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Lipid peroxidation-induced chemical modifications of insulin signaling proteins

Lipid peroxidation-induced chemical modifications of insulin signaling proteins
脂质过氧化诱导的胰岛素信号蛋白化学修饰
批准号:
8119876
负责人:
Krisztian Stadler
金额:
$24.9万
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:
2010-09-15 至 2013-08-31
关键词:
4 hydroxynonenalAcuteAftercareAldehyde ReductaseAldehydesAnimal ModelAnimalsAtherosclerosisAttenuatedCardiovascular systemCause of DeathCellsChemicalsChronicComplications of Diabetes MellitusDataDetectionDevelopmentDiabetes MellitusDiabetic NephropathyDietDiseaseElectron Spin Resonance SpectroscopyEnzymesFatty acid glycerol estersFree Radical FormationFree RadicalsGlucoseHealthHeart failureHumanHydroxyl RadicalHyperglycemiaImageImpairmentIn SituIncidenceInflammationInflammatoryInjection of therapeutic agentInsulinInsulin ReceptorInsulin ResistanceInsulin Signaling PathwayInsulin-Dependent Diabetes MellitusKidneyLaboratoriesLeadLipid PeroxidationLipid PeroxidesLipidsLiverMediatingMetabolic DiseasesMethodologyMethodsMitochondriaModelingModificationMusNADPNeuropathyNitrogenNon-Insulin-Dependent Diabetes MellitusObesityOxidantsOxidative StressOxygenParticipantPathogenesisPathway interactionsPatientsPatternPeroxonitritePhosphorylationPreventionProcessProductionProteinsRattusReceptor SignalingRetinal DiseasesRodentRoleSchemeSignal PathwaySignal TransductionSignaling ProteinSiteSkeletal MuscleSourceSpin TrappingStagingStreptozocinStressTechniquesTestingTherapeutic AgentsTimeTissuesWorkWorld Health OrganizationXanthinesZucker Ratsbaseclinically relevantdiabeticdiabetic patientdiabetic ratglycationhuman NOS2A proteinimprovedin vivoinhibitor/antagonistinsightinsulin receptor substrate 1 proteininsulin sensitivityinsulin signalinginsulin tolerancemacrophagenitrationnoveloral glucose toleranceoverexpressionoxidationpolyolpublic health relevanceresearch studyrestorationrosiglitazonetype I and type II diabetestype I diabetic

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Lipid peroxidation-induced chemical modifications of insulin signaling proteins
Lipid peroxidation-induced chemical modifications of insulin signaling proteins
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