Serotonin transporter gene variation is associated with alcohol sensitivity in rhesus macaques exposed to early-life stress

被引:131
作者
Barr, CS
Newman, TK
Becker, ML
Champoux, M
Lesch, KP
Suomi, SJ
Goldman, D
Higley, JD
机构
[1] NIAAA, Clin Studies Lab, Primate Unit, NIH,Anim Ctr, Poolesville, MD 20837 USA
[2] NICHHD, Comparat Ethol Lab, NIH, Poolesville, MD 20837 USA
[3] NIAAA, Neurogenet Lab, NIH, Rockville, MD 20852 USA
[4] Univ Wurzburg, Clin & Mol Psychobiol Dept Psychiat & Psychothera, Wurzburg, Germany
关键词
nonhuman primate; serotonin transporter; environment; stress; alcohol sensitivity;
D O I
10.1097/01.ALC.0000067976.62827.ED
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
Background: Decreased sensitivity to alcohol has been demonstrated to be a predictor of alcoholism in humans, and variation in the gene-linked polymorphic region of the serotonin transporter (5-HTTLPR) is associated with the response to the motor-impairing effects of alcohol. In a nonhuman primate model of excessive alcohol intake, we have shown that decreased serotonin turnover is associated with both lower initial sensitivity to alcohol and higher prospective alcohol consumption using rhesus macaques. In addition, we have demonstrated that macaques separated from their mothers and reared in peer-only groups are more likely to consume alcohol as adults. Method: To examine the relationship between serotonin transporter genotype, early rearing experience, and initial sensitivity to alcohol, peer- and mother-reared, adolescent, alcohol-naive rhesus macaques (n=123) were rated for intoxication after intravenous administration of ethanol (2.2 g/kg and 2.0 g/kg for males and females, respectively) during two testing periods. Serotonin transporter (rh5-HTTLPR) genotype was determined using polymerase chain reaction followed by gel electrophoresis, and data were analyzed using ANOVA and the Mann-Whitney U test. Results: Our analyses demonstrate an effect of serotonin transporter gene variation on ethanol sensitivity, such that animals homozygous for the l allele exhibited decreased sensitivity to the ataxic and sedating effects of alcohol, This effect remained after correction for blood ethanol concentrations and birth cohort. When animals were segregated according to rearing condition, serotonin transporter gene variation predicted intoxication scores among peer-reared animals. Conclusions: As in some human reports, this study demonstrates a diminution in the response to alcohol in animals homozygous for the l rh5-HTTLPR allele. The phenotypic expression of this genotype in l/s animals, however. is environmentally dependent.
引用
收藏
页码:812 / 817
页数:6
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