Adiponectin signaling in mood regulation
Adiponectin signaling in mood regulation
批准号:
8687748
负责人:
Xin-Yun Lu
金额:
$37.08万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-07-01 至 2018-04-30
关键词:
AblationAdipose tissueAdultAffectAnimal ModelAntidepressive AgentsBehaviorBehavioralBehavioral MechanismsBiologicalBrainBrain regionChronicClinicalClinical ResearchDevelopmentDiabetes MellitusDiabetic mouseDietFatty acid glycerol estersFunctional disorderGlycogen Synthase Kinase 3GoalsHippocampus (Brain)HormonesIn VitroIndividualInjection of therapeutic agentLeadMedialMediatingMedicalMental DepressionMental disordersMetabolic DiseasesModelingMolecularMood DisordersMusNeuronsNon-Insulin-Dependent Diabetes MellitusObesityPathogenesisPatternPhenotypePhosphorylation SitePhosphotransferasesPlasmaPlayPopulationPredispositionPrefrontal CortexPrevalencePropertyProtein IsoformsRiskRisk FactorsRoleSeveritiesSignal PathwaySignal TransductionStagingStressSymptomsTestingTherapeuticTimeWeightadiponectinadult neurogenesisbaseclinically significantdepressive symptomsdiabeticin vivoinsightkinase inhibitormood regulationneurogenesisneuromechanismnew therapeutic targetnon-diabeticnovelpreclinical studypublic health relevancereceptorresponsesevere mental illnesssocialtherapeutic targettreatment strategy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Depression is a severe and common mental disorder and often coexists with metabolic disorders such as diabetes. Therefore, the identification and characterization of therapeutic targets that are potentially beneficial for the treatment of both depression and diabetes would be of great clinical significance. Adiponectin, a hormone secreted almost exclusively by white adipose tissue, is well recognized as an anti-diabetic adipokine. We have demonstrated that adiponectin insufficiency increases susceptibility to depression-like symptoms. By contrast, administration of exogenous adiponectin to the brain produces antidepressant-like effects in normal weight mice and in obese diabetic mice, suggesting a critical role for adiponectin in depressive-like behaviors. The goal of this project i to define the molecular and cellular mechanisms of adiponectin actions on depressive behaviors. Adiponectin receptors, AdipoR1 and AidpoR2, display distinct expression patterns in the hippocampus and medial prefrontal cortex (mPFC), two key brain regions implicated in depression and the therapeutic actions of antidepressants. Central injection of adiponectin induces neuronal activation and stimulates p38MAPK, an upstream activator of the inhibitory phosphorylation site of GSK-3b. Moreover, adiponectin has been shown to stimulate hippocampal neurogenesis in vitro. Based upon these findings, we hypothesize that adiponectin regulates depressive behaviors in a brain-region, receptor-specific manner through distinct molecular and cellular mechanisms. We propose to determine the region-specific roles of AdipoR1 and AdipoR2 in the development of depressive-like behaviors and in mediating the antidepressant-like effect of adiponectin, identify the signaling cascade that mediates actions of adiponectin on depressive-like behaviors, and determine whether neurogenesis contributes to the behavioral effect of adiponectin. These studies will provide novel insights into adipokine regulation of mood-related behaviors and lead to the development of novel therapies for depression.
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