Portland Alcohol Research Center, Department of Behavioral Neuroscience at Oregon Health & Science University and Veterans Administration Portland Health Care System, Portland, OR, United States.
Portland Alcohol Research Center, Department of Behavioral Neuroscience at Oregon Health & Science University and Veterans Administration Portland Health Care System, Portland, OR, United States.
Alcohol. 2021 Jun;93:45-56. doi: 10.1016/j.alcohol.2021.02.001. Epub 2021 Feb 6.
The High Drinking in the Dark mouse lines (HDID-1 and HDID-2) were selectively bred to achieve high blood ethanol concentrations (BECs) in the Drinking in the Dark (DID) task, a widely used model of binge-like intake of 20% ethanol. There are several components that differentiate DID from other animal models of ethanol intake: time of day of testing, length of ethanol access, single-bottle access, and individual housing. Here, we sought to determine how some of these individual factors contribute to the high ethanol intake observed in HDID mice. HDID-1, HDID-2, and non-selected HS/NPT mice were tested in a series of DID experiments where one of the following factors was manipulated: length of ethanol access, fluid choice, number of ethanol bottles, and housing condition. We observed that 1) HDID mice achieve intoxicating BECs in DID, even when they are group-housed; 2) HDID mice continue to show elevated ethanol intake relative to HS/NPT mice during an extended access session, but this is most apparent during the first 4 h of access; and 3) offering a water choice during DID prevents elevated intake in the HDID-1 mice, but not necessarily in HDID-2 mice. Together, these results suggest that the lack of choice in the DID paradigm, together with the length of ethanol access, are important factors contributing to elevated ethanol intake in the HDID mice. These results further suggest important differences between the HDID lines in response to procedural manipulations of housing condition and ethanol bottle number in the DID paradigm, highlighting the distinct characteristics that each of these lines possess, despite being selectively bred for the same phenotype.
高饮酒黑暗小鼠品系(HDID-1 和 HDID-2)被选择性繁殖,以在饮酒黑暗(DID)任务中达到高血液乙醇浓度(BEC),这是一种广泛使用的狂欢样摄入 20%乙醇的模型。DID 与其他乙醇摄入动物模型有几个不同之处:测试时间、乙醇访问时间、单瓶访问和个体饲养。在这里,我们试图确定这些个体因素中的一些如何导致 HDID 小鼠观察到的高乙醇摄入。HDID-1、HDID-2 和非选择性 HS/NPT 小鼠在一系列 DID 实验中进行测试,其中一个因素被操纵:乙醇访问时间、液体选择、乙醇瓶数量和饲养条件。我们观察到:1)HDID 小鼠在 DID 中达到醉酒的 BEC,即使它们是群体饲养;2)HDID 小鼠在延长的访问期间相对于 HS/NPT 小鼠继续表现出升高的乙醇摄入,但这在访问的前 4 小时最为明显;3)在 DID 中提供水选择可防止 HDID-1 小鼠摄入增加,但不一定防止 HDID-2 小鼠摄入增加。这些结果表明,在 DID 范式中缺乏选择,加上乙醇访问时间的长短,是导致 HDID 小鼠乙醇摄入升高的重要因素。这些结果进一步表明,在 DID 范式中,HDID 品系对饲养条件和乙醇瓶数量的程序操作的反应存在重要差异,突出了每个品系所具有的独特特征,尽管它们是为相同的表型选择性繁殖的。