GABA B agonists revisited: Brain, behavioral and genetic effects in smokers

重新审视 GABA B 激动剂：吸烟者的大脑、行为和遗传影响

• 批准号: 8237990
• 负责人: TERESA R FRANKLIN
• 金额: $ 29.84万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-09-15 至 2017-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8237990
• 关键词: Affect; Agonist; Amygdaloid structure; Anterior; Baclofen; Behavior; Behavioral; Behavioral Genetics; Brain; Candidate Disease Gene; Catechol O-Methyltransferase; Cessation of life; Cigarette; Cognitive; Consumption; Cues; DNA; Data; Decision Making; Dopamine; Dopamine Agonists; Dorsal; Economic Burden; Emotional; Exhibits; Functional Magnetic Resonance Imaging; GABA Agonists; Genes; Genetic; Genetic Polymorphism; Genotype; Goals; Health; Homozygote; Image; Individual; Insula of Reil; Intervention; Knowledge; Lateral; Life; Link; Longitudinal Studies; Measurement; Medial; Mediating; Medicine; Methods; Methyltransferase Gene; Modeling; Modification; Monitor; National Institute of Drug Abuse; Nicotine; Nicotine Withdrawal; Perfusion; Pharmaceutical Preparations; Placebos; Play; Population; Predisposition; Publishing; Randomized; Regimen; Relapse; Relative (related person); Reporting; Research Design; Rest; Rewards; Role; Sample Size; Sampling; Smoke; Smoker; Smoking; Smoking Behavior; Societies; Structure; Subgroup; Synapses; Techniques; Testing; Time; Tobacco Dependence; Treatment outcome; Variant; Ventral Striatum; Withdrawal; Withholding Treatment; addiction; combat; craving; cue reactivity; design; dopamine transporter; drug reward; endophenotype; gamma-Aminobutyric Acid; gene interaction; improved; innovation; meetings; novel; relating to nervous system; response; smoking cessation; smoking relapse; tobacco abuse; transmission process; treatment strategy

DESCRIPTION (provided by applicant): Cigarette addiction is the leading cause of preventable death in our nation. Despite the life-threatening health consequences of smoking and the substantial heavy economic burden on society, close to 25% of the population continues to smoke. Two major factors contribute to continued smoking and relapse: craving elicited by smoking cues (SCs) and craving elicited by nicotine withdrawal (WD). Inability to combat WD-induced craving, which declines within a month, plays a major role in EARLY relapse. However, smokers report that SCs can trigger relapse months or even years after quitting. Existing smoking cessation medications alleviate WD and/or reduce nicotine reward, and are helpful for subgroups of smokers. However, other 'cue-vulnerable' smokers receive less benefit evincing the critical need to identify agents that target SC reactivity. A number of factors, including genetic variance, may underlie the relative contribution of SCs and WD to susceptibility to relapse. Indeed, we have found a profound effect of variance in the dopamine transporter SLC6A3 (DAT) gene on SC reactivity. Our findings are consistent with the well-established role of dopamine (DA) in drug reward and drug-associated cues. GABA B agonists modulate DA and have shown promise as drug cue blocking agents. Evidence suggests that the GABA B agonist, baclofen modulates drug seeking and taking behavior and thus may be a 'prototypical probe' to examine the effects of GABA B agonists on SC reactivity. The goal of this proposal is to identify a SC-vulnerable pharmaco-responsive endophenotype. Towards this goal, we will: AIM 1, confirm a SC-vulnerable endophenotype mediated by variance in functional DA-modulating candidate genes AIM 2, utilize our innovative brain/behavioral/genetic paradigm to link 'baclofen-induced' neural responses during SC exposure with behavioral correlates to identify a pharmaco-responsive endophenotype~ and Exploratory AIM: explore the interaction between allelic variance in DA-modulating genes and baclofen- induced brain and behavioral responses. Our model will employ the quantitative technique of perfusion fMRI, which facilitates the measurement of medication-induced (longitudinal) neural modifications, both in the brain 'at rest' and during cognitive and emotional tasks. Thus, we will acquire resting baseline and SC exposure data in smokers prior to and following a 3-week medication regimen. Smoking behavior will be monitored using 'novel naturalistic methods'. DNA samples will be analyzed for allelic variance in DA-regulating genes. Ultimately, the goal for contemporary medicine is to establish brain/behavioral/genetic endophenotypes that predict medication response, such that treatments are tailored to manage individual vulnerabilities (i.e., Personalized Medicine). The proposed studies will provide knowledge about genetic influences and GABA agonist mechanisms on a major relapse predictor: SC reactivity. This will have a sustained and lasting impact on smoking treatment strategies and will aid in meeting a major goal set by NIDA, which is to "Eradicate Tobacco Abuse and Addiction". PUBLIC HEALTH RELEVANCE: The proposed project will utilize perfusion fMRI, a functional candidate gene association approach (of dopaminergic addictions-targeted polymorphisms), and the dopamine-modulating and GABA B agonist, baclofen to examine the brain and behavioral responses in smokers to appetitive smoking reminders (cues that motivate continued smoking and relapse). These studies will provide a means to identify an appetitive cue- sensitive pharmaco-responsive endophenotype. Once brain/behavioral/genetic endophenotypes can be determined prior to treatment, smoking cessation treatments can be structured to meet individual needs, which will significantly improve treatment outcome.

描述（由申请人提供）：吸烟成瘾是我国可预防死亡的主要原因。尽管吸烟对健康造成了威胁生命的后果，并给社会带来了沉重的经济负担，但仍有近25%的人口继续吸烟。两个主要因素导致继续吸烟和复吸：吸烟线索引起的渴望（SC）和尼古丁戒断引起的渴望（WD）。 无法对抗WD引起的渴望，这种渴望在一个月内下降，在早期复发中起着重要作用。然而，吸烟者报告说，SC可以在戒烟后数月甚至数年内引发复发。现有的戒烟药物缓解WD和/或减少尼古丁奖励，并对吸烟者亚组有帮助。然而，其他“线索脆弱”的吸烟者获得的益处较少，表明迫切需要确定靶向SC反应性的药剂。许多因素，包括遗传变异，可能是SC和WD对复发易感性的相对贡献的基础。事实上，我们已经发现了多巴胺转运蛋白SLC 6A 3（DAT）基因的变异对SC反应性的深刻影响。我们的研究结果与多巴胺（DA）在药物奖励和药物相关线索中的既定作用一致。GABA B激动剂调节DA，并已显示出作为药物线索阻断剂的前景。有证据表明，GABA B激动剂巴氯芬调节药物寻求和服用行为，因此可能是一个“原型探针”，以检查GABA B激动剂对SC反应性的影响。本提案的目标是确定SC易感的药物反应性内表型。为了实现这一目标，我们将：AIM 1，确认由功能性DA调节候选基因AIM 2的变异介导的SC易感性内表型，利用我们创新的脑/行为/遗传范式将SC暴露期间的“细菌诱导的”神经反应与行为相关性联系起来，以鉴定药物反应性内表型~和探索性AIM：探索DA调节基因中等位基因变异与巴氯芬诱导的脑和行为反应之间的相互作用。我们的模型将采用定量技术灌注功能磁共振成像，这有利于测量药物引起的（纵向）神经修改，无论是在大脑“休息”和认知和情感任务。因此，我们将在3周药物治疗方案之前和之后采集吸烟者的静息基线和SC暴露数据。吸烟行为将使用“新颖的自然主义方法”进行监测。将分析DNA样本中DA调节基因的等位基因变异。最终，当代医学的目标是建立预测药物反应的大脑/行为/遗传内表型，使得治疗被定制以管理个体脆弱性（即，个性化医疗）。 拟议的研究将提供有关遗传影响和GABA激动剂机制对一个主要的复发预测因子：SC反应性的知识。这将对吸烟治疗战略产生持续和持久的影响，并将有助于实现NIDA设定的一个主要目标，即“根除烟草滥用和成瘾”。 公共卫生相关性：拟议的项目将利用灌注功能磁共振成像，一种功能性候选基因关联方法（多巴胺能成瘾靶向多态性），以及多巴胺调节和GABA B激动剂巴氯芬来检查吸烟者对食欲吸烟提醒（激励继续吸烟和复吸的线索）的大脑和行为反应。这些研究将提供鉴定食欲线索敏感的药物响应性内表型的方法。 一旦在治疗前确定了大脑/行为/遗传内表型，戒烟治疗就可以满足个人需求，这将显着改善治疗结果。