Alpha 5 nAChR is a Risk Factor within the Dopamine System for Nicotine Addiction

Alpha 5 nAChR 是多巴胺系统内尼古丁成瘾的危险因素

• 批准号: 9686812
• 负责人: John A. Dani
• 金额: $ 12.91万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-05-01 至 2020-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9686812
• 关键词: Acute; Addictive Behavior; Area; Behavior Control; Behavioral; Cessation of life; Chronic; Corpus striatum structure; Data; Dopamine; Dorsal; Dose; Drosophila acetylcholine receptor alpha-subunit; Event; Experimental Designs; Genes; Human Genetics; In Vitro; Knockout Mice; Link; Malignant neoplasm of lung; Measures; Mediating; Methodology; Microdialysis; Midbrain structure; Modeling; Mus; Mutant Strains Mice; Nicotine; Nicotine Dependence; Nicotine Withdrawal; Nicotinic Receptors; Nucleus Accumbens; Organism; Periodicity; Phase; Physiology; Preparation; Process; Psychological reinforcement; Research; Rewards; Risk; Risk Factors; Rodent; Role; Scanning; Self Administration; Signal Transduction; Single Nucleotide Polymorphism; Smoker; Smoking; Source; Substance Withdrawal Syndrome; Synapses; System; Time; Tobacco; Tobacco Dependence; Tobacco use; Translating; United States; Ventral Tegmental Area; Wild Type Mouse; Withdrawal; addiction; base; dopamine system; dopaminergic neuron; drinking water; expectation; experience; genome wide association study; high risk; in vivo; neuroadaptation; nicotine exposure; nicotine use; premature; preventable death; public health relevance; response; reward processing; smoking cessation; therapy development

DESCRIPTION (provided by applicant): Genome-wide association studies identified a nonsynonymous SNP (rs16969968) within the CHRNA5 gene that encodes for the �5 nicotinic receptor (nAChR) subunit. This SNP produces a twofold higher risk for heavy smoking and increases the risk for lung cancer. Consistent with the human genetics, our preliminary studies showed that the �5 nAChR is necessary for the expression of the nicotine withdrawal syndrome. The �5 nAChR also regulates sensitive to nicotine-induced behaviors and controls nicotine self-administration at high doses. In these proposed studies, we will investigate �5's mechanistic action on the midbrain dopamine (DA) systems that reinforce rewarding and addictive behaviors. We will examine the effect of the rs16969968 SNP on DA signaling from its source in the midbrain to its main targets in the striatum, including the nucleus accumbens (NAc) which is important for processing reward. Our in vivo multi-tetrode recordings show that nicotine increases the phasic burst firing of DA neurons, and our cyclic voltammetry and in vivo microdialysis data show that nicotine-induced changes in DA neuron firing are translated in a target-specific manner in areas that process reinforcement and reward, including the NAc core and shell. However, little is known about the role of the �5 subunit or the rs16969968 SNP and about the role of the �5-subunit in regulating the relationship between DA neuron firing and DA release in targets. Our working hypothesis is that nicotine acts via the �5-nAChR subunit to modulate DA signaling both at the source (i.e., DA neurons in the midbrain) and at the targets (including the NAc and the dorsal striatum). The aims examine the hypothesis that nicotine-induced changes in the DA system evolve during chronic nicotine exposure and during the withdrawal period. The significance of the study originates from the expectation that these nicotine-induced activities and changes in the DA system contribute to the transition from initial nicotine use to addiction. Tobacco use remains the leading cause of preventable death in the United States, and these studies provide a mechanistic basis for nicotine addiction and for developing therapies to aid smoking cessation.

描述（由申请人提供）：全基因组关联研究在编码β 5烟碱受体（nAChR）亚基的CHRNA 5基因内发现了一个非同义SNP（rs 16969968）。这种SNP会使重度吸烟的风险增加两倍，并增加肺癌的风险。与人类遗传学一致，我们的初步研究表明，5 nAChR是尼古丁戒断综合征表达所必需的。5 nAChR还调节对尼古丁诱导的行为的敏感性，并控制高剂量尼古丁的自我给药。在这些拟议的研究中，我们将调查5对中脑多巴胺（DA）系统的机制作用，这些系统加强了奖励和成瘾行为。我们将研究rs 16969968 SNP对DA信号传导的影响，从中脑的来源到纹状体的主要靶点，包括对处理奖励很重要的丘脑核（NAc）。我们的体内多四极记录显示，尼古丁增加DA神经元的相位爆发放电，我们的循环伏安法和体内微透析数据显示，尼古丁诱导的DA神经元放电变化在处理强化和奖励的区域（包括NAc核心和外壳）中以靶向特异性方式进行翻译。然而，关于β 5亚基或rs 16969968 SNP的作用以及β 5亚基在调节DA神经元放电和靶点DA释放之间的关系中的作用知之甚少。我们的工作假设是，尼古丁通过β 5-nAChR亚基在源头（即，中脑中的DA神经元）和靶点（包括NAc和背侧纹状体）。其目的是研究尼古丁诱导的DA系统变化在慢性尼古丁暴露期间和戒断期演变的假设。这项研究的意义源于这样一种预期，即这些尼古丁诱导的活动和DA系统的变化有助于从最初的尼古丁使用到成瘾的转变。烟草使用仍然是美国可预防死亡的主要原因，这些研究为尼古丁成瘾和开发帮助戒烟的疗法提供了机制基础。