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Anti-apoptotic and antioxidant effects of 3-epi-iso- seco-tanapartholide isolated from artemisia argyi against iodixanol-induced kidney epithelial cell death

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dc.contributor.authorLee D.-
dc.contributor.authorKim K.O.-
dc.contributor.authorLee D.-
dc.contributor.authorKang K.S.-
dc.date.available2020-08-10T00:36:34Z-
dc.date.created2020-06-17-
dc.date.issued2020-06-
dc.identifier.issn2218-273X-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/76192-
dc.description.abstractIodixanol is a non-ionic iso-osmolar contrast agent, but it is a risk factor for kidney damage and increases morbidity and mortality. In this study, we investigated the effect of 9 sesquiterpenes isolated from mugwort (Artemisia argyi) in contrast agent-induced cytotoxicity in LLC-PK1 cells. Cells were exposed to nine sesquiterpene compounds for 2 h, followed by incubation with iodixanol for 3 h. Cell viability was assessed using the Ez-Cytox assay. The level of reactive oxygen species was measured using 2′,7′-dichlorodihydrofluorescein diacetate staining. Apoptotic cell death was detected using annexin V/PI staining. In addition, immunofluorescence staining and western blotting were performed using antibodies against proteins related to apoptosis, oxidative stress, and MAPK pathways. The most effective 3-epi-iso-seco-tanapartholide (compound 8) among the 9 sesquiterpene compounds protected LLC-PK1 cells from iodixanol-induced cytotoxicity, oxidative stress, and apoptotic cell death. Pretreatment with compound 8 reversed iodixanol-induced increases in the expression of JNK, ERK, p38, Bax, caspase-3, and caspase-9. It also reversed the iodixanol-induced decrease in Bcl-2 expression. Furthermore, pretreatment with compound 8 caused nuclear translocation of Nrf2 and upregulated HO-1 via the Nrf2 pathway in iodixanol-treated LLC-PK1 cells. Thus, we demonstrated here that compound 8 isolated from A. argyi has the potential to effectively prevent iodixanol-induced kidney epithelial cell death via the caspase- 3/MAPK pathways and HO-1 via the Nrf2 pathway. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI AG-
dc.relation.isPartOfBiomolecules-
dc.titleAnti-apoptotic and antioxidant effects of 3-epi-iso- seco-tanapartholide isolated from artemisia argyi against iodixanol-induced kidney epithelial cell death-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000550863800001-
dc.identifier.doi10.3390/biom10060867-
dc.identifier.bibliographicCitationBiomolecules, v.10, no.6, pp.1 - 18-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85086176083-
dc.citation.endPage18-
dc.citation.startPage1-
dc.citation.titleBiomolecules-
dc.citation.volume10-
dc.citation.number6-
dc.contributor.affiliatedAuthorLee D.-
dc.contributor.affiliatedAuthorKang K.S.-
dc.type.docTypeArticle-
dc.subject.keywordAuthorApoptosis-
dc.subject.keywordAuthorContrast agent-
dc.subject.keywordAuthorCytotoxicity-
dc.subject.keywordAuthorIodixanol-
dc.subject.keywordAuthorOxidative stress-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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