A critical role for rapid estrogen signaling in alcohol addiction and anxiety

快速雌激素信号在酒精成瘾和焦虑中的关键作用

• 批准号: 10190744
• 负责人: Kristen Elizabeth Pleil
• 金额: $ 46.58万
• 依托单位: WEILL MEDICAL COLL OF CORNELL UNIV
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-09-10 至 2024-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10190744
• 关键词: Acute; Adopted; Alcohol consumption; Alcohol dependence; Alcohol withdrawal syndrome; Alcohols; Amygdaloid structure; Anatomy; Anxiety; Anxiety Disorders; Automobile Driving; Behavior; Behavior Control; Behavioral; Behavioral Mechanisms; Biological Availability; Biosensor; Brain; Calcium; Cell Nucleus; Cells; Corticotropin-Releasing Hormone; Data; Disease; Dose; Drug usage; E211; Electrophysiology (science); Estradiol; Estrogen Receptors; Estrogens; Estrus; Experimental Designs; Female; Fiber; Glutamates; Gonadal Steroid Hormones; Hormones; Image; In Situ Hybridization; Interneuron function; Lasers; Lead; Mass Spectrum Analysis; Measures; Membrane; Menstrual cycle; Neurons; Neuropeptides; Optics; Output; Periodicity; Peripheral; Pharmacology; Phenotype; Photometry; Play; Population; Prevention; RNA Interference; Recording of previous events; Research; Resolution; Risk; Risk Factors; Role; Signal Transduction; Slice; Source; Stress; Structure of terminal stria nuclei of preoptic region; Synapses; Technology; Time; Woman; Work; addiction; alcohol comorbidity; alcohol exposure; alcohol use disorder; binge drinking; drinking; drinking behavior; experimental study; in vivo; male; men; negative affect; neural circuit; neurophysiology; neuropsychiatric disorder; novel; novel therapeutic intervention; optogenetics; receptor; receptor binding; recruit; relating to nervous system; reproductive; response; sensor; sex; stress reactivity; stressor; synaptic function; tool; transmission process

Project Summary/Abstract Binge alcohol drinking and high stress reactivity are leading risk factors for anxiety and alcohol use disorders, and women are at twice the risk for co-expression of these diseases. The sex hormone estrogen has been implicated in playing a modulatory role in anxiety and alcohol/drug use and may be related to the telescoping of addiction observed in women by amplifying the positive and negative components of binge alcohol consumption and withdrawal. Further, alcohol consumption itself may be able to stimulate estrogen synthesis to promote drinking behavior, suggesting that estrogen signaling may be an important mechanism in addiction for both males and females. However, the mechanisms by which estrogen regulates neuronal function to control these behaviors is unknown. We hypothesize that estrogen signals at membrane-bound receptors located at discrete synaptic nodes of limbic circuitry to modulate their control of behavior, and that this mechanism is prominent at baseline in females but becomes more important in males across alcohol drinking exposure. In the proposed work, we examine the locus and mechanism of endogenous estrogen signaling, its effect on circuit function and corresponding behavior, and alcohol-induced plasticity in estrogen modulation in both males and females.

项目摘要/摘要 酗酒和高度应激反应是焦虑和酒精使用障碍的主要风险因素， 而女性同时患有这些疾病的风险是女性的两倍。性激素雌激素一直是 在焦虑和酒精/药物使用中起调节作用，并可能与伸缩有关 通过放大酗酒的积极和消极成分在女性中观察到的成瘾 消费和撤退。此外，饮酒本身可能会刺激雌激素的合成。 促进饮酒行为，提示雌激素信号可能是成瘾的重要机制 无论是男性还是女性。然而，雌激素调节神经功能的机制 控制这些行为是未知的。我们假设雌激素信号在膜结合受体上 位于边缘回路的离散突触节点，调节它们对行为的控制，这 这种机制在女性的基线上很突出，但在男性饮酒后变得更加重要 曝光。在拟议的工作中，我们研究了内源性雌激素信号转导的位置和机制，其 酒精对雌性大鼠神经回路功能和行为的影响及酒精诱导的可塑性 无论是雄性还是雌性。