Direct measurement of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) enzyme levels in obesity using a novel positron emissiontomography radioligand
Direct measurement of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) enzyme levels in obesity using a novel positron emissiontomography radioligand
批准号:
10888092
负责人:
Jason Bini
金额:
$7.69万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-07-01 至 2024-12-31
关键词:
11-beta-Hydroxysteroid DehydrogenasesAdipocytesAdipose tissueAffectAnimalsAreaAwardBindingBiological AssayBody WeightBody Weight decreasedBrainClinical EndocrinologyCommunitiesCortisoneCushing SyndromeDataDepositionDoseEducationEndocrinologyEnzymesFunctional disorderGluconeogenesisGlucoseGlycosylated hemoglobin AGoalsHealthHepatic TissueHumanHydrocortisoneHydroxysteroid DehydrogenasesHyperglycemiaImaging TechniquesImpairmentIn VitroIndividualInsulinInsulin ResistanceK-Series Research Career ProgramsKineticsKnock-outKnowledgeLearningLiverMeasurementMeasuresMentorsMentorshipMetabolicMetabolic DiseasesMetabolic syndromeMetabolismMethodsModelingMusMuscleMyoblastsNADH dehydrogenase (ubiquinone)ObesityPancreasPhenotypePhysiologyPlasmaPopulationPositronPositron-Emission TomographyPre-Clinical ModelPrevalencePublishingQuality of lifeRat StrainsRattusReportingResearchResearch DesignResearch MethodologyResearch PersonnelResistanceRodentRoleSkeletal MuscleSocietiesSteroidsStructureThinnessTissuesTrainingTraining ProgramsUnited StatesVisceralWeightWeight Gainadipocyte differentiationage relatedcareerdesigndietary controleffective therapyexperiencefasting glucosehepatic veinhuman subjectimage translationimaging studyimprovedin vivoinnovationinsulin secretioninsulin sensitivitynon-diabeticnovelobese personpharmacologicphase II trialprogramsradioligandresponseskillsstable isotopesteroid hormonesubcutaneoustooltreatment strategyuptakeurinarywhole body imaging
中文摘要
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY
The prevalence of obesity in the United States population is over 30%, predisposing a large portion of
the population to metabolic diseases. Cortisol, a steroid hormone, is of critical importance in obesity, as it is
responsible for stimulating gluconeogenesis in the liver and promoting adipocyte differentiation and maturation.
Cortisol is activated from cortisone by the intracellular enzyme 11β-hydroxysteroid dehydrogenase type 1 (11β-
HSD1).
The overall aim of this proposal is to examine whole-body 11β-HSD1 enzyme distribution levels during
normal physiology and in response to weight gain, insulin resistance and obesity using the novel 18F-FMOZAT
PET radioligand in rodent and human populations. Whole-body PET imaging can provide a direct measure of
the distribution of 11β-HSD1 allowing comparison to conventional methods using urinary or plasma cortisol
metabolites in both lean and non-diabetic obese human individuals. We propose an obese Zucker fatty (ZF) rat
model that will allow direct in vivo PET imaging of 11β-HSD1 levels in various tissues during progression to
obesity (Aim 1). We also propose to examine 11β-HSD1 levels in lean and non-diabetic obese individuals with
18F-FMOZAT PET to assess tissue-specific variability in whole-body 11β-HSD1 enzyme levels, and compare
these novel direct measures with current methods using urinary metabolites of cortisol (Aim 2).
The program of research and training described in this K01 Mentored Career Development Award
application will provide the candidate with the requisite skills and experience to become an independent
investigator in the field of endocrinology (obesity). Under the mentorship of field-leading experts in
endocrinology and obesity, and PET imaging, the proposed aims will afford training in the design, conduct and
analysis of novel translational PET imaging techniques to be uniquely applied to metabolic syndromes in
endocrinology, such as obesity. In pursuit of this goal, the candidate proposes to undertake further training in
three primary areas 1) build expertise in clinical endocrinology (obesity) research 2) receive education in the
pathophysiology of obesity and 3) continue to enhance my knowledge of cutting-edge whole-body PET
imaging.
The opportunities afforded by this award would enable the candidate to embark on a comprehensive,
structured 5-year program of training and research designed to develop an expertise in innovative
endocrinology research methods toward a career as an independent investigator.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
Noninvasive Quantitative PET Imaging in Humans of the Pancreatic Beta-Cell Mass Biomarkers VMAT2 and Dopamine D2/D3 Receptors In Vivo.
人体胰腺 β 细胞群生物标志物 VMAT2 和多巴胺 D2/D3 受体的无创定量 PET 成像。
DOI:
10.1007/978-1-0716-2807-2_4
发表时间:
2023
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
作者:
[Bini,Jason, Carson,RichardE, Cline,GaryW]
通讯作者:
Cline,GaryW
Direct measurement of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) enzyme levels in obesity using a novel positron emissiontomography radioligand
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批准号:10426245
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项目类别:
-
资助金额:$15.38万
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财政年份:2019
-
负责人:Jason Bini
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依托单位:
Direct measurement of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) enzyme levels in obesity using a novel positron emissiontomography radioligand
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批准号:10197114
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项目类别:
-
资助金额:$15.38万
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财政年份:2019
-
负责人:Jason Bini
-
依托单位:
Direct measurement of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) enzyme levels in obesity using a novel positron emissiontomography radioligand
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批准号:10641851
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项目类别:
-
资助金额:$15.38万
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财政年份:2019
-
负责人:Jason Bini
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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
-
负责人:陶凌
-
依托单位: