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肿瘤坏死因子-α抑制对实验性糖尿病大鼠尿白蛋白排泄的影响。

Effect of TNF-alpha inhibition on urinary albumin excretion in experimental diabetic rats.

作者信息

Moriwaki Yuji, Inokuchi Taku, Yamamoto Asako, Ka Tsuneyoshi, Tsutsumi Zenta, Takahashi Sumio, Yamamoto Tetsuya

机构信息

Division of Endocrinology and Metabolism, Department of Internal Medicine, Hyogo College of Medicine, Mukogawa-cho 1-1, Nishinomiya, 663-8501 Hyogo, Japan.

出版信息

Acta Diabetol. 2007 Dec;44(4):215-8. doi: 10.1007/s00592-007-0007-6. Epub 2007 Sep 1.

Abstract

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.

摘要

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。

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