Lawrence G M, Brewer D B
J Pathol. 1983 Feb;139(2):115-40. doi: 10.1002/path.1711390204.
Biochemical, immunological, histochemical and electron microscope morphometric techniques were used to monitor the changes in urinary protein composition, albumin clearance and glomerular ultrastructure induced in female Wistar rats following i.p. injection of puromycin aminonucleoside (PAN) or bovine albumin (BSA). BSA injected rats maintained a high degree of selectivity with albumin constituting 90 per cent. of the total protein excreted even when mean protein excretion was in the order of 500 mg/24 hr. A similar degree of selectivity was only evident in PAN nephrotic rats at low levels of proteinuria. Levels of 500 mg/24 hr only 57 per cent. of the total protein was albumin. These differences correlated well with the increased number of glomeruli from PAN nephrotics compared with hyperalbuminaemic rats which, at these high levels of proteinuria, had bare areas of glomerular basement membrane caused by epithelial cell detachment (88 and 7 per cent. respectively). Detailed electron microscope morphometric and immunohistochemical studies showed that there were also important quantitative differences in a number of superficially similar glomerular structural alterations. In PAN nephrotic rats all glomeruli showed very marked epithelial cell foot process loss and reduced staining with colloidal iron. In glomeruli from hyperalbuminaemic rats there was a wide variation in the extent of epithelial cell foot process loss and reduced colloidal iron staining was only demonstrable in those glomeruli which had swollen epithelial containing large numbers of vacuoles and protein droplets. Similarly, while protein droplets were smaller and less numerous in glomeruli from PAN-injected rats, they were present in most glomeruli whereas their distribution was much more variable in glomeruli from BSA-injected rats. All the data collected therefore indicated that there were important differences in the types of proteinuria and glomerular ultrastructural damage present in PAN nephrotic and hyperalbuminaemic rats and suggested that their induction may have involved entirely different mechanisms. Evidence gathered from one experimental model should thus only be used with extreme caution to aid in interpretation of data obtained from the other.
采用生化、免疫、组织化学及电子显微镜形态计量技术,监测雌性Wistar大鼠腹腔注射嘌呤霉素氨基核苷(PAN)或牛血清白蛋白(BSA)后尿蛋白成分、白蛋白清除率及肾小球超微结构的变化。注射BSA的大鼠保持高度选择性,白蛋白占总排泄蛋白的90%。即使平均蛋白排泄量约为500mg/24小时,情况亦是如此。仅在PAN肾病大鼠蛋白尿水平较低时,才出现类似程度的选择性。当蛋白排泄量为500mg/24小时时,白蛋白仅占总蛋白的57%。与高白蛋白血症大鼠相比,PAN肾病大鼠的肾小球数量增加,这些差异与上述情况密切相关。在这些高蛋白尿水平下,高白蛋白血症大鼠由于上皮细胞脱离导致肾小球基底膜出现裸露区域(分别为88%和7%)。详细的电子显微镜形态计量和免疫组织化学研究表明,一些表面相似的肾小球结构改变在数量上也存在重要差异。在PAN肾病大鼠中,所有肾小球均显示出非常明显的上皮细胞足突消失,胶体铁染色减弱。在高白蛋白血症大鼠的肾小球中,上皮细胞足突消失的程度差异很大,仅在那些上皮细胞肿胀且含有大量空泡和蛋白滴的肾小球中,才显示出胶体铁染色减弱。同样,虽然注射PAN大鼠的肾小球中蛋白滴较小且数量较少,但大多数肾小球中都有蛋白滴,而注射BSA大鼠的肾小球中蛋白滴的分布则更具变异性。因此,收集到的所有数据表明,PAN肾病大鼠和高白蛋白血症大鼠的蛋白尿类型和肾小球超微结构损伤存在重要差异,提示其诱导机制可能完全不同。因此,从一个实验模型收集的证据仅应极其谨慎地用于辅助解释从另一个模型获得的数据。