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患有遗传性肾小球病的萨摩耶犬肾小球毛细血管基底膜中阴离子位点的定量分析。

Quantitation of anionic sites in glomerular capillary basement membranes of Samoyed dogs with hereditary glomerulopathy.

作者信息

Thorner P S, Jansen B, Liang J, Baumal R, Valli V

出版信息

Virchows Arch A Pathol Anat Histopathol. 1987;411(1):79-85. doi: 10.1007/BF00734518.

Abstract

Samoyed hereditary glomerulopathy (SHG) is an X-linked dominant disease characterized by proteinuria and renal failure in affected male dogs. Electron microscopic examination of glomerular capillary basement membranes (GCBM) shows widespread multilaminar splitting of the lamina densa, identical to that in Alport's syndrome. Anionic sites in GCBM of three affected males and five unaffected dogs were labeled using polyethyleneimine to determine whether proteinuria was associated with an alteration in their number. No significant differences were noted in the number of anionic sites in the lamina rara externa, whereas small but statistically significant increases were seen in the number of sites in the lamina rara interna of affected males. In the lamina densa, affected males showed a striking increase in anionic sites, particularly in regions of GCBM which were split. Thus, although proteinuria in some glomerular diseases has been attributed to a reduction in anionic sites in GCBM, this was not so in SHG.

摘要

萨摩耶遗传性肾小球病(SHG)是一种X连锁显性疾病,其特征为患病雄性犬出现蛋白尿和肾衰竭。对肾小球毛细血管基底膜(GCBM)进行电子显微镜检查显示,致密层广泛出现多层分裂,这与阿尔波特综合征中的情况相同。使用聚乙烯亚胺对三只患病雄性犬和五只未患病犬的GCBM中的阴离子位点进行标记,以确定蛋白尿是否与其数量改变有关。在外侧稀疏层中,阴离子位点的数量未观察到显著差异,而在患病雄性犬的内侧稀疏层中,位点数量虽有小幅增加,但具有统计学意义。在致密层中,患病雄性犬的阴离子位点显著增加,尤其是在GCBM发生分裂的区域。因此,尽管某些肾小球疾病中的蛋白尿被认为是由于GCBM中阴离子位点减少所致,但在SHG中并非如此。

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