Sakatoku H, Kawai K, Kamiya H, Sakurai M
Gan To Kagaku Ryoho. 1986 Feb;13(2):239-46.
Experimental studies were designed in order to ameliorate cisplatin-induced nephrotoxicity. Cisplatin was injected intravenously into DS mice at a dose of 5.0 mg/kg. Plasma platinum levels declined in a biphasic fashion and were undetectable after 5 days post-infusion. Renal platinum levels decreased in the same manner as the plasma levels and revealed detectable plateau levels 5 days after single injection. Cisplatin was administer once a week for 3 consecutive weeks; serial plasma and renal platinum levels and BUN were measured 7 days after each injection. The results showed that there was no significant change in the levels of plasma platinum and BUN but that the renal platinum levels increased progressively (1.6 +/- 0.3, 3.1 +/- 0.4, 4.8 +/- 2.7 micrograms/g wet wt.). After another 6 successive weeks of cisplatin administration, 55% of mice died. The renal platinum levels and BUN of the survivors were highly increased. The renal tissue revealed histologically acute renal failure. However the renal concentration of platinum was decreased to a low level of 1.1 +/- 0.4 micrograms/g wet wt. 4 weeks after the third injection. These results suggested that cisplatin-induced nephrotoxicity could be ameliorated by adequate intervals of cisplatin administration.
开展实验研究以改善顺铂诱导的肾毒性。将顺铂以5.0毫克/千克的剂量静脉注射到DS小鼠体内。血浆铂水平呈双相下降,输注后5天检测不到。肾铂水平与血浆水平以相同方式下降,单次注射后5天显示出可检测的平稳水平。连续3周每周给药一次顺铂;每次注射后7天测量系列血浆和肾铂水平以及血尿素氮(BUN)。结果显示血浆铂和BUN水平无显著变化,但肾铂水平逐渐升高(1.6±0.3、3.1±0.4、4.8±2.7微克/克湿重)。在连续另外6周给予顺铂后,55%的小鼠死亡。存活小鼠的肾铂水平和BUN大幅升高。肾组织组织学显示为急性肾衰竭。然而,第三次注射后4周,肾铂浓度降至1.1±0.4微克/克湿重的低水平。这些结果表明,通过适当间隔给予顺铂可改善顺铂诱导的肾毒性。