Indiana Alcohol Research Center and Department of Psychology, Indiana University - Purdue University Indianapolis, Indianapolis, IN 46202, United States.
Indiana Alcohol Research Center and Department of Psychology, Indiana University - Purdue University Indianapolis, Indianapolis, IN 46202, United States.
Alcohol. 2022 Dec;105:43-51. doi: 10.1016/j.alcohol.2022.09.005. Epub 2022 Oct 12.
After an extended alcohol-drinking history, alcohol use can transition from controlled to compulsive, causing deleterious consequences. Alcohol use can be segregated into two distinct behaviors, alcohol seeking and alcohol taking. Expression of habitual and compulsive alcohol seeking depends on the dorsolateral striatum (DLS), a brain region thought to engage after extended alcohol access. However, it is unknown whether the DLS is also involved in compulsive-like alcohol taking. The purpose of this experiment was to identify whether the DLS gates compulsive-like binge alcohol drinking. To ask this question, we gave adult male and female C57BL/6J mice a binge-like alcohol-drinking history, which we have previously demonstrated to produce compulsive-like alcohol drinking (Bauer, McVey, & Boehm, 2021), or a water-drinking history. We then tested the involvement of the DLS on gating binge-like alcohol drinking and compulsive-like quinine-adulterated alcohol drinking via intra-DLS AMPA receptor antagonism. We hypothesized that pharmacological lesioning of the DLS would reduce compulsive-like quinine-adulterated alcohol (QuA) drinking, but not non-adulterated alcohol drinking, in male and female C57BL/6J mice. Three important findings were made. First, compulsive-like alcohol drinking is significantly blunted in cannulated mice. Because of this, we conclude that we were not able to adequately assess the effect of intra-DLS lesioning on compulsive-like alcohol drinking. Second, we found that the DLS gates binge-like alcohol drinking initially, which replicates findings in our previous work (Bauer, McVey, Germano, Zhang, & Boehm, 2022). However, following an extended alcohol history, the DLS no longer drives this behavior. Finally, alcohol and QuA front-loading is DLS-dependent in alcohol-history mice. Intra-DLS NBQX altered these drinking behaviors without altering ambulatory locomotor activity. These data demonstrate the necessity of the DLS in binge-like alcohol drinking before, but not following, an extended binge-like alcohol-drinking history and in alcohol front-loading in alcohol-history mice.
在长期饮酒后,饮酒行为可能从自控转变为强迫性,从而导致有害后果。饮酒可以分为两种截然不同的行为,即寻找酒精和饮酒。习惯性和强迫性饮酒寻求的表达取决于背外侧纹状体(DLS),这是一个被认为在长期饮酒后参与的大脑区域。然而,尚不清楚 DLS 是否也参与强迫性 binge 饮酒。本实验的目的是确定 DLS 是否控制强迫性 binge 饮酒。为了提出这个问题,我们让成年雄性和雌性 C57BL/6J 小鼠进行 binge 样饮酒史,我们之前的研究表明,这种饮酒史会导致强迫性 binge 饮酒(Bauer、McVey 和 Boehm,2021),或水饮用史。然后,我们通过 DLS 内 AMPA 受体拮抗剂测试 DLS 在控制 binge 样饮酒和强迫性奎宁污染酒精(QuA)饮酒中的作用。我们假设 DLS 的药理学损伤会减少雄性和雌性 C57BL/6J 小鼠的强迫性奎宁污染酒精(QuA)饮酒,但不会减少非污染酒精的饮酒。有三个重要发现。首先,在插管小鼠中,强迫性 binge 饮酒显著减弱。因此,我们得出结论,我们无法充分评估 DLS 内损伤对强迫性 binge 饮酒的影响。其次,我们发现 DLS 最初控制 binge 样饮酒,这与我们之前的研究结果一致(Bauer、McVey、Germano、Zhang 和 Boehm,2022)。然而,在长期饮酒后,DLS 不再驱动这种行为。最后,酒精和 QuA 前置加载在酒精史小鼠中依赖于 DLS。DLS 内 NBQX 改变了这些饮酒行为,而不改变自主运动活动。这些数据表明,在长期 binge 样饮酒史之前,DLS 对 binge 样饮酒是必需的,但在长期 binge 样饮酒史后则不是,并且在酒精史小鼠中,酒精和 QuA 前置加载需要 DLS。