Publication:
Protection against cisplatin-induced nephrotoxicity in mice by Curcuma comosa Roxb. ethanol extract

dc.contributor.authorSurawat Jariyawaten_US
dc.contributor.authorPranida Kigpitucken_US
dc.contributor.authorKanoknetr Suksenen_US
dc.contributor.authorAporn Chuncharuneeen_US
dc.contributor.authorArusa Chaovanalikiten_US
dc.contributor.authorPawinee Piyachaturawaten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.date.accessioned2018-09-13T06:30:22Z
dc.date.available2018-09-13T06:30:22Z
dc.date.issued2009-10-01en_US
dc.description.abstractThe protective effect of an ethanol extract of Curcuma comosa against cisplatin-induced renal toxicity in mice was studied. Adult male mice were pretreated for 4 days with the ethanol extract of C. comosa [100-200 mg/kg body weight (BW), orally (p.o.)] before injection of cisplatin (12.5 mg/kg BW, intraperitoneally (i.p.)). Five days later the mice were killed, and blood samples were collected to determine blood urea nitrogen (BUN) and plasma creatinine levels. Kidneys were examined histopathologically and levels of lipid peroxidation, gluthathione (GSH) content, and superoxide dismutase (SOD), gluthathione peroxidase (GPx), and catalase (CAT) activities were determined. Histological examinations revealed degenerative changes and tubular necrosis in mice treated with cisplatin, which were improved by pretreatment with C. comosa ethanol extract. Cisplatin raised BUN, creatinine, and kidney lipid peroxidation levels, and lowered kidney GSH content and levels of GPx, SOD, and CAT activities, all of which (except SOD and CAT) could be restored to normal values by pretreatment with 200 mg/kg BW of C. comosa ethanol extract. In addition, the ethanol extract of C. comosa and its isolated diarylheptanoid compound also exhibited radical scavenging activities. The results suggest that the ethanol extract of C. comosa exhibits effective protection against cisplatin-induced nephrotoxicity mediated through its antioxidant activity. © 2009 The Japanese Society of Pharmacognosy and Springer.en_US
dc.identifier.citationJournal of Natural Medicines. Vol.63, No.4 (2009), 430-436en_US
dc.identifier.doi10.1007/s11418-009-0345-5en_US
dc.identifier.issn18610293en_US
dc.identifier.issn13403443en_US
dc.identifier.other2-s2.0-69949132511en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/27394
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=69949132511&origin=inwarden_US
dc.subjectChemistryen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleProtection against cisplatin-induced nephrotoxicity in mice by Curcuma comosa Roxb. ethanol extracten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=69949132511&origin=inwarden_US

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