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CDr10b inhibits the expression of cyclooxygenase-2 and inducible nitric oxide synthase induced by lipopolysaccharide

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dc.contributor.authorGu, Gyo-Jeong-
dc.contributor.authorLim, Se-Jin-
dc.contributor.authorAhn, Sang-il-
dc.contributor.authorLee, Sung-Chan-
dc.contributor.authorChang, Young-Tae-
dc.contributor.authorChoi, Tae Hyun-
dc.contributor.authorKim, Byoung Soo-
dc.contributor.authorEom, Yong-Bin-
dc.contributor.authorLee, Na Kyung-
dc.contributor.authorYoun, Hyung-Sun-
dc.date.accessioned2021-08-11T21:46:49Z-
dc.date.available2021-08-11T21:46:49Z-
dc.date.issued2014-11-05-
dc.identifier.issn0014-2999-
dc.identifier.issn1879-0712-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/11701-
dc.description.abstractThe pathophysiological processes of inflammation can lead to a host of diseases, such as periodontitis, atherosclerosis, rheumatoid arthritis, and even cancer. The dysregulated inducible nitric oxide synthase ( iNOS) and cyclooxygenase-2 ( COX- 2) activation play important roles in the development of certain inflammatory diseases. Here, we investigated the effects of CDr10b which is originally developed for a microglia staining probe on inflammation, by modulating NF-kappa B activation and iNOS and COX-2 expression induced by lipopolysaccharide (LPS) in murine macrophages. The CDr10b suppressed NF-kappa B activation and iNOS and COX-2 expression induced by LPS. All the results suggest that CDr10b is a promising novel agent for the treatment of inflammatory diseases. (C) 2014 Elsevier B.V. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleCDr10b inhibits the expression of cyclooxygenase-2 and inducible nitric oxide synthase induced by lipopolysaccharide-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ejphar.2014.08.036-
dc.identifier.scopusid2-s2.0-84922242002-
dc.identifier.wosid000345526600006-
dc.identifier.bibliographicCitationEuropean Journal of Pharmacology, v.742, pp 42 - 46-
dc.citation.titleEuropean Journal of Pharmacology-
dc.citation.volume742-
dc.citation.startPage42-
dc.citation.endPage46-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusTOLL-LIKE RECEPTOR-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusSIGNALING PATHWAYS-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusINNATE IMMUNITY-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusTLR4-
dc.subject.keywordPlusHOMODIMERIZATION-
dc.subject.keywordPlusPHYTOCHEMICALS-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorNuclearfactor-kappa B-
dc.subject.keywordAuthorCyclooxygenase-2-
dc.subject.keywordAuthorInducible nitric oxide synthase-
dc.subject.keywordAuthorCDr10b-
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