Department of Molecular Physiology and Biophysics , Vanderbilt University , Nashville , Tennessee 37212 , United States.
ACS Chem Neurosci. 2018 Sep 19;9(9):2188-2204. doi: 10.1021/acschemneuro.8b00200. Epub 2018 Jun 8.
Developing efficacious treatments for alcohol use disorder (AUD) has proven difficult. The insidious nature of the disease necessitates a deep understanding of its underlying biology as well as innovative approaches to ameliorate ethanol-related pathophysiology. Excessive ethanol seeking and relapse are generated by long-term changes to membrane properties, synaptic physiology, and plasticity throughout the limbic system and associated brain structures. Each of these factors can be modulated by metabotropic glutamate (mGlu) receptors, a diverse set of G protein-coupled receptors highly expressed throughout the central nervous system. Here, we discuss how different components of the mGlu receptor family modulate neurotransmission in the limbic system and other brain regions involved in AUD etiology. We then describe how these processes are dysregulated following ethanol exposure and speculate about how mGlu receptor modulation might restore such pathophysiological changes. To that end, we detail the current understanding of the behavioral pharmacology of mGlu receptor-directed drug-like molecules in animal models of AUD. Together, this review highlights the prominent position of the mGlu receptor system in the pathophysiology of AUD and provides encouragement that several classes of mGlu receptor modulators may be translated as viable treatment options.
开发有效的酒精使用障碍(AUD)治疗方法一直很困难。该疾病的隐匿性特征需要深入了解其潜在的生物学特性,以及改善乙醇相关病理生理学的创新方法。长期以来,膜特性、突触生理学和边缘系统及相关脑结构的可塑性的改变导致了过度的乙醇寻求和复发。代谢型谷氨酸(mGlu)受体可以调节这些因素中的每一个,mGlu 受体是一组多样化的 G 蛋白偶联受体,在中枢神经系统中高度表达。在这里,我们讨论了 mGlu 受体家族的不同成分如何调节边缘系统和其他与 AUD 病因相关的脑区的神经传递。然后,我们描述了乙醇暴露后这些过程是如何失调的,并推测 mGlu 受体调节可能如何恢复这种病理生理变化。为此,我们详细介绍了目前对 AUD 动物模型中 mGlu 受体靶向药物样分子的行为药理学的理解。综上所述,本综述强调了 mGlu 受体系统在 AUD 病理生理学中的突出地位,并为几种 mGlu 受体调节剂可能被转化为可行的治疗选择提供了依据。