Mouse inbred strain differences in ethanol drinking to intoxication

被引:270
作者
Rhodes, J. S.
Ford, M. M.
Yu, C. -H.
Brown, L. L.
Finn, D. A.
Garland, T., Jr.
Crabbe, J. C.
机构
[1] Univ Illinois, Beckman Inst, Dept Psychol, Urbana, IL 61801 USA
[2] Oregon Hlth Sci Univ, Dept Behav Neurosci, Portland Alcohol Res Ctr, Portland, OR 97201 USA
[3] VA Med Ctr, Portland, OR USA
[4] Univ Calif Riverside, Dept Biol, Riverside, CA 92521 USA
关键词
C57BL/6J; drinking pattern; drinking; ethanol; inbred mouse strains; intoxication; Mouse Phenome Project; pharmacogenetics; phylogenetically independent contrasts;
D O I
10.1111/j.1601-183X.2006.00210.x
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Recently, we described a simple procedure, Drinking in the Dark (DID), in which C57BL/6J mice self-administer ethanol to a blood ethanol concentration (BEC) above 1 mg/ml. The test consists of replacing the water with 20% ethanol in the home cage for 4 h early during the dark phase of the light/dark cycle. Three experiments were conducted to explore this high ethanol drinking model further. In experiment 1, a microanalysis of C57BL/6J behavior showed that the pattern of ethanol drinking was different from routine water intake. In experiment 2, drinking impaired performance of C57BL/6J on the accelerating rotarod and balance beam. In experiment 3, 12 inbred strains were screened to estimate genetic influences on DID and correlations with other traits. Large, reliable differences in intake and BEC were detected among the strains, with C57BL/6J showing the highest values. Strain means were positively correlated with intake and BEC in the standard (24 h) and a limited (4 h) two-bottle ethanol vs. water test, but BECs reached higher levels for DID. Strain mean correlations with other traits in the Mouse Phenome Project database supported previously reported genetic relationships of high ethanol drinking with low chronic ethanol withdrawal severity and low ethanol-conditioned taste aversion. We extend these findings by showing that the correlation estimates remain relatively unchanged even after correcting for phylogenetic relatedness among the strains, thus relaxing the assumption that the strain means are statistically independent. We discuss applications of the model for finding genes that predispose pharmacologically significant drinking in mice.
引用
收藏
页码:1 / 18
页数:18
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