Matsukawa W, Hara S, Yoshida F, Suzuki N, Fukatsu A, Yuzawa Y, Sakamoto N, Matsuo S
Third Department of Internal Medicine, Nagoya University School of Medicine, Japan.
J Lab Clin Med. 1992 Feb;119(2):116-23.
FK506 is a recently-developed immunosuppressive drug. The aim of the present work was to investigate the effects of FK506 in experimental autoimmune glomerulonephritis (active Heymann nephritis) in rats. Active Heymann nephritis was induced in female Lewis rats by two immunizations with the homologous brush border vesicles (BBVs) at day 0 and day 28 (groups I, II, V, and VI). Rats of groups III and IV received the third immunization at day 56. In rats of groups I and III, FK506 was injected (1 mg/kg/day IM) from day 0 for 14 days. In rats of groups II and IV, significant proteinuria was observed (group II, 112.8 mg/16 hours; group IV, 55.4 mg/16 hours) at the time the rats were killed (day 84). Coarse subepithelial immune deposits (IDs) were found in these rats. In contrast, urinary protein excretion remained within normal range (less than 3.0 mg/16 hours) in groups I and III rats, and tiny subepithelial IDs were only occasionally seen. Circulating anti-BBV antibody levels were markedly lower in group I and III rats than in those of groups II and IV during the period between day 14 and day 56. To investigate the effects of FK506 on the proteinuric rats, FK506 (1 mg/kg/day, IM) was administered every day for 2 weeks beginning on day 56 (group V).(ABSTRACT TRUNCATED AT 250 WORDS)
FK506是一种最近研发的免疫抑制药物。本研究的目的是调查FK506对大鼠实验性自身免疫性肾小球肾炎(活动性海曼肾炎)的影响。在第0天和第28天,用同源刷状缘小泡(BBV)对雌性Lewis大鼠进行两次免疫,诱导出活动性海曼肾炎(I、II、V和VI组)。III组和IV组大鼠在第56天接受第三次免疫。I组和III组大鼠从第0天开始注射FK506(1毫克/千克/天,肌肉注射),持续14天。II组和IV组大鼠在处死时(第84天)出现明显蛋白尿(II组,112.8毫克/16小时;IV组,55.4毫克/16小时)。在这些大鼠中发现了粗大的上皮下免疫沉积物(ID)。相比之下,I组和III组大鼠的尿蛋白排泄仍在正常范围内(小于3.0毫克/16小时),仅偶尔可见微小的上皮下ID。在第14天至第56天期间,I组和III组大鼠的循环抗BBV抗体水平明显低于II组和IV组。为了研究FK506对蛋白尿大鼠的影响,从第56天开始,每天给V组大鼠注射FK506(1毫克/千克/天,肌肉注射),持续2周。(摘要截短于250字)