Isolation of maltol derivatives from Stellera chamaejasme and the anti-atopic properties of maltol on skin lesions in DNCB-stimulated mice

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dc.contributor.authorB G Jo-
dc.contributor.authorN J Park-
dc.contributor.authorS N Kim-
dc.contributor.authorJ Jegal-
dc.contributor.authorSangho Choi-
dc.contributor.authorSang Woo Lee-
dc.contributor.authorL W Yi-
dc.contributor.authorS R Lee-
dc.contributor.authorK H Kim-
dc.contributor.authorM H Yang-
dc.date.accessioned2019-04-09T16:30:11Z-
dc.date.available2019-04-09T16:30:11Z-
dc.date.issued2019-
dc.identifier.issn2046-2069-
dc.identifier.uri10.1039/C8RA09743Gko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18425-
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)-β-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.publisherRoyal Soc Chem-
dc.titleIsolation of maltol derivatives from Stellera chamaejasme and the anti-atopic properties of maltol on skin lesions in DNCB-stimulated mice-
dc.title.alternativeIsolation of maltol derivatives from Stellera chamaejasme and the anti-atopic properties of maltol on skin lesions in DNCB-stimulated mice-
dc.typeArticle-
dc.citation.titleRsc Advances-
dc.citation.number4-
dc.citation.endPage2132-
dc.citation.startPage2125-
dc.citation.volume9-
dc.contributor.affiliatedAuthorSangho Choi-
dc.contributor.affiliatedAuthorSang Woo Lee-
dc.contributor.alternativeName조범근-
dc.contributor.alternativeName박노준-
dc.contributor.alternativeName김수남-
dc.contributor.alternativeName제갈종환-
dc.contributor.alternativeName최상호-
dc.contributor.alternativeName이상우-
dc.contributor.alternativeNameYi-
dc.contributor.alternativeName이성락-
dc.contributor.alternativeName김기현-
dc.contributor.alternativeName양민혜-
dc.identifier.bibliographicCitationRsc Advances, vol. 9, no. 4, pp. 2125-2132-
dc.identifier.doi10.1039/C8RA09743G-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > International Biological Material Research Center > 1. Journal Articles
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