Genetics of GABAergic signaling in nicotine and alcohol dependence

被引:25
作者
Cui, Wen-Yan [2 ,3 ]
Seneviratne, Chamindi [1 ]
Gu, Jun [3 ]
Li, Ming D. [1 ,2 ]
机构
[1] Univ Virginia, Dept Psychiat & Neurobehav Sci, Charlottesville, VA 22911 USA
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis, Hangzhou 310003, Zhejiang, Peoples R China
[3] Peking Univ, Coll Life Sci, Natl Key Lab Prot & Plant Gene Res, Beijing 100871, Peoples R China
关键词
GENOME-WIDE ASSOCIATION; GABA(B) RECEPTOR MODULATION; LINKAGE SCAN; ENVIRONMENT INTERACTIONS; SUSCEPTIBILITY LOCI; EUROPEAN-AMERICANS; AFRICAN-AMERICANS; CENTRAL AMYGDALA; CANDIDATE GENE; COMBINATORIAL APPROACH;
D O I
10.1007/s00439-011-1108-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Both nicotine and alcohol addictions are common chronic brain disorders that are of great concern to individuals and society. Although genetics contributes significantly to these disorders, the susceptibility genes and variants underlying them remain largely unknown. Many years of genome-wide linkage and association studies have implicated a number of genes and pathways in the etiology of nicotine and alcohol addictions. In this communication, we focus on current evidence, primarily from human genetic studies, supporting the involvement of genes and variants in the GABAergic signaling system in the etiology of nicotine dependence and alcoholism based on linkage, association, and gene-by-gene interaction studies. Current efforts aim not only to replicate these findings in independent samples, but also to identify which variant contributes to the detected associations and through what molecular mechanisms.
引用
收藏
页码:843 / 855
页数:13
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