Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14910
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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.identifier.issn13403443
dc.identifier.other2-s2.0-69949132511
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14910-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-69949132511&doi=10.1007%2fs11418-009-0345-5&partnerID=40&md5=443e5aae721908615464cfcc99bd90a7
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.subjectalcohol
dc.subjectantioxidant
dc.subjectascorbic acid
dc.subjectcatalase
dc.subjectcisplatin
dc.subjectcreatinine
dc.subjectCurcuma comosa extract
dc.subjectglutathione
dc.subjectglutathione peroxidase
dc.subjectplant extract
dc.subjectscavenger
dc.subjectsuperoxide dismutase
dc.subjecttrolox C
dc.subjectunclassified drug
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectblood sampling
dc.subjectcontrolled study
dc.subjectcreatinine blood level
dc.subjectCurcuma comosa
dc.subjectdegeneration
dc.subjectdrug structure
dc.subjecthistopathology
dc.subjectkidney tubule necrosis
dc.subjectlipid peroxidation
dc.subjectmale
dc.subjectmedicinal plant
dc.subjectmouse
dc.subjectnephrotoxicity
dc.subjectnonhuman
dc.subjecturea nitrogen blood level
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectCatalase
dc.subjectCisplatin
dc.subjectCurcuma
dc.subjectEthanol
dc.subjectGlutathione
dc.subjectGlutathione Peroxidase
dc.subjectKidney
dc.subjectMale
dc.subjectMice
dc.subjectMolecular Structure
dc.subjectPlant Extracts
dc.subjectSuperoxide Dismutase
dc.titleProtection against cisplatin-induced nephrotoxicity in mice by Curcuma comosa Roxb. ethanol extract
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of Natural Medicines. Vol 63, No.4 (2009), p.430-436
dc.identifier.doi10.1007/s11418-009-0345-5
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