Brenner B M, Hostetter T H, Humes H D
Am J Physiol. 1978 Jun;234(6):F455-60. doi: 10.1152/ajprenal.1978.234.6.F455.
The formation of glomerular ultrafiltrate is dependent on the interplay of glomerular pressures and flows as well as the intrinsic permselectivity properties of the glomerular capillary wall. These intrinsic permeability properties serve to exclude macromolecules from the urinary space, based on size as well as net molecular charge discrimination. Neutral dextrans with molecular radii less than 20 A cross the glomerular wall without measurable restriction, whereas dextrans with radii greater than 42 A are almost completely barred. For any given size, negatively charged macromolecules are restricted to a greater extent than neutral molecules. Additionally, positively charged molecules are enhanced in their ability to cross the glomerular wall compared to similarly sized neutral polymers. The concept of a charge barrier, due to fixed negative charges within the glomerular wall, is also supported by morphological studies. Glomerular injury, leading to proteinuria, has been associated with loss of the charge-selective properties of these capillaries. Loss of glomerular fixed negative charges may also result in the foot process fusion and mesangial cell dysfunction often observed in proteinuric states.
肾小球超滤液的形成取决于肾小球压力和血流的相互作用,以及肾小球毛细血管壁固有的选择通透性特性。这些固有的通透性特性基于大小和净分子电荷区分,起到将大分子排除在尿液空间之外的作用。分子半径小于20 Å的中性右旋糖酐可毫无可测限制地穿过肾小球壁,而半径大于42 Å的右旋糖酐几乎完全被阻挡。对于任何给定大小,带负电荷的大分子比中性分子受到更大程度的限制。此外,与大小相似的中性聚合物相比,带正电荷的分子穿过肾小球壁的能力增强。形态学研究也支持由于肾小球壁内固定负电荷而形成电荷屏障的概念。导致蛋白尿的肾小球损伤与这些毛细血管电荷选择性特性的丧失有关。肾小球固定负电荷的丧失也可能导致蛋白尿状态下常见的足突融合和系膜细胞功能障碍。