A new strategy for protection from cerebral ischemia
A new strategy for protection from cerebral ischemia
批准号:
7581636
负责人:
YING XIA
金额:
$41.38万
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
项目状态:
已结题
起止时间:
2009-02-01 至 2014-01-31
关键词:
Acupuncture procedureAttentionAttenuatedAwardBlood flowBrainBrain InfarctionBrain InjuriesCell Membrane ProteinsCerebral IschemiaCerebrovascular CirculationCerebrumCessation of lifeComplementary and alternative medicineDataEarly treatmentEmployee StrikesEventFamilyFundingGrantHome environmentHomeostasisHospitalsHypoxiaIndividualInflammatoryInflammatory ResponseInjuryInvestigationIschemiaIschemic Brain InjuryKnowledgeLeadLightMediatingMiddle Cerebral Artery OcclusionModalityMolecularNational Center for Complementary and Alternative MedicineNeedlesNeurologicNeuronsOpioidOpioid ReceptorOutcomePatientsPlayPreventionProductionReceptor ActivationReceptor Down-RegulationReceptor InhibitionReceptor Up-RegulationRecoveryRegulationResearchRiskRoleScienceScientistSignal TransductionSimulateSolutionsSomatosensory Evoked PotentialsStrokeStudy SectionSystemTechniquesTestingTherapeuticTransgenic ModelTransgenic OrganismsTravelUnited StatesUnited States National Institutes of HealthUp-RegulationWorkacute strokeattenuationbasecostcytokinedelta opioid receptordesigndisabilityeffective therapyexperienceneuron apoptosisnovelnovel strategiesnovel therapeuticspreventpublic health relevancereceptor expression
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Ischemic brain injury such as stroke is a leading cause of neurological disability and death in the States. There is, however, no effective strategy to protect the brain from ischemic injury. Recently, we have made exciting observations on effect of electro-acupuncture (EA) on cerebral ischemia. The most striking finding is that EA remarkably reduces brain infarction due to the occlusion of middle cerebral artery, which is dependent on the EA-triggered cellular/molecular events in the brain. Since our studies and those of others have shown that 1) activation of delta-opioid receptor (DOR) attenuates hypoxic/ischemic disruption of ionic homeostasis that triggers neuronal apoptosis and death; 2) DOR up-regulation enhances intracellular survival signals; 3) opioid receptor activation inhibits inflammatory responses, e.g., production of inflammatory cytokines that plays a critical role in ischemic injury; and 4) DOR inhibition largely attenuates the EA-induced protection against ischemic injury, it is likely that the EA-induced protection represents the outcome of cellular and molecular regulation at multiple levels in the brain. Specifically, it may depend on DOR up-regulation and the DOR-mediated stabilization of ionic homeostasis and modulation of survival/death signals. The general hypothesis of this proposal is that EA protects against cerebral ischemia mainly through DOR up-regulation and the DOR-mediated modulation of cellular and molecular signaling in neurons.. With molecular, transgenic and electrophysiological approaches, this proposal is designed to accomplish 3 specific aims: 1) to investigate if EA protects the brain from cerebral ischemia via DOR up-regulation; 2) to investigate if the EA protection is mediated by DOR-based stabilization of ionic homeostasis; and 3) to investigate if the EA protection relies on DOR-mediated inhibition of inflammatory responses to ischemia. The outcome data of this project may yield important information on the mechanism underlying the EA-induced protection from cerebral ischemia and may provide novel clues for therapeutic solutions of stroke. PUBLIC HEALTH RELEVANCE:
Stroke is a leading cause of neurological disability and death in the United States. However, there is no effective therapy to date to protect the brain from stroke-induced brain injury. To seek novel approaches to prevent/treat stroke, we have recently made exciting observations on the effect of electro- acupuncture (EA) on stroke-induced injury. The most striking and surprising finding is that EA, through little needles without any other treatment, remarkably reduces stroke-induced brain injury via the regulation of delta-opioid receptor (a cell membrane protein). Also, functional studies showed that EA promotes the recovery of brain function after stroke. Our finding thus suggests important therapeutic potential for EA in stroke. In this application, we propose to use modern techniques including molecular, transgenic and electrophysiological approaches to test three specific hypotheses for exploring mechanisms underlying the EA protection against stroke. Our preliminary studies have shown that this proposal is feasible and will very likely yield important information on the EA-induced protection and eventually shed light on new therapeutic modalities of stroke.
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