Mechanisms of Dietary Restriction mediated by Creb-binding Protein in Mice
Mechanisms of Dietary Restriction mediated by Creb-binding Protein in Mice
批准号:
8628018
负责人:
Cesar Llogari Moreno
金额:
$3.1万
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:
2012-03-02 至 2016-03-01
关键词:
AblationAcuteAddressAffectAfferent NeuronsAgeAge-MonthsAgingAlzheimer&aposs DiseaseAnimal ModelBinding ProteinsBiological AssayCREB-binding proteinCaenorhabditis elegansCardiovascular DiseasesCharacteristicsChronicComplexConsensusCorticosteroneCustomDevelopmentDiabetes MellitusDietDiseaseEmbryoEnergy IntakeFutureGene ExpressionGene Expression ProfileGene TargetingGenesGenetic MarkersGlucoseHourHumanHypothalamic structureLaboratoriesLifeLiquid ChromatographyLiverLongevityMalignant NeoplasmsMalnutritionMass Spectrum AnalysisMediatingMetabolicMolecularMonitorMouse StrainsMusNeuronsNeurosecretory SystemsNutritionalOne-Step dentin bonding systemPathologyPhysiologicalPhysiologyPropertyProtein BindingProteinsProtocols documentationReportingReverse Transcriptase Polymerase Chain ReactionRoleSensoryTissuesTranscriptional RegulationTranslatingWorkage relatedbasechromatin immunoprecipitationclinical applicationclinically relevantdeprivationdetection of nutrientdietary restrictionhuman CREBBP proteininterestjuvenile animalmortalitynoveloxidationpostnatalpreventprotective effectprotein expressionresponsesenescencetransgenic model of alzheimer disease
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英文摘要
DESCRIPTION (provided by applicant): Dietary Restriction is a manipulation that reduces caloric intake and subsequently extends lifespan and protects against age-related diseases in animal models. The protective spectrum of this manipulation includes prevalent diseases such as cancer, diabetes, cardiovascular disease, and Alzheimer's disease. It is therefore imperative to understand the underlying metabolic mechanisms of this paradigm. CBP is a transcriptional regulator that has been implicated in both the protective and age-extending properties of dietary restriction. Of importance, evidence suggests CBP exerts these effects by mainly acting in the hypothalamus, a sensory center of metabolic state. The purpose of these studies is to study the role of CBP and the metabolic profile of dietary restriction with an emphasis in hypothalamic responses. To carry these studies we will develop mice that lack CBP post-natally. These mice will then be subjected to either acute (8 weeks) or chronic (18 month) dietary restriction. Following this period, relevant tissues will be collected and analyzed for metabolic profiles. Specifically, we will 1) monitor metabolic gene expression changes using custom qPCR plates; 2) observe metabolic gene targeting changes of CBP using Chromatin immunoprecipitation followed by RT-PCR; 3) quantify metabolite usage by liquid chromatography followed by mass spectrometry. These assays will be performed in both chronic and acute groups. Additionally, we will assess the chronically dietary restricted mice using genetic markers of senescence, which will help discern if the protective effects are attributable to CBP expression in the hypothalamus. Other neuroendocrine responses will be monitored for all groups further characterizing the physiology of this dietary manipulation. Upon completion of this project it is expected that a clearer metabolic and transcriptional profile of dietary restriction will be established, taking us one step closer to the development of clinical applications.
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Mechanisms of Dietary Restriction mediated by Creb-binding Protein in Mice
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批准号:8319814
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项目类别:
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资助金额:$3.42万
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财政年份:2012
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负责人:Cesar Llogari Moreno
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依托单位:
Mechanisms of Dietary Restriction mediated by Creb-binding Protein in Mice
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批准号:8795150
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项目类别:
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资助金额:$0.77万
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财政年份:2012
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负责人:Cesar Llogari Moreno
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依托单位:
Mechanisms of Dietary Restriction mediated by Creb-binding Protein in Mice
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批准号:8445691
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项目类别:
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资助金额:$3.3万
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财政年份:2012
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负责人:Cesar Llogari Moreno
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依托单位:
海外基金