Center for Renal Medicine, Division of Nephrology.
Division of Diabetes, Department of Medicine.
JCI Insight. 2021 Feb 8;6(3):143619. doi: 10.1172/jci.insight.143619.
The role of insulin receptor (IR) activated by hyperinsulinemia in obesity-induced kidney injury is not well understood. We hypothesized that activation of kidney proximal tubule epithelial IR contributes to obesity-induced kidney injury. We administered normal-fat diet (NFD) or high-fat diet (HFD) to control and kidney proximal tubule IR-knockout (KPTIRKO) mice for 4 months. Renal cortical IR expression was decreased by 60% in male and female KPTIRKO mice. Baseline serum glucose, serum creatinine, and the ratio of urinary albumin to creatinine (ACR) were similar in KPTIRKO mice compared to those of controls. On HFD, weight gain and increase in serum cholesterol were similar in control and KPTIRKO mice; blood glucose did not change. HFD increased the following parameters in the male control mice: renal cortical contents of phosphorylated IR and Akt, matrix proteins, urinary ACR, urinary kidney injury molecule-1-to-creatinine ratio, and systolic blood pressure. Renal cortical generation of hydrogen sulfide was reduced in HFD-fed male control mice. All of these parameters were ameliorated in male KPTIRKO mice. Interestingly, female mice were resistant to HFD-induced kidney injury in both genotypes. We conclude that HFD-induced kidney injury requires renal proximal tubule IR activation in male mice.
高胰岛素血症激活的胰岛素受体(IR)在肥胖诱导的肾损伤中的作用尚不清楚。我们假设肾脏近端小管上皮细胞 IR 的激活导致肥胖诱导的肾损伤。我们用正常脂肪饮食(NFD)或高脂肪饮食(HFD)喂养对照组和肾脏近端小管 IR 敲除(KPTIRKO)小鼠 4 个月。雄性和雌性 KPTIRKO 小鼠的肾脏皮质 IR 表达减少了 60%。与对照组相比,KPTIRKO 小鼠的基础血清葡萄糖、血清肌酐和尿白蛋白与肌酐比值(ACR)相似。在 HFD 喂养下,对照组和 KPTIRKO 小鼠的体重增加和血清胆固醇升高相似;血糖没有变化。HFD 增加了雄性对照组小鼠的以下参数:肾脏皮质磷酸化 IR 和 Akt、基质蛋白、尿 ACR、尿肾损伤分子-1 与肌酐比值和收缩压。HFD 喂养的雄性对照组小鼠肾脏皮质产生的硫化氢减少。所有这些参数在雄性 KPTIRKO 小鼠中均得到改善。有趣的是,两种基因型的雌性小鼠均对 HFD 诱导的肾损伤具有抗性。我们得出结论,HFD 诱导的肾损伤需要雄性小鼠肾脏近端小管 IR 的激活。