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Time-dependent inhibition of oxygen radical induced lung injury

dc.contributor.authorJohnson, Kent J.en_US
dc.contributor.authorVarani, Jamesen_US
dc.contributor.authorGannon, David E.en_US
dc.contributor.authorHe, Xuanminen_US
dc.contributor.authorWard, Peter A.en_US
dc.date.accessioned2006-09-11T14:54:14Z
dc.date.available2006-09-11T14:54:14Z
dc.date.issued1990-10en_US
dc.identifier.citationGannon, David E.; He, Xuanmin; Ward, Peter A.; Varani, James; Johnson, Kent J.; (1990). "Time-dependent inhibition of oxygen radical induced lung injury." Inflammation 14(5): 509-522. <http://hdl.handle.net/2027.42/44504>en_US
dc.identifier.issn0360-3997en_US
dc.identifier.issn1573-2576en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44504
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2249886&dopt=citationen_US
dc.description.abstractExperimental acute lung injury mediated by reactive metabolites of oxygen can be inhibited by the antioxidant enzymes catalase and Superoxide dismutase (SOD). However, the specific time interval during which these enzymes must be present in order to cause protection is not well defined. Using two experimental models of oxidant-dependent acute lung injury, one involving the intratracheal injection of glucose, glucose oxidase, and lactoperoxidase and the other involving the intravenous injection of cobra venom factor (CVF), we investigated the effects of delaying antioxidant administration on the outcome of the inflammatory response. In both cases, the protective effects of catalase and SOD were rapidly attenuated when their administration was delayed for a short period of time. For example, intratracheal catalase resulted in 98% protection when given simultaneously with the glucose oxidase and lactoperoxidase, but only 13% protection when the catalase was delayed 4 min. Likewise, in the CVF-induced lung injury model, intravenous catalase resulted in 40% protection when given simultaneously with the CVF, but only 2% protection when the catalase was delayed 20 min, even though the peak of the injury occurred hours after the initiation of the injury. A similar time dependence was seen with SOD. These results indicate that antioxidant therapy is required early in the course of oxygen radical-mediated acute lung injury for effective protection.en_US
dc.format.extent1375935 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherInternal Medicineen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherPathologyen_US
dc.subject.otherRheumatologyen_US
dc.titleTime-dependent inhibition of oxygen radical induced lung injuryen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPathologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Medicine, University of Vermont College of Medicine, Given Medical Building, 05405-0068, Burlington, Vermonten_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid2249886en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44504/1/10753_2004_Article_BF00914272.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00914272en_US
dc.identifier.sourceInflammationen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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