Bertani T, Poggi A, Pozzoni R, Delaini F, Sacchi G, Thoua Y, Mecca G, Remuzzi G, Donati M B
Lab Invest. 1982 Jan;46(1):16-23.
Adriamycin has been suspected of causing experimental nephrotoxicity. We report here that adriamycin induces a nephrotic syndrome in rats, proteinuria beginning 4 to 5 days after a single intravenous injection (7.5 mg. per kg. of body weight). The full expression of the syndrome develops 13 to 15 days later. Minimal alterations at light microscopy, negative immunofluorescence, and only some focal "fusion" of foot processes can be observed by electron microscopy in the early phase after injection (28 hours). At 13 days, loss of foot process architecture, and replacement by flattened epithelial cytoplasm, was invariably found. These ultrastructural findings became extensive at 28 days follow-up. Colloidal iron staining of kidney biopsies revealed loss of glomerular polyanions as early as 3 hours and very marked loss at 28 hours after adriamycin injection. Polyanions were totally absent at 13 days and were still undetectable at 28 days. Thus, the loss of polyanionic charges associated with the sialic acid coat precedes the ultrastructural changes and the onset of proteinuria. These changes appeared similar to those reported in rats treated with daunomycin or puromycin animonucleoside. The present study supports in a different animal model the concept that both morphologic changes and proteinuria are the consequence of a common primary event that is the loss of glomerular fixed negative charges.
阿霉素一直被怀疑会引起实验性肾毒性。我们在此报告,阿霉素可在大鼠中诱发肾病综合征,单次静脉注射(每千克体重7.5毫克)后4至5天开始出现蛋白尿。该综合征的完全表现13至15天后出现。注射后早期(28小时),光镜下改变轻微,免疫荧光阴性,电镜下仅见一些局灶性足突“融合”。在13天时,总是发现足突结构丧失,被扁平的上皮细胞质取代。在28天的随访中,这些超微结构改变变得广泛。肾活检的胶体铁染色显示,阿霉素注射后3小时肾小球多阴离子就开始丢失,28小时时丢失非常明显。13天时多阴离子完全缺失,28天时仍检测不到。因此,与唾液酸包被相关的多阴离子电荷丢失先于超微结构改变和蛋白尿的发生。这些改变与用柔红霉素或嘌呤霉素氨基核苷处理的大鼠中报道的改变相似。本研究在不同的动物模型中支持了这样一种观点,即形态学改变和蛋白尿都是一个共同的原发事件的结果,这个原发事件就是肾小球固定负电荷的丢失。