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Hemeoxygenase 1 partly mediates the anti-inflammatory effect of dieckol in lipopolysaccharide stimulated murine macrophages

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dc.contributor.authorYayeh, Taddesse-
dc.contributor.authorIm, Eun Ju-
dc.contributor.authorKwon, Tae-Hyung-
dc.contributor.authorRoh, Seong-Soo-
dc.contributor.authorKim, Suk-
dc.contributor.authorKim, Ji Hye-
dc.contributor.authorHong, Seung-Bok-
dc.contributor.authorCho, Jae Youl-
dc.contributor.authorPark, Nyun-Ho-
dc.contributor.authorRhee, Man Hee-
dc.date.accessioned2022-12-26T23:02:18Z-
dc.date.available2022-12-26T23:02:18Z-
dc.date.issued2014-09-
dc.identifier.issn1567-5769-
dc.identifier.issn1878-1705-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/18799-
dc.description.abstractEisenia bicyclis is edible brown algae recognized as a rich source of bioactive derivatives mainly phlorotannins reported for their anti-oxidant properties. Of all phlorotannins identified so far, dieckol has shown the most potent effect in anti-inflammatory, radical scavenging and neuroprotective functions. However, whether dieckol up-regulates hemeoxygenase 1 (HO-1) and this mediates its anti-inflammatory effect in murine macrophages remains poorly understood. Dieckol (12.5-50 mu M) inhibited nitric oxide production and attenuated inducible nitric oxide synthase, phospho (p)-PI-3 K, p-Akt, p-IKK-alpha/beta, p-I kappa B-alpha and nuclear p-NF-kappa Bp65 protein expressions, and NF-kappa B transcriptional activity in LPS (0.1 mu g/ml) stimulated murine macrophages. On the other hand, dieckol up-regulated HO-1 which partly mediated its anti-inflammatory effect in murine macrophages. Thus, dieckol appeared to be a potential therapeutic agent against inflammation through HO-1 up-regulation. (C) 2014 Elsevier B.V. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titleHemeoxygenase 1 partly mediates the anti-inflammatory effect of dieckol in lipopolysaccharide stimulated murine macrophages-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.intimp.2014.06.009-
dc.identifier.scopusid2-s2.0-84903752736-
dc.identifier.wosid000340849700006-
dc.identifier.bibliographicCitationINTERNATIONAL IMMUNOPHARMACOLOGY, v.22, no.1, pp 51 - 58-
dc.citation.titleINTERNATIONAL IMMUNOPHARMACOLOGY-
dc.citation.volume22-
dc.citation.number1-
dc.citation.startPage51-
dc.citation.endPage58-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusMARINE BROWN ALGA-
dc.subject.keywordPlusNITRIC-OXIDE-
dc.subject.keywordPlusECKLONIA-STOLONIFERA-
dc.subject.keywordPlusHEME OXYGENASE-1-
dc.subject.keywordPlusPHLOROTANNINS-
dc.subject.keywordPlusLPS-
dc.subject.keywordPlusANTIOXIDANT-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordAuthorDieckol-
dc.subject.keywordAuthorHO-1-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorMurine macrophages-
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