Chronic Alcohol Induced Dysregulation of Central Anti-Stress Systems

慢性酒精引起中枢抗应激系统失调

• 批准号: 8606723
• 负责人: Thomas L. Kash
• 金额: $ 17.94万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-02-10 至 2017-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8606723
• 关键词: Alcohol abuse; Alcohol withdrawal syndrome; Alcoholism; Alcohols; Allopregnanolone; Amygdaloid structure; Anxiety; Anxiety Disorders; Attenuated; Behavior; Behavioral; Biological; Brain; Brain region; Buffers; Cell physiology; Chronic; Chronic stress; Complex; Corticotropin-Releasing Hormone; Electrophysiology (science); Emotional; Goals; Health; Hypothalamic structure; Knowledge; Lead; Literature; Mediating; Methods; Neurons; Pharmaceutical Preparations; Play; Positioning Attribute; Regulation; Relapse; Reporting; Research; Resources; Rhodopsin; Risk; Role; Signal Transduction; Societies; Stress; Structure of terminal stria nuclei of preoptic region; System; Technical Expertise; Testing; Virus; Work; alcohol behavior; alcohol exposure; alcoholism therapy; drinking behavior; experience; gamma-Aminobutyric Acid; insight; neuronal circuitry; neuropeptide Y; neurosteroids; novel; optogenetics; recombinase; transmission process

DESCRIPTION (provided by applicant): Alcoholism and alcohol abuse are major health problems and represent a tremendous financial burden on our society. A growing literature indicates that chronic alcohol exposure leads to an imbalance between central stress and anti-stress systems in key brain circuits that regulate emotional behavior. These imbalances can lead to pathological behavior, including increased anxiety, stress-responsivity and enhanced risk of relapse. Despite these advances identifying the role these systems play in alcohol related behaviors, there remains a gap in our knowledge of the fundamental biological, cellular and circuit mechanisms that contribute to this dysregulated behavior. In order to more effectively treat alcohol abuse, it is necessary to define the impact of chronic alcohol exposure on the in the circuitry that is critical for regulation of this behavior. Here, we propose to characterize the impact of chronic alcohol exposure on anti-stress systems, specifically neuropeptide Y (NPY) and GABAergic neuroactive steroids, in the amygdala and extended amygdala, brain regions critical for regulation of stress and anxiety-like behavior. Additionally, we will utilize inducible channel rhodopsin viruses in combination with neurochemically specific Cre-recombinase driver lines to determine the impact of chronic alcohol exposure on GABAergic circuits in these brain regions. In total, the proposed work will begin to define specific alcohol-induced cellular and circuit adaptations that are likely to play key roles in pathological behaviors associated with alcoholism.

描述（由申请人提供）：酗酒和酗酒是主要的健康问题，对我们的社会造成了巨大的经济负担。越来越多的文献表明，长期饮酒会导致调节情绪行为的关键大脑回路中的中枢压力和抗压力系统之间的不平衡。这些不平衡可能导致病态行为，包括焦虑增加，压力反应和复发风险增加。尽管这些进展确定了这些系统在酒精相关行为中的作用，但我们对导致这种失调行为的基本生物学，细胞和电路机制的认识仍然存在差距。为了更有效地治疗酒精滥用，有必要确定慢性酒精暴露对调节这种行为的关键电路的影响。在这里，我们建议的特点，慢性酒精暴露对抗压力系统的影响，特别是神经肽Y（NPY）和GABA能神经活性类固醇，在杏仁核和扩展杏仁核，大脑区域的压力和焦虑样行为的调节至关重要。此外，我们将利用诱导通道视紫红质病毒与神经化学特异性Cre重组酶驱动线相结合，以确定慢性酒精暴露对这些脑区GABA能回路的影响。总的来说，拟议的工作将开始，以确定特定的酒精诱导的细胞和电路的适应，可能发挥关键作用的病理行为与酗酒。