Department of Basic Neurosciences, Medical Faculty, and Clinic of Neurology, Geneva University Hospital, CH-1211 Geneva, Switzerland.
Neuron. 2010 Feb 25;65(4):445-59. doi: 10.1016/j.neuron.2010.01.016.
Many excitatory synapses express Group 1, or Gq coupled, metabotropic glutamate receptors (Gp1 mGluRs) at the periphery of their postsynaptic density. Activation of Gp1 mGluRs typically occurs in response to strong activity and triggers long-term plasticity of synaptic transmission in many brain regions, including the neocortex, hippocampus, midbrain, striatum, and cerebellum. Here we focus on mGluR-induced long-term synaptic depression (LTD) and review the literature that implicates Gp1 mGluRs in the plasticity of behavior, learning, and memory. Moreover, recent studies investigating the molecular mechanisms of mGluR-LTD have discovered links to mental retardation, autism, Alzheimer's disease, Parkinson's disease, and drug addiction. We discuss how mGluRs lead to plasticity of neural circuits and how the understanding of the molecular mechanisms of mGluR plasticity provides insight into brain disease.
许多兴奋性突触在后突触密度的外围表达 1 组或 Gq 偶联的代谢型谷氨酸受体 (Gp1 mGluRs)。Gp1 mGluRs 的激活通常发生在强烈活动的情况下,并触发包括新皮层、海马体、中脑、纹状体和小脑在内的许多脑区的突触传递的长期可塑性。在这里,我们重点关注 mGluR 诱导的长时程突触抑制 (LTD),并回顾了表明 Gp1 mGluRs 参与行为、学习和记忆可塑性的文献。此外,最近研究 mGluR-LTD 的分子机制的研究发现与智力迟钝、自闭症、阿尔茨海默病、帕金森病和药物成瘾有关。我们讨论了 mGluRs 如何导致神经网络的可塑性,以及对 mGluR 可塑性的分子机制的理解如何为大脑疾病提供了深入的认识。