Brain Apolipoprotein AIV, Food Intake and Obesity
Brain Apolipoprotein AIV, Food Intake and Obesity
批准号:
7169243
负责人:
Min Liu
金额:
$24.11万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-04-01 至 2009-01-31
关键词:
AddressAdipose tissueAnimal ModelAnimalsApolipoproteins AAppetite DepressantsAppetitive BehaviorAreaBehavioralBiochemistryBloodBlood - brain barrier anatomyBody WeightBrainCarbohydratesCategoriesCellsChronicConsumptionCountryDataDevelopmentDietDietary FatsEatingEnergy MetabolismEnvironmentEquilibriumEtiologyFacultyFatty acid glycerol estersFeeding behaviorsGastrointestinal tract structureGene ExpressionGoalsHealthHomeostasisHumanHypothalamic structureImpairmentIncidenceIndividualIntestinesInvestigationKnockout MiceKnowledgeLaboratoriesLeadLipidsMalignant NeoplasmsMessenger RNAMethodsMolecularNeuraxisNeuronsNeuropeptidesNon-Insulin-Dependent Diabetes MellitusNumbersObesityOutcomes ResearchPathway interactionsPeptidesPeripheralPersonal SatisfactionPhysiologicalPositioning AttributePrevention approachPreventivePrincipal InvestigatorProteinsPurposeRangeRattusRegulationRelative (related person)ResearchResistanceResource SharingRiskRisk FactorsRoleSatiationSignal TransductionSocietiesSourceSucroseSystemTechniquesTestingTherapeuticTherapeutic InterventionUniversitiesWorkapolipoprotein A-IVbasefeedinghypertensive heart diseaseinnovationmembermortalitynovelobesity treatmentprogramsresearch studyresponsesize
中文摘要
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英文摘要
Apolipoprotein AIV (apo AIV) is a circulating signal released from intestinal cells in response to lipid feeding,
and it contributes to the anorectic effect of a lipid meal. We have demonstrated that apo AIV is also
synthesized in the hypothalamus, and that hypothalamic apo AIV gene expression is regulated
physiologically. Our long-range goal is to understand the role of hypothalamic apo AIV in the development
of obesity and how it can be modulated for preventive and therapeutic purposes. The objective of this
application is to evaluate three hypotheses. 1) When hypothalamic apo AIV function is reduced, meal size is
chronically increased and obesity develops. Obese animals will, therefore, have lower hypothalamic apo
AIV levels and/or lower responsivity of hypothalamic apo AIV to dietary lipids relative to lean animals. 2)
Peripheral apo AIV contributes to the central action of apo AIV after crossing the blood-brain barrier (BBB).
Therefore, impaired transport across the BBB may result in reduced hypothalamic apo AIV levels and action
in obese animals. 3) Hypothalamic apo AIV interacts with other regulatory neuropeptides to exert its
physiological function. These hypotheses will be evaluated with the following three specific aims: 1) To
determine hypothalamic apo AIV gene expression and protein levels and the responsivity of hypothalamic
apo AIV to dietary lipids in several strains of obese and lean animals. We will further determine the
response to chronic high-fat feeding in apo AIV knockout mice. 2) To characterize the transport of apo AIV
from blood into the central nervous system (CNS) and to assess the areas in the brain that are activated by
apo AIV administered either centrally or intravenously. 3) To determine the interaction of apo AIV with other
regulatory peptides within the hypothalamus. The proposed work is innovative because it addresses
important unanswered questions. In addition, the proposed research takes advantage of the availability of
experimental methods and several unique animal models. Finally, the outcomes of the research will be
significant because it is expected that these studies will contribute to broader understanding of the role of
apo AIV in the regulation of energy homeostasis. This new knowledge may lead to novel targets for
preventive and therapeutic interventions that will be particularly important to the growing numbers of obese
persons in this country.
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海外基金