Role of the lateral hypothalamic area in leptin action
Role of the lateral hypothalamic area in leptin action
批准号:
7540464
负责人:
Martin G Myers
金额:
$32.9万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-01-01 至 2012-12-31
关键词:
AccountingAdipose tissueAffectAnimalsAreaArousalBehaviorBehavioralBiological AssayBody WeightBrainCell NucleusDataDesire for foodDevelopmentDiabetes MellitusDietEnergy MetabolismEpidemicFoodGene ExpressionGene Expression RegulationGeneticHealthHealth Care CostsHomeostasisHormonesHumanHypothalamic structureIncentivesIncidenceIndividualLateral Hypothalamic AreaLeptinLife ExpectancyMediatingNeural PathwaysNeuronsNeurotensinObesityPathogenesisPhenotypePhysiologicalPhysiologyPlayPopulationRegulationRewardsRodentRoleSignal TransductionSiteStructure of nucleus infundibularis hypothalamiSystemTestingUnited StatesVentral Tegmental Areadefined contributiondesignenergy balancefeedinghedonichypocretininsightleptin receptormelanin-concentrating hormonemesolimbic systemmotivated behaviorneurophysiologynovelpreventpublic health emergencypublic health relevanceresponsetherapeutic targetventromedial hypothalamic nucleus
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The ongoing epidemic of obesity in the United States represents a public health emergency that remains unchecked and without specific therapy. To design specific treatments to prevent and treat obesity, we must first understand the mechanisms that regulate feeding and energy expenditure in order to identify potential therapeutic targets. In this proposal, entitled, Role of the lateral hypothalamic area in leptin action, we will analyze novel leptin-regulated neural pathways in the lateral hypothalamic area (LHA) that likely contribute to body energy homeostasis. We have defined the existence of a novel population of LRb-expressing, leptin-responsive LHA neurons that project locally as well as densely innervating the ventral tegmental area (VTA). We hypothesize that LRb-mediated signaling in the LHA is crucial to the regulation of the VTA and activity of the mesolimbic dopamine system, and thereby for the regulation of feeding and energy balance. We will thus study the regulation of LHA LRb neurons and their role in the regulation of physiology by leptin. We propose the following specific aims: 1. Understand the regulation of LHA LRb neurons. Analyze the regulation of gene expression and activity of LHA LRb neurons, and define the mechanisms by which leptin and other factors mediate this regulation. 2. Define the action of LHA LRb neurons on downstream neurons. Define the downstream target neurons of LHA LRb neurons and the role of LHA LRb neurons in the regulation of these downstream neurons, including the mesolimbic dopamine system. 3. Determine the function of LHA LRb neurons in physiologic leptin action. Examine the physiologic function of LHA LRb neurons by examining energy balance and behavior in animals following a variety of genetic and pharmacologic manipulations directed at these neurons. These studies will enable us to understand the mechanisms by which leptin regulates LHA function, and the mechanisms by which LHA LRb neurons interact with other areas of the CNS in order to contribute to the regulation of feeding and energy balance. This information will in turn lay the groundwork for understanding mechanisms by which LHA-driven feeding may be regulated, which is crucial as we seek to determine the pathogenesis of, and potential therapeutic targets for the ongoing epidemic of obesity. PUBLIC HEALTH RELEVANCE: The ongoing epidemic of obesity in the United States represents a public health emergency that remains unchecked and without specific therapy. To design specific treatments to prevent and treat obesity, we must first understand the mechanisms that regulate feeding and energy expenditure in order to identify potential therapeutic targets. In this proposal, we will analyze novel neural pathways in the brain that likely contribute to body energy homeostasis in order to define these mechanisms and the potential therapeutic targets that they represent.
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批准号:10263950
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资助金额:$41.97万
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财政年份:2019
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A Leptin-Regulated Brainstem Pathway That Controls Glucose and Energy Homeostasis
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批准号:8652155
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资助金额:$33.82万
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财政年份:2013
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A Leptin-Regulated Brainstem Pathway That Controls Glucose and Energy Homeostasis
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批准号:8786551
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资助金额:$33.82万
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财政年份:2013
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负责人:Martin G Myers
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依托单位:
Comprehensive Laboratory Animal Monitoring System for Core Facility
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批准号:7791669
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项目类别:
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资助金额:$17.87万
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财政年份:2010
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负责人:Martin G Myers
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依托单位:
Molecular mechanisms of leptin receptor/Jak2 action
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批准号:7998415
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项目类别:
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资助金额:$18.36万
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财政年份:2009
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负责人:Martin G Myers
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依托单位:
Role of the Lateral Hypothalamic Area in Leptin Action
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批准号:9223687
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项目类别:
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资助金额:$37.44万
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财政年份:2008
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负责人:Martin G Myers
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依托单位:
Role of the lateral hypothalamic area in leptin action
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批准号:8030417
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项目类别:
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资助金额:$32.24万
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财政年份:2008
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依托单位:
Role of the Lateral Hypothalamic Area in Leptin Action
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批准号:8720920
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资助金额:$37.44万
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依托单位:
Role of the Lateral Hypothalamic Area in Leptin Action
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批准号:8231461
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资助金额:$32.24万
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负责人:Martin G Myers
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依托单位:
Role of the Lateral Hypothalamic Area in Leptin Action
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批准号:7810340
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资助金额:$23.44万
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财政年份:2008
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负责人:Martin G Myers
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依托单位:
LEPTIN RECEPTOR PATHWAYS IN MAMMALIAN PHYSIOLOGY
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批准号:6381818
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项目类别:
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资助金额:$37.46万
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财政年份:2000
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负责人:Martin G Myers
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依托单位:
Mechanisms of Leptin Receptors Signal Attenuation
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批准号:7026944
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项目类别:
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资助金额:$32.27万
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财政年份:2000
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负责人:Martin G Myers
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依托单位:
Developmental mechanisms of leptin resistance
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批准号:7835492
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项目类别:
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资助金额:$54.07万
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财政年份:2000
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负责人:Martin G Myers
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依托单位:
Developmental mechanisms of leptin resistance
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批准号:7659882
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项目类别:
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资助金额:$53.44万
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财政年份:2000
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负责人:Martin G Myers
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依托单位:
LEPTIN RECEPTOR PATHWAYS IN MAMMALIAN PHYSIOLOGY
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批准号:6090865
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项目类别:
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资助金额:$36.61万
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财政年份:2000
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负责人:Martin G Myers
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依托单位:
LEPTIN RECEPTOR PATHWAYS IN MAMMALIAN PHYSIOLOGY
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项目类别:
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资助金额:$31.88万
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财政年份:2000
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负责人:Martin G Myers
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依托单位:
海外基金