Microcirculation in Health and Disease
健康与疾病中的微循环
基本信息
- 批准号:7808044
- 负责人:
- 金额:$ 37万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-05-01 至 2013-02-28
- 项目状态:已结题
- 来源:
- 关键词:AcuteAnimal ModelAnimalsArachidonic AcidsAttenuatedBiochemicalBlood GlucoseBlood VesselsBlood flowBody WeightCardiovascular DiseasesCardiovascular systemChronicClinical TrialsDataDiseaseEpoprostenolExerciseGlucoseGoalsHealthHumanHyperemiaHyperglycemiaHyperlipidemiaHypertensionIn VitroInsulinInsulin ResistanceLaboratoriesLinkLipidsMediatingMetabolicMetabolismMicrocirculationModelingMuscleNon-Insulin-Dependent Diabetes MellitusObesityOxidative StressPartner in relationshipPatientsPersonsPhysiologicalPotassium ChannelProstaglandin H2Prostaglandins IPublishingReactive Oxygen SpeciesReceptor ActivationReportingRisk FactorsSkeletal MuscleTechniquesTestingThromboxane ReceptorThromboxanesTissuesTrainingUnited StatesUnited States National Institutes of HealthVasoconstrictor AgentsVasodilationWeight maintenance regimenWorkZucker Ratsarteriolebaseblood glucose regulationimprovedin vivoinsightmuscle metabolismpreventprogramspublic health relevancereceptorresearch studyresponsetempolvasoconstriction
项目摘要
DESCRIPTION (provided by applicant): The long-term goal of our laboratory is to define the physiological mechanisms linking muscle blood flow to the metabolic state of the tissue. In response to exercise, skeletal muscle blood flow increases dramatically through a functional vasodilation of the arterioles. We have demonstrated that arachidonic acid metabolites are important in the control of muscle blood flow. The studies in the current proposal will extend these studies and determine the mechanisms by which chronic exercise improves functional vasodilatory in obesity. Obesity is increasing at an alarming rate in the United States and is a major risk factor for a variety of cardiovascular diseases. NIH has initiated clinical trials to determine if exercise training improves cardiovascular health in persons who have both Type 2 diabetes and hypertension, conditions that are prevalent in obesity. Obese humans have an impaired ability to increase muscle blood flow in response to exercise, and the mechanisms underlying this abnormal increase in blood flow (functional hyperemia) are unclear. An impaired functional hyperemia could potentially prevent the obese patient from adequate exercise, a therapy known to improve glucose, lipid and weight control. Therefore, a better understanding of the mechanisms underlying improved functional hyperemia by chronic exercise training in obesity is important. Our recent work has demonstrated that, in obesity, there is an altered arachidonic acid metabolism, resulting in an impaired blood flow response to acute exercise. We have also demonstrated that chronic exercise training improves functional vasodilatory responses in an animal model of obesity. Based on our published and preliminary data the overall goal of this proposal is to test the central hypothesis that chronic exercise training will improve functional vasodilation through improvements in PGI2 vasodilatory responses and decreases in thromboxane vasoconstrictor responses. We propose that these alterations in arachidonic acid metabolism are due to hyperglycemic/hyperlipidemic induced increases in reactive oxygen species. The proposed studies will utilize in vivo and in vitro microcirculatory techniques to provide new and important insights into mechanisms by which chronic exercise training improves functional vasodilatory responses in obesity. PUBLIC HEALTH RELEVANCE: Obesity is increasing at an alarming rate in the United States and is a major risk factor for a variety of cardiovascular diseases. Obese humans have an impaired ability to increase muscle blood flow in response to exercise, which could prevent the obese patient from adequate exercise, a therapy known to improve the elevated glucose, lipids and body weight associated with obesity. Therefore, a better understanding of the mechanisms by which chronic exercise training improves muscle blood flow in obesity is important.
描述(由申请人提供):我们实验室的长期目标是确定将肌肉血流与组织代谢状态联系起来的生理机制。为了响应运动,骨骼肌血流量通过小动脉的功能性血管舒张而急剧增加。我们已经证明花生四烯酸代谢物对于控制肌肉血流很重要。当前提案中的研究将扩展这些研究,并确定长期运动改善肥胖症功能性血管舒张的机制。在美国,肥胖正在以惊人的速度增长,并且是多种心血管疾病的主要危险因素。美国国立卫生研究院 (NIH) 已启动临床试验,以确定运动训练是否可以改善患有 2 型糖尿病和高血压(肥胖症中常见的疾病)的患者的心血管健康。肥胖的人因运动而增加肌肉血流量的能力受损,并且这种血流量异常增加(功能性充血)的机制尚不清楚。功能性充血受损可能会妨碍肥胖患者进行充分的运动,而运动是一种已知可以改善血糖、血脂和体重控制的疗法。因此,更好地了解肥胖症患者通过长期运动训练改善功能性充血的机制非常重要。我们最近的工作表明,在肥胖症中,花生四烯酸代谢发生改变,导致对剧烈运动的血流反应受损。我们还证明,长期运动训练可以改善肥胖动物模型的功能性血管舒张反应。根据我们已发表的初步数据,该提案的总体目标是检验以下中心假设:长期运动训练将通过改善 PGI2 血管舒张反应和减少血栓素血管收缩反应来改善功能性血管舒张。我们认为花生四烯酸代谢的这些改变是由于高血糖/高血脂引起的活性氧的增加。拟议的研究将利用体内和体外微循环技术,为长期运动训练改善肥胖症功能性血管舒张反应的机制提供新的重要见解。公共健康相关性:肥胖在美国正以惊人的速度增长,并且是多种心血管疾病的主要危险因素。肥胖者因运动而增加肌肉血流量的能力受损,这可能会妨碍肥胖患者进行充分的运动,而运动是一种已知可以改善与肥胖相关的血糖、血脂和体重升高的疗法。因此,更好地了解长期运动训练改善肥胖患者肌肉血流量的机制非常重要。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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ROBERT L HESTER其他文献
ROBERT L HESTER的其他文献
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{{ truncateString('ROBERT L HESTER', 18)}}的其他基金
COMPUTER SERVICES, ELECTRONICS, AND INSTRUMENTATION
计算机服务、电子产品和仪器仪表
- 批准号:
8208834 - 财政年份:2010
- 资助金额:
$ 37万 - 项目类别:
COMPUTER SERVICES, ELECTRONICS, AND INSTRUMENTATION
计算机服务、电子产品和仪器仪表
- 批准号:
8147937 - 财政年份:2009
- 资助金额:
$ 37万 - 项目类别:
Computer Services, Electronics and Instrumentation
计算机服务、电子和仪器仪表
- 批准号:
7596576 - 财政年份:2008
- 资助金额:
$ 37万 - 项目类别:
Core-Computer Sciences, Electronics, and Instrumentation Core
核心-计算机科学、电子和仪器仪表核心
- 批准号:
7062944 - 财政年份:2004
- 资助金额:
$ 37万 - 项目类别:
Core-Computer Sciences, Electronics, and Instrumentation Core
核心-计算机科学、电子和仪器仪表核心
- 批准号:
6781630 - 财政年份:2003
- 资助金额:
$ 37万 - 项目类别:
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