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Deficiency of hypoxia inducible factor-1α promoted progression of diabetic nephropathy with hypertension

机译:缺氧诱导因子-1α缺乏促进糖尿病肾病合并高血压

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摘要

The present study was designed to investigate the effect of hypoxia inducible factor-1α (HIF-1α) on diabetic nephropathy (DN) with hypertension. HIF-1α deficient mice (Mx/HIF-1α−/−) were constructed and treated with streptozotocin (STZ) injection for hypertensive DN induction. Normal C57BL/6 mice received STZ or no treatment (normal) were considered as controls. Three days post STZ administration; body weight, fasting blood glucose (FBG), 24 h urinary albumin and systolic blood pressure (SBP) were measured weekly. Periodic acid-Schiff's staining was performed for histologic analysis of glomeruli damage. In comparison with the normal control, significant upregulation and downregulation of HIF-1α was, respectively, detected in diabetic and HIF-1α−/− mice (P<0.01). In comparison with STZ-induced diabetic mice, HIF-1α−/− + STZ mice displayed reduced body weight, and increased FBG, urinary albumin and SBP. PAS showed HIF-1α−/− + STZ mice had damaged kidney tissues, with more renal fibrosis and apparent glomerular hypertrophy. These results demonstrated that HIF-1α deficiency accelerated DN progression with increasing hypertension in mice.
机译:本研究旨在研究缺氧诱导因子-1α(HIF-1α)对高血压合并糖尿病肾病(DN)的影响。构建HIF-1α缺陷小鼠(Mx /HIF-1α-/-),并用链脲佐菌素(STZ)注射治疗高血压DN。接受STZ或未接受治疗(正常)的正常C57BL / 6小鼠被视为对照组。 STZ管理后三天;每周测量体重,空腹血糖(FBG),24 h尿白蛋白和收缩压(SBP)。进行高碘酸-希夫氏染色以对肾小球损伤进行组织学分析。与正常对照组相比,在糖尿病和HIF-1α-/-小鼠中分别检测到HIF-1α显着上调和下调(P <0.01)。与STZ诱导的糖尿病小鼠相比,HIF-1α-/- + STZ小鼠体重减轻,FBG,尿白蛋白和SBP升高。 PAS显示HIF-1α-/- + STZ小鼠的肾脏组织受损,肾脏纤维化更多,肾小球肥大。这些结果表明,HIF-1α缺乏症会随着小鼠高血压的增加而加速DN的发展。

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