Role of SGLTs in Glucose Homeostasis and Tissue Metabolism
Role of SGLTs in Glucose Homeostasis and Tissue Metabolism
批准号:
8055502
负责人:
ERNEST M WRIGHT
金额:
$32.07万
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 2013-03-31
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 metabolismglucose transportglucose uptakehuman subjecthuman subject protectionhydroxyl groupinhibitor/antagonistinterestneglectneuronal cell bodyradiotracersugarsymportertumoruptake
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。长期过量摄入葡萄糖会导致体重增加,增加患糖尿病的风险。血糖被控制在较窄的范围内,以平衡能量的供给和需求,而控制血糖的一个主要因素是将多余的葡萄糖转运到肌肉和脂肪中储存。葡萄糖转运蛋白分为GLUTs和SGLTs两类,但对健康和疾病中葡萄糖转运的研究主要集中在GLUTs上。SGLTs基因在全身表达,表明这些转运体在将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SGLTs(钠/葡萄糖共转运体)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。本建议的具体目的是:1)。设计适合SGLTs的PET探针;2). [F-18]标记sglt探针的合成和3)。使用PET成像与这些新的葡萄糖探针来检查sglt在动物和人类受试者中的生理作用。SGLT1和SGLT2在葡萄糖摄取中的作用将通过纳入SGLTs基因突变患者、葡萄糖-半乳糖-吸收不良患者和家族性肾性糖尿患者来测试。同时,我们将使用2-FDG进行研究,以确定GLUTs和SGLTs在感兴趣器官葡萄糖摄取中的相对重要性。研究还将在现有的啮齿动物以及SGLT和GLUT敲除小鼠上使用SGLT和GLUT探针进行,以补充对患者的研究。显然,要充分了解健康和疾病中的能量平衡,就需要确定细胞摄取葡萄糖的所有途径。本项目旨在测试钠葡萄糖共转运体在葡萄糖稳态中被严重忽视的作用。相关声明:本研究旨在确定钠/葡萄糖共转运体(SGLTs)在葡萄糖稳态中的作用。sglt在全身表达,但直到现在,它们在肠肾外的作用一直被忽视。该研究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/葡萄糖共转运体(SGLTs)在葡萄糖稳态中的作用。sglt在全身表达,但直到现在,它们在肠道和肾脏外的作用一直被忽视。该研究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.
期刊论文(3)
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Role of SGLTs in Glucose Homeostasis and Tissue Metabolism
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批准号:7576872
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项目类别:
-
资助金额:$32.73万
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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:
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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:
-
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:
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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:
-
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:
-
资助金额:$19.18万
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财政年份:1992
-
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