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dc.contributor.authorDORJSEMBE, BANZRAGCH-
dc.contributor.authorNho, Chu Won-
dc.contributor.authorChoi, Yong soo-
dc.contributor.authorKim, Jin-Chul-
dc.date.accessioned2024-01-12T03:31:11Z-
dc.date.available2024-01-12T03:31:11Z-
dc.date.created2022-04-27-
dc.date.issued2022-05-
dc.identifier.issn1420-3049-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/76734-
dc.description.abstractBlack soybean has been used in traditional medicine to treat inflammatory diseases, cancer, and diabetes and as a nutritional source since ancient times. We found that Korean black soybean cultivar A63 has more cyanidin-3-O-glucoside, (C3G), procyanidin B2 (PB2), and epicatechin (EPC) contents than other cultivars and has beneficial effects on cell viability and anti-oxidation. Given the higher concentration of anthocyanidins and their strong anti-oxidant activity, we predicted that A63 extract could relieve inflammatory disease symptoms, including those of atopic dermatitis (AD). Here, we evaluated the anti-AD activity of A63 extract in an oxazolone (OXA)-induced mouse model. A63 extract treatment significantly reduced epidermal thickness and inflammatory cell infiltration, downregulated the expression of AD gene markers, including Interleukin (IL)-4 and IL-5, and restored damaged skin barrier tissues. Furthermore, A63 extract influenced the activation of the signal transducer and activator of transcription (STAT) 3 and STAT6, extracellular regulatory kinase (ERK), and c-Jun N-terminal kinase (JNK) signaling pathways, which play a crucial role in the development of AD. Altogether, our results suggest that A63 can ameliorate AD-like skin inflammation by inhibiting inflammatory cytokine production and STAT3/6 and Mitogen-activated protein kinase (MAPK) signaling and restoring skin barrier function.-
dc.languageEnglish-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleExtract from Black Soybean Cultivar A63 Extract Ameliorates Atopic Dermatitis-like Skin Inflammation in an Oxazolone-Induced Murine Model-
dc.typeArticle-
dc.identifier.doi10.3390/molecules27092751-
dc.description.journalClass1-
dc.identifier.bibliographicCitationMolecules, v.27, no.9-
dc.citation.titleMolecules-
dc.citation.volume27-
dc.citation.number9-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000794656500001-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusKERATINOCYTES-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusDISEASES-
dc.subject.keywordPlusWILD-
dc.subject.keywordAuthorblack soybean A63-
dc.subject.keywordAuthoratopic dermatitis-
dc.subject.keywordAuthorGlycine max L-
dc.subject.keywordAuthorHS human dermal fibroblast cells (HS68)-
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