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dc.contributor.authorJo, Beom-Geun-
dc.contributor.authorPark, No-June-
dc.contributor.authorKim, Su-Nam-
dc.contributor.authorJegal, Jonghwan-
dc.contributor.authorChoi, Sangho-
dc.contributor.authorLee, Sang Woo-
dc.contributor.authorYi, Li Wan-
dc.contributor.authorLee, Seoung Rak-
dc.contributor.authorKim, Ki Hyun-
dc.contributor.authorYang, Min Hye-
dc.date.accessioned2024-01-19T21:02:52Z-
dc.date.available2024-01-19T21:02:52Z-
dc.date.created2022-01-25-
dc.date.issued2019-01-
dc.identifier.issn2046-2069-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/120505-
dc.description.abstractThe aim of this study was to isolate maltol derivatives from S. chamaejasme and to investigate the anti-atopic dermatitis (anti-AD) effect of maltol in a 2,4-dinitrochlorobenzene (DNCB)-sensitized mouse model of AD. A novel compound, maltol 3-O-(4'-O-cis-p-coumaroyl)-beta-D-glucoside (named isosoyamaloside I), and two known maltol derivatives (maltol and soyamaloside I) were isolated from S. chamaejasme using chromatographic methods. Dermal application of maltol to DNCB-sensitized AD mice reduced erythema, pruritus, and lichenification scores. Histopathological examinations revealed significant decline in mast cell infiltration in maltol-treated AD mice. In addition, maltol accelerated skin barrier recovery by reducing TEWL and skin pH and increasing skin hydration. Maltol was also found to suppress atopy-induced IL-4 and IgE elevations in serum, which are known to be essential for the development of atopy. The results of this study show that maltol is a potential therapeutic candidate for the treatment of AD-related skin diseases.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleIsolation of maltol derivatives from Stellera chamaejasme and the anti-atopic properties of maltol on skin lesions in DNCB-stimulated mice-
dc.typeArticle-
dc.identifier.doi10.1039/c8ra09743g-
dc.description.journalClass1-
dc.identifier.bibliographicCitationRSC ADVANCES, v.9, no.4, pp.2125 - 2132-
dc.citation.titleRSC ADVANCES-
dc.citation.volume9-
dc.citation.number4-
dc.citation.startPage2125-
dc.citation.endPage2132-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000457783900042-
dc.identifier.scopusid2-s2.0-85060288417-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusDERMATITIS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCYTOKINES-
dc.subject.keywordPlusMODULATION-
dc.subject.keywordPlusTACROLIMUS-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusBARRIER-
dc.subject.keywordPlusDRUG-
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