AMYGDALA GLUCOCORTICOID RECEPTOR FUNCTION IN STRESS
AMYGDALA GLUCOCORTICOID RECEPTOR FUNCTION IN STRESS
批准号:
7578658
负责人:
Louis J Muglia
金额:
$39.67万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-02-13 至 2013-12-31
关键词:
Adrenal GlandsAmygdaloid structureAnxietyAnxiety DisordersBehaviorBehavioralBiologicalBipolar DisorderCell NucleusCircadian RhythmsCorticosteroneCorticotropinCorticotropin-Releasing HormoneCorticotropin-Releasing Hormone ReceptorsDevelopmentDiseaseEndocrineEnkephalinsFeedbackFrightFunctional disorderGene ExpressionGlucocorticoid ReceptorGlucocorticoidsHealthHumanHyperactive behaviorHypothalamic structureInfectionKnock-outLearningMajor Depressive DisorderMeasuresMediatingMemoryMental disordersMineralocorticoid ReceptorModelingMotorMusNeuronsNeurosecretory SystemsNodalPerformancePituitary GlandProcessProductionProsencephalonPublic HealthRegulationReporterResearchRoleRosaSchizophreniaSignal TransductionSiteStressStructureSubfamily lentivirinaeSwimmingSystemTail SuspensionTarget PopulationsTestingUnited StatesVasopressinsbiological adaptation to stressbrain pathwayconditioned fearconditioningdepressiongenetic manipulationhypothalamic-pituitary-adrenal axisindexinginsightnovelnovel therapeutic interventionpublic health relevancereceptor functionresponse
中文摘要
描述(申请人提供):我们研究的长期目标是确定下丘脑-垂体-肾上腺(HPA)轴和通过糖皮质激素受体(GR)的信号在正常应激反应和精神疾病中的生物学作用。HPA轴功能障碍是一种内分泌应激反应,与严重抑郁症、双相情感障碍、焦虑症和精神分裂症的易感性特别相关。杏仁核是整合神经内分泌和行为应激反应的关键前脑结构,在人类抑郁和HPA高分泌状态下会发生杏仁核过度活动。此外,杏仁核中央核(CEA)的糖皮质激素作用被认为参与了一个正反馈环路的调节,该环路增强了HPA轴的活动、焦虑,以及情绪显著记忆的获得或表达。这些过程发生的机制仍然知之甚少,部分原因是对CEA功能的遗传操纵没有足够的具体手段。我们将验证CEA中的糖皮质激素受体通过控制促肾上腺皮质激素释放激素(CRH)基因在该部位的表达来调节行为和肾上腺应激反应的假设。我们的具体目标将寻求建立一个新的CEA特异性GR基因敲除系统,确定CEA中GR功能丧失对HPA轴调节和行为的表型后果,并确定CRH表达的变化是否通过CRH的区域替代而导致行为和肾上腺轴的改变。最终,我们的努力旨在加深对与精神疾病相关的神经内分泌回路的了解,并促进这些主要健康疾病的新治疗方法的开发。公共卫生相关性据估计,美国有4000万人患有精神障碍,造成了巨大的社会和公共卫生负担。我们计划的关于糖皮质激素受体功能在杏仁核中作用的研究结果,有望为调节对压力的反应以及精神疾病的发生和治疗的大脑通路提供新的见解。
英文摘要
DESCRIPTION (provided by applicant): The long-term objective of our studies is to define the biological role of the hypothalamic-pituitary-adrenal (HPA) axis and signaling through the glucocorticoid receptor (GR) in both the normal stress response and in psychiatric disease. Dysfunction HPA axis, the endocrine stress response, is specifically associated with vulnerability to major depression, bipolar disorder, anxiety disorders, and schizophrenia. The amygdala is a key nodal forebrain structure for integrating neuroendocrine and behavioral responses to stress, and amygdalar hyperactivity occurs in human depression and HPA hypersecretory states. Moreover, glucocorticoid action in the central nucleus of the amygdala (CeA) has been implicated in mediating a positive feedback loop that potentiates activity of the HPA axis, anxiety, and acquisition or expression of emotionally salient memory. The mechanisms by which these processes occur remain poorly understood, in part because of inadequately specific means for genetic manipulation of CeA function. We will test the hypotheses that glucocorticoid receptors in the CeA regulate behavioral and adrenal responses to stress by control of corticotropin-releasing hormone (CRH) gene expression at this site. Our specific aims will seek to establish a novel CeA-specific GR knockout system, determine the phenotypic consequences of loss of GR function in the CeA for HPA axis regulation and behavior, and determine whether alteration in CRH expression contributes to the resulting behavioral and adrenal axis changes by regional replacement of CRH. Ultimately, our efforts aim to further the understanding of neuroendocrine circuits relevant for psychiatric diseases and promote development of novel therapeutic approaches for these major health disorders. PUBLIC HEALTH RELEVANCE An estimated 40 million people in the United States suffer from a psychiatric disorder, generating an enormous societal and public health burden. The results of our planned studies on the role of glucocorticoid receptor function in the amygdala hold promise for new insights into brain pathways regulating the responses to stress and the genesis and treatment of mental illness.
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