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Taraxacum coreanum Nakai extract attenuates lipopolysaccharide-induced inflammatory responses and intestinal barrier dysfunction in Caco-2 cells

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dc.contributor.authorHan, Seok Hee-
dc.contributor.authorLee, Hak-Dong-
dc.contributor.authorLee, Sanghyun-
dc.contributor.authorLee, Ah Young-
dc.date.accessioned2023-09-22T02:40:39Z-
dc.date.available2023-09-22T02:40:39Z-
dc.date.issued2024-01-
dc.identifier.issn0378-8741-
dc.identifier.issn1872-7573-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/67938-
dc.description.abstractEthnopharmacological relevance: Taraxacum coreanum Nakai (TC) is a dandelion native to Korea that has long been used as a medicinal herb with antioxidant and anti-inflammatory properties. Intestinal inflammation is closely associated with intestinal epithelial barrier disruption, which leads to the progression of various intestinal diseases. Aim of the study: The aim of this study was to investigate the protective effects of TC extract on inflammatory responses and intestinal barrier dysfunction in lipopolysaccharide (LPS)-stimulated Caco-2 cells. Materials and methods: The inhibitory effect of TC on nitric oxide (NO) and pro-inflammatory cytokines production were determined by Griess reagent and enzyme-linked immunosorbent assay, respectively. The epithelial permeability was evaluated by transepithelial electrical resistance (TEER) assay, and inflammation- and tight junction (TJ)-related protein expression were analyzed by Western blotting. In addition, the presence of ten active compounds was identified and quantified using UHPLC-ESI-MS and HPLC-DAD analyses. Results: Treatment with TC significantly reduced NO production and pro-inflammatory cytokines production [interleukin (IL)-6 and tumor necrosis factor (TNF)-α] compared to the group treated with LPS only, particularly at 100 μg/mL. TC significantly decreased monolayer permeability as detected by TEER. In addition, the transmission of fluorescein isothiocyanate-dextran 4 across the barrier was decreased after treatment with TC. Inflammation-related proteins (inducible NO synthase, cyclooxygenase-2, TNF-α, IL-6, and IL-1β) were down-regulated after treatment with TC. In contrast, TC significantly increased the protein levels of the TJ-related protein, claudin-5. Ten phytochemicals (protocatechuic acid, chlorogenic acid, caffeic acid, scopoletin, chicoric acid, hyperoside, nicotiflorin, luteoloside, sophoricoside, and luteolin) were identified by UHPLC-ESI-MS and HPLC-DAD analysis. Conclusion: Our findings suggest that ethanolic extract of TC could attenuate the LPS-induced intestinal barrier dysfunction by increasing the TJ protein and suppressing inflammatory responses. © 2023 Elsevier B.V.-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleTaraxacum coreanum Nakai extract attenuates lipopolysaccharide-induced inflammatory responses and intestinal barrier dysfunction in Caco-2 cells-
dc.typeArticle-
dc.publisher.location아일랜드-
dc.identifier.doi10.1016/j.jep.2023.117105-
dc.identifier.scopusid2-s2.0-85170246220-
dc.identifier.wosid001071824900001-
dc.identifier.bibliographicCitationJournal of Ethnopharmacology, v.319-
dc.citation.titleJournal of Ethnopharmacology-
dc.citation.volume319-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPlant Sciences-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaIntegrative & Complementary Medicine-
dc.relation.journalWebOfScienceCategoryPlant Sciences-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryIntegrative & Complementary Medicine-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusTIGHT JUNCTIONS-
dc.subject.keywordPlusMOUSE MODEL-
dc.subject.keywordPlusPERMEABILITY-
dc.subject.keywordPlusLPS-
dc.subject.keywordPlusPOLYSACCHARIDE-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusINTEGRITY-
dc.subject.keywordPlusCYTOKINES-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordAuthorCaco-2 cells-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorLipopolysaccharide-
dc.subject.keywordAuthorTaraxacum coreanum Nakai-
dc.subject.keywordAuthorTight junction-
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