Anti-itching and anti-inflammatory effects of kushenol F via the inhibition of TSLP production

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dc.contributor.authorSeongyea Cho-
dc.contributor.authorE Y Gong-
dc.contributor.authorWonbeak Yoo-
dc.contributor.authorHyunji Choi-
dc.contributor.authorD Jung-
dc.contributor.authorKyung Hee Noh-
dc.contributor.authorS Kim-
dc.contributor.authorS H Kim-
dc.contributor.authorHyeong Kyu Lee-
dc.date.accessioned2022-11-11T16:32:29Z-
dc.date.available2022-11-11T16:32:29Z-
dc.date.issued2022-
dc.identifier.issn1424-8247-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/30580-
dc.description.abstractAtopic dermatitis (AD) is a chronic inflammatory skin disease that results from eczema, itching, disrupted barrier function and aberrant cutaneous immune responses. The aim of the present study was to assess the efficacy of kushenol F as an effective treatment for AD via the suppression of thymic stromal lymphopoietin (TSLP) production. The results of the present study demonstrated that the clinical symptoms of AD were less severe and there was reduced ear thickening and scratching behavior in kushenol F-treated Dermatophagoides farinae extract (DFE)/1-chloro-2,4-dinitrochlorobenzene (DNCB)-induced AD mice. Histopathological analysis demonstrated that kushenol F decreased the DFE/DNCB-induced infiltration of eosinophil and mast cells and TSLP protein expression levels. Furthermore, kushenol F-treated mice exhibited significantly lower concentrations of serum histamine, IgE and IgG2a compared with the DFE/DNCB-induced control mice. Kushenol F also significantly decreased phosphorylated NF-κB and IKK levels and the mRNA expression levels of IL-1β and IL-6 in cytokine combination-induced human keratinocytes. The results of the present study suggested that kushenol F may be a potential therapeutic candidate for the treatment of AD via reducing TSLP levels.-
dc.publisherMDPI-
dc.titleAnti-itching and anti-inflammatory effects of kushenol F via the inhibition of TSLP production-
dc.title.alternativeAnti-itching and anti-inflammatory effects of kushenol F via the inhibition of TSLP production-
dc.typeArticle-
dc.citation.titlePharmaceuticals-
dc.citation.number11-
dc.citation.endPage1347-
dc.citation.startPage1347-
dc.citation.volume15-
dc.contributor.affiliatedAuthorSeongyea Cho-
dc.contributor.affiliatedAuthorWonbeak Yoo-
dc.contributor.affiliatedAuthorHyunji Choi-
dc.contributor.affiliatedAuthorKyung Hee Noh-
dc.contributor.affiliatedAuthorHyeong Kyu Lee-
dc.contributor.alternativeName조성예-
dc.contributor.alternativeName공은영-
dc.contributor.alternativeName유원백-
dc.contributor.alternativeName최현지-
dc.contributor.alternativeName정다나-
dc.contributor.alternativeName노경희-
dc.contributor.alternativeName김석호-
dc.contributor.alternativeName김상현-
dc.contributor.alternativeName이형규-
dc.identifier.bibliographicCitationPharmaceuticals, vol. 15, no. 11, pp. 1347-1347-
dc.identifier.doi10.3390/ph15111347-
dc.subject.keywordKushenol F-
dc.subject.keywordAtopic dermatitis-
dc.subject.keywordThymic stromal lymphopoietin (TSLP)-
dc.subject.keywordItching-
dc.subject.keywordInflammation-
dc.subject.localKushenol F-
dc.subject.localAtopic Dermatitis-
dc.subject.localAtopic dermatitis-
dc.subject.localatopic dermatitis-
dc.subject.localatopic dermatitis (AD)-
dc.subject.localAtopic dermatitis (AD)-
dc.subject.localthymic stromal lymphopoietin-
dc.subject.localThymic stromal lymphopoietin (TSLP)-
dc.subject.localItching-
dc.subject.localInflammation-
dc.subject.localinflammation-
dc.subject.localnflammation-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Genomic Medicine Research Center > 1. Journal Articles
Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
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