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dc.contributor.authorCho, Young-Chang-
dc.contributor.authorLee, Sung Ho-
dc.contributor.authorYoon, Goo-
dc.contributor.authorKim, Hyung-Seok-
dc.contributor.authorNa, Joo Young-
dc.contributor.authorChoi, Hyun Jin-
dc.contributor.authorCho, Cheng-Weon-
dc.contributor.authorCheon, Seung Hoon-
dc.contributor.authorKang, Bok Yun-
dc.date.accessioned2024-01-20T18:34:01Z-
dc.date.available2024-01-20T18:34:01Z-
dc.date.created2021-09-05-
dc.date.issued2010-09-
dc.identifier.issn1567-5769-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/131136-
dc.description.abstractLicochalcone, a constituent of licorice, has antitumor, antimicrobial, and anti-inflammatory effects. Recently, licochalcone E was isolated from the roots of Glycyrrhiza inflata and its biological functions are not fully examined. In this study, we investigated its ability to modulate production of IL-12p40, a common subunit of IL-12 and IL-23. Licochalcone E dose-dependently inhibited IL-12p40 production from lipopolysaccharide-stimulated RAW264.7 macrophage cells. The repressive effect was mapped to a region in the IL-12 gene promoter containing a binding site for NF-kappa B. Furthermore, licochalcone E decreased binding to the NF-kappa B site in RAW264.7 macrophage cells. Using a chronic allergic contact dermatitis model induced by repeated application of oxazolone, we showed that licochalcone E inhibited the increased IL-12p40 expression and ear thickness induced by oxazolone. Taken together, licochalcone E inhibits IL-12p40 production and has therapeutic potential to reduce skin inflammation. (C) 2010 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectGLYCYRRHIZA-INFLATA-
dc.subjectT-CELLS-
dc.subjectPARASITE MITOCHONDRIA-
dc.subjectPSORIASIS-VULGARIS-
dc.subjectINTERFERON-GAMMA-
dc.subjectINTERLEUKIN-12-
dc.subjectCYTOKINE-
dc.subjectIL-23-
dc.subjectP40-
dc.subjectEXPRESSION-
dc.titleLicochalcone E reduces chronic allergic contact dermatitis and inhibits IL-12p40 production through down-regulation of NF-kappa B-
dc.typeArticle-
dc.identifier.doi10.1016/j.intimp.2010.06.015-
dc.description.journalClass1-
dc.identifier.bibliographicCitationINTERNATIONAL IMMUNOPHARMACOLOGY, v.10, no.9, pp.1119 - 1126-
dc.citation.titleINTERNATIONAL IMMUNOPHARMACOLOGY-
dc.citation.volume10-
dc.citation.number9-
dc.citation.startPage1119-
dc.citation.endPage1126-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000281981600018-
dc.identifier.scopusid2-s2.0-77955920339-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusGLYCYRRHIZA-INFLATA-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusPARASITE MITOCHONDRIA-
dc.subject.keywordPlusPSORIASIS-VULGARIS-
dc.subject.keywordPlusINTERFERON-GAMMA-
dc.subject.keywordPlusINTERLEUKIN-12-
dc.subject.keywordPlusCYTOKINE-
dc.subject.keywordPlusIL-23-
dc.subject.keywordPlusP40-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorLicochalcone E-
dc.subject.keywordAuthorInteleukin-12p40-
dc.subject.keywordAuthorNF-kappa B-
dc.subject.keywordAuthorAllergic contact dermatitis-
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