Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jo, Beom-Geun | - |
dc.contributor.author | Park, No-June | - |
dc.contributor.author | Kim, Su-Nam | - |
dc.contributor.author | Jegal, Jonghwan | - |
dc.contributor.author | Choi, Sangho | - |
dc.contributor.author | Lee, Sang Woo | - |
dc.contributor.author | Yi, Li Wan | - |
dc.contributor.author | Lee, Seoung Rak | - |
dc.contributor.author | Kim, Ki Hyun | - |
dc.contributor.author | Yang, Min Hye | - |
dc.date.accessioned | 2024-01-19T21:02:52Z | - |
dc.date.available | 2024-01-19T21:02:52Z | - |
dc.date.created | 2022-01-25 | - |
dc.date.issued | 2019-01 | - |
dc.identifier.issn | 2046-2069 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/120505 | - |
dc.description.abstract | The 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.language | English | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.title | Isolation of maltol derivatives from Stellera chamaejasme and the anti-atopic properties of maltol on skin lesions in DNCB-stimulated mice | - |
dc.type | Article | - |
dc.identifier.doi | 10.1039/c8ra09743g | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | RSC ADVANCES, v.9, no.4, pp.2125 - 2132 | - |
dc.citation.title | RSC ADVANCES | - |
dc.citation.volume | 9 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 2125 | - |
dc.citation.endPage | 2132 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000457783900042 | - |
dc.identifier.scopusid | 2-s2.0-85060288417 | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | DERMATITIS | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | CYTOKINES | - |
dc.subject.keywordPlus | MODULATION | - |
dc.subject.keywordPlus | TACROLIMUS | - |
dc.subject.keywordPlus | DISEASE | - |
dc.subject.keywordPlus | BARRIER | - |
dc.subject.keywordPlus | DRUG | - |
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