A murine model of toluene diisocyanate-induced asthma can be treated with matrix metalloproteinase inhibitor

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dc.contributor.authorLee, YCko
dc.contributor.authorSong, CHko
dc.contributor.authorLee, HBko
dc.contributor.authorOh, JLko
dc.contributor.authorRhee, YKko
dc.contributor.authorPark, HSko
dc.contributor.authorKoh, Gou Youngko
dc.date.accessioned2013-03-03T10:15:36Z-
dc.date.available2013-03-03T10:15:36Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-12-
dc.identifier.citationJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , v.108, pp.1021 - 1026-
dc.identifier.issn0091-6749-
dc.identifier.urihttp://hdl.handle.net/10203/78337-
dc.description.abstractBackground: Toluene diisocyanate (TDI) is a leading cause of occupational asthma. TDI-induced asthma is an inflammatory disease of the airways that is associated with airway remodeling. However, there are little data available on the role of matrix metalloproteinases (MMPs) in TDI-induced asthma. Objective: We. evaluated whether MMP-9 participates in the airway inflammation in TDI-induced asthma. An additional aim of the present study was to determine whether MMP inhibitors could be effective therapeutic agents for TDI-induced asthma. Methods: We developed a murine model of TDI-induced asthma to examine the involvement of MMPs by performing 2 sensitizations with 3% TDI and 1 challenge with 1% TDI using ultrasonic nebulization. Results: Marine TDI-induced asthma includes findings of (1) increased inflammatory cells, including neutrophils, lymphocytes, and eosinophils; (2) histologic changes, including infiltration of inflammatory cells around bronchioles, thickened airway epithelium, and accumulation of mucus and debris in the bronchioles; (3) increased MMP-9 activity in inflammatory cells in the airway lumen; and (4) airway hyperresponsiveness. Administration of an MMP inhibitor remarkably reduced all these pathophysiologic findings. Conclusion: We conclude that TDI-induced occupational asthma is associated with the induction of MMP-9 in inflammatory cells, and the inhibition of MMP-9 may be a good therapeutic strategy.-
dc.languageEnglish-
dc.publisherMosby-Elsevier-
dc.titleA murine model of toluene diisocyanate-induced asthma can be treated with matrix metalloproteinase inhibitor-
dc.typeArticle-
dc.identifier.wosid000172938400020-
dc.identifier.scopusid2-s2.0-0035217088-
dc.type.rimsART-
dc.citation.volume108-
dc.citation.beginningpage1021-
dc.citation.endingpage1026-
dc.citation.publicationnameJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-
dc.identifier.doi10.1067/mai.2001.120132-
dc.contributor.localauthorKoh, Gou Young-
dc.contributor.nonIdAuthorLee, YC-
dc.contributor.nonIdAuthorSong, CH-
dc.contributor.nonIdAuthorLee, HB-
dc.contributor.nonIdAuthorOh, JL-
dc.contributor.nonIdAuthorRhee, YK-
dc.contributor.nonIdAuthorPark, HS-
dc.type.journalArticleArticle-
dc.subject.keywordAuthortoluene diisocyanate-
dc.subject.keywordAuthormatrix metalloproteinase-
dc.subject.keywordAuthorasthma-
dc.subject.keywordAuthorairway hyperresponsiveness-
dc.subject.keywordPlusTISSUE INHIBITOR-
dc.subject.keywordPlusPOLYMORPHONUCLEAR NEUTROPHILS-
dc.subject.keywordPlusBASEMENT-MEMBRANE-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusCOLLAGENASE-
dc.subject.keywordPlusMODULATION-
dc.subject.keywordPlusMIGRATION-
dc.subject.keywordPlusFIBROSIS-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusSPUTUM-
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