Metabotropic Glutamate Receptors in Alcohol Use Disorder: Physiology, Plasticity, and Promising Pharmacotherapies

被引:24
|
作者
Joffe, Max E. [1 ,2 ,3 ]
Centanni, Samuel W. [3 ,4 ]
Jaramillo, Anel A. [3 ,4 ]
Winder, Danny G. [1 ,3 ,4 ]
Conn, P. Jeffrey [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Dept Pharmacol, 12475E MRB4, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Vanderbilt Ctr Neurosci Drug Discovery, 1205 Light Hall, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Vanderbilt Ctr Addict Res, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37212 USA
来源
ACS CHEMICAL NEUROSCIENCE | 2018年 / 9卷 / 09期
基金
美国国家卫生研究院;
关键词
Alcohol use disorder; metabotropic glutamate receptor; synaptic plasticity; prefrontal cortex; nucleus accumbens; bed nucleus of the stria terminalis; LONG-TERM DEPRESSION; MGLUR5 ANTAGONIST MPEP; CONDITIONED PLACE PREFERENCE; PREFERRING P RATS; POSITIVE ALLOSTERIC MODULATORS; INTERMITTENT ETHANOL EXPOSURE; NUCLEUS-ACCUMBENS SYNAPSES; BETA-ADRENERGIC-RECEPTORS; CUE-INDUCED REINSTATEMENT; DORSOLATERAL BED NUCLEUS;
D O I
10.1021/acschemneuro.8b00200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2188 / 2204
页数:17
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