Kreisberg J I, Karnovsky M J
Am J Pathol. 1978 Sep;92(3):637-52.
We have examined the nature of focal glomerular sclerosis (FGS) in fawn-hooded (FH) rats. The fawn-hooded rat develops pathologic features similar to those observed in steroid-resistant focal glomerular sclerosis, ie, by light microscopy some of the glomeruli appear normal but others show areas of solidification confined to one or two lobules of the tuft. The pathogenesis of this disease is not well known and there is a great need for an animal model. In the FH animal, a marked difference in the development of the lesion was noted between male and female rats. Fifty percent of 4-month-old males had proteinuria in excess of 10 mg/day (none of the females had significant proteinuria), while all 12-month-old males had proteinuria in excess of 45 mg/day (female 12-month-old FH rats had mean proteinuria of 7 mg/day). At 6 months of age continuing through 12 months of age, male FH rats had mesangial deposits of IgG, IgM, and, occasionally, C3, demonstrable by immunofluorescence, whether or not FGS was present. Subepithelial electron-dense deposits were never seen by electron microscopy either at 6 of 12 months. Six-month-old animals frequently did not exhibit FGS. Instead, the glomerular epithelial cells, exhibited fusion of foot processes, vacuolization, and, in some areas, focal loss of the epithelial covering on the glomerular basement membrane (GBM). Six-month-old males with proteinuria exhibited focal loss of negative charge from all layers of the filtration barrier. The GBM from sclerotic glomeruli of 12-month-old rats was commonly denuded of epithelium. None of the animals in this study was uremic. FH rats demonstrated FGS associated with progressive glomerular epithelial cell injury.
我们研究了淡黄褐毛(FH)大鼠局灶性肾小球硬化(FGS)的性质。淡黄褐毛大鼠出现的病理特征与在激素抵抗性局灶性肾小球硬化中观察到的相似,即通过光学显微镜观察,一些肾小球看起来正常,但其他肾小球显示出局限于肾小球丛一两个小叶的硬化区域。这种疾病的发病机制尚不清楚,非常需要一种动物模型。在FH动物中,注意到雄性和雌性大鼠在病变发展上存在显著差异。4个月大的雄性大鼠中有50%蛋白尿超过10毫克/天(雌性大鼠均无明显蛋白尿),而所有12个月大的雄性大鼠蛋白尿超过45毫克/天(12个月大的雌性FH大鼠平均蛋白尿为7毫克/天)。在6个月至12个月大期间,雄性FH大鼠无论是否存在FGS,通过免疫荧光均可显示IgG、IgM以及偶尔的C3在系膜沉积。在6个月或12个月时,电子显微镜检查从未发现上皮下电子致密沉积物。6个月大的动物通常不表现出FGS。相反,肾小球上皮细胞出现足突融合、空泡化,并且在某些区域,肾小球基底膜(GBM)上的上皮覆盖物局部缺失。有蛋白尿的6个月大雄性大鼠在滤过屏障的所有层均表现出负电荷局部缺失。12个月大的大鼠硬化肾小球的GBM通常上皮剥脱。本研究中没有动物出现尿毒症。FH大鼠表现出与进行性肾小球上皮细胞损伤相关的FGS。