Chronic coronary occlusion, exercise training and NO
Chronic coronary occlusion, exercise training and NO
批准号:
7651232
负责人:
CRISTINE L HEAPS
金额:
$35.32万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-07-01 至 2011-07-31
关键词:
AddressAgonistAnimalsAreaArteriesAttentionAttenuatedBindingBiochemicalBiological AvailabilityBlood VesselsBlood flowCalciumCardiacCardiovascular DiseasesCessation of lifeChronicCoronaryCoronary ArteriosclerosisCoronary OcclusionsCoronary arteryDataDeveloped CountriesDeveloping CountriesDistalEndothelial CellsEndotheliumEnzymesEventExerciseExhibitsFamily suidaeFunctional disorderGene ExpressionGoalsHealthHeartHydrogen PeroxideImageMediatingModelingMolecularMyocardial IschemiaMyocardial perfusionMyocardiumMyosin ATPaseNitric OxideOxidesPathogenesisPatientsPerfusionPhosphorylationPhysical activityProductionProteinsReactive Oxygen SpeciesRelaxationResearchResearch PersonnelRho-associated kinaseRoleSuperoxide DismutaseSuperoxidesTestingTrainingTraining ProgramsVasodilationVasodilator AgentsVasomotorarterioleartery occlusioncatalaseconstrictionextracellularimprovedimproved functioningmRNA Expressionmyosin phosphataseprogramsrelease of sequestered calcium ion into cytoplasmrestorationrhosedentarytherapeutic target
中文摘要
描述(由申请方提供):内皮功能障碍是冠状动脉疾病发病机制的主要因素,也是改善缺血性心脏病心肌灌注的潜在治疗靶点。有规律的运动在改善内皮功能障碍中的作用已经越来越受到研究人员和临床医生的关注,作为一种机制,可以大大改善冠状动脉疾病患者的心肌灌注和功能。然而,运动训练逆转内皮功能障碍的机制还没有很好的定义。本申请中提出的研究的总体目标是确定负责运动训练诱导的慢性闭塞心脏的侧支依赖性冠状动脉和小动脉内皮功能改善的特定细胞/分子机制。我们的中心假设是,运动训练通过增强一氧化氮的生物利用度恢复冠心病患者的内皮依赖性血管舒张。具体而言,具体目标1将确定运动训练对负责侧支依赖性冠状动脉和小动脉中内皮源性一氧化氮产生的细胞和分子机制的影响;具体目标2将确定运动训练对活性氧在侧支依赖性冠状动脉和小动脉中激动剂介导的一氧化氮依赖性舒张中的作用的影响;具体目标3将确定运动训练对闭塞心脏的侧支依赖性冠状动脉中一氧化氮生物利用度和Rho激酶活性的相互作用的影响。为了解决这些问题,我们将确定运动训练对慢性冠状动脉闭塞的猪模型血管内皮功能的影响。这些研究将检查功能性血管对内皮依赖性血管扩张剂的反应性,有助于内皮功能的酶和因子的蛋白质和mRNA表达,以及内皮细胞内游离钙浓度和一氧化氮的产生。相关性:冠状动脉疾病造成超过50%的心血管疾病相关死亡,这是全世界发达国家的突出健康问题。本申请中提出的研究将确定运动/身体活动改善冠状动脉功能的适应性,从而增加疾病患者心脏受损区域的血流量。
英文摘要
DESCRIPTION (provided by applicant): Endothelial dysfunction is a major contributor to the pathogenesis of coronary artery disease and a potential therapeutic target to improve myocardial perfusion in ischemic heart disease. The role of regular exercise in the improvement of endothelial dysfunction has garnered increasing attention from both researchers and clinicians as a mechanism by which myocardial perfusion and function can be substantially improved in patients with coronary artery disease. However, the mechanisms by which exercise training reverses endothelium dysfunction are not well defined. The overall goal of the research proposed in this application is to define the specific cellular/molecular mechanisms responsible for exercise training-induced improvements in endothelium function in collateral-dependent coronary arteries and arterioles of chronically occluded hearts. Our central hypothesis is that exercise training restores endothelium-dependent vasodilatation in coronary artery disease via enhanced nitric oxide bioavailability. Specifically, Specific Aim 1 will determine the effects of exercise training on cellular and molecular mechanisms responsible for endothelium-derived nitric oxide production in collateral-dependent coronary arteries and arterioles; Specific Aim 2 will determine the effects of exercise training on the role of reactive oxygen species in agonist-mediated, nitric oxide-dependent relaxation in collateral-dependent coronary arteries and arterioles; Specific Aim 3 will determine the effects of exercise training on the interaction of nitric oxide bioavailability and Rho-kinase activity in collateral-dependent coronary arteries of occluded hearts. To address these issues, we will determine the effects of exercise training on vascular endothelial function in the well-established porcine model of chronic coronary artery occlusion. These studies will examine functional vasomotor reactivity to endotheliumdependent vasodilators, protein and mRNA expression of enzymes and factors that contribute to endothelium function, and intracellular free calcium concentration and nitric oxide production in endothelial cells. Relevance: Coronary artery disease produces more than 50% of cardiovascular disease-related deaths, the preeminant health problem of developed countries worldwide. The research proposed in this application will determine the adaptations by which exercise/physical activity improves the function of the coronary arteries and thereby increases blood flow to compromised areas of the heart in diseased patients.
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专著(0)
科研奖励(0)
会议论文
Exercise training-enhanced reactive oxygen species as protective mechanisms in the coronary microcirculation
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批准号:9914125
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项目类别:
-
资助金额:$60.33万
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财政年份:2018
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负责人:CRISTINE L HEAPS
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依托单位:
Adenosine-activation of voltage-dependent K+ currents
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批准号:6584215
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项目类别:
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资助金额:$4.81万
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财政年份:2003
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负责人:CRISTINE L HEAPS
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依托单位:
Adenosine-activation of voltage-dependent K+ currents
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批准号:6693853
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项目类别:
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资助金额:$4.68万
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财政年份:2002
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负责人:CRISTINE L HEAPS
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依托单位:
Chronic coronary occlusion, exercise training and NO
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批准号:7267078
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项目类别:
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资助金额:$35.32万
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财政年份:2000
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负责人:CRISTINE L HEAPS
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依托单位:
Chronic coronary occlusion, exercise training and NO
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批准号:7880939
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项目类别:
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资助金额:$35.32万
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财政年份:2000
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负责人:CRISTINE L HEAPS
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依托单位:
Chronic coronary occlusion, exercise training and NO
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批准号:7099840
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项目类别:
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资助金额:$36.38万
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财政年份:2000
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负责人:CRISTINE L HEAPS
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依托单位:
Chronic coronary occlusion, exercise training and NO
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批准号:7468466
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项目类别:
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资助金额:$35.32万
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财政年份:2000
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负责人:CRISTINE L HEAPS
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依托单位:
国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
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批准号:32000851
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项目类别:青年科学基金项目
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资助金额:24.0万元
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批准年份:2020
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负责人:乔安娜
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依托单位: