Neural regulation of protein ingestion
Neural regulation of protein ingestion
批准号:
7785633
负责人:
Christopher D Morrison
金额:
$33.3万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-06-01 至 2015-05-31
关键词:
5&apos-AMP-activated protein kinaseAdolescenceAdolescentAmino AcidsAnimalsAreaBiologicalBrainBranched-Chain Amino AcidsCellsDataDietDietary ProteinsEatingEnergy IntakeEquilibriumFeeding behaviorsFoundationsGene ExpressionGenetic ModelsGoalsGrowthHyperphagiaHypothalamic structureIn VitroIncidenceIngestionIntakeInterventionLeadLeucineLifeMacronutrients NutritionMediatingMetabolismModelingNeuronsNeuropeptide GeneNeuropeptidesObesityProteinsPublicationsRegulationRelative (related person)Set proteinSignal PathwaySignal TransductionSignaling MoleculeStructure of nucleus infundibularis hypothalamiSystemTestingThird ventricle structureVariantWorkbasebrain metabolismenergy balanceexperiencefeedingin vivomTOR proteinmeetingsmind controlmouse modelneuroregulationnovel strategiespublic health relevancerapid growthresearch studyresponse
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A number of observations support the existence of regulatory systems which assess endogenous protein/amino acid demand and alter food intake to meet this demand. Settings of negative protein balance lead to significant increases in food intake, resulting in excess energy intake and increased body adiposity as the animal attempts to meet the demand for protein. Thus regulatory systems governing protein intake are sufficient to override systems governing energy intake. Yet little is known about the mechanisms contributing to the regulation of protein intake or their relationship to energy balance and obesity. The long term goal of this project is to define the neuronal systems regulating food intake in response to varied protein balance. Results of recent studies indicate that amino acids, and specifically the branched-chain amino acid leucine, act locally in the hypothalamus to inhibit food intake and the expression of the orexigenic neuropeptides Npy and Agrp. At least two signaling pathways appear to mediate this response. One involves the intracellular signaling molecules mTOR (mammalian target of rapamycin) and AMP-activated protein kinase (AMPK); the second involves the local brain metabolism of leucine. The current project will 1) Test the hypothesis that reduced amino acid signaling within specific areas of the hypothalamus contributes to the hyperphagia induced by negative protein balance, and 2) Test the hypothesis that mTOR signaling, AMPK signaling, and/or branched-chain amino acid metabolism mediate the effect of amino acids on food intake and neuropeptide gene expression. Completion of these studies will dramatically increase our understanding of macronutrient composition and its impact on food intake and could lay the foundation for new interventions to control or reverse obesity.
PUBLIC HEALTH RELEVANCE: The current project seeks to clarify the biological basis whereby the brain controls feeding behavior in response to variations in protein balance. This work is especially important considering that protein balance takes priority over energy balance, and thus tapping into this regulatory system will reveal novel approaches to regulate food intake and treat obesity. Protein intake is robustly regulated relative to other macronutrients, yet very little is known about the mechanisms by which the brain senses and regulates protein intake. Considering that this regulatory system is particularly important in periods of rapid growth and high protein demand and that many adolescents consume low quality diets, mechanisms regulating protein intake and their interaction with energy intake may have direct relevance to adolescent obesity.
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科研奖励(0)
会议论文
Preclinical
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批准号:10569511
-
项目类别:
-
资助金额:$40.49万
-
财政年份:2020
-
负责人:Christopher D Morrison
-
依托单位:
FGF21-dependent mechanisms driving changes in energy expenditure during dietary protein restriction
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批准号:10359751
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项目类别:
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资助金额:$37.0万
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财政年份:2020
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负责人:Christopher D Morrison
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依托单位:
Neural circuits coordinating protein intake: Role of FGF21
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批准号:10263297
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项目类别:
-
资助金额:$33.3万
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财政年份:2020
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负责人:Christopher D Morrison
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依托单位:
Preclinical
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批准号:10333352
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项目类别:
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资助金额:$31.29万
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财政年份:2020
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负责人:Christopher D Morrison
-
依托单位:
FGF21-dependent mechanisms driving changes in energy expenditure during dietary protein restriction
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批准号:10578837
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项目类别:
-
资助金额:$37.0万
-
财政年份:2020
-
负责人:Christopher D Morrison
-
依托单位:
FGF21-dependent mechanisms driving changes in energy expenditure during dietary protein restriction
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批准号:10161777
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项目类别:
-
资助金额:$37.0万
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财政年份:2020
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负责人:Christopher D Morrison
-
依托单位:
Neural circuits coordinating protein intake: Role of FGF21
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批准号:10662472
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项目类别:
-
资助金额:$33.3万
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财政年份:2020
-
负责人:Christopher D Morrison
-
依托单位:
Neural circuits coordinating protein intake: Role of FGF21
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批准号:10449404
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项目类别:
-
资助金额:$33.3万
-
财政年份:2020
-
负责人:Christopher D Morrison
-
依托单位:
FGF21-dependent mechanisms driving changes in energy expenditure during dietary protein restriction
-
批准号:9973291
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项目类别:
-
资助金额:$37.0万
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财政年份:2020
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负责人:Christopher D Morrison
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依托单位:
Sable Systems Promethion for Mouse Metabolic Analysis
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批准号:9281302
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项目类别:
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资助金额:$62.58万
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财政年份:2017
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负责人:Christopher D Morrison
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依托单位:
FGF21 is an endocrine signal of protein restriction
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批准号:9388340
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项目类别:
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资助金额:$33.3万
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财政年份:2015
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负责人:Christopher D Morrison
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依托单位:
FGF21 is an endocrine signal of protein restriction
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批准号:9274081
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项目类别:
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资助金额:$3.45万
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财政年份:2015
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负责人:Christopher D Morrison
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依托单位:
LOUISIANA COBRE: P4: MECHANISMS OF AGING-INDUCED LEPTIN RESISTANCE AND OBESITY
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批准号:8167952
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项目类别:
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资助金额:$20.58万
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财政年份:2010
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负责人:Christopher D Morrison
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依托单位:
Neural regulation of protein ingestion
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批准号:8049740
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项目类别:
-
资助金额:$28.52万
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财政年份:2010
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负责人:Christopher D Morrison
-
依托单位:
Neural regulation of protein ingestion
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批准号:8664366
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项目类别:
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资助金额:$27.49万
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财政年份:2010
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负责人:Christopher D Morrison
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依托单位:
Neural regulation of protein ingestion
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批准号:8468686
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项目类别:
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资助金额:$26.54万
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财政年份:2010
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负责人:Christopher D Morrison
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依托单位:
Neural regulation of protein ingestion
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批准号:8280397
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项目类别:
-
资助金额:$27.52万
-
财政年份:2010
-
负责人:Christopher D Morrison
-
依托单位:
LOUISIANA COBRE: P4: MECHANISMS OF AGING-INDUCED LEPTIN RESISTANCE AND OBESITY
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批准号:7959987
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项目类别:
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资助金额:$23.41万
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财政年份:2009
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负责人:Christopher D Morrison
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依托单位:
LOUISIANA COBRE: P4: MECHANISMS OF AGING-INDUCED LEPTIN RESISTANCE AND OBESITY
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批准号:7720514
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项目类别:
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资助金额:$21.13万
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财政年份:2008
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负责人:Christopher D Morrison
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依托单位:
LOUISIANA COBRE: P4: MECHANISMS OF AGING-INDUCED LEPTIN RESISTANCE AND OBESITY
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批准号:7610784
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项目类别:
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资助金额:$20.96万
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财政年份:2007
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负责人:Christopher D Morrison
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依托单位:
海外基金