Rankin G O, Yang D J, Cressey-Veneziano K, Brown P I
Toxicol Lett. 1985 Jan;24(1):99-105. doi: 10.1016/0378-4274(85)90146-8.
The nephrotoxic potential of N-(3,5-dichlorophenyl)succinimide (NDPS) was examined, in male Fischer-344 rats. Rats were administered NDPS (0.1, 0.2, 0.4 or 1.0 mmol/kg intraperitoneally (i.p.) or sesame oil (2.5 ml/kg, i.p.), and renal function was monitored at 24 and 48 h. NDPS (0.1 mmol/kg) stimulated organic ion uptake at 48 h. NDPS (0.2 mmol/kg) produced diuresis but did not alter blood urea nitrogen (BUN), kidney weight or organic ion uptake by renal cortical slices at 48 h. High-dose NDPS (0.4 and 1.0 mmol/kg) administration produced diuresis, decreased accumulation of p-aminohippurate (PAH) and tetraethylammonium (TEA), increased BUN and kidney weight and caused acute tubular necrosis. At 24 h, NDPS (0.2 mmol/kg) decreased uptake of PAH and TEA and tended to increase BUN. These results are similar to previous reports of NDPS-induced nephrotoxicity in Sprague-Dawley rats and suggest that either rat model would be suitable for future studies on the mechanism(s) of NDPS-induced nephropathy.
在雄性Fischer - 344大鼠中检测了N - (3,5 - 二氯苯基)琥珀酰亚胺(NDPS)的肾毒性潜力。给大鼠腹腔注射NDPS(0.1、0.2、0.4或1.0 mmol/kg)或芝麻油(2.5 ml/kg,腹腔注射),并在24小时和48小时监测肾功能。NDPS(0.1 mmol/kg)在48小时时刺激有机离子摄取。NDPS(0.2 mmol/kg)产生利尿作用,但在48小时时未改变血尿素氮(BUN)、肾脏重量或肾皮质切片对有机离子的摄取。高剂量NDPS(0.4和1.0 mmol/kg)给药产生利尿作用,降低对氨基马尿酸(PAH)和四乙铵(TEA)的蓄积,增加BUN和肾脏重量,并导致急性肾小管坏死。在24小时时,NDPS(0.2 mmol/kg)降低PAH和TEA的摄取,并倾向于增加BUN。这些结果与之前关于NDPS诱导Sprague - Dawley大鼠肾毒性的报道相似,表明这两种大鼠模型都适合未来关于NDPS诱导肾病机制的研究。