Jiao Yuejiang, Jiang Hongwei, Lu Haibo, Yang Yiping, Zhang Yanfang, Zhang Kun, Liu Hui
Department of Endocrinology, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang, Henan 471009, P.R. China.
Department of Endocrinology, The 1st Affiliated Hospital of Henan University of Science and Technology, Luoyang, Henan 471033, P.R. China.
Exp Ther Med. 2018 Oct;16(4):3658-3662. doi: 10.3892/etm.2018.6621. Epub 2018 Aug 20.
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.
本研究旨在探讨缺氧诱导因子-1α(HIF-1α)对糖尿病肾病(DN)合并高血压的影响。构建HIF-1α基因缺陷小鼠(Mx/HIF-1α),并通过注射链脲佐菌素(STZ)诱导高血压性糖尿病肾病。将正常C57BL/6小鼠接受STZ注射或不接受任何处理(正常组)作为对照。STZ给药后3天,每周测量体重、空腹血糖(FBG)、24小时尿白蛋白和收缩压(SBP)。采用高碘酸-希夫氏染色法对肾小球损伤进行组织学分析。与正常对照组相比,糖尿病小鼠和HIF-1α基因缺陷小鼠中分别检测到HIF-1α显著上调和下调(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染色显示HIF-1α + STZ小鼠肾组织受损,肾纤维化增多,肾小球明显肥大。这些结果表明,HIF-1α缺乏会加速小鼠糖尿病肾病进展并加重高血压。