Suppr超能文献

组氨酸三联核苷酸结合蛋白-1(HINT1)基因变异与尼古丁依赖的关联。

Association of the histidine-triad nucleotide-binding protein-1 (HINT1) gene variants with nicotine dependence.

机构信息

Department of Psychiatry and Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.

出版信息

Pharmacogenomics J. 2011 Aug;11(4):251-7. doi: 10.1038/tpj.2010.41. Epub 2010 Jun 1.

Abstract

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.

摘要

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。

相似文献

4

引用本文的文献

3
The Many Faces of Histidine Triad Nucleotide Binding Protein 1 (HINT1).组氨酸三联体核苷酸结合蛋白1(HINT1)的多种面貌
ACS Pharmacol Transl Sci. 2023 Jul 20;6(10):1310-1322. doi: 10.1021/acsptsci.3c00079. eCollection 2023 Oct 13.
5
HINT1 neuropathy: Expanding the genotype and phenotype spectrum.神经病变:扩大基因型和表型谱。
Clin Genet. 2022 Nov;102(5):379-390. doi: 10.1111/cge.14198. Epub 2022 Aug 16.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验