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神经元烟碱型乙酰胆碱受体基因的α4和β2亚基与日本人群中的甲基苯丙胺使用障碍无关。

Alpha4 and beta2 subunits of neuronal nicotinic acetylcholine receptor genes are not associated with methamphetamine-use disorder in the Japanese population.

作者信息

Kishi Taro, Ikeda Masashi, Kitajima Tsuyoshi, Yamanouchi Yoshio, Kinoshita Yoko, Kawashima Kunihiro, Inada Toshiya, Harano Mutsuo, Komiyama Tokutaro, Hori Toru, Yamada Mitsuhiko, Iyo Masaomi, Sora Ichiro, Sekine Yoshimoto, Ozaki Norio, Ujike Hiroshi, Iwata Nakao

机构信息

Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan.

出版信息

Ann N Y Acad Sci. 2008 Oct;1139:70-82. doi: 10.1196/annals.1432.023.

Abstract

The mesolimbic system is thought to be involved in the reinforcing action of many addictive drugs and the release of dopamine modulated by neuronal nicotine cholinergic receptors (nAChRs). Several investigations suggested that nAChRs on dopaminergic terminals play an important role in the development of some long-lasting adaptations associated with drug abuse. A majority of high-affinity nicotine binding sites in the brain have been showed in heteropentameric alpha4 (alpha4) and beta2 subunit (beta2) of nAChRs. Therefore, we conducted a genetic association analysis of the alpha4 gene (CHRNA4) and beta2 gene (CHRNB2) with methamphetamine (METH)-use disorder (191 cases and 753 controls). We first evaluated the linkage disequilibrium (LD) structure of these genes and selected 7 and 5 tagging SNPs (tag SNPs) on CHRNA4 and CHRNB2, respectively. Some tag SNPs were significantly associated with total METH-use disorder and METH-induced psychosis; however, these associations were no longer statistically significant after Bonferroni's correction for multiple testing. In conclusion, our results suggest that neither CHRNA4 nor CHRNB2 plays a major role in Japanese METH-use disorder.

摘要

中脑边缘系统被认为与许多成瘾性药物的强化作用以及由神经元烟碱胆碱能受体(nAChRs)调节的多巴胺释放有关。多项研究表明,多巴胺能终末上的nAChRs在与药物滥用相关的一些持久适应性变化的发展中起重要作用。大脑中大多数高亲和力尼古丁结合位点已显示存在于nAChRs的异源五聚体α4(α4)和β2亚基(β2)中。因此,我们对α4基因(CHRNA4)和β2基因(CHRNB2)与甲基苯丙胺(METH)使用障碍(191例病例和753例对照)进行了基因关联分析。我们首先评估了这些基因的连锁不平衡(LD)结构,并分别在CHRNA4和CHRNB2上选择了7个和5个标签单核苷酸多态性(标签SNP)。一些标签SNP与总的METH使用障碍和METH诱发的精神病显著相关;然而,在进行多重检验的Bonferroni校正后,这些关联不再具有统计学意义。总之,我们的结果表明,CHRNA4和CHRNB2在日本人群的METH使用障碍中均不发挥主要作用。

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