Role of SGLTs in Glucose Homeostasis and Tissue Metabolism
Role of SGLTs in Glucose Homeostasis and Tissue Metabolism
批准号:
7576872
负责人:
ERNEST M WRIGHT
金额:
$32.73万
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:
2008-04-01 至 2012-03-31
关键词:
AnimalsBiological AssayBlood GlucoseCancer DetectionCellsControl AnimalDefectDiabetes MellitusDiagnostic Neoplasm StagingDiseaseDrug Delivery SystemsEnsureEquilibriumEuglycemic ClampingExerciseFatty acid glycerol estersGalactoseGeneric DrugsGenesGlucoseGlucose ClampGlucose TransporterGoalsHealthHomeostasisHumanHuman bodyImageIn VitroInheritedInsulinIntakeIntestinal AbsorptionIntestinesKidneyKineticsKnockout MiceLabelLifeMalabsorption SyndromesMediatingMedicalMetabolismMethodsMolecularMonitorMuscleMutationNormal CellObesityOocytesOrganPathway interactionsPatientsPhasePhlorhizinPhysiologicalPhysiologyPlayPositron-Emission TomographyProtein IsoformsRadiationRadiometryRadiopharmaceuticalsRelative (related person)ResearchResearch DesignRiskRodentRoleSLC2A1 geneSodiumSpecificityStagingSubstrate SpecificityTestingTissuesToxicologyTracerWeight GainXenopus laevisbaseblood glucose regulationdesignenergy balanceglucose transportglucose uptakehuman subjecthuman subject protectionhydroxyl groupinhibitor/antagonistinterestneglectneuronal cell bodypublic health relevanceradiotracersugarsymportertumoruptake
中文摘要
描述(由申请人提供):葡萄糖是身体的主要燃料,必须保持足够的供应以支持器官和组织的正常功能。从长远来看,过量的葡萄糖摄入会导致体重增加,增加患糖尿病的风险。血糖保持在狭窄的范围内以平衡能量的供应和需求,并且这种控制的主要因素是将过量的葡萄糖运输到肌肉和脂肪中以进行储存。有两类葡萄糖转运蛋白,GLUT和SGLT,但对健康和疾病中葡萄糖转运的研究主要集中在GLUT上。SGLTs基因在整个身体中表达,表明这些转运蛋白在葡萄糖转运到细胞中的作用比预期的要大。目的是利用正电子发射断层扫描(PET)阐明SGLT(钠/葡萄糖协同转运蛋白)在人体葡萄糖稳态和代谢生理学中的重要性。葡萄糖探针2-FDG和PET的引入彻底改变了人体器官和组织中葡萄糖摄取和代谢的研究。在临床上,这对癌症的检测、分期和治疗产生了巨大的影响。然而,2-FDG不是SGLT的底物,这限制了我们对正常细胞和肿瘤中葡萄糖转运和代谢的理解。本提案的具体目标是:1)。设计专用于SGLT的PET探头; 2).合成[F-18]标记的SGLT探针;和3)。使用这些新的葡萄糖探针进行PET成像,以检查SGLT在动物和人类受试者中的生理作用。将通过纳入SGLT基因突变患者、葡萄糖-半乳糖-吸收不良和家族性肾性糖尿患者来检测SGLT 1和SGLT 2在葡萄糖摄取中的作用。同时,我们将使用2-FDG进行研究,以确定GLUT和SGLT在感兴趣器官的葡萄糖摄取中的相对重要性。还将使用SGLT和GLUT探针对现有啮齿动物和SGLT和GLUT敲除小鼠进行研究,以补充对患者的研究。显然,要充分理解健康和疾病中的能量平衡,就需要确定葡萄糖摄取到细胞中的所有途径。本研究旨在检测钠/葡萄糖协同转运蛋白(SGLTs)在葡萄糖稳态中的作用。相关声明:本研究旨在确定钠/葡萄糖协同转运蛋白(SGLTs)在葡萄糖稳态中的作用。SGLT在整个身体中表达,但迄今为止,它们在肠肾外的作用一直被忽视。这项研究的结果可能为糖尿病和肥胖症提供新的药物靶点,并开发新的PET示踪剂来检测和分期癌症。 公共卫生相关性:本研究旨在确定钠/葡萄糖协同转运蛋白(SGLT)在葡萄糖稳态中的作用。 SGLT在整个身体中表达,但迄今为止,它们在肠道和肾脏外的作用一直被忽视。 这项研究的结果可能为糖尿病和肥胖症提供新的药物靶点,并开发新的PET示踪剂来检测和分期癌症。
英文摘要
DESCRIPTION (provided by applicant): Glucose is the primary fuel for the body and adequate supplies must be maintained to support the normal function of organs and tissues. Over the long term an excess of glucose intake results in weight gain and added risk for developing diabetes. Blood glucose is held within narrow limits to balance the supply and demand for energy and a major factor in this control is the transport of excess glucose into muscle and fat for storage. There are two classes of glucose transporters, GLUTs and SGLTs, but research on glucose transport in health and disease has focused on the GLUTs. SGLTs genes are expressed throughout the body indicating a larger role of these transporters in the transport of glucose into cells than anticipated. The goal is to elucidate the importance of SGLTs (sodium/glucose cotransporters) in the human physiology of glucose homeostasis and metabolism using Positron Emission Tomography (PET). The Introduction of the glucose probe 2-FDG and PET has revolutionized studies of glucose uptake and metabolism in organs and tissues in the human body. Clinically this has had an enormous impact in cancer detection, staging and therapy. However, 2-FDG is not a substrate for SGLTs and this has limited our understanding of glucose transport and metabolism in normal cells and tumors. The specific aims of this proposal are to: 1). Design PET probes specific for SGLTs; 2). Synthesize [F-18]-labeled probes for SGLTs; and 3). Use PET imaging with these new glucose probes to examine the physiological role of SGLTs in animal and human subjects. The role of SGLT1 and SGLT2 in glucose uptakes will be tested by including in the study patients with mutations in the SGLTs genes, patients with Glucose- Galactose-Malabsorption and Familial Renal Glucosuria. In parallel, we will conduct studies using 2-FDG to determine the relative importance of GLUTs and SGLTs in glucose uptakes in organs of interest. Studies will also be carried out with both SGLT and GLUT probes on available rodents and SGLT and GLUT knockout mice to compliment the studies on patients. Clearly, identification of all the pathways for glucose uptake into cells is required for a full understanding of energy balance in health and disease. This project is designed to test the sorely neglected role of sodium glucose cotransporters in glucose homeostasis.Relevance Statement: This study of designed to determine the role of sodium/glucose cotransporters (SGLTs) in glucose homeostasis. SGLTs are expressed throughout the body but until now their role outside the intestinal kidneys has been neglected. The results of this study may provide new drug targets for diabetes and obesity and develop new PET tracers to detect and stage cancer. PUBLIC HEALTH RELEVANCE: This study is designed to determine the role of sodium/glucose cotransporters (SGLTs) in glucose homeostasis. SGLTs are expressed throughout the body but until now their role outside the intestine and kidneys has been neglected. The results of this study may provide new drug targets for diabetes and obesity and develop new PET tracers to detect and stage cancer.
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Role of SGLTs in Glucose Homeostasis and Tissue Metabolism
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批准号:8055502
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项目类别:
-
资助金额:$32.07万
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财政年份:2008
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负责人:ERNEST M WRIGHT
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依托单位:
MOLECULAR CLONING OF BLOOD/BRAIN BARRIER NUTRIENT TRANSPORTERS
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批准号:6112291
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项目类别:
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资助金额:$0.0万
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财政年份:1998
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负责人:ERNEST M WRIGHT
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依托单位:
MOLECULAR CLONING OF BLOOD/BRAIN BARRIER NUTRIENT TRANSPORTERS
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批准号:6217918
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项目类别:
-
资助金额:$16.89万
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财政年份:1998
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负责人:ERNEST M WRIGHT
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依托单位:
MOLECULAR CLONING OF BLOOD-BRAIN BARRIER NUTRIENT TRANSPORTERS
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批准号:6243624
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项目类别:
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资助金额:$17.18万
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财政年份:1997
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE/GALACTOSE MALABSORPTION
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批准号:2143891
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项目类别:
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资助金额:$20.43万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE/GALACTOSE MALABSORPTION
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批准号:2143892
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项目类别:
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资助金额:$5.96万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE/GALACTOSE MALABSORPTION
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批准号:2143894
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项目类别:
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资助金额:$1.19万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
MOLECULAR ARCHITECTURE OF THE NA/GLUCOSE COTRANSPORTER
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批准号:2143912
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项目类别:
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资助金额:$21.64万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE GALACTOSE MALABSORPTION
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批准号:6380708
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项目类别:
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资助金额:$28.1万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
MOLECULAR ARCHITECTURE OF THE NA+/GLUCOSE COTRANSPORTER
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批准号:6177002
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项目类别:
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资助金额:$21.15万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
MOLECULAR ARCHITECTURE OF THE NA+/GLUCOSE COTRANSPORTER
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批准号:2693164
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项目类别:
-
资助金额:$19.81万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE-GALACTOSE MALABSORPTION
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批准号:3246112
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项目类别:
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资助金额:$7.4万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
Molecular Architecture of the Na+/Glucose Cotransporter
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批准号:6897465
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项目类别:
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资助金额:$25.16万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE/GALACTOSE MALABSORPTION
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批准号:2143893
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项目类别:
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资助金额:$21.25万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE-GALACTOSE MALABSORPTION
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批准号:3246111
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项目类别:
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资助金额:$19.18万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE GALACTOSE MALABSORPTION
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批准号:6176997
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项目类别:
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资助金额:$27.41万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE GALACTOSE MALABSORPTION
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批准号:2905469
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项目类别:
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资助金额:$26.65万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
FAMILIAL GLUCOSE GALACTOSE MALABSORPTION
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批准号:2016478
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项目类别:
-
资助金额:$24.93万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
MOLECULAR ARCHITECTURE OF THE NA/GLUCOSE COTRANSPORTER
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批准号:3246131
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项目类别:
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资助金额:$20.01万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
MOLECULAR ARCHITECTURE OF THE NA+/GLUCOSE COTRANSPORTER
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批准号:6380710
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项目类别:
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资助金额:$21.78万
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财政年份:1992
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负责人:ERNEST M WRIGHT
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依托单位:
海外基金