Human γ-aminobutyric acid A receptor α2 gene moderates the acute effects of alcohol and brain mRNA expression

被引:46
|
作者
Haughey, H. M. [1 ]
Ray, L. A. [1 ]
Finan, P. [1 ]
Villanueva, R. [1 ]
Niculescu, M. [1 ]
Hutchison, K. E. [1 ]
机构
[1] Univ Colorado, Dept Psychol, Boulder, CO 80309 USA
关键词
alcohol; alcoholism; endophenotype; GABA; GABRA2; haplotype; mRNA; polymorphism; SNP;
D O I
10.1111/j.1601-183X.2007.00369.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
gamma-aminobutyric acid A (GABA(A)) receptors moderate several of the behavioral effects of alcohol. In fact, recent studies have shown an association between the gene for the alpha 2-subunit of the GABA(A) receptor (GABRA2) and alcoholism. In the present study, we examined the functional relevance of the GABRA2 gene in alcohol dependence by assessing brain GABRA2 mRNA and GABA(A) alpha 2-subunit protein levels in post-mortem prefrontal cortical tissue collected from control and alcohol-dependent individuals. In addition, using an endophenotype approach, we tested whether the GABRA2 gene moderates sensitivity to the acute effects of alcohol in two independent samples from distinct human alcohol challenge studies. Results indicated that GABRA2 mRNA levels significantly differed by GABRA2 genotype. GABRA2 single nucleotide polymorphisms (rs573400, rs279871 and rs279858) were significantly associated with sensitivity to the acute effects of alcohol. Specifically, there was a significant main effect of GABRA2 x breath alcohol concentration on several measures of subjective responses to alcohol, including the hedonic value of alcohol. Importantly, reanalysis of a previous intravenous alcohol administration study confirmed the results of the oral alcohol challenge study. In summary, these results extend previous findings and provide new insights into the putative biobehavioral mechanisms that may moderate the association between the GABRA2 gene, sensitivity to the acute effects of alcohol and ultimately alcohol dependence.
引用
收藏
页码:447 / 454
页数:8
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