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Antioxidant and Anti-Inflammatory Effects of 3-Dehydroxyceanothetric Acid 2-Methyl Ester Isolated from Ziziphus jujuba Mill. against Cisplatin-Induced Kidney Epithelial Cell Death

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dc.contributor.authorLee, Dahae-
dc.contributor.authorKang, Kyo Bin-
dc.contributor.authorHwang, Gwi Seo-
dc.contributor.authorChoi, You-Kyoung-
dc.contributor.authorKim, Tae Kon-
dc.contributor.authorKang, Ki Sung-
dc.date.accessioned2021-12-06T01:40:58Z-
dc.date.available2021-12-06T01:40:58Z-
dc.date.created2021-11-05-
dc.date.issued2021-11-
dc.identifier.issn2218-273X-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/82856-
dc.description.abstractCisplatin is a platinum-based chemotherapeutic agent for treating solid tumors; however, it presents a risk factor for nephropathy. In the present study, we investigated the antioxidant and anti-inflammatory effects of 3-dehydroxyceanothetric acid 2-methyl ester (3DC2ME) isolated from Ziziphus jujuba Mill. in LLC-PK1 cells following cisplatin-induced cytotoxicity. These cells were exposed to 3DC2ME for 2 h, followed by treatment with cisplatin for 24 h. The treated cells were subjected to cell viability analysis using the Ez-Cytox assay. Reactive oxygen species (ROS) were detected via 2′, 7′-dichlorodihydrofluorescein diacetate (DCFH-DA) staining. In addition, western blotting and fluorescent immunostaining were performed to evaluate protein expressions related to oxidative stress and inflammation pathways. Pretreatment with 3DC2ME protected LLC-PK1 cells from cisplatin-induced cytotoxicity and oxidative stress. In addition, pretreatment with 3DC2ME upregulated heme oxygenase 1 (HO-1) via the nuclear factor erythroid 2-related factor 2 (Nrf2) pathway in the cisplatin-treated LLC-PK1 cells. Furthermore, the increase in the expressions of IκB kinase α/β (IKKα/β), inhibitor of kappa B alpha (IκBα), nuclear factor kappa B (NF-κB), inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2) in these cells was inhibited. These results provide basic scientific evidence for understanding the antioxidant and anti-inflammatory effects of 3DC2ME isolated from Z. jujuba against cisplatin-induced kidney epithelial cell death. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI-
dc.relation.isPartOfBiomolecules-
dc.titleAntioxidant and Anti-Inflammatory Effects of 3-Dehydroxyceanothetric Acid 2-Methyl Ester Isolated from Ziziphus jujuba Mill. against Cisplatin-Induced Kidney Epithelial Cell Death-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000723880700001-
dc.identifier.doi10.3390/biom11111614-
dc.identifier.bibliographicCitationBiomolecules, v.11, no.11-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85118224289-
dc.citation.titleBiomolecules-
dc.citation.volume11-
dc.citation.number11-
dc.contributor.affiliatedAuthorLee, Dahae-
dc.contributor.affiliatedAuthorHwang, Gwi Seo-
dc.contributor.affiliatedAuthorChoi, You-Kyoung-
dc.contributor.affiliatedAuthorKang, Ki Sung-
dc.type.docTypeArticle-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorLLC-PK1-
dc.subject.keywordAuthorNephrotoxicity-
dc.subject.keywordAuthorOxidative stress-
dc.subject.keywordAuthorZiziphus jujuba Mill-
dc.subject.keywordPlusNRF2/HO-1 SIGNALING PATHWAY-
dc.subject.keywordPlusINDUCED NEPHROTOXICITY-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusMECHANISMS-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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