Jones S E, White K E, Flyvbjerg A, Marshall S M
Diabetes Research Group, School of Clinical Medical Sciences, University Of Newcastle upon Tyne, Newcastle upon Tyne, UK.
Diabetologia. 2006 Jan;49(1):191-9. doi: 10.1007/s00125-005-0052-z. Epub 2005 Dec 9.
AIMS/HYPOTHESIS: We tested the hypothesis that diabetic glomerulosclerosis would develop more rapidly in animals with fewer glomeruli.
We studied the female offspring of Wistar rats that had been fed a low-protein diet (LPD) containing 6% protein or a normal-protein diet (NPD) containing 18% protein during pregnancy. Streptozotocin diabetes was induced at 12 weeks and animals were killed at 40 weeks.
Non-diabetic LPD offspring were of lower birthweight than the NPD offspring (5.19+/-0.64 vs 6.45+/-0.67 g, p<0.001) and had fewer glomeruli (27,402+/-3,137 vs 34,203+/-6,471, p<0.05). Glomerular volume correlated inversely with glomerular number (r=-0.64, p=0.035), but total glomerular filtration surface area was reduced in the LPD animals (4,770+/-541 vs 5,779+/-1,302 mm(2), p=0.05). Other renal structural and functional parameters were similar. In LPD and NPD diabetic animals, glomerular volume and basement membrane width were significantly increased compared to their respective controls. Podocyte density was lowest in the LPD diabetic animals (not significant), and the area covered by each podocyte was greater in the LPD diabetic group (2.40+/-0.693 x10(-3) mm(2)) than in the LPD control group (1.68+/-0.374 x10(-3) mm(2), p<0.001) and in the NPD diabetic animals (1.71+/-0.291 x 10(-3) mm(2), p<0.05). There was no difference in any other structural or functional parameter between the LPD and NPD diabetic animals.
CONCLUSIONS/INTERPRETATION: A decrease in glomerular number was not deleterious to renal structure and function over 40 weeks in this animal model. Further work in models with progressive renal impairment and hypertension is necessary to clarify the impact of glomerular number on the development of renal disease.
目的/假设:我们检验了肾小球数量较少的动物糖尿病性肾小球硬化发展更快这一假设。
我们研究了孕期喂食含6%蛋白质的低蛋白饮食(LPD)或含18%蛋白质的正常蛋白饮食(NPD)的Wistar大鼠的雌性后代。在12周时诱导链脲佐菌素糖尿病,40周时处死动物。
非糖尿病LPD后代出生体重低于NPD后代(5.19±0.64 vs 6.45±0.67 g,p<0.001),肾小球数量更少(27,402±3,137 vs 34,203±6,471,p<0.05)。肾小球体积与肾小球数量呈负相关(r=-0.64,p=0.035),但LPD动物的总肾小球滤过表面积减少(4,770±541 vs 5,779±1,302 mm²,p=0.05)。其他肾脏结构和功能参数相似。在LPD和NPD糖尿病动物中,与各自对照组相比,肾小球体积和基底膜宽度显著增加。LPD糖尿病动物的足细胞密度最低(无显著性差异),LPD糖尿病组每个足细胞覆盖的面积(2.40±0.693×10⁻³ mm²)大于LPD对照组(1.68±0.374×10⁻³ mm²,p<0.001)和NPD糖尿病动物(1.71±0.291×10⁻³ mm²,p<0.05)。LPD和NPD糖尿病动物在任何其他结构或功能参数上均无差异。
结论/解读:在该动物模型中,40周内肾小球数量减少对肾脏结构和功能无害。有必要在进行性肾功能损害和高血压模型中开展进一步研究,以阐明肾小球数量对肾脏疾病发展的影响。