Discovery of New Anti-Inflammatory Agents to Treat COPD
Discovery of New Anti-Inflammatory Agents to Treat COPD
批准号:
9194162
负责人:
SCHROEDER M NOBLE
金额:
$62.03万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-06-01 至 2020-04-30
关键词:
AminopeptidaseAnatomyAnimal ModelAnimalsAnti-Inflammatory AgentsAnti-inflammatoryApoptosisBindingBiologyChronic Obstructive Airway DiseaseDevelopmentDiseaseDisease ProgressionEnzymatic BiochemistryEnzymesEpithelial CellsExhibitsFocus GroupsGenerationsGlycineHumanIL8RB geneImmunologicsInflammationInflammatoryKineticsKnowledgeLeadLigandsLungLung diseasesMaintenanceMeasuresMediatingModelingMorbidity - disease rateMusNeutrophil InfiltrationNeutrophiliaOutcomePathogenesisPathway interactionsPatientsPeptide HydrolasesPharmaceutical PreparationsPharmacotherapyPhysiologicalPlayPrevalenceProcessProlinePropertyPublishingPulmonary EmphysemaPulmonary InflammationRecombinantsResolutionRespiratory FailureRoleSeveritiesStructureTherapeuticTissuesValidationWorkX-Ray Crystallographybasecigarette smoke-inducedcigarette smokingclinically relevantdesignenvironmental tobacco smoke exposureenzyme structurein vitro activityin vivoleukotriene A4 hydrolasemortalitymouse modelnovelpreventresponsesmall molecule
中文摘要
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英文摘要
Emphysematous chronic obstructive pulmonary disease (COPD) is an irreversible lung disease of increasing
prevalence for which effective disease modifying therapy is not available. Patients with COPD exhibit
dysregulated and exaggerated inflammatory and immunologic responses. Recent studies have shown that the
aminopeptidase activity of the leukotriene A4 hydrolase (LTA4H) enzyme may play crucial roles in the process
of resolving inflammation. We have independently demonstrated effective protection of murine lungs against
COPD by selectively augmenting the LTA4H aminopeptidase activity with 4MDM, a selective small molecule
activator of the LTA4H aminopeptidase activity. When COPD was induced with cigarette smoke, treatment with
4MDM significantly reduced severity of COPD as determined by pre-mortem physiologic and post-mortem
anatomic assessment. On the basis of these findings, we believe that 4MDM can serve as a lead molecule for
the discovery of novel anti-inflammatory agents to treat COPD. Therefore, we propose specific aims to better
understand the target LTA4H enzyme structure, discover new activators of the LTA4H aminopeptidase activity,
and determine the effect of these compounds in the pathogenesis of COPD. We believe that our proposed
work and expected outcomes will provide potential first-in-class drugs to treat patients with COPD.
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