Appenroth D, Winnefeld K, Bräunlich H
Institute of Pharmacology and Toxicology, Friedrich Schiller University, DDR, Jena.
Biomed Biochim Acta. 1988;47(8):791-7.
Wistar rats (10 and 55 days old) were administered a single dose of 0.6 mg cisplatinum (CP) 100 g body wt. intraperitoneally. Urinary volume, p-aminohippurate and total protein excretion were determined. Separation of urinary proteins was performed by sodium dodecylsulfate polyacrylamide gel electrophoresis. Significant symptoms of nephrotoxicity (oliguria, reduced PAH-excretion, heavy proteinuria, changes in urinary protein composition) were detected in adult rats 72 h after CP. At that time young rats did not show distinct signs of nephrotoxicity. Experiments on time dependence of nephrotoxicity showed that in young rats symptoms occurred already 6 h after CP-administration, and 72 h after CP the damage was nearly completely repaired. Pt-determination in serum, kidney tissue, and urine showed a shorter t1/2 in serum, lower concentrations in kidney tissue as well as higher Pt-concentrations in urine of young compared with adult rats.
给10日龄和55日龄的Wistar大鼠腹腔注射单剂量每100克体重0.6毫克顺铂(CP)。测定尿量、对氨基马尿酸和总蛋白排泄量。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳对尿蛋白进行分离。在成年大鼠注射CP后72小时检测到明显的肾毒性症状(少尿、对氨基马尿酸排泄减少、重度蛋白尿、尿蛋白组成改变)。此时幼鼠未表现出明显的肾毒性迹象。肾毒性时间依赖性实验表明,幼鼠在注射CP后6小时就出现症状,而在注射CP后72小时损伤几乎完全修复。与成年大鼠相比,幼鼠血清、肾组织和尿液中的铂测定显示血清中的半衰期更短,肾组织中的浓度更低,尿液中的铂浓度更高。