Impaired adipogenesis in insulin resistance: pilot clinical and in-vitro studies
Impaired adipogenesis in insulin resistance: pilot clinical and in-vitro studies
批准号:
7359827
负责人:
RICHARD E PRATLEY
金额:
$22.19万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-03-15 至 2010-02-28
关键词:
AccountingAdipocytesAdipose tissueAffectAgeAgonistAmericanBiopsyBlood VesselsBody CompositionBody Weight decreasedBuffersCCL2 geneCaliberCellsChoristomaClinicalClinical ResearchComplexConditionDEXADNADevelopmentDiabetes MellitusDifferentiation and GrowthEconomicsEndocannabinoidsEndocrineEnergy IntakeEnergy MetabolismEpidemicEthnic groupExerciseExposure toFacilities and Administrative CostsFailureFatty AcidsFatty acid glycerol estersFeedbackFeeding behaviorsFunctional disorderGenderGene ExpressionGlucose ClampGrowthHumanHypertrophyImmunityImpairmentIn VitroIndividualInflammatoryInsulinInsulin ResistanceInterleukin-6LabelLeadLeptinLinkLipodystrophyLiverLongitudinal StudiesMeasurementMeasuresMetabolicMetabolismMorbidity - disease rateNon-Insulin-Dependent Diabetes MellitusNonesterified Fatty AcidsNutritional statusObesityOrganOverweightPathway interactionsPharmaceutical PreparationsPhenotypePhysiologicalPilot ProjectsPopulationPreventionPublic HealthPuncture biopsyRateRecruitment ActivityRegulationRelative (related person)ResearchReverse Transcriptase Polymerase Chain ReactionRiskRisk FactorsRoleRole playing therapySecondary toSignal TransductionSignaling MoleculeSiteSkeletal MuscleStaining methodStainsStandards of Weights and MeasuresStratificationSystemTechniquesTestingThinkingTimeTissue SampleTissuesTitleTriglyceridesVisceraladipocyte differentiationadipokinesadiponectinautocrinebaseconceptcytokinediabetes riskimprovedin vivoinsightinsulin sensitivitylipid biosynthesismacrophagemortalitynon-diabeticnovel strategiesnutritionoral glucose toleranceparacrinepreventresearch studyresponsesizestable isotopesubcutaneoustheoriestherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Obesity is the strongest acquired risk factor for type 2 diabetes (T2DM), however the precise mechanisms linking these conditions are not known. The central hypothesis of this pilot project is that a failure to differentiate new subcutaneous adipocytes in response to over nutrition leads to the development of hypertrophic adipocytes that manifest alterations in the expression and secretion of adipokines. These changes, including increases in pro-inflammatory cytokines and decreases in adiponectin, provide feedback through both paracrine and endocrine axes to limit further fat accretion, at the expense of worsening metabolic dysfunction. Four specific aims will be tested in obese insulin resistant subjects (OIR, N = 15) and obese insulin sensitive subjects (OIS, N = 15) to determine: 1) whether preadipocyte proliferation or differentiation is impaired in vivo in OIR vs. OIS, 2) whether preadipocyte proliferation or differentiation is impaired in vitro in OIR vs. OIS, 3) whether impairments in preadipocyte proliferation are associated with hypertrophic adipocytes and a pro-inflammatory phenotype and 4) the role of the endocannabinoid system in regulating preadipocyte proliferation and differentiation. Subjects will undergo measurement of body composition (DEXA), oral glucose tolerance, insulin sensitivity (glucose clamp) and percutaneous needle biopsies of subcutaneous fat. Adipogenesis will be measured in vivo by determining turnover rates of adipocytes and stromal-vascular cells using 2H2O to label DNA. Proliferation and differentiation of preadipocytes in vitro will be measured in primary cultures derived from each subject. Adipocyte size, expression of pro-inflammatory cytokines and the expression of genes involved in the endocannabinoid pathway will be compared in OIR and OIS subjects and related to measures of proliferation and differentiation. Understanding the mechanisms whereby obesity leads to T2DM may improve risk stratification and may suggest novel approaches to prevent and treat T2DM and its complications.
Project Narrative: Obesity is a potent risk factor for developing type 2 diabetes. This study tests whether differences in the growth rates of fat cells are related to the risk for diabetes in obese individuals. Results from this study could suggest new prevention / treatment strategies.
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科研奖励(0)
会议论文
NATURAL HISTORY STUDY OF THE DEVELOPMENT OF TYPE I DIABETES
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批准号:8166968
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项目类别:
-
资助金额:$0.77万
-
财政年份:2010
-
负责人:RICHARD E PRATLEY
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依托单位:
CLINICAL TRIAL: EFFECTS OF PIOGLITAZONE ON INCRETIN AXIS IN PTS W TYPE 2 DIABETE
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批准号:8166982
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项目类别:
-
资助金额:$15.32万
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财政年份:2010
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负责人:RICHARD E PRATLEY
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依托单位:
IMPAIRED ADIPOGENESIS IN INSULIN RESISTANCE: PILOT CLINICAL AMP IN VITRO STUDIES
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批准号:8166981
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项目类别:
-
资助金额:$16.35万
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财政年份:2010
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负责人:RICHARD E PRATLEY
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依托单位:
CLINICAL TRIAL: EFFECTS OF SITAGLIPTIN ON BONE TURNOVER IN PTS WITH TYPE 2 DIABE
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批准号:8166983
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项目类别:
-
资助金额:$7.1万
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财政年份:2010
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负责人:RICHARD E PRATLEY
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依托单位:
CLINICAL TRIAL: EFFECTS OF PIOGLITAZONE ON INCRETIN AXIS IN PTS W TYPE 2 DIABETE
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批准号:7952123
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项目类别:
-
资助金额:$3.08万
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财政年份:2009
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负责人:RICHARD E PRATLEY
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依托单位:
WEIGHT LOSS & ASTHMA
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批准号:7959624
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项目类别:
-
资助金额:$32.39万
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财政年份:2009
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负责人:RICHARD E PRATLEY
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依托单位:
IMPAIRED ADIPOGENESIS IN INSULIN RESISTANCE
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批准号:7952122
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项目类别:
-
资助金额:$2.42万
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财政年份:2009
-
负责人:RICHARD E PRATLEY
-
依托单位:
NATURAL HISTORY STUDY OF THE DEVELOPMENT OF TYPE I DIABETES
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批准号:7952105
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项目类别:
-
资助金额:$1.03万
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财政年份:2009
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负责人:RICHARD E PRATLEY
-
依托单位:
Impaired adipogenesis in insulin resistance: pilot clinical and in-vitro studies
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批准号:8001118
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项目类别:
-
资助金额:$3.9万
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财政年份:2009
-
负责人:RICHARD E PRATLEY
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依托单位:
NON-INVASIVE GLUCOSE MONITORING USING EXHALED BREATH CONDENSATE
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批准号:7952116
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项目类别:
-
资助金额:$1.03万
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财政年份:2009
-
负责人:RICHARD E PRATLEY
-
依托单位:
CLINICAL TRIAL: EFFECTS OF SITAGLIPTIN ON BONE TURNOVER IN PTS WITH TYPE 2 DIABE
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批准号:7952124
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项目类别:
-
资助金额:$2.15万
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财政年份:2009
-
负责人:RICHARD E PRATLEY
-
依托单位:
Impaired adipogenesis in insulin resistance: pilot clinical and in-vitro studies
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批准号:7586169
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项目类别:
-
资助金额:$18.81万
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财政年份:2008
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负责人:RICHARD E PRATLEY
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依托单位:
WEIGHT LOSS & ASTHMA
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批准号:7720878
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项目类别:
-
资助金额:$31.85万
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财政年份:2008
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负责人:RICHARD E PRATLEY
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依托单位:
WEIGHT LOSS & ASTHMA
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批准号:7609702
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项目类别:
-
资助金额:$29.7万
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财政年份:2007
-
负责人:RICHARD E PRATLEY
-
依托单位:
NATURAL HISTORY STUDY OF THE DEVELOPMENT OF TYPE I DIABETES
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批准号:7605814
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项目类别:
-
资助金额:$1.3万
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财政年份:2007
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负责人:RICHARD E PRATLEY
-
依托单位:
ADIPOSE TISSUE MCP-1 AND MIF: ROLE IN OBESITY-ASSOCIATED INFLAMMATION
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批准号:7605813
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项目类别:
-
资助金额:$4.81万
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财政年份:2007
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负责人:RICHARD E PRATLEY
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依托单位:
ADIPOSE TISSUE MCP-1 AND MIF: RELATION TO GLUCOSE TOLERANCE, INSULIN ACTION
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批准号:7378601
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项目类别:
-
资助金额:$0.32万
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财政年份:2006
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负责人:RICHARD E PRATLEY
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依托单位:
EFFECTS OF LAF237 ON MAX INSULIN SECRETION IN PTS WITH TYPE 2 DIABETES
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批准号:7378594
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项目类别:
-
资助金额:$3.94万
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财政年份:2006
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负责人:RICHARD E PRATLEY
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依托单位:
WEIGHT LOSS & ASTHMA
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批准号:7381080
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项目类别:
-
资助金额:$33.0万
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财政年份:2006
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负责人:RICHARD E PRATLEY
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依托单位:
EFFECTS OF LAF237 ON MAX INSULIN SECRETION IN PTS WITH TYPE 2 DIABETES
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批准号:7206973
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项目类别:
-
资助金额:$1.66万
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财政年份:2005
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负责人:RICHARD E PRATLEY
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依托单位:
国内基金
海外基金
支链氨基酸代谢紊乱调控“Adipocytes - Macrophages Crosstalk”诱发2型糖尿病脂肪组织功能和结构障碍的作用及机制
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批准号:81970721
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项目类别:面上项目
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资助金额:55.0万元
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批准年份:2019
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负责人:陶凌
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依托单位: