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Anti-Inflammatory Effects of the LK5 Herbal Complex on LPS- and IL-4/IL-13-Stimulated HaCaT Cells and a DNCB-Induced Animal Model of Atopic Dermatitis in BALB/c Mice

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dc.contributor.authorKim, Hyun-Jeong-
dc.contributor.authorKim, So-Yeon-
dc.contributor.authorBae, Ho Jung-
dc.contributor.authorChoi, Yu-Yeong-
dc.contributor.authorAn, Ju-Yeon-
dc.contributor.authorCho, Ye Eun-
dc.contributor.authorCho, So-Young-
dc.contributor.authorLee, Su-Jung-
dc.contributor.authorLee, Sanghyun-
dc.contributor.authorSin, MinSub-
dc.contributor.authorYun, Young Min-
dc.contributor.authorLee, Jong Ryul-
dc.contributor.authorPark, Se Jin-
dc.date.accessioned2024-03-13T05:00:22Z-
dc.date.available2024-03-13T05:00:22Z-
dc.date.issued2024-01-
dc.identifier.issn1999-4923-
dc.identifier.issn1999-4923-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/72804-
dc.description.abstractAtopic dermatitis (AD) is a chronic inflammatory skin disease influenced by a complex interplay of genetic and environmental factors. The activation of the JAK-STAT pathway increases the expression of inflammatory cytokines such as IL-4 and IL-13, further deteriorating AD. Therefore, for the treatment of AD, the JAK-STAT pathway is emerging as a significant target, alongside inflammatory cytokines. This study investigates the potential therapeutic effects of a novel herbal complex, LK5, composed of Scutellaria baicalensis, Liriope platyphylla, Sophora flavescens, Dictammus dasycarpus, and Phellodendron schneider, known for their anti-inflammatory and immune-modulating properties. We examined the anti-inflammatory and anti-AD effects of the LK5 herbal complex in HaCaT cells stimulated by LPS and IL-4/IL-13, as well as in a mouse model of AD induced by DNCB. In HaCaT cells stimulated with LPS or IL-4/IL-13, the LK5 herbal complex demonstrated anti-inflammatory effects by inhibiting the expression of inflammatory cytokines including TNF-α, IL-6, and IL-1β, and downregulating the phosphorylation of STAT proteins. In a murine AD-like model induced by DNCB, administration of the LK5 herbal complex significantly ameliorated clinical symptoms, including dermatitis, ear thickness, and TEWL. Histological analysis revealed a reduction in epidermal thickness and mast cell infiltration. The LK5 herbal complex also inhibited pruritus induced by compound 48/80. Furthermore, the LK5 herbal complex treatment significantly decreased the levels of inflammatory cytokines such as TSLP, IL-6, and IgE in plasma and ear tissue of AD-induced mice. These findings suggest that the LK5 herbal complex may modulate the immune response and alleviate AD symptoms by inhibiting STAT pathways. © 2023 by the authors.-
dc.language영어-
dc.language.isoENG-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleAnti-Inflammatory Effects of the LK5 Herbal Complex on LPS- and IL-4/IL-13-Stimulated HaCaT Cells and a DNCB-Induced Animal Model of Atopic Dermatitis in BALB/c Mice-
dc.typeArticle-
dc.identifier.doi10.3390/pharmaceutics16010040-
dc.identifier.bibliographicCitationPharmaceutics, v.16, no.1-
dc.description.isOpenAccessY-
dc.identifier.wosid001151307800001-
dc.identifier.scopusid2-s2.0-85183130040-
dc.citation.number1-
dc.citation.titlePharmaceutics-
dc.citation.volume16-
dc.type.docTypeArticle-
dc.publisher.location스위스-
dc.subject.keywordAuthoranti-inflammation-
dc.subject.keywordAuthoratopic dermatitis-
dc.subject.keywordAuthoritching-
dc.subject.keywordAuthorLK5 herbal complex-
dc.subject.keywordAuthorsignal transducers and activators of transcription-
dc.subject.keywordPlus48/80-INDUCED SCRATCHING BEHAVIOR-
dc.subject.keywordPlusITCH-RELATED RESPONSES-
dc.subject.keywordPlusSCUTELLARIA-BAICALENSIS-
dc.subject.keywordPlusLIRIOPE-PLATYPHYLLA-
dc.subject.keywordPlusSOPHORA-FLAVESCENS-
dc.subject.keywordPlusCHLOROGENIC ACID-
dc.subject.keywordPlusARTHRITIS-
dc.subject.keywordPlusEXTRACT-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusBARRIER-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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