Constitutional mechanisms of vulnerability and resilience to nicotine dependence

被引:20
作者
Hiroi, N. [1 ,2 ]
Scott, D. [2 ]
机构
[1] Albert Einstein Coll Med, Dept Psychiat & Behav Sci, Lab Mol Psychobiol, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dominick P Purpura Dept Neurosci, Bronx, NY 10461 USA
关键词
smoking; addiction; knockout mice; translational model; comorbidity; genetic susceptibility; MONOAMINE-OXIDASE-A; CONDITIONED PLACE PREFERENCE; DEFICIT HYPERACTIVITY DISORDER; ADOLESCENT SMOKING TRAJECTORIES; CATECHOL-O-METHYLTRANSFERASE; DOPAMINE METABOLIC ENZYMES; GENOME-WIDE ASSOCIATION; CIGARETTE-SMOKING; DEVELOPMENTAL TRAJECTORIES; PSYCHIATRIC-DISORDERS;
D O I
10.1038/mp.2009.16
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The core nature of nicotine dependence is evident in wide variations in how individuals become and remain smokers. Individuals with pre-existing behavioral traits are more likely to develop nicotine dependence and experience difficulty when attempting to quit. Many molecular factors likely contribute to individual variations in the development of nicotine dependence and behavioral traits in complex manners. However, the identification of such molecules has been hampered by the phenotypic complexity of nicotine dependence and the complex ways molecules affect elements of nicotine dependence. We hypothesize that nicotine dependence is, in part, a result of interactions between nicotine and pre-existing behavioral traits. This perspective suggests that the identification of the molecular bases of such pre-existing behavioral traits will contribute to the development of effective methods for reducing smoking dependence and for helping smokers to quit. Molecular Psychiatry (2009) 14, 653-667; doi:10.1038/mp.2009.16; published online 24 February 2009
引用
收藏
页码:653 / 667
页数:15
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