Behavioral actions of alcohol: phenotypic relations from multivariate analysis of mutant mouse data

被引:31
作者
Blednov, Y. A. [1 ]
Mayfield, R. D. [1 ]
Belknap, J. [2 ]
Harris, R. A. [1 ]
机构
[1] Univ Texas Austin, Inst Cell & Mol Biol, Waggoner Ctr Alcohol & Addict Res, Inst Neurosci,Sect Neurobiol, Austin, TX 78712 USA
[2] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Portland Alcohol Res Ctr, Portland, OR 97201 USA
关键词
Alcohol behaviors; correlation analyses; mutant mice; FYN-KINASE GENE; ETHANOL-CONSUMPTION; NULL MUTANT; STRAIN DIFFERENCES; BETA-2; SUBUNIT; DEFICIENT MICE; RECEPTOR; DELETION; SENSITIVITY; RESPONSES;
D O I
10.1111/j.1601-183X.2012.00780.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
Behavioral studies on genetically diverse mice have proven powerful for determining relationships between phenotypes and have been widely used in alcohol research. Most of these studies rely on naturally occurring genetic polymorphisms among inbred strains and selected lines. Another approach is to introduce variation by engineering single-gene mutations in mice. We have tested 37 different mutant mice and their wild-type controls for a variety (31) of behaviors and have mined this data set by K-means clustering and analysis of correlations. We found a correlation between a stress-related response (activity in a novel environment) and alcohol consumption and preference for saccharin. We confirmed several relationships detected in earlier genetic studies, including positive correlation of alcohol consumption with saccharin consumption and negative correlations with conditioned taste aversion and alcohol withdrawal severity. Introduction of single-gene mutations either eliminated or greatly diminished these correlations. The three tests of alcohol consumption used (continuous two-bottle choice and two limited access tests: drinking in the dark and sustained high alcohol consumption) share a relationship with saccharin consumption, but differ from each other in their correlation networks. We suggest that alcohol consumption is controlled by multiple physiological systems where single-gene mutations can disrupt the networks of such systems.
引用
收藏
页码:424 / 435
页数:12
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