通道(负责快速兴奋性传递)不同,mGlu受体可调节和微调突触传递的效能。mGlu受体是G蛋白偶联受体,构成了治疗各种中枢神经系统疾病的一组新的“可成药”靶点。最近发现的能选择性结合I组(mGlu1和mGlu5)和II组(mGlu2和mGlu3)受体的小分子,使我们在理解这些受体在包括焦虑在内的脑功能和功能障碍中的作用方面取得了重大进展。尽管对III组(mGlu4、6、7和8)受体作用的研究进展较少,但基因操作动物的产生以及亚型选择性化合物鉴定方面的最新进展,已揭示了对这组受体治疗潜力的一些初步认识。