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

dc.contributor.authorJariyawat S.
dc.contributor.authorKigpituck P.
dc.contributor.authorSuksen K.
dc.contributor.authorChuncharunee A.
dc.contributor.authorChaovanalikit A.
dc.contributor.authorPiyachaturawat P.
dc.date.accessioned2021-04-05T04:32:06Z
dc.date.available2021-04-05T04:32:06Z
dc.date.issued2009
dc.date.issuedBE2552
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.
dc.format.mimetypeapplication/pdf
dc.identifier.citationJournal of Natural Medicines. Vol 63, No.4 (2009), p.430-436
dc.identifier.doi10.1007/s11418-009-0345-5
dc.identifier.issn13403443
dc.identifier.other2-s2.0-69949132511
dc.identifier.urihttps://hdl.handle.net/20.500.14740/4251
dc.rights.holderScopus
dc.subject.otherAlcohol
dc.subject.otherAntioxidant
dc.subject.otherAscorbic acid
dc.subject.otherCatalase
dc.subject.otherCisplatin
dc.subject.otherCreatinine
dc.subject.otherCurcuma comosa extract
dc.subject.otherGlutathione
dc.subject.otherGlutathione peroxidase
dc.subject.otherPlant extract
dc.subject.otherScavenger
dc.subject.otherSuperoxide dismutase
dc.subject.otherTrolox C
dc.subject.otherUnclassified drug
dc.subject.otherAnimal experiment
dc.subject.otherAnimal tissue
dc.subject.otherAntioxidant activity
dc.subject.otherArticle
dc.subject.otherBlood sampling
dc.subject.otherControlled study
dc.subject.otherCreatinine blood level
dc.subject.otherCurcuma comosa
dc.subject.otherDegeneration
dc.subject.otherDrug structure
dc.subject.otherHistopathology
dc.subject.otherKidney tubule necrosis
dc.subject.otherLipid peroxidation
dc.subject.otherMale
dc.subject.otherMedicinal plant
dc.subject.otherMouse
dc.subject.otherNephrotoxicity
dc.subject.otherNonhuman
dc.subject.otherUrea nitrogen blood level
dc.subject.otherAnimals
dc.subject.otherAntioxidants
dc.subject.otherCatalase
dc.subject.otherCisplatin
dc.subject.otherCurcuma
dc.subject.otherEthanol
dc.subject.otherGlutathione
dc.subject.otherGlutathione Peroxidase
dc.subject.otherKidney
dc.subject.otherMale
dc.subject.otherMice
dc.subject.otherMolecular Structure
dc.subject.otherPlant Extracts
dc.subject.otherSuperoxide Dismutase
dc.titleProtection against cisplatin-induced nephrotoxicity in mice by Curcuma comosa Roxb. ethanol extract
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-69949132511&doi=10.1007%2fs11418-009-0345-5&partnerID=40&md5=443e5aae721908615464cfcc99bd90a7

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