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Therapeutic Effect of Rumex japonicus Houtt. on DNCB-Induced Atopic Dermatitis-Like Skin Lesions in Balb/c Mice and Human Keratinocyte HaCaT Cells

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dc.contributor.authorYang, Hye Ryeon-
dc.contributor.authorLee, Hyunkyoung-
dc.contributor.authorKim, Jong-Hyun-
dc.contributor.authorHong, Il-Hwa-
dc.contributor.authorHwang, Du Hyeon-
dc.contributor.authorRho, Il Rae-
dc.contributor.authorKim, Gon Sup-
dc.contributor.authorKim, Euikyung-
dc.contributor.authorKang, Changkeun-
dc.date.accessioned2022-12-26T15:04:03Z-
dc.date.available2022-12-26T15:04:03Z-
dc.date.issued2019-03-07-
dc.identifier.issn2072-6643-
dc.identifier.issn2072-6643-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/9346-
dc.description.abstractRumex japonicus Houtt. (RJ) is traditionally used in folk medicines to treat patients suffering from skin disease in Korea and other parts of East Asia. However, the beneficial effect of RJ extract on atopic dermatitis (AD) has not been thoroughly examined. Therefore, this study aimed to investigate the anti-inflammatory effects of RJ on AD in vitro and in vivo. Treatment with RJ inhibited the phosphorylation of mitogen-activated protein kinase (MAPK) as well as the activation of nuclear factor-kappa B (NF-kappa B) in tumor necrosis factor-alpha (TNF-alpha) stimulated in HaCaT cells. The five-week-old Balb/c mice were used as an AD-like mouse model by treating them with 1-chloro-2, 4-dinitrobenzene (DNCB). Topical administration of RJ to DNCB-treated mice significantly reduced clinical dermatitis severity, epidermal thickness, and decreased mast cell and eosinophil infiltration into skin and ear tissue. These results suggest that RJ inhibits the development of AD-like skin lesions by regulating the skin inflammation responses in HaCaT cells and Balb/c mice. Thus, RJ may be a potential therapeutic agent for AD.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleTherapeutic Effect of Rumex japonicus Houtt. on DNCB-Induced Atopic Dermatitis-Like Skin Lesions in Balb/c Mice and Human Keratinocyte HaCaT Cells-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/nu11030573-
dc.identifier.scopusid2-s2.0-85062891822-
dc.identifier.wosid000464376900004-
dc.identifier.bibliographicCitationNUTRIENTS, v.11, no.3-
dc.citation.titleNUTRIENTS-
dc.citation.volume11-
dc.citation.number3-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNutrition & Dietetics-
dc.relation.journalWebOfScienceCategoryNutrition & Dietetics-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCYCLOOXYGENASE-2-
dc.subject.keywordPlusPATHOGENESIS-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusCYTOKINE-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusVIVO-
dc.subject.keywordAuthorRumex japonicus Houtt-
dc.subject.keywordAuthoratopic dermatitis-
dc.subject.keywordAuthorDNCB-
dc.subject.keywordAuthorskin lesion-
dc.subject.keywordAuthorMAPK-
dc.subject.keywordAuthorNF-kappa B-
dc.subject.keywordAuthorTNF-alpha-
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