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dc.contributor.authorBaşaran, A
dc.contributor.authorErol, K
dc.contributor.authorBaşaran, N
dc.contributor.authorGüneş, Hasan Veysi
dc.contributor.authorAçıkalın, E
dc.contributor.authorTimuralp, G
dc.contributor.authorTomatir, Ag
dc.date.accessioned2019-10-22T20:08:16Z
dc.date.available2019-10-22T20:08:16Z
dc.date.issued1993
dc.identifier.issn0009-3157
dc.identifier.urihttps://hdl.handle.net/11421/22524
dc.descriptionWOS: A1993LF33200005en_US
dc.descriptionPubMed ID: 8508688en_US
dc.description.abstractIn the present study, ciprofloxacin, a fluoroquinolone antibiotic, was evaluated in vivo. The toxic effects of ciprofloxacin (20 and 200 mg/kg/day) on kidney and liver functions, and on chromosomes were investigated in rats. 20 mg/kg/day ciprofloxacin did not significantly affect urine composition, serum enzyme levels and the haematocrit, affecting only creatinine clearance. The 200 mg/kg/day dose increased urine volume, serum creatinine and and creatinine clearance. Ciprofloxacin at both doses had no significant numerical effect on chromosomes, but there was a statistically significant dose-dependent increase in chromatid-type breakage. Significant histological changes in the liver and kidney were not observed.en_US
dc.language.isoengen_US
dc.publisherKargeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChromatid-Type Breakageen_US
dc.subjectCiprofloxacinen_US
dc.subjectCreatinine Clearanceen_US
dc.titleEffects of Ciprofloxacin on Chromosomes, and Hepatic and Renal Functions in Ratsen_US
dc.typearticleen_US
dc.relation.journalChemotherapyen_US
dc.contributor.departmentAnadolu Üniversitesi, Tıp Fakültesi, Farmakoloji Anabilim Dalıen_US
dc.identifier.volume39en_US
dc.identifier.issue3en_US
dc.identifier.startpage182en_US
dc.identifier.endpage188en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]


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