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Cited 26 time in webofscience Cited 29 time in scopus
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Beneficial Effects of Bioactive Compounds in Mulberry Fruits against Cisplatin-Induced Nephrotoxicity

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dc.contributor.authorLee, Dahae-
dc.contributor.authorYu, Jae Sik-
dc.contributor.authorLee, Seoung Rak-
dc.contributor.authorHwang, Gwi Seo-
dc.contributor.authorKang, Ki Sung-
dc.contributor.authorPark, Jae Gyu-
dc.contributor.authorKim, Hyun Young-
dc.contributor.authorKim, Ki Hyun-
dc.contributor.authorYamabe, Noriko-
dc.date.accessioned2022-12-26T17:03:33Z-
dc.date.available2022-12-26T17:03:33Z-
dc.date.issued2018-04-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/11734-
dc.description.abstractMulberry, the fruit of white mulberry tree (Morus alba L., Moraceae), is commonly used in traditional Chinese medicines as a sedative, tonic, laxative, and emetic. In our continuing research of the bioactive metabolites from mulberry, chemical analysis of the fruits led to the isolation of five compounds, 1-5. The compounds were identified as butyl pyroglutamate (1), quercetin 3-O-beta-D-glucoside (2), kaempferol 3-O-beta-D-rutinoside (3), rutin (4), and 2-phenylethyl D-rutinoside (5) by spectroscopic data analysis, comparing their nuclear magnetic resonance (NMR) data with those in published literature, and liquid chromatography-mass spectrometry analysis. The isolated compounds 1-5 were evaluated for their effects on anticancer drug-induced side effects by cell-based assays. Compound 1 exerted the highest protective effect against cisplatin-induced kidney cell damage. This effect was found to be mediated through the attenuation of phosphorylation of c-Jun N-terminal kinase, extracellular signal-regulated kinase, p38, mitogen-activated protein kinase, and caspase-3 in cisplatin-induced kidney cell damage.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleBeneficial Effects of Bioactive Compounds in Mulberry Fruits against Cisplatin-Induced Nephrotoxicity-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/ijms19041117-
dc.identifier.scopusid2-s2.0-85045223343-
dc.identifier.wosid000434978700196-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.19, no.4-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.volume19-
dc.citation.number4-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusCERVICAL-CANCER-
dc.subject.keywordPlusKIDNEY-CELLS-
dc.subject.keywordPlusINDUCED CYTOTOXICITY-
dc.subject.keywordPlusINDUCED APOPTOSIS-
dc.subject.keywordPlusL.-
dc.subject.keywordPlusEXTRACTS-
dc.subject.keywordPlusTOXICITY-
dc.subject.keywordPlusANALOGS-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusINJURY-
dc.subject.keywordAuthormulberry-
dc.subject.keywordAuthorMorus alba-
dc.subject.keywordAuthorcisplatin-
dc.subject.keywordAuthornephrotoxicity-
dc.subject.keywordAuthormitogen-activated protein kinases-
dc.subject.keywordAuthorcaspase-3-
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