Zhai Limin, Gu Junfei, Yang Di, Hu Wen, Wang Wei, Ye Shandong
Department of Endocrinology, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China.
Department of Pathology, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China.
J Diabetes. 2017 May;9(5):510-517. doi: 10.1111/1753-0407.12437. Epub 2016 Sep 12.
Previous studies found that metformin provided some renoprotection for diabetic renal damage. In the present study, we evaluated the effects of different doses of metformin on the expression of renal tissue nephrin in type 2 diabetes mellitus (T2DM) model rats and the possible mechanism underlying its protective effect in kidney podocytes.
A high-fat diet combined with a low dose of streptozotocin was used to induce T2DM model rats. Diabetic rats were treated with 150, 300, or 500 mg/kg metformin for 8 weeks. At the end of the study, urine and blood samples were collected for measurement of different indices. Light microscopy and transmission electron microscopy were used to identify morphological changes. Renal expression of nephrin protein was assayed by immunohistochemical staining, whereas real-time polymerase chain reaction was used to detect renal nephrin (Nphs1) mRNA expression.
Metformin treatment of T2DM rats produced dose-dependent significant reductions in urinary albumin and nephrin concentrations, glomerular basement membrane thickness (GBMT), and the foot process fusion rate (FPFR) compared with control T2DM model rats, whereas renal expression of nephrin protein and Nphs1 mRNA was dose-dependently increased by metformin treatment.
Metformin protects kidney podocytes in T2DM model rats by dose-dependently adjusting renal nephrin expression.
先前的研究发现二甲双胍对糖尿病肾损伤具有一定的肾脏保护作用。在本研究中,我们评估了不同剂量二甲双胍对2型糖尿病(T2DM)模型大鼠肾组织nephrin表达的影响及其对肾足细胞保护作用的潜在机制。
采用高脂饮食联合低剂量链脲佐菌素诱导T2DM模型大鼠。糖尿病大鼠分别用150、300或500mg/kg二甲双胍治疗8周。在研究结束时,收集尿液和血液样本以测量不同指标。用光镜和透射电镜鉴定形态学变化。通过免疫组织化学染色检测nephrin蛋白的肾表达,而实时聚合酶链反应用于检测肾nephrin(Nphs1)mRNA表达。
与对照T2DM模型大鼠相比,二甲双胍治疗T2DM大鼠可使尿白蛋白和nephrin浓度、肾小球基底膜厚度(GBMT)和足突融合率(FPFR)呈剂量依赖性显著降低,而二甲双胍治疗可使肾nephrin蛋白和Nphs1 mRNA的表达呈剂量依赖性增加。
二甲双胍通过剂量依赖性调节肾nephrin表达来保护T2DM模型大鼠的肾足细胞。