作者: Ken-ichiro Nan-ya , Masatomo Kajihara , Natsuki Kojima , Masakuni Degawa
DOI: 10.1002/JAT.2999
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摘要: We explored biomarkers suitable for monitoring sub-chronic kidney injury using the three rat models of cisplatin (CDDP)-induced injury, which were designed to extend current knowledge beyond sub-acute exposure period. In pilot study, a single intravenous administration 1.5 mg kg(-1) CDDP rats was confirmed result in no histopathological changes. Subsequently, intravenously administered at dose 4 days 24-h intervals (Experimental model 1) and up 10 weeks weekly 2 3), changes blood urine components, such as recently recommended urinary (Kim-1, clusterin so on) traditional (blood urea nitrogen serum creatinine), examined together with renal tissues during development each model. these experimental models, significant increase Kim-1 observed prior tissues, retained after adverse Significant all other occurred along addition, treatment reduced time-dependent manner cessation drug. The present findings indicate that is most useful biomarker CDDP-induced among examined.