Tune B M, Wu K Y, Fravert D, Holtzman D
J Pharmacol Exp Ther. 1979 Jul;210(1):98-100.
The effects of the nephrotoxic antibiotic, cephaloridine, were studied in rabbit renal cortical mitochondria. Mitochondria from animals which received a toxic dose of 200 mg/kg of the drug 2 hr before sacrifice (in vivo exposure) had significantly decreased rates of respiration compared with those of mitochondria from untreated control animals. In vitro exposure of normal mitochondria to cephaloridine resulted in a qualitatively similar decrease of respiration. With both in vivo and in vitro exposure, inhibition was greatest with ADP-dependent respiration using succinate as substrate. The severity of in vitro inhibition of respiration showed some correlation to the degree of in situ cytotoxicity at different cephaloridine concentrations. The results are in agreement with the finding of a reduction of rates of respiration in renal tubule suspensions after similar in vivo and in vitro exposure to cephaloridine. These studies provide preliminary evidence that cephaloridine nephrotoxicity may be mediated through an inhibitory effect on mitochondrial respiration.
研究了肾毒性抗生素头孢噻啶对兔肾皮质线粒体的影响。处死前2小时接受200mg/kg药物毒性剂量(体内暴露)的动物的线粒体,与未处理的对照动物的线粒体相比,呼吸速率显著降低。正常线粒体在体外暴露于头孢噻啶后,呼吸也出现了定性相似的降低。体内和体外暴露时,以琥珀酸为底物的ADP依赖性呼吸的抑制作用最大。不同头孢噻啶浓度下,体外呼吸抑制的严重程度与原位细胞毒性程度存在一定相关性。这些结果与在体内和体外相似暴露于头孢噻啶后肾小管悬浮液中呼吸速率降低的发现一致。这些研究提供了初步证据,表明头孢噻啶肾毒性可能通过对线粒体呼吸的抑制作用介导。