Department of Psychiatry and Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Pharmacogenomics J. 2011 Aug;11(4):251-7. doi: 10.1038/tpj.2010.41. Epub 2010 Jun 1.
The histidine triad nucleotide-binding protein-1 gene (HINT1) is implicated in schizophrenia and in the behavioral effects of morphine and amphetamine. Because nicotine dependence (ND) is highly comorbid with schizophrenia and other substance abuse, we examined the association of HINT1 with ND. Association analyses from two independent samples show that HINT1 gene variants are associated with ND phenotypes. Furthermore, human postmortem mRNA expression shows that smoking status and genotype influence HINT1 expression in the brain. In animal studies, western blot analyses show an increase of HINT1 protein level in the mouse nucleus accumbens (NAc) after chronic nicotine exposure. This increase was reduced after treatment with the nicotinic-receptor antagonist mecamylamine, and 24 and 72 h after cessation of nicotine treatment. These results indicate a genetic association between HINT1 variants and ND, and indicate that nicotine-induced modulation of HINT1 level may be involved in mechanisms of excess smoking.
组氨酸三联核苷酸结合蛋白 1 基因(HINT1)与精神分裂症以及吗啡和安非他命的行为效应有关。由于尼古丁依赖(ND)与精神分裂症和其他物质滥用高度共病,我们研究了 HINT1 与 ND 的关联。来自两个独立样本的关联分析表明,HINT1 基因变异与 ND 表型相关。此外,人类死后的 mRNA 表达显示吸烟状况和基因型会影响大脑中的 HINT1 表达。在动物研究中,Western blot 分析显示,慢性尼古丁暴露后,小鼠伏隔核(NAc)中的 HINT1 蛋白水平增加。在用烟碱型受体拮抗剂美加明治疗后,以及在停止尼古丁治疗 24 和 72 小时后,这种增加减少。这些结果表明 HINT1 变体与 ND 之间存在遗传关联,并表明尼古丁诱导的 HINT1 水平调节可能参与了过量吸烟的机制。