Alcohol preference drinking in a mouse line selectively bred for high drinking in the dark

被引:59
作者
Crabbe, John C. [1 ]
Spence, Stephanie E.
Brown, Lauren L.
Metten, Pamela
机构
[1] Oregon Hlth & Sci Univ, Portland Alcohol Res Ctr, Dept Behav Neurosci, Portland, OR 97239 USA
关键词
Selected mouse lines; High Drinking in the Dark (HDID) mice; Ethanol preference; Pharmacogenetics; Binge drinking; Limited access; VOLUNTARY ETHANOL INTAKE; STRAIN DIFFERENCES; SCHEDULED ACCESS; MICE; CONSUMPTION; GENETICS; INTOXICATION; GENES; RATS;
D O I
10.1016/j.alcohol.2010.12.001
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
We have selectively bred mice that reach very high blood ethanol concentrations (BECs) after drinking from a single bottle of 20% ethanol. High Drinking in the Dark (HDID-1) mice drink nearly 6 g/kg ethanol in 4 h and reach average BECs of more than 1.0 mg/mL. Previous studies suggest that DID and two-bottle preference for 10% ethanol with continuous access are influenced by many of the same genes. We therefore asked whether HDID-1 mice would differ from the HS/Npt control stock on two-bottle preference drinking. We serially offered mice access to 3-40% ethanol in tap water versus tap water. For ethanol concentrations between 3 and 20%, HDID-1 and HS/Npt controls did not differ in two-bottle preference drinking. At the highest concentrations, the HS/Npt mice drank more than the HDID-1 mice. We also tested the same mice for preference for two concentrations each of quinine, sucrose, and saccharin. Curiously, the mice showed preference ratios (volume of tastant/total fluid drunk) of about 50% for all tastants and concentrations. Thus, neither genotype showed either preference or avoidance for any tastant after high ethanol concentrations. Therefore, we compared naive groups of HDID-1 and HS/Npt mice for tastant preference. Results from this test showed that ethanol-naive mice preferred sweet fluids and avoided quinine but the genotypes did not differ. Finally, we tested HDID-1 and HS mice for an extended period for preference for 15% ethanol versus water during a 2-h access period in the dark. After several weeks, HDID-1 mice consumed significantly more than HS. We conclude that drinking in the dark shows some genetic overlap with other tests of preference drinking, but that the degree of genetic commonality depends on the model used. Published by Elsevier Inc.
引用
收藏
页码:427 / 440
页数:14
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