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dc.contributor.authorAn, SJ-
dc.contributor.authorPae, HO-
dc.contributor.authorOh, GS-
dc.contributor.authorChoi, BM-
dc.contributor.authorJeong, S-
dc.contributor.authorJang, SI-
dc.contributor.authorOh, H-
dc.contributor.authorKwon, TO-
dc.contributor.authorSong, CE-
dc.contributor.authorChung, HT-
dc.date.accessioned2024-01-21T10:31:52Z-
dc.date.available2024-01-21T10:31:52Z-
dc.date.created2021-09-01-
dc.date.issued2002-07-
dc.identifier.issn1567-5769-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139417-
dc.description.abstractCatalposide, the major iridoid glycoside isolated from the stem bark of Catalpa ovata G. Don (Bignoniaceae), was found to inhibit the productions of tumor necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), and interleukin-6 (IL-6), and the activation of nuclear factor kappaB (NF-kappaB) in RAW 264.7 macrophages activated with lipopolysaccharide (LPS). Catalposide also inhibited the expressions of TNF-alpha, IL-1beta, and IL-6 genes and the nuclear translocation of p65 subunit of NF-kappaB in LPS-activated RAW 264.7 cells. Flow cytometric analysis revealed that catalposide suppressed the binding of FITC-conjugated LPS to CD 14 on the surface of cells, probably resulting in the inhibitory effects on TNT-alpha, IL- 1beta, and IL-6 productions and NF-kappaB activation. These findings suggest that catalposide could be an attractive candidate for adjunctive therapy in Gram-negative bacterial infections. (C) 2002 Elsevier Science B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectENDOTOXIN-SHOCK-
dc.subjectMOLECULAR MECHANISM-
dc.subjectSEVERE SEPSIS-
dc.subjectSEPTIC SHOCK-
dc.subjectHYPERSENSITIVITY-
dc.subjectPATHOPHYSIOLOGY-
dc.subjectCHROMATOGRAPHY-
dc.subjectCYTOKINES-
dc.subjectSYSTEM-
dc.subjectCD14-
dc.titleInhibition of TNF-alpha, IL-1 beta, and IL-6 productions and NF-kappa B activation in lipopolysaccharide-activated RAW 264.7 macrophages by catalposide, an iridoid glycoside isolated ftom Catalpa ovata G. Don (Bignoniaceae)-
dc.typeArticle-
dc.identifier.doi10.1016/S1567-5769(02)00085-1-
dc.description.journalClass1-
dc.identifier.bibliographicCitationINTERNATIONAL IMMUNOPHARMACOLOGY, v.2, no.8, pp.1173 - 1181-
dc.citation.titleINTERNATIONAL IMMUNOPHARMACOLOGY-
dc.citation.volume2-
dc.citation.number8-
dc.citation.startPage1173-
dc.citation.endPage1181-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000178179300014-
dc.identifier.scopusid2-s2.0-0035993221-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusENDOTOXIN-SHOCK-
dc.subject.keywordPlusMOLECULAR MECHANISM-
dc.subject.keywordPlusSEVERE SEPSIS-
dc.subject.keywordPlusSEPTIC SHOCK-
dc.subject.keywordPlusHYPERSENSITIVITY-
dc.subject.keywordPlusPATHOPHYSIOLOGY-
dc.subject.keywordPlusCHROMATOGRAPHY-
dc.subject.keywordPlusCYTOKINES-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusCD14-
dc.subject.keywordAuthorLPS-
dc.subject.keywordAuthorTNF-alpha-
dc.subject.keywordAuthorIL-1 beta-
dc.subject.keywordAuthorIL-6-
dc.subject.keywordAuthorNF-kappa B-
dc.subject.keywordAuthorcatalposide-
dc.subject.keywordAuthorCatalpa ovata-
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