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Cited 47 time in webofscience Cited 53 time in scopus
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Sulfated Chitosan Oligosaccharides Suppress LPS-Induced NO Production via JNK and NF-κB Inactivation

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dc.contributor.authorKim, Jung-Hyun-
dc.contributor.authorKim, Yon-Suk-
dc.contributor.authorHwang, Jin-Woo-
dc.contributor.authorHan, Young-Ki-
dc.contributor.authorLee, Jung-Suck-
dc.contributor.authorKim, Se-Kwon-
dc.contributor.authorJeon, You-Jin-
dc.contributor.authorMoon, Sang-Ho-
dc.contributor.authorJeon, Byong-Tae-
dc.contributor.authorBahk, Young Yil-
dc.contributor.authorPark, Pyo-Jam-
dc.date.accessioned2025-03-19T06:00:13Z-
dc.date.available2025-03-19T06:00:13Z-
dc.date.issued2014-11-
dc.identifier.issn1420-3049-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/77454-
dc.description.abstractVarious biological effects have been reported for sulfated chitosan oligosaccharides, but the molecular mechanisms of action of their anti-inflammatory effects are still unknown. This study aimed to evaluate the anti-inflammatory effects of sulfated chitosan oligosaccharides and to elucidate the possible mechanisms of action. The results showed that pretreated low molecular weight sulfated chitosan oligosaccharides inhibited the production of nitric oxide (NO) and inflammatory cytokines such as IL-6 and TNF-alpha in lipopolysaccharide (LPS)-activated RAW264.7 cells. The sulfated chitosan oligosaccharides also suppressed inducible nitric oxide synthase (iNOS), phosphorylation of JNK and translocation of p65, a subunit of NF-kappa B, into the nucleus by inhibiting degradation of I kappa B-alpha. Our investigation suggests sulfated chitosan oligosaccharides inhibit IL-6/TNF-alpha in LPS-induced macrophages, regulated by mitogen-activated protein kinases (MAPKs) pathways dependent on NF-kappa B activation.-
dc.format.extent16-
dc.language영어-
dc.language.isoENG-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleSulfated Chitosan Oligosaccharides Suppress LPS-Induced NO Production via JNK and NF-κB Inactivation-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/molecules191118232-
dc.identifier.scopusid2-s2.0-84912535702-
dc.identifier.wosid000345564300067-
dc.identifier.bibliographicCitationMolecules, v.19, no.11, pp 18232 - 18247-
dc.citation.titleMolecules-
dc.citation.volume19-
dc.citation.number11-
dc.citation.startPage18232-
dc.citation.endPage18247-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusNITRIC-OXIDE SYNTHASE-
dc.subject.keywordPlusRAW 264.7 MACROPHAGES-
dc.subject.keywordPlusSIGNALING PATHWAYS-
dc.subject.keywordPlusANTIOXIDANT ACTIVITY-
dc.subject.keywordPlusSENTICOSUS EXTRACT-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCHITOOLIGOSACCHARIDES-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordAuthorsulfated chitosan oligosaccharides-
dc.subject.keywordAuthorRAW264.7 cells-
dc.subject.keywordAuthorMAPKs pathways-
dc.subject.keywordAuthoranti-inflammatory-
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