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Physiological Consequences of Hypoxia and Lung Disease

Physiological Consequences of Hypoxia and Lung Disease
缺氧和肺部疾病的生理后果
批准号:
7451070
负责人:
PETER D WAGNER
金额:
$60.39万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-08-20 至 2009-06-30
关键词:
AblationAconitate HydrataseAddressAdultAffectAgeAgingAntioxidantsApoptosisAttenuatedBackBindingBinding ProteinsBiologicalBiological AssayBiopsy SpecimenBlood capillariesBlood flowBreathingBreedingCalcineurinCapillarityCardiacCellsChronicChronic Obstructive Airway DiseaseCollaborationsConditionConsensusDNADNA-Binding ProteinsDeferoxamineDiseaseElectric StimulationElectrophoretic Mobility Shift AssayElementsEngineeringEnvironmentExerciseFK506FiberFluorescent ProbesFunctional ImagingFutureGastrocnemius MuscleGene ActivationGenerationsGenetic TranscriptionGoalsHealthHourHumanHydrogen PeroxideHydroxyl RadicalHypoxemiaHypoxiaImageImmunosuppressive AgentsIn VitroInflammatoryInjection of therapeutic agentJUN geneKneeLegLengthLinkLiving WillsLocalizedLuciferasesLung diseasesMaintenanceMapsMeasurementMeasuresMessenger RNAMethodsMitochondriaMolecularMolecular BiologyMouse StrainsMusMuscleMuscle ContractionMuscle FibersNG-Nitroarginine Methyl EsterNeuronal PlasticityNeurophysiology - biologic functionNitric OxideOrganOxidantsOxygenPathway interactionsPatientsPhysiologicalPrincipal InvestigatorPromoter RegionsProteinsProtocols documentationRangeRateReactive Oxygen SpeciesReporterReporter GenesResearchRespiratory physiologyRestRoleSP1 geneSignal PathwaySignal TransductionSiteSite-Directed MutagenesisSkeletal MuscleSpin TrappingSteroidsStimulusStructureSuperoxide DismutaseSuperoxidesTestingTissuesTrainingTrans-ActivatorsTransactivationTranscription factor genesTranscriptional ActivationTransgenic MiceTransgenic OrganismsTransplantationVascular Endothelial Growth FactorsViralWeekWorkactivating transcription factoradeno-associated viral vectorage effectangiogenesisattenuationbasecapillarycaspase-3catalase-polyethylene glycolcaveolin 1cytokinein vivoinhibitor/antagonistinterestmorphometryphosphorescenceprogramspromoterrecombinaseresponsesizetooltranscription factor

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中文摘要
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英文摘要
The most important consequence of lung disease is hypoxemia resulting in impaired oxygen supply to the tissues, diminishing organ function. This research program continues its commitment to understanding the causes and effects of hypoxemia in health and disease. Three of the five projects address this at the level of the skeletal muscles. A fourth deals with cardiac consequences of hypoxia, and a fifth with neural plasticity in hypoxia. The same five project'leadersare proposed as in the current cycle (years 26-30), lending continuity to a productive program. However, experimental approaches have evolved to focus more onfundamental mechanisms of the hypoxic response. Yet there are also studies proposed to link these back to humans as a function of age and disease, making for an integrated approach to the problem of hypoxia. Project 1 (Wagner) focuses on the basic molecular mechanisms of muscle angiogenesis in response to hypoxia in health and disease; Project 2 (Mathieu-Costello) uses modern morphometric methods to assess regional myocardialOz availability and the impact of chronic hypoxia and aging on this; Project 3 (Richardson) examines the effects of aging on human muscle structure and function using integrative methods ranging from macroscopic imaging to molecular biological; Project 4 (Powell) addresses the effects of hypoxia on neural function involved in ventilatory control, integrating molecular and physiological tools; Project 5 (Hogan) investigates the role of Oaavailability on single muscle fiber function in vitro using a combination of imaging, functional, and molecular methods. The projects interact extensively,many formally asjoint efforts between project leaders with overlapping interests, and are supported by three cores (Tissue Imaging and Morphometry; Molecular Biology; Administration). Our collective goals are to better understand how Oatransport between the environment and the mitochondria of several key organs is regulated as a function of aging and disease, and in turn, how hypoxia itself modulates its own availability and thereby affects organ function in these same conditions. ^
期刊论文(11)
专著(0)
科研奖励(0)
会议论文
Rapid intravenous infusion of 20 ml/kg saline does not impair resting pulmonary gas exchange in the healthy human lung.
快速静脉输注 20 ml/kg 生理盐水不会损害健康人肺的静息肺气体交换。
DOI: 10.1152/japplphysiol.00787.2009
发表时间: 2010
期刊: Journal of applied physiology (Bethesda, Md. : 1985)
影响因子: --
作者: [Prisk,GKim, Olfert,IMark, Arai,TatsuyaJ, Wagner,PeterD, Hopkins,SusanR]
通讯作者: Hopkins,SusanR
DOI: 10.1002/jcp.21955
发表时间: 2010-03
期刊: Journal of cellular physiology
影响因子: 5.6
作者: [Tang K, Wagner PD, Breen EC]
通讯作者: Breen EC
DOI: 10.1113/jphysiol.2007.150128
发表时间: 2008
期刊: The Journal of physiology
影响因子: --
作者: [Vogiatzis,Ioannis, Zakynthinos,Spyros, Boushel,Robert, Athanasopoulos,Dimitris, Guenette,JordanA, Wagner,Harrieth, Roussos,Charis, Wagner,PeterD]
通讯作者: Wagner,PeterD
Administrative
Mechanisms of skeletal muscle adaptation in COPD
Administrative
Mechanisms of skeletal muscle adaptation in COPD