Anti-inflammatory activity of (-)-aptosimon isolated from Daphne genkwa in RAW264.7 cells = 압토시몬의 항염효과

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dc.contributor.authorM Y Lee-
dc.contributor.authorB Y Park-
dc.contributor.authorOk-Kyoung Kwon-
dc.contributor.authorJi Eun Yuk-
dc.contributor.authorSei Ryang Oh-
dc.contributor.authorHui-Seong Kim-
dc.contributor.authorHyeong Kyu Lee-
dc.contributor.authorKyung Seop Ahn-
dc.date.accessioned2017-04-19T09:13:53Z-
dc.date.available2017-04-19T09:13:53Z-
dc.date.issued2009-
dc.identifier.issn1567-5769-
dc.identifier.uri10.1016/j.intimp.2009.03.012ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8984-
dc.description.abstractIn the present study, we investigated that (-)-aptosimon, isolated from flower buds of Daphne genkwa, inhibited cyclooxygenase-2 (COX-2) and inducible nitric oxide (NO) synthase (iNOS) expression in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Similarly, (-)-aptosimon suppressed tumor necrosis factor (TNF)-α production. Our results clearly indicated that (-)-aptosimon inhibited LPS-induced nuclear factor-κB (NF-κB) activation, by preventing degradation of the inhibitor kappa B-alpha (IκB-α). (-)-Aptosimon also inhibited interleukin-4 (IL-4) and interleukin-13 (IL-13) production in ConA-induced splenocytes. In conclusion, the anti-inflammatory effects of (-)-aptosimon are attributed to the suppression of pro-inflammatory cytokines and mediators by blocking NF-κB activation. These data suggest that (-)-aptosimon as a potential therapeutic agent for inflammation-associated disorders.-
dc.publisherElsevier-
dc.titleAnti-inflammatory activity of (-)-aptosimon isolated from Daphne genkwa in RAW264.7 cells = 압토시몬의 항염효과-
dc.title.alternativeAnti-inflammatory activity of (-)-aptosimon isolated from Daphne genkwa in RAW264.7 cells-
dc.typeArticle-
dc.citation.titleInternational Immunopharmacology-
dc.citation.number7-
dc.citation.endPage885-
dc.citation.startPage878-
dc.citation.volume9-
dc.contributor.affiliatedAuthorOk-Kyoung Kwon-
dc.contributor.affiliatedAuthorJi Eun Yuk-
dc.contributor.affiliatedAuthorSei Ryang Oh-
dc.contributor.affiliatedAuthorHui-Seong Kim-
dc.contributor.affiliatedAuthorHyeong Kyu Lee-
dc.contributor.affiliatedAuthorKyung Seop Ahn-
dc.contributor.alternativeName이미영-
dc.contributor.alternativeName박보영-
dc.contributor.alternativeName권옥경-
dc.contributor.alternativeName육지은-
dc.contributor.alternativeName오세량-
dc.contributor.alternativeName김희성-
dc.contributor.alternativeName이형규-
dc.contributor.alternativeName안경섭-
dc.identifier.bibliographicCitationInternational Immunopharmacology, vol. 9, no. 7, pp. 878-885-
dc.identifier.doi10.1016/j.intimp.2009.03.012-
dc.subject.keyword(-)-aptosimon-
dc.subject.keywordanti-inflammatory-
dc.subject.keywordCOX-2-
dc.subject.keywordIL-13-
dc.subject.keywordIL-4-
dc.subject.keywordiNOS-
dc.subject.local(-)-aptosimon-
dc.subject.localanti-inflammatory-
dc.subject.localAnti-inflammatory-
dc.subject.localCOX-2-
dc.subject.localCox-2-
dc.subject.localIL-13-
dc.subject.localIL-4-
dc.subject.localInducible nitric oxide synthase (iNOS)-
dc.subject.localInducible nitric oxide synthase-
dc.subject.localinducible nnitric oxide synthase-
dc.subject.localiNOS-
dc.subject.localInducible nitric oxide synthease (iNOS)-
dc.subject.localINOS-
dc.subject.localinducible nitric oxide synthase-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Bio-Resource Central Bank > 1. Journal Articles
Ochang Branch Institute > 1. Journal Articles
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
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