Sharp Burt M, Chen Hao
Department of Genetics, Genomics and Informatics, College of Medicine, University of Tennessee Health Science Center, 19 S. Manassas, CRB #220, Memphis, TN, 38103, USA.
Department of Pharmacology, University of Tennessee Health Science Center, Memphis, TN, USA.
Eur J Neurosci. 2019 Aug;50(3):2164-2179. doi: 10.1111/ejn.14171. Epub 2018 Oct 25.
The single most preventable cause of disease, disability, and death in the United States is tobacco use. Decades of study show that the risk of becoming addicted to smoked cigarettes varies greatly amongst individuals and is heritable, yet environmental factors are also important contributors. In this review, we consider a wide range of methodologies and key published reports that have defined the inheritance of different stages of nicotine-dependent smoking behavior, including preference, initiation, regular use, withdrawal and dependence as well as cessation and relapse. Major findings from both animal and human studies are discussed. Current findings converge primarily on the role of nicotinic cholinergic receptor subunits, although other neurotransmitter systems as well as nicotine metabolism enzymes are implicated. Various stages of nicotine addiction may share common genetic mechanisms, yet several lines of evidence indicate that each stage also has its own unique genetic determinants. Studies on the heritability of smoking initiation demonstrate substantial evidence for gene-environment interaction, although the precise molecular genetic mechanism(s) remains unknown. Considering the relatively few genes identified so far and the small to modest fraction of the variance in risk for a particular smoking phenotype (e.g., smoking initiation in late adolescence) attributable to these genes, a large gap remains to be filled in order to account for the heritability of key phenotypes involved in each stage of addiction to smoked tobacco. Looking forward, new research strategies involving both human and animal studies will produce the fundamental genetic insights that are the foundation for the precision medical treatment of individuals addicted to smoked tobacco.
在美国,疾病、残疾和死亡的最可预防的单一原因是烟草使用。数十年的研究表明,对吸烟上瘾的风险在个体之间差异很大且具有遗传性,但环境因素也是重要的促成因素。在本综述中,我们考虑了广泛的方法和已发表的关键报告,这些方法和报告界定了尼古丁依赖吸烟行为不同阶段的遗传情况,包括偏好、开始吸烟、经常吸烟、戒断和依赖以及戒烟和复吸。讨论了动物和人类研究的主要发现。目前的研究结果主要集中在烟碱型胆碱能受体亚基的作用上,不过其他神经递质系统以及尼古丁代谢酶也与之有关。尼古丁成瘾的各个阶段可能有共同的遗传机制,但有几条证据表明每个阶段也有其独特的遗传决定因素。关于开始吸烟遗传性的研究表明存在基因 - 环境相互作用的大量证据,尽管确切的分子遗传机制仍然未知。鉴于迄今为止鉴定出的基因相对较少,以及特定吸烟表型(例如青春期后期开始吸烟)风险变异中可归因于这些基因的比例较小,为了解释吸烟成瘾每个阶段所涉及关键表型的遗传性,仍有很大差距有待填补。展望未来,涉及人类和动物研究的新研究策略将产生基本的遗传学见解,这些见解是对吸烟成瘾个体进行精准医疗的基础。