Luft F C, Bloch R, Sloan R S, Yum M N, Costello R, Maxwell D R
J Infect Dis. 1978 Oct;138(4):541-5. doi: 10.1093/infdis/138.4.541.
Netilmicin, gentamicin, tobramycin, amikacin, kanamycin, streptomycin, and sisomicin were given daily for 15 days to groups of rats at three dosage levels corresponding to 10, 15, or 25 times the dose recommended for humans on a weight basis. Decreased urinary osmolality and increased urinary excretion of protein and beta-N-acetyl hexosaminidase were dose-related features of nephrotoxicity. Decreased tubular resorption of glucose and phosphate were observed with the most toxic regimens after extensive renal damage had occurred. All aminoglycosides accumulated in renal tissue; however, the concentration of drug in the renal cortex at the time the rats were killed was not useful for the prediction of renal impairment. Streptomycin and netilmicin exhibited a flat dose-reponse curve with respect to histological damage, as compared with the curves for the other drugs. Results of studies of creatinine clearance and examination of renal tissue suggested the following order of increasing toxicity of the treatment regimens: (1) 0.9% NaCl and uninjected controls; (2) streptomycin; (3) netilmicin; (4) tobramycin; (5) sisomicin, amikacin, and kanamycin; and (6) gentamicin.
将奈替米星、庆大霉素、妥布霉素、阿米卡星、卡那霉素、链霉素和西索米星按相当于人类推荐剂量的10倍、15倍或25倍这三个剂量水平,每日给药大鼠15天。尿渗透压降低、尿蛋白和β-N-乙酰己糖胺酶排泄增加是肾毒性的剂量相关特征。在广泛的肾损伤发生后,最具毒性的给药方案出现了肾小管对葡萄糖和磷酸盐重吸收减少的情况。所有氨基糖苷类药物都在肾组织中蓄积;然而,大鼠处死时肾皮质中的药物浓度对预测肾功能损害并无帮助。与其他药物的曲线相比,链霉素和奈替米星在组织学损伤方面呈现出平缓的剂量反应曲线。肌酐清除率研究和肾组织检查结果表明,各给药方案的毒性递增顺序如下:(1) 0.9%氯化钠溶液和未注射对照组;(2) 链霉素;(3) 奈替米星;(4) 妥布霉素;(5) 西索米星、阿米卡星和卡那霉素;(6) 庆大霉素。