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FK506对棕色挪威大鼠自身免疫性肾小球肾炎的治疗作用。

Effect of FK 506 in the treatment of autoimmune glomerulonephritis in Brown Norway rats.

作者信息

Nakahama H, Obata K, Sugita M, Horio M, Oka K, Moriyama T

机构信息

Fifth Department of Internal Medicine, Hyogo College of Medicine, Hyogo, Japan.

出版信息

Nephron. 1999;81(4):421-7. doi: 10.1159/000045326.

Abstract

Mercuric chloride (HgCl2) induces a lymphoproliferative disorder and autoimmune glomerulonephritis in Brown Norway (BN) rats. The effects of a new immunosuppressant, FK 506, on this model of glomerulonephritis were studied. BN rats were treated with HgCl2 according to a standard protocol (HgCl2 1 mg/kg s.c. 3 times/week). FK 506 was inoculated subcutaneously daily from day 15 to day 28. Animals were divided into 4 groups: group 1, rats were treated with normal saline alone and sacrificed on day 28; group 2, rats were treated with HgCl2 alone and sacrificed on day 14; group 3, rats were treated with HgCl2 alone and sacrificed on day 28, and group 4, rats were treated with HgCl2 and FK 506 (from day 15 to day 28) and sacrificed on day 28. Rats developed proteinuria by day 7, which reached a plateau level by day 14. On day 14, renal histology showed prominent mesangial cellular proliferation and the expansion of mesangial matrix. Electron microscopic study showed the effacement of visceral epithelial foot processes and the microvillous transformation of the visceral epithelium. Immunofluorescence study showed strong linear staining for IgG and the adhesion molecule ICAM-1 in all glomeruli. Treatment with FK 506 (1 mg/kg s.c. daily) resulted in a remarkable reduction in proteinuria on day 28 (493.5 +/- 48.3 vs. 24.4 +/- 13.5 mg/day) and an improvement in the morphological lesions. These findings suggest that FK 506 could be useful in the treatment of some human glomerulonephritides.

摘要

氯化汞(HgCl2)可诱导棕色挪威(BN)大鼠发生淋巴细胞增生性疾病和自身免疫性肾小球肾炎。本研究探讨了新型免疫抑制剂FK 506对该肾小球肾炎模型的影响。按照标准方案(HgCl2 1 mg/kg皮下注射,每周3次)用HgCl2处理BN大鼠。从第15天至第28天每天皮下接种FK 506。动物分为4组:第1组,仅用生理盐水处理大鼠,并在第28天处死;第2组,仅用HgCl2处理大鼠,并在第14天处死;第3组,仅用HgCl2处理大鼠,并在第28天处死;第4组,用HgCl2和FK 506处理(从第15天至第28天),并在第28天处死。大鼠在第7天出现蛋白尿,至第14天达到平台期水平。在第14天,肾脏组织学显示系膜细胞显著增生和系膜基质扩张。电子显微镜研究显示脏层上皮足突消失和脏层上皮微绒毛化。免疫荧光研究显示所有肾小球中IgG和黏附分子ICAM-1呈强线性染色。用FK 506(1 mg/kg皮下注射,每日1次)治疗导致第28天蛋白尿显著减少(493.5 +/- 48.3 vs. 24.4 +/- 13.5 mg/天),形态学病变改善。这些发现提示FK 506可能对治疗某些人类肾小球肾炎有用。

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