Combination Therapy of Aspirin and Apyrase for Stroke
Combination Therapy of Aspirin and Apyrase for Stroke
批准号:
7996413
负责人:
RIDONG CHEN
金额:
$28.76万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-28 至 2013-08-31
关键词:
AcademyAcuteAmericanAmerican Heart AssociationAnimal ModelAnimalsAnti-Inflammatory AgentsAnti-inflammatoryAntiplatelet DrugsApyraseAspirinAutologousBloodBlood ClotBlood PlateletsBlood VesselsBlood coagulationBrainCardiovascular systemCause of DeathCell Culture TechniquesCell LineCell surfaceCerebral hemisphere hemorrhageCerebrovascular DisordersCerebrumChinese Hamster Ovary CellClinicClinicalClinical DataClinical TrialsCombined Modality TherapyComputer AssistedCulture MediaDoseEndothelial CellsEngineeringEnzymesExhibitsFibrinolytic AgentsFundingFutureGoalsGrantGuidelinesHemorrhageHospitalizationHourHumanIndustryInfarctionInjuryInterventionIntracranial HemorrhagesIschemiaIschemic StrokeLaboratoriesLilly brand of abciximabLung TransplantationMetastatic Neoplasm to the BoneModelingModificationMorbidity - disease rateNervous System PhysiologyNeurologicNeurologyNeuronsNitric OxideOutcomePathogenesisPatientsPhasePhase II Clinical TrialsPhase III Clinical TrialsPlatelet ActivationPlayPreclinical TestingProductionPropertyProstaglandins IProteinsRattusRecoveryRegimenReperfusion InjuryResearchRestRiskRoleSafetySecondary PreventionSecureSerumStagingStrokeTexasTherapeuticTherapeutic EffectThromboxanesTimeTissuesUniversitiesabciximabbasebrain tissueclinically relevantclopidogreldesigndisabilityeffective therapyefficacy testingfluiditygastrointestinalimprovedinterestmeetingsmortalityneuroprotectionnovelpercutaneous coronary interventionpublic health relevanceresearch studystroke therapy
中文摘要
描述(由申请人提供):人apyrase是一种非常有前途的治疗急性缺血性中风的方法,急性缺血性中风是导致死亡和残疾的主要原因,对大多数患者几乎没有有效的治疗方法。这种酶强烈抑制血小板的激活和聚集,有适度的出血风险。我们将验证假设,在大鼠脑卒中血栓栓塞模型中,在短期和长期实验中,ASA + apyrase联合治疗在不增加脑出血的情况下,比单独使用ASA或apyrase提供更有效的保护。
英文摘要
DESCRIPTION (provided by applicant): Human apyrase represents a highly promising therapy for acute ischemic stroke which is a leading cause of death and disability with almost no effective therapy for most patients. This enzyme strongly inhibits platelet activation and aggregation with modest bleeding risk. We will validate hypothesis that in thromboembolic model of stroke in rats, combination treatment of ASA plus apyrase at acute stage provides more effective protection than ASA or apyrase alone in short term as well as long-term experiments without increasing intracerebral hemorrhage.
PUBLIC HEALTH RELEVANCE: We will utilize clinically relevant embolic stroke models in rats to assess neuroprotective effect of aspirin and apyrase treatment.
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