Silber P M, Gandolfi A J, Brendel K
Drug Chem Toxicol. 1986;9(3-4):285-303. doi: 10.3109/01480548608998281.
The progression of changes in rabbit kidney function following dosing with the nephrotoxin S-(1,2-dichlorovinyl)-L-cysteine (DCVC, 20-50 mg/kg) was determined. Proteinuria was observed 0.5-1 hr after administration of DCVC at doses of 20-50 mg/kg. Blood urea nitrogen levels, glomerular filtration rates, urinary glucose excretion, and urine volume were also altered following DCVC dosing; however, these parameters were less sensitive than proteinuria as markers of early renal dysfunction. None of these latter four indicators were affected by low DCVC doses, nor were they altered by high DCVC doses until 1.5-2.5 hr after dosing. Dose-dependent morphological changes to kidney structure were also observed 5 hr after DCVC administration. Low doses caused damage restricted to brush border membranes in the pars recta, while higher doses produced a necrotic lesion encompassing all regions of the proximal tubule. This study indicates that DCVC can cause rapid renal dysfunctional changes which are first detected by elevated urinary protein excretion.
测定了给兔子注射肾毒素S-(1,2-二氯乙烯基)-L-半胱氨酸(DCVC,20-50毫克/千克)后肾功能变化的进展情况。在以20-50毫克/千克的剂量注射DCVC后0.5-1小时观察到蛋白尿。注射DCVC后,血尿素氮水平、肾小球滤过率、尿糖排泄和尿量也发生了改变;然而,作为早期肾功能障碍的标志物,这些参数比蛋白尿的敏感性要低。后四个指标中的任何一个都不受低剂量DCVC的影响,在高剂量DCVC给药后1.5-2.5小时之前,它们也没有发生改变。在注射DCVC 5小时后,还观察到肾脏结构的剂量依赖性形态学变化。低剂量导致损伤局限于直部的刷状缘膜,而高剂量则产生包括近端小管所有区域的坏死性病变。这项研究表明,DCVC可导致快速的肾功能障碍变化,这种变化首先通过尿蛋白排泄增加而被检测到。