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实验性原位性肾炎的药物防治研究
引用本文:许光辉,黄文聪,何柏林,李士梅,蓝辉耀,胡缓芳. 实验性原位性肾炎的药物防治研究[J]. 中山大学学报(医学科学版), 1988, 0(4)
作者姓名:许光辉  黄文聪  何柏林  李士梅  蓝辉耀  胡缓芳
作者单位:中山医科大学第一附属医院内科肾脏病研究室(许光辉,黄文聪,何柏林,李士梅),中山医科大学病理解剖学教研室(蓝辉耀),中山医科大学病理解剖学教研室(胡缓芳)
摘    要:本文用抑制TxA_2合成酶的药物——苄基咪唑(BIm)和抑制血小板聚集的活血化瘀中药藏红花、毛冬青甲素和丹参对实验性原位性肾炎模型进行了干扰,结果显示BIm,藏红花和毛冬青甲素组动物的尿蛋白显著低于对照组,肾小球中的免疫复合物吸收加速,病理组织损害亦较对照组有显著的改善,尿毒症的死亡率较对照组减少。但丹参组和对照组比较则无显著性差别。结论;藏红花、毛冬青甲素和BIm对实验性原位性肾炎有治疗作用。提示血小板和TxA_2在原位性肾炎发病机理和病情发展中起着重要的致病作用。

关 键 词:原位性肾炎  血栓素A_2合成酶抑制剂  血小板聚集抑制剂

Experimental Study on Drug Prophylaxis and Treatment of in Situ Immune Complex Glomerulonephritis in Rabbits
Xu Guanghui Huang Wencong He Bailin LI Shimei. Experimental Study on Drug Prophylaxis and Treatment of in Situ Immune Complex Glomerulonephritis in Rabbits[J]. Journal of Sun Yatsen University(Medical Sciences), 1988, 0(4)
Authors:Xu Guanghui Huang Wencong He Bailin LI Shimei
Abstract:The effects of a selective thromboxane A 2 synthetase inhibitor, i-benzylimidazole (BIm) and antiplatelet agents, traditional Chinese herbs Crocus Sativus (CS), Ilexonin A (IA), and Radix Salviae Miltiorrhizae (RSM) on in situ immune complex glomerulonephritis (GN) in rabbits were evaluated. Cationic bovine serum albumin (c-BSA) (PI =8.7) was injected intravenously to induce membranous nephropathy in immunized rabbits for Q weeks. 40 animals were divided into 5 groups, 4 groups treated with agents and one untreated (control). After 2 week dosage of c-BSA injection, the agents were administered for 10 weeks repectiv-ely. It was showed that BIm, CS and IA could significantly reduce the amount of urinary protein. As the c-BSA nephritis developed, serum creatinine (Cr), serum urea nitrogen (Sun), and creatinine clearance (Ccr) v/ere worsen in control, but the administration of BIm to c-BSA nephritis had beneficial effects on Ccr. Histological examination by immunofluorescence, light microscopy and electron microscopy revealed glomerular deposition of IgG and Cs was less intense after treatment; glomerular capillary wall-thickening, mesangial cell proliferation and mesangial matrix increasing were milder in treated animals; BIm-treated group also showed significantly less formation of glomerular epithelial crescent. The rate of uremic death in animals treated with BIm, CS and IA was significantly lower than that in nontreated animals. In our study, it showed BIm, CS and IA couldn't effectively prevent the immune complex deposition in GN induced by c-BSA, but it is suggested that BIm, CS and IA could be more effective than RSM against the in situ immune complex GN in rabbits.
Keywords:In situ immune complex Glomerulonephritis Thromboxane A2 inhibitor Antiplate- let agents
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