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Anti-inflammatory effect of erdosteine in lipopolysaccharide-stimulated RAW 264.7 cells

DC Field Value Language
dc.contributor.authorPark, Jong Sun-
dc.contributor.authorPark, Mi-Young-
dc.contributor.authorCho, Young-Jae-
dc.contributor.authorLee, Jae Ho-
dc.contributor.authorYoo, Chul-Gyu-
dc.contributor.authorLee, Choon-Taek-
dc.contributor.authorLee, Sang-Min-
dc.date.accessioned2025-02-20T07:55:40Z-
dc.date.available2025-02-20T07:55:40Z-
dc.date.created2018-09-05-
dc.date.created2018-09-05-
dc.date.issued2016-08-
dc.identifier.citationInflammation, Vol.39 No.4, pp.1573-1581-
dc.identifier.issn0360-3997-
dc.identifier.urihttps://hdl.handle.net/10371/217056-
dc.description.abstractErdosteine is widely used as a mucolytic agent and also has free radical scavenging and antioxidant activities. However, little is known about the mechanisms of the anti-inflammatory effect of erdosteine. We investigated the effect of erdosteine on the activation of the nuclear factor (NF)-kB/inhibitor of NFkB (IkB), and the mitogen-activated protein kinase (MAPK) and Akt pathways in the mouse macrophage cell line RAW 264.7. Cultured RAW 264.7 cells were pretreated with erdosteine and stimulated with lipopolysaccharide (LPS). In Western blotting, pretreatment with erdosteine inhibited the IkB alpha degradation induced in RAW 264.7 cells by LPS. LPS-induced IkB kinase (IKK) activity and NF-kB transcription were inhibited by pretreatment with erdosteine. Production of IL-6 and IL-1 beta was also inhibited by erdosteine pretreatment. However, erdosteine did not inhibit LPS-induced phosphorylation of Akt and MAPKs. These results suggest that the anti-inflammatory effect of erdosteine in mouse macrophages is mediated through inhibition of LPS-induced NF-kB activation.-
dc.language영어-
dc.publisherKluwer Academic/Plenum Publishers-
dc.titleAnti-inflammatory effect of erdosteine in lipopolysaccharide-stimulated RAW 264.7 cells-
dc.typeArticle-
dc.identifier.doi10.1007/s10753-016-0393-4-
dc.citation.journaltitleInflammation-
dc.identifier.wosid000380232200033-
dc.identifier.scopusid2-s2.0-84975105939-
dc.citation.endpage1581-
dc.citation.number4-
dc.citation.startpage1573-
dc.citation.volume39-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorPark, Jong Sun-
dc.contributor.affiliatedAuthorLee, Jae Ho-
dc.contributor.affiliatedAuthorYoo, Chul-Gyu-
dc.contributor.affiliatedAuthorLee, Choon-Taek-
dc.contributor.affiliatedAuthorLee, Sang-Min-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusACUTE LUNG INJURY-
dc.subject.keywordPlusALVEOLAR MACROPHAGES-
dc.subject.keywordPlusANTIOXIDANT ACTIVITY-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusSEPTIC SHOCK-
dc.subject.keywordPlusP65 SUBUNIT-
dc.subject.keywordPlusACETYLCYSTEINE-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusKINASE-
dc.subject.keywordAuthorerdosteine-
dc.subject.keywordAuthorNF-kB/IkB-
dc.subject.keywordAuthoranti-inflammatory effect-
dc.subject.keywordAuthorMAPK-
dc.subject.keywordAuthorAkt-
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  • College of Medicine
  • Department of Medicine
Research Area Interstitial lung disease, Pneumonia, Pulmonary fibrosis, 간질성 폐질환, 폐렴, 폐섬유증

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