Okamoto K, Ito M, Suzuki Y
Jpn J Pharmacol. 1984 Jan;34(1):33-41. doi: 10.1254/jjp.34.33.
Crescentic-type nephritis was induced in rats by immunizing with rabbit gamma-globulin following i.v. injection of rabbit anti-rat glomerular basement membrane (anti-GBM) serum. The antinephritic effect of mizoribine was compared to that of azathioprine by administration from the 2nd day after the injection of anti-GBM serum to the 23rd day (Experiment I) and from the 15th to the 38th day (Experiment II). The experiment I assessment on the 24th day revealed that mizoribine at a dose of 7.5 mg/kg/day p.o. remarkably reduced plasma cholesterol level, wet kidney weight and glomerular histopathological changes (i.e., crescent formation and fibrinoid deposition). In addition, mizoribine at this dose also tended to reduce urinary protein excretion and the adhesion of capillary walls to Bowman's capsule. At a dose of 5 mg/kg/day p.o., mizoribine significantly reduced kidney weight and crescent formation. On the other hand, azathioprine at a dose of 20 mg/kg/day p.o. had a tendency to reduce these biochemical and histopathological parameters. In the experiment II assessment on the 39th day, the effects of both drugs were somewhat diminished compared to those in experiment I. Mizoribine strikingly inhibited the crescent formation with 5 and 7.5 mg/kg/day p.o. and inhibited the fibrinoid deposition with a dose of 7.5 mg/kg/day p.o. Azathioprine at a dose of 20 mg/kg/day p.o. was prone to reduce histopathological parameters. The above data indicate that mizoribine may be a useful new immunosuppressive agent for rapidly progressive glomerulonephritis, which is characterized by severe glomerular lesion with the extensive formation of crescents.
通过静脉注射兔抗大鼠肾小球基底膜(抗GBM)血清后用兔γ球蛋白免疫大鼠,诱导其发生新月体型肾炎。从注射抗GBM血清后的第2天至第23天(实验I)以及从第15天至第38天(实验II)给予咪哩立宾,将其抗肾炎作用与硫唑嘌呤进行比较。实验I在第24天的评估显示,口服剂量为7.5mg/kg/天的咪哩立宾显著降低了血浆胆固醇水平、肾脏湿重和肾小球组织病理学变化(即新月体形成和纤维蛋白样沉积)。此外,该剂量的咪哩立宾还倾向于减少尿蛋白排泄以及毛细血管壁与鲍曼囊的粘连。口服剂量为5mg/kg/天的咪哩立宾显著降低了肾脏重量和新月体形成。另一方面,口服剂量为20mg/kg/天的硫唑嘌呤有降低这些生化和组织病理学参数的趋势。在实验II第39天的评估中,与实验I相比,两种药物的作用均有所减弱。口服5mg/kg/天和7.5mg/kg/天的咪哩立宾显著抑制了新月体形成,口服剂量为7.5mg/kg/天的咪哩立宾抑制了纤维蛋白样沉积。口服剂量为20mg/kg/天的硫唑嘌呤易于降低组织病理学参数。上述数据表明,咪哩立宾可能是一种用于快速进展性肾小球肾炎的有用的新型免疫抑制剂,快速进展性肾小球肾炎的特征是严重的肾小球病变并伴有广泛的新月体形成。