[大鼠肾小球硬化发病机制的超微结构和放射自显影研究[作者简介]。

W Romen
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引用次数: 0

摘要

在衰老过程中、肾大部切除、肾静脉收缩和n -亚硝基氨基吗啡中毒后,研究了大鼠肾小球的光镜和电镜变化。尽管使用了四种不同的实验模型,但在肾小球中总是发现相同的变化。形态学上表现为肾小球基底膜弥漫性增厚,系膜基质增加,但肾小球细胞不增生。尽管肾小球基底膜增厚,但可以观察到肾小球毛细血管对大蛋白的渗透性增加,表现为中度蛋白尿。对于这些形态学变化,建议用“肾小球硬化”一词;它们被解释为肾小球对多种不同影响引起的损害的非特异性、非炎性反应。从这里提出的肾小球硬化的正式发病机制的研究可以得出结论,在个别实验模型中,以不同的方式获得了相同的结果。肾小球硬化发生的一种可能是基底膜和系膜基质成分的增加。这似乎是肾切除术后所遵循的途径。另一种可能是减缓基质和膜的分解。在衰老过程中,在缺氧和毒性变化后发生的肾小球硬化似乎就是这种情况。这可能是由于负责基底膜和基质破裂的系膜细胞功能紊乱所致。另一方面,人们可能不得不考虑这些结构的大分子的主要改变,正如从化学上密切相关的胶原蛋白的研究中已经知道的那样。通过对正常肾小球和病变肾小球的光镜和电镜观察,我们对肾小球基底膜和系膜基质的起源和形成有了一定的认识。为了扩大研究范围,在大鼠肾小球的超薄和半薄切片上进行了3h -脯氨酸和3h -亮氨酸的放射自显影研究。本文的研究结果表明,在肾小球的三种细胞类型中,脏上皮细胞(足细胞,“Deckzellen”)可能参与肾小球基底膜的形成,而系膜细胞似乎负责系膜基质的合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[On the pathogenesis of the glomerulosclerosis ultrastructural and autoradiographic investigations on the rat kidney (author's transl)].

The light- and electron microscopic changes in the glomeruli of the rat's kidney have been investigated in the course of ageing and after subtotal nephrectomy, constriction of the renal vein, and intoxication by N-nitrosomorpholine. In spite of the fact that four different experimental models have been used, identical changes were always found in the glomeruli. Morphologically they consisted of a diffuse thickening of the glomerular basement membrane and of an increase in the mesangial matrix without a proliferation of the glomerular cells. Despite this thickening of the glomerular basement membrane, functionally an increased permeability of the glomerular capillaries for macroproteins could be observed, shown by a moderate proteinuria. For these morphological changes the term "glomerulosclerosis" is suggested; they are interpreted as a non-specific, non-inflammatory reaction of the glomerulus to an impairment caused by a number of varied influences. From the study of the formal pathogenesis of the glomerulosclerosis presented here one can conclude that in the individual experimental models the same result has been achieved in different ways. One possibility in the development of glomerulosclerosis is an increased production of the components of the basement membrane and of the mesangial matrix. This is the pathway which appears to be followed after nephrectomy. Another possibility is a slowing down of the breakdown of both the matrix and the membrane. This seems to be the case in the glomerulosclerosis occuring in the course of ageing, and after hypoxic and toxic changes. It could be accounted for by a functional disturbance of, presumably, the mesangial cells responsible for the breakdown of the basement membrane and of the matrix. On the other hand, one may have to consider a primary alteration of the macromolecules of these structures, as is already known from studies of the, chemically closely related, collagen. The light- and electron microscopic studies of the normal and of the altered glomeruli have led to certain conclusions concerning the origin and the fomation of the glomerular basement membrane and the mesangial matrix. In order to widen the scope of the studies, additional autoradiographic investigations with 3H-proline and 3H-leucine have been performed in ultrathin and semithin sections of the rat's glomeruli. The results of the studies presented here suggest that of the three cell types of the glomerulus the visceral epithelial cells (podocytes, "Deckzellen") may participate on the formation of the glomerular basement membrane, whereas the mesangial cells appear to be responsible for the synthesis of the mesangial matrix.

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