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dc.contributor.author서은경*
dc.contributor.author황은숙*
dc.contributor.author한아름*
dc.date.accessioned2016-08-29T12:08:31Z-
dc.date.available2016-08-29T12:08:31Z-
dc.date.issued2014*
dc.identifier.issn1612-1872*
dc.identifier.otherOAK-14367*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/230265-
dc.description.abstractRhizomes of Curcuma phaeocaulis Valeton (Zingiberaceae) have traditionally been used for controlling inflammatory conditions. Numerous studies have aimed to isolate and characterize the bioactive constituents of C. phaeocaulis. It has been reported that its anti-inflammatory properties are a result of cyclooxygenase-2 inhibition; however, its effect on the T-cell function remains to be elucidated. In this study, four known sesquiterpenoids, viz., ar-turmerone (TM), germacrone (GM), (+)-(4S,5S)-germacrone-4,5-epoxide (GE), and curzerenone (CZ), were isolated from C. phaeocaulis rhizomes and evaluated for their effects on the CD4+ T-cell function. While GM, GE, and CZ had no effect on the activation of splenic T cells or CD4+ T cells, TM suppressed the interferon (IFN)-γ production, without affecting the interleukin (IL)-4 expression. TM also decreased the expression of IL-2 in CD4+ T cells, but did not change their cell-division rates upon stimulation. These results suggest that TM, a major constituent of C. phaeocaulis rhizomes selectively exerts potent anti-inflammatory effects via suppression of the inflammatory cytokines IFN-γ and IL-2. Copyright © 2014 Verlag Helvetica Chimica Acta AG, Zürich.*
dc.languageEnglish*
dc.publisherWiley-VCH Verlag*
dc.subjectAnti-inflammatory activity*
dc.subjectar-Turmerone*
dc.subjectCurcuma phaeocaulis*
dc.subjectIFN-γ*
dc.subjectIL-2*
dc.subjectRhizomes*
dc.titleSuppression of inflammatory cytokine production by ar-turmerone isolated from Curcuma phaeocaulis*
dc.typeArticle*
dc.relation.issue7*
dc.relation.volume11*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1034*
dc.relation.lastpage1041*
dc.relation.journaltitleChemistry and Biodiversity*
dc.identifier.doi10.1002/cbdv.201300397*
dc.identifier.wosidWOS:000340670200005*
dc.identifier.scopusid2-s2.0-84904468057*
dc.author.googleOh S.*
dc.author.googleHan A.R.*
dc.author.googlePark H.R.*
dc.author.googleJang E.J.*
dc.author.googleKim H.K.*
dc.author.googleJeong M.G.*
dc.author.googleSong H.*
dc.author.googlePark G.H.*
dc.author.googleSeo E.K.*
dc.author.googleHwang E.S.*
dc.contributor.scopusid서은경(7005953758)*
dc.contributor.scopusid황은숙(8688011100)*
dc.contributor.scopusid한아름(56278315000;34769874800)*
dc.date.modifydate20240130112016*
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약학대학 > 약학과 > Journal papers
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