Moriwaki Yuji, Inokuchi Taku, Yamamoto Asako, Ka Tsuneyoshi, Tsutsumi Zenta, Takahashi Sumio, Yamamoto Tetsuya
Division of Endocrinology and Metabolism, Department of Internal Medicine, Hyogo College of Medicine, Mukogawa-cho 1-1, Nishinomiya, 663-8501 Hyogo, Japan.
Acta Diabetol. 2007 Dec;44(4):215-8. doi: 10.1007/s00592-007-0007-6. Epub 2007 Sep 1.
The objective is to assess the effect of TNF-alpha inhibition on urinary albumin excretion in experimental diabetic rats. Male Wistar rats, 8-week-old, were categorized into four groups, which were the control (n = 9), diabetes (n = 9), infliximab-treated diabetes (n = 10), and FR167653-treated diabetes (n = 9) groups. Diabetes was induced by intraperitoneal injection of STZ (40 mg/kg). Thereafter, infliximab was injected intraperitoneally once a month (5.5 mg/kg) and FR167653 was administered orally by mixing with the rat chow (0.08%). The effects of infliximab and FR167653 on urinary albumin excretion were observed for 12 weeks. Body weight, blood sugar, 24-h urinary TNF-alpha, and 24-h urinary albumin/creatinine ratio (Ualb/Ucr) levels were determined at 1, 4, 8, and 12 weeks after the STZ-injection. Treatment of rats with STZ caused a significant loss of body weight, as well as polyuria and hyperglycemia within 1 week, while the urinary excretions of albumin and TNF-alpha were increased. Neither infliximab nor FR167653 affected body weight or blood sugar levels, whereas both decreased urinary albumin excretion, together with a modest decrease in the urinary excretion of TNF-alpha. These results suggest a role of TNF-alpha in the pathogenesis of diabetic nephropathy and show that TNF-alpha inhibition is a potential therapeutic strategy.
目的是评估肿瘤坏死因子-α(TNF-α)抑制对实验性糖尿病大鼠尿白蛋白排泄的影响。8周龄雄性Wistar大鼠被分为四组,即对照组(n = 9)、糖尿病组(n = 9)、英夫利昔单抗治疗糖尿病组(n = 10)和FR167653治疗糖尿病组(n = 9)。通过腹腔注射链脲佐菌素(STZ,40 mg/kg)诱导糖尿病。此后,每月腹腔注射一次英夫利昔单抗(5.5 mg/kg),并将FR167653与大鼠饲料混合口服给药(0.08%)。观察英夫利昔单抗和FR167653对尿白蛋白排泄的影响,持续12周。在注射STZ后的第1、4、8和12周测定体重、血糖、24小时尿TNF-α以及24小时尿白蛋白/肌酐比值(Ualb/Ucr)水平。用STZ处理大鼠导致体重显著减轻,以及在1周内出现多尿和高血糖,同时白蛋白和TNF-α的尿排泄增加。英夫利昔单抗和FR-167653均未影响体重或血糖水平,但两者均降低了尿白蛋白排泄,同时尿TNF-α排泄略有下降。这些结果表明TNF-α在糖尿病肾病发病机制中起作用,并表明抑制TNF-α是一种潜在的治疗策略。