Chronic Alcohol Induced Dysregulation of Central Anti-Stress Systems
Chronic Alcohol Induced Dysregulation of Central Anti-Stress Systems
批准号:
8231077
负责人:
Thomas L. Kash
金额:
$18.5万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-02-10 至 2017-01-31
关键词:
Alcohol abuseAlcohol withdrawal syndromeAlcoholismAlcoholsAllopregnanoloneAmygdaloid structureAnxietyAnxiety DisordersAttenuatedBehaviorBehavioralBiologicalBrainBrain regionBuffersCell physiologyChronicChronic stressComplexCorticotropin-Releasing HormoneElectrophysiology (science)EmotionalGoalsHealthHypothalamic structureKnowledgeLeadLiteratureMediatingMethodsNeuronsPharmaceutical PreparationsPlayPositioning AttributeRegulationRelapseReportingResearchResourcesRhodopsinRiskRoleSignal TransductionSocietiesStressStructure of terminal stria nuclei of preoptic regionSystemTechnical ExpertiseTestingVirusWorkalcohol behavioralcohol exposurealcoholism therapydrinking behaviorexperiencegamma-Aminobutyric Acidinsightneuronal circuitryneuropeptide Yneurosteroidsnoveloptogeneticsrecombinasetransmission process
中文摘要
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英文摘要
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.
PUBLIC HEALTH RELEVANCE: The focus of this project is to understand how alcohol exposure alters emotional behavior. Successful completion of this project will result in a greater understanding of how alcohol changes brain function. Further, these studies may provide insight as to how to develop more useful treatments for alcoholism and anxiety disorders.
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会议论文
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Core 1: Brain Circuit Validation Core
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The role of corticotropin releasing factor in binge-like ethanol drinking
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The role of corticotropin releasing factor in binge-like ethanol drinking
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资助金额:$34.99万
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依托单位:
Chronic Alcohol Induced Dysregulation of Central Anti-Stress Systems
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批准号:8423705
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项目类别:
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资助金额:$17.21万
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依托单位:
5/8 INIA Stress and Chronic Alcohol Interactions: Probing brain circuits that regulate alcohol stress interactions
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批准号:10574573
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资助金额:$44.87万
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依托单位:
5/8 INIA Stress and Chronic Alcohol Interactions: Probing brain circuits that regulate alcohol stress interactions
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批准号:10411787
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依托单位:
6/8: INIA Stress and Chronic Alcohol Interactions: Deconstructing the role of extended amygdala circuits in stress regulated alcohol drinking
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批准号:9241569
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资助金额:$38.0万
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依托单位:
6/8: INIA Stress and Chronic Alcohol Interactions: Deconstructing the role of extended amygdala circuits in stress regulated alcohol drinking
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依托单位:
The Role of Serotonin in Alcohol-Withdrawal Induced Anxiety
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依托单位:
海外基金