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新型合成蛋白酶抑制剂FUT-175对(NZB×NZW)F1小鼠狼疮性肾炎发展的影响。

Effect of FUT-175, a new synthetic protease inhibitor, on the development of lupus nephritis in (NZB x NZW) F1 mice.

作者信息

Ikehara S, Shimamura K, Aoyama T, Fujii S, Hamashima Y

出版信息

Immunology. 1985 Aug;55(4):595-600.

Abstract

FUT-175 (6-amidino-2-naphthyl p-guanidinobenzoate dimethanesulphonate), a new synthetic protease inhibitor, was administrated to (NZB x NZB) F1 mice in order to examine its influence on the development of autoimmune diseases. A dose (400 mg/kg of body weight) of FUT-175 has both prophylactic and curative effects on the development of lupus nephritis: mice showed a significantly low percentage of proteinuria, a marked decrease in BUN levels, and the lowest degree of glomerular damages. Dexamethasone had almost the same effect as FUT-175 (400 mg/kg), but it was slightly less effective than FUT-175. These results suggest that the administration of FUT-175 may become a viable strategy for the treatment of human autoimmune diseases.

摘要

FUT - 175(6 - 脒基 - 2 - 萘基对 - 胍基苯甲酸盐二甲磺酸盐),一种新型合成蛋白酶抑制剂,被给予(新西兰黑鼠×新西兰黑鼠)F1代小鼠,以研究其对自身免疫性疾病发展的影响。FUT - 175剂量为400毫克/千克体重时,对狼疮性肾炎的发展具有预防和治疗作用:小鼠蛋白尿百分比显著降低,血尿素氮水平明显下降,肾小球损伤程度最低。地塞米松与FUT - 175(400毫克/千克)效果几乎相同,但稍逊于FUT - 175。这些结果表明,给予FUT - 175可能成为治疗人类自身免疫性疾病的可行策略。

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Etiopathogenesis of murine SLE.小鼠系统性红斑狼疮的病因发病机制。
Immunol Rev. 1981;55:179-216. doi: 10.1111/j.1600-065x.1981.tb00343.x.

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