Imaging Biomarkers for Evaluating Mitochondrial Function in Diabetes
Imaging Biomarkers for Evaluating Mitochondrial Function in Diabetes
批准号:
8111516
负责人:
GEOFFREY DAVID CLARKE
金额:
$16.83万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-01 至 2014-08-31
关键词:
Adenosine TriphosphateAffectAreaBackBiochemicalBiochemical ProcessBiochemistryBiological AssayBiological MarkersBiologyBloodBlood GlucoseBlood flowCharacteristicsChemicalsClinicalClinical MedicineClinical ResearchComplementComputer SimulationConcentration measurementCreatineCreatine KinaseDataDeoxyglucoseDevelopmentDiabetes MellitusEnergy-Generating ResourcesExerciseFamilyFatty acid glycerol estersFluorineFunctional disorderFutureGenerationsGlucoseGlycogenGoalsHumanHydrogenHyperglycemiaImageImaging TechniquesImaging technologyInsulinInsulin ResistanceKineticsKnowledgeLaboratory ResearchLeadLiverMagnetic Resonance ImagingMeasurementMeasuresMedical ImagingMetabolicMetabolismMethodsMitochondriaModelingMolecularMolecular ModelsMuscleMyocardiumNMR SpectroscopyNon-Insulin-Dependent Diabetes MellitusNonesterified Fatty AcidsObesityOutcomeOxygenPathogenesisPatientsPerfusionPhosphocreatinePhosphorusPhysicsPhysiologicalPlasmaPositioning AttributePositron-Emission TomographyPrevalenceProcessProductionReactionReactive Oxygen SpeciesRecoveryResearchResearch PersonnelResearch TrainingResistanceRestSkeletal MuscleSyndromeTestingTissue SampleTissuesTrainingTransmission Electron MicroscopyWaterWorkcareerdensitydesigndiabeticdiabetic patientexperiencefatty acid oxidationfeedingglucose metabolismglucose uptakeimaging modalityimprovedin vivoinorganic phosphateinterestmagnetic fieldmagnetic resonance spectroscopic imagingminimally invasivemitochondrial dysfunctionmolecular modelingmuscle metabolismoxidationreaction rateresponseskillstherapy developmenttool
中文摘要
描述(由申请人提供):申请人以前的研究经验主要集中在研究医学成像的基础物理和技术进展,特别是MRI物理。由于候选人的家庭中糖尿病的患病率和疾病的增加,他对应用他的技术技能来研究2型糖尿病(T2DM)的发病机制产生了兴趣。本提案的总体目标是扩大候选人在代谢生物学和临床医学领域的培训和实践经验,使他能够利用成像方法研究胰岛素抵抗和糖尿病背景下线粒体功能障碍的过程。培训的重点如下。胰岛素是葡萄糖代谢的重要调节剂,通过刺激葡萄糖从血液中摄取并促进其作为糖原储存在肝脏和肌肉中,从而影响肝脏、肌肉和脂肪组织。当胰岛素水平正常时,葡萄糖摄取异常低是一种被称为胰岛素抵抗(IR)的情况。骨骼肌胰岛素抵抗增加在瘦型和肥胖型糖尿病患者中都很常见。糖尿病患者葡萄糖水平升高导致线粒体产生活性氧,这可能会损害线粒体产生足够胰岛素抵抗能量的能力。胰岛素抵抗在骨骼肌代谢中的作用是糖尿病研究的热点,研究人员正在努力建立一个整体的理论框架来理解这一过程。这种类型的计算机建模将受益于直接从活体组织中获得的细胞内代谢数据。无创成像技术可以测量一系列生理条件下的代谢过程,从而改进模型。这些数据将补充从切除组织样本中获得的更具侵入性的分析信息,包括透射电子显微镜和台式生化分析。磷-31核磁共振波谱可用于证明胰岛素抵抗受试者的代谢受损。然而,所使用的方法需要校准和优化,以提供高度准确的生理模型信息。此外,正电子发射断层扫描已广泛用于测量骨骼肌的葡萄糖利用和组织血流量。拟议项目的总体目标是开发这些成像方法来测量骨骼肌中作为重要代谢中介的各种化学物质的浓度,测量重要反应的进展速度,测量肌肉血流量和测量葡萄糖利用率,同时,血糖水平被严格控制,以开发和完善糖尿病患者骨骼肌中胰岛素抵抗的分子和生化机制的计算机模型。人们希望这些工具能够提高对糖尿病发病的理解,并开发出能够减轻与糖尿病相关的胰岛素抵抗状况的治疗方法。
英文摘要
DESCRIPTION (provided by applicant): The candidate's previous research experience has focused on studying the basic physics and technological advances of medical imaging, particularly MRI physics. Due to the increasing prevalence of diabetes and afflictions in the own candidate's family, he has become interested in applying his technical skills to investigate the pathogenesis of type 2 diabetes mellitus (T2DM). The overall goal of this proposal is to expand the candidate's training and practical experience in areas of metabolic biology and clinical medicine to position him for a research career using imaging methods to study the processes involved in mitochondrial dysfunction in the setting of insulin resistance and diabetes. The focus of this training is described below. Insulin is an important regulator of glucose metabolism that affects liver, muscle and fat tissue by stimulating glucose uptake from blood and promoting its storage as glycogen in liver and muscle. Abnormally low uptake of glucose, when there are normal insulin levels, is a condition known as insulin resistance (IR). Increased insulin resistance in skeletal muscle is common in both lean and obese diabetic subjects. The increased glucose levels in diabetes lead to production of reactive oxygen species in mitochondria, which probably impairs the ability of mitochondria to produce adequate energy in insulin resistance. The action of insulin resistance in skeletal muscle metabolism is of intense interest in diabetes research and investigators are working on an overall theoretical framework to understand the processes. This type of computer modeling would benefit from intracellular metabolic data acquired directly from the tissues of livings subjects. Noninvasive imaging technologies can measure metabolic processes under a range of physiological conditions, allowing refinement of the models. These data would supplement information obtained from more invasive analyses from excised tissue samples, including transmission electron microscopy and bench top biochemical assays. Phosphorus-31 nuclear magnetic resonance spectroscopy can be used to demonstrate impaired metabolism in subjects with insulin resistance. However the methods used need to be calibrated and optimized to supply highly accurate information for physiological models. Also, positron emission tomography has been used extensively to measure glucose utilization and tissue blood flow in skeletal muscle. The overall goals of the proposed project are to develop these imaging methods to measure the concentrations of various chemicals in skeletal muscle that are important intermediaries of metabolism, measure the rate at which important reactions progress, measure muscle blood flow and measure glucose utilization rate, while the blood glucose level is being strictly controlled in order to develop and refine computer models of molecular and biochemical mechanisms that contribute to insulin resistance in the skeletal muscle of diabetic patients. It is hoped that these tools will lead to improved understanding of the onset of diabetes and allow development of therapies that can alleviate the insulin resistant condition associated with diabetes.
PUBLIC HEALTH RELEVANCE: This research examines factors necessary for producing data on humans, noninvasively using magnetic resonance spectroscopic imaging (MRS) and positron emission tomography (PET). The information obtained will be used to evaluate mitochondrial function in patients with insulin resistance syndrome and diabetes. The project consists of a training regime that that is designed to increase the knowledge of contemporary biochemistry to a graduate level. This will be complemented by laboratory and clinical research training in the use of clinical measures of insulin resistance, PET imaging with oxygen-15-water and fluorine-18- deoxyglucose, assays of the metabolism of isolated mitochondria. The project includes a plan to develop, validate and employ both phosphorus-31 MRS imaging and PET imaging to evaluate the metabolic status of the mitochondria in patients and insulin resistant subjects in a minimally invasive manner.
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