Cartmell J, Schoepp D D
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN 46285, USA.
J Neurochem. 2000 Sep;75(3):889-907. doi: 10.1046/j.1471-4159.2000.0750889.x.
The G protein-coupled metabotropic glutamate (mGlu) receptors are differentially localized at various synapses throughout the brain. Depending on the receptor subtype, they appear to be localized at presynaptic and/or postsynaptic sites, including glial as well as neuronal elements. The heterogeneous distribution of these receptors on glutamate and nonglutamate neurons/cells thus allows modulation of synaptic transmission by a number of different mechanisms. Electrophysiological studies have demonstrated that the activation of mGlu receptors can modulate the activity of Ca(2+) or K(+) channels, or interfere with release processes downstream of Ca(2+) entry, and consequently regulate neuronal synaptic activity. Such changes evoked by mGlu receptors can ultimately regulate transmitter release at both glutamatergic and nonglutamatergic synapses. Increasing neurochemical evidence has emerged, obtained from in vitro and in vivo studies, showing modulation of the release of a variety of transmitters by mGlu receptors. This review addresses the neurochemical evidence for mGlu receptor-mediated regulation of neurotransmitters, such as excitatory and inhibitory amino acids, monoamines, and neuropeptides.
G蛋白偶联的代谢型谷氨酸(mGlu)受体在整个大脑的各种突触中呈差异分布。根据受体亚型的不同,它们似乎定位于突触前和/或突触后位点,包括神经胶质细胞和神经元成分。这些受体在谷氨酸能和非谷氨酸能神经元/细胞上的异质性分布,使得突触传递能够通过多种不同机制进行调节。电生理学研究表明,mGlu受体的激活可以调节Ca(2+)或K(+)通道的活性,或干扰Ca(2+)内流下游的释放过程,从而调节神经元的突触活性。mGlu受体引起的这种变化最终可以调节谷氨酸能和非谷氨酸能突触处的递质释放。从体外和体内研究中获得的越来越多的神经化学证据表明,mGlu受体可以调节多种递质的释放。本综述阐述了mGlu受体介导的对神经递质(如兴奋性和抑制性氨基酸、单胺和神经肽)调节作用的神经化学证据。