Mechanisms of Optic Nerve Stroke Neuroprotection
Mechanisms of Optic Nerve Stroke Neuroprotection
批准号:
9334599
负责人:
STEVEN L BERNSTEIN
金额:
$38.38万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-08-01 至 2019-08-31
关键词:
AcuteAffectAge-YearsAgonistAnterior Ischemic Optic NeuropathyAxonBiologicalBlindnessCell SurvivalCell surfaceCellsCellular InfiltrationCessation of lifeClinicalClinical TrialsCompartment syndromesDiseaseDown-RegulationEdemaElectrophysiology (science)EquilibriumEventFunctional disorderFundingGene ExpressionHourImmunomodulatorsIndividualInfarctionInfiltrationInflammationInflammatoryInflammatory ResponseInterventionInvadedIschemiaIschemic Optic NeuropathyLaboratoriesLeadModelingMolecularMyelinNF-kappa BNatural regenerationOligodendrogliaOptic DiskOptic NerveOutcomePathway interactionsPatientsPhysiciansPlayPrimatesProcessProstaglandinsProteinsRecoveryResearch DesignRetinal Ganglion CellsRodentRodent ModelSpinal cord injuryStrokeTechniquesTestingTimeTransgenic MiceTransgenic ModelTranslatingUp-RegulationVisualaxon injuryclinical developmentclinically relevantclinically translatablecytokinedesigneffective therapyexperiencefallsimmunoregulationimprovedin vivoischemic lesionmacrophagemodel developmentneuroprotectionnovel strategiespublic health relevancereceptorregenerativerepairedresponse
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Nonarteritic anterior ischemic optic neuropathy (NAION) is an optic nerve (ON) infarct, and the most common cause of sudden optic nerve (ON) related vision loss, NAION affects ~15,000 individuals/year and has no effective treatments. Little is known about the mechanisms in NAION pathophysiology. Our lab developed the first rodent and primate NAION models that have been validated for nearly every finding found in NAION, and us to critically dissect NAIONs likely processes. We have determined that early and late inflammatory changes play a key role in NAION model development and damage. Soon after NAION model induction, ON head edema and a compartment syndrome occur along with soluble inflammatory cytokine expression and progressive ischemia. Later (>3d) changes include significant cellular inflammatory infiltration, with increased M1 (degenerative macrophage response) and decreased M2 (regenerative macrophage response) activities, and progressive axon- and oligodendrocyte damage. These responses ultimately result in retinal ganglion cell (RGC) and oligodendrocyte death. We identified prostaglandin J2 (PGJ2) as the first agent that can potentially treat early stage disease. In aim 1, we will separately evaluate PGJ2's neuroprotective mechanisms, confirming their individual identities and their maximal effects. We will then determine whether these mechanisms act synergistically, to maximize neuroprotection. In aim 2, we will determine whether selectively immunomodulating the neuroprotective M2 macrophage inflammatory response will reduce RGC and myelin dysfunction and cellular death, and improve post-infarct recovery. Results of these interventions will be evaluated using a variety of techniques, to quantify effects at the gene expression level, histochemically and functionally. This combination early and later approaches is designed to maximize development of clinically effective treatments for NAION and related diseases, and greatly improve post- NAION recovery.
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批准号:8762089
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资助金额:$38.38万
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依托单位:
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批准号:7528671
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资助金额:$37.5万
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依托单位:
海外基金