Guo Min, Ricardo Sharon D, Deane James A, Shi Ming, Cullen-McEwen Luise, Bertram John F
Department of Anatomy and Cell Biology, School of Biomedical Sciences, Monah University, Clayton, Victoria, Australia.
J Anat. 2005 Dec;207(6):813-21. doi: 10.1111/j.1469-7580.2005.00492.x.
In diabetic nephropathy, glomerular hypertrophy is evident early in response to hyperglycaemia. Alterations of capillary length and vascular remodelling that may contribute to glomerular hypertrophy and the subsequent development of glomerulosclerosis remain unclear. The present study used the db/db mouse model of Type 2 diabetes to examine the glomerular microvascular changes apparent with long-term diabetic complications. Unbiased stereological methods and high-resolution light microscopy were used to estimate glomerular volume, and glomerular capillary dimensions including length and surface area in 7-month-old db/db diabetic mice and age-matched db/m control mice. The db/db diabetic mice showed significant glomerular hypertrophy, corresponding with elevated blood glucose levels, and increased body weight and kidney weight, compared with db/m control mice. Glomerular enlargement in db/db mice was associated with increases in the surface area (5.387 +/- 0.466 x 10(4) microm2 vs. 2.610 +/- 0.287 x 10(4) microm2; P < 0.0005) and length (0.3343 +/- 0.022 x 10(4) microm vs. 0.1549 +/- 0.017 x 10(4) microm; P < 0.0001) of capillaries per glomerulus, compared with non-diabetic mice. Stereological assessment at the electron microscopic level revealed increased glomerular volume density of mesangial cells and mesangial matrix, and thickening of the glomerular basement membrane in db/db mice. These results demonstrate that glomerular hypertrophy evident in advanced diabetic nephropathy in this model is associated with increased length and surface area of glomerular capillaries. The contribution of angiogenesis and vasculogenesis to the glomerular microvascular alterations in response to hyperglycaemia remain to be determined.
在糖尿病肾病中,肾小球肥大在对高血糖的早期反应中就很明显。毛细血管长度的改变和血管重塑可能导致肾小球肥大以及随后的肾小球硬化,但目前尚不清楚。本研究使用2型糖尿病的db/db小鼠模型来检查长期糖尿病并发症中明显的肾小球微血管变化。采用无偏体视学方法和高分辨率光学显微镜来估计7月龄db/db糖尿病小鼠和年龄匹配的db/m对照小鼠的肾小球体积以及包括长度和表面积在内的肾小球毛细血管尺寸。与db/m对照小鼠相比,db/db糖尿病小鼠表现出显著的肾小球肥大,这与血糖水平升高、体重和肾脏重量增加相对应。db/db小鼠的肾小球增大与每个肾小球毛细血管的表面积增加(5.387±0.466×10⁴μm²对2.610±0.287×10⁴μm²;P<0.0005)和长度增加(0.3343±0.022×10⁴μm对0.1549±0.017×10⁴μm;P<0.0001)有关。电子显微镜水平的体视学评估显示,db/db小鼠的系膜细胞和系膜基质的肾小球体积密度增加,以及肾小球基底膜增厚。这些结果表明,该模型中晚期糖尿病肾病中明显的肾小球肥大与肾小球毛细血管长度和表面积增加有关。血管生成和血管发生对高血糖反应中肾小球微血管改变的作用仍有待确定。