Neurochemical Bases for the Rewarding Effects of Ethanol

描述（由申请人提供）：长期以来，人们一直认为酒精的行为效应取决于γ-氨基丁酸（GABA）神经传递。最近，GABAA受体亚型，1424，已提出介导的影响，酒精在低至中等浓度。目前的建议将通过测试1424 GABAA受体介导乙醇的增强特性的各个方面，从而对乙醇的自愿摄入做出重要贡献的假设来研究这种可能性。我们将使用病毒介导的RNA干扰来敲低参与奖励和强化过程的脑区中脑核中14和4个GABAA受体亚基的表达，以探测1424 GABAA受体对大鼠乙醇饮酒行为的贡献。在我们的实验目标，我们将测试该受体的贡献，口服乙醇消耗，以及仪器响应乙醇。我们还将开始研究的机制，乙醇在NAC与1424 GABAA受体相互作用，使用体外电生理技术。总之，这些研究将有助于确定GABAAR的两个独特亚基在大脑奖励回路的主要区域NAc中的作用，以增强乙醇的作用。了解调节乙醇强化作用的神经机制对于开发药物治疗酒精滥用和酒精中毒至关重要。支持饮酒的神经递质和受体系统的阐明对于理解酒精的药理作用如何导致自愿摄入酒精（包括在滥用条件下）至关重要。如果在本提案的实验中研究的GABAA受体被发现有助于饮酒，那么未来的研究可能通过与该受体相互作用来减少饮酒的药物方法将被指示。

DESCRIPTION (provided by applicant): The behavioral effects of alcohol have long been considered to depend on gamma-amino-butyric acid (GABA) neurotransmission. Recently, the GABAA receptor isoform, 1424, has been proposed to mediate effects of alcohol at low-to-moderate concentrations. The current proposal will examine this possibility by testing the hypothesis that the 1424 GABAA receptor mediates aspects of the reinforcing properties of ethanol, thereby critically contributing to voluntary intake of ethanol. We will use viral-mediated RNA interference to knock down expression of the 14 and 4 GABAA receptor subunits in the nucleus accumbens, a brain region involved in processes of reward and reinforcement, to probe the contribution of the 1424 GABAA receptor to ethanol drinking behaviors by rats. Within our experimental aims we will test the contribution of this receptor to oral ethanol consumption, as well as to instrumental responding for ethanol. We will also initiate studies of the mechanism whereby ethanol in the NAc interacts with the 1424 GABAA receptor, using in vitro electrophysiogical techniques. Together, these studies will serve to define a role for two unique subunits of the GABAAR in a primary region of the brain reward circuitry, the NAc, in the reinforcing effects of ethanol. Understanding the neural mechanisms that mediate ethanol's reinforcing effects is critical for the development of treatments to assist in pharmacological therapies for alcohol abuse and alcoholism. PUBLIC HEALTH RELEVANCE The elucidation of the neurotransmitter and receptor systems that support alcohol drinking is critical for understanding how the pharmacological actions of alcohol lead to voluntary intake of alcohol, including under conditions of abuse. If the GABAA receptor studied in the experiments in this proposal is found to contribute to alcohol drinking, then future research on possible pharmaceutical approaches to reduce drinking by interacting with this receptor would be indicated.