Hypothermia for Cardiac Arrest: Optimizing Akt-Nitric Oxide Synthase Signaling
Hypothermia for Cardiac Arrest: Optimizing Akt-Nitric Oxide Synthase Signaling
批准号:
7530599
负责人:
David Gustav Beiser
金额:
$12.42万
依托单位:
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:
2008-08-20 至 2013-06-30
关键词:
AbbreviationsAnimal ExperimentsAnimalsAttenuatedBioavailableBiologyBiomedical EngineeringBlood CirculationBrainCardiacCardiac MyocytesCardiogenic ShockCardiopulmonary ResuscitationCardiovascular PhysiologyCardiovascular systemCaringCell DeathCellsCessation of lifeChicagoClinicalCommunitiesConditionDataDevelopmentDihematoporphyrin EtherDiseaseElectron Spin Resonance SpectroscopyEmergency MedicineEmergency SituationEnzyme ActivationEquilibriumFamilyFamily suidaeFluorescent ProbesFolateFree RadicalsFunctional disorderGenerationsHealedHeartHeart ArrestHospitalsHourHumanInjuryInstitutesInsulinIschemiaIsomerismKnock-outLaboratoriesLaboratory miceLocalizedMeasuresMechanicsMediatingMedicineMentorsMentorshipMitochondriaModelingMolecularMolecular BiologyMusMyocardialMyocardial dysfunctionNG-Nitroarginine Methyl EsterNOS1 geneNOS1 protein, humanNOS3 geneNamesNervous System PhysiologyNervous System TraumaNeurological outcomeNeuronsNitric OxideNitric Oxide SynthaseNitric Oxide Synthase Type INumbersOutcomeOxidantsOxidasesPathway interactionsPatientsPharmaceutical PreparationsPharmacologic SubstancePhasePhosphorylationPhysiciansPhysiological reperfusionPrincipal InvestigatorProcessProductionProtein IsoformsProtein KinaseQuality of lifeReactive Nitrogen SpeciesReactive Oxygen SpeciesRefractoryRelative (related person)Reperfusion InjuryReperfusion TherapyResearchResearch PersonnelResuscitationRoleScientistSeriesSignal PathwaySignal TransductionSourceStressSuperoxide DismutaseSuperoxidesSyndromeTemperatureTestingTherapeuticTherapeutic InterventionThreonineTimeTissuesTrainingTraining ProgramsTranslational ResearchUniversitiesWorkXDH geneXanthine Dehydrogenaseaortic balloon pumparginine methyl esterbasecardiovascular injurycareercofactordesignexperiencehealinghuman NOS3 proteinimprovedin vitro Modelin vivoindexinginhibitor/antagonistinnovationinterestmembermortalitymouse modelmovienatural hypothermianoveloxidationpreventprogramsprotective effectskillstetrahydrobiopterintherapy developmentvasoactive agent
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This proposal is a natural extension of the candidate's background in Emergency Medicine and Biomedical Engineering. His unique background and passion for translational science has already contributed to animal resuscitation research. This innovative work models early post-cardiac arrest reperfusion injury in our patients, i.e. cardiovascular collapse despite initial return of spontaneous circulation (ROSC). The training program will enhance the mouse modeling already done by formally training the applicant in the best molecular biology approaches for study of nitric oxide signaling and uncoupling. The applicant will benefit from multi-disciplinary mentorship within the Emergency Resuscitation Center, building upon expertise in heart oxidant injury and adaptation, and free radical biology. The sponsors Drs. Vanden Hoek and McNally are experienced physician-scientists. They are also collaborators interested in oxidantmediated heart contractile dysfunction and death in cardiomyocyte and mouse models. This Career Development Project builds upon the strengths of the applicant, the training program and institutional support and mentorship. We hypothesize that protective hypothermia following cardiac arrest increases Akt-related constitutive nitric oxide synthase (cNOS) NO-signaling, while attenuating cNOS uncoupling and generation of damaging reactive oxygen species (ROS). Specifically, in a mouse model of cardiac arrest we will: (Aim 1) Optimize the target temperature of protective hypothermia based on heart Akt and cNOS activity; (Aim 2) Test the relative importance of NOS1/NOS3 in post-cardiac arrest injury, NO and ROS generation, and hypothermia protection using selective-inhibitor and knockout strategies; and (Aim 3). Test whether hypothermia protection can be reproduced by NOS substrate/cofactor repletion strategies. The University of Chicago Department of Medicine and Section of Emergency Medicine have a track-record of successful mentoring using the K08 physician-scientist training program. The proposed training will provide Dr. Beiser with additional skills to become a leading independent physician-scientist in his field. From a layperson perspective, cardiac arrest (when the heart stops) is different than depicted on TV or the movies-most people initially resuscitated do not survive. This work will help understand how cooling the body a few degrees can actually increase a type of oxidant stress that helps the body heal itself.
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Hypothermia for Cardiac Arrest: Optimizing Akt-Nitric Oxide Synthase Signaling
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批准号:8294612
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项目类别:
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资助金额:$12.42万
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财政年份:2008
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负责人:David Gustav Beiser
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依托单位:
Hypothermia for Cardiac Arrest: Optimizing Akt-Nitric Oxide Synthase Signaling
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批准号:7862489
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项目类别:
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资助金额:$12.42万
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财政年份:2008
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负责人:David Gustav Beiser
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依托单位:
Hypothermia for Cardiac Arrest: Optimizing Akt-Nitric Oxide Synthase Signaling
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批准号:8098021
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项目类别:
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资助金额:$12.42万
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财政年份:2008
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负责人:David Gustav Beiser
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依托单位:
Hypothermia for Cardiac Arrest: Optimizing Akt-Nitric Oxide Synthase Signaling
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批准号:7676749
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项目类别:
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资助金额:$12.42万
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财政年份:2008
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负责人:David Gustav Beiser
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依托单位:
海外基金