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Therapeutic potential of ginseng leaf extract in inhibiting mast cell-mediated allergic inflammation and atopic dermatitis-like skin inflammation in DNCB-treated mice

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dc.contributor.authorOh, Jung-Mi-
dc.contributor.authorYoon, HyunHo-
dc.contributor.authorJoo, Jae-Yeol-
dc.contributor.authorIm, Wan-Taek-
dc.contributor.authorChun, Sungkun-
dc.date.accessioned2024-05-29T02:00:30Z-
dc.date.available2024-05-29T02:00:30Z-
dc.date.issued2024-05-
dc.identifier.issn1663-9812-
dc.identifier.issn1663-9812-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/119136-
dc.description.abstractGinseng leaves are known to contain high concentrations of bioactive compounds, such as ginsenosides, and have potential as a treatment for various conditions, including fungal infections, cancer, obesity, oxidative stress, and age-related diseases. This study assessed the impact of ginseng leaf extract (GLE) on mast cell-mediated allergic inflammation and atopic dermatitis (AD) in DNCB-treated mice. GLE reduced skin thickness and lymph node nodules and suppressed the expression and secretion of histamine and pro-inflammatory cytokines. It also significantly lowered the production of inflammatory response mediators including ROS, leukotriene C4 (LTC4), prostaglandin E2 (PGE2), cyclooxygenase-2 (COX-2), and inducible nitric oxide synthase (iNOS). GLE inhibited the phosphorylation of MAPKs (ERK, P38, JNK) and the activation of NF-κB, which are both linked to inflammatory cytokine expression. We demonstrated that GLE’s inhibitory effect on mast cell-mediated allergic inflammation is due to the blockade of the NF-κB and inflammasome pathways. Our findings suggest that GLE can be an effective therapeutic agent for mast-cell mediated and allergic inflammatory conditions.-
dc.format.extent20-
dc.language영어-
dc.language.isoENG-
dc.publisherFrontiers Media S.A.-
dc.titleTherapeutic potential of ginseng leaf extract in inhibiting mast cell-mediated allergic inflammation and atopic dermatitis-like skin inflammation in DNCB-treated mice-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3389/fphar.2024.1403285-
dc.identifier.scopusid2-s2.0-85195090708-
dc.identifier.wosid001238205200001-
dc.identifier.bibliographicCitationFrontiers in Pharmacology, v.15, no.15, pp 1 - 20-
dc.citation.titleFrontiers in Pharmacology-
dc.citation.volume15-
dc.citation.number15-
dc.citation.startPage1-
dc.citation.endPage20-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusRED GINSENG-
dc.subject.keywordPlusNLRP3 INFLAMMASOME-
dc.subject.keywordPlusPANAX-GINSENG-
dc.subject.keywordPlusINNATE IMMUNITY-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusIGE-
dc.subject.keywordPlusPROSTAGLANDIN-E2-
dc.subject.keywordPlusGINSENOSIDES-
dc.subject.keywordAuthoranti-inflammatory-
dc.subject.keywordAuthordegranulation-
dc.subject.keywordAuthorginseng leaf extract-
dc.subject.keywordAuthorinflammasome-
dc.subject.keywordAuthorMAPK-
dc.subject.keywordAuthorNF-κB-
dc.subject.keywordAuthorpro-inflammatory cytokines-
dc.identifier.urlhttps://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2024.1403285/full-
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