Schafer J A
Department of Physiology and Biophysics, University of Alabama, Birmingham 35294.
Annu Rev Physiol. 1990;52:709-26. doi: 10.1146/annurev.ph.52.030190.003425.
The weight of current evidence indicates that the proximal tubule has a high transepithelial osmotic water permeability in the range of 3500-6000 microns/sec, which is attributable in large part to the high water permeabilities of the cell membranes. Water movement through these membranes may occur through specialized, proteinaceous channels that can be blocked by sulfhydryl reagents. The water channels probably exclude even the smallest solutes and allow only single file movement of the water molecules as do the water channels previously described in the red blood cell and vasopressin-responsive epithelia. If a significant fraction of the water flow also occurs through the junctional complexes, it seems likely that these junctions could be a site for solute solvent coupling which would contribute to solute absorption by solvent drag and which would be responsible for non-unity reflection coefficients for some solutes such as Na+ and Cl-. This possibility is still a matter of vigorous debate. Since the transepithelial water permeability is high, only a very small osmolality difference (1-10 mOsM) is required to drive normally observed rates of volume absorption both in vivo and in vitro. The osmolality difference is produced at least in part by dilution of the luminal fluid and is possibly augmented by the development of interstitial hyperosmolality because of the rapid transport of preferentially absorbed solutes. In the future it is likely that the most important work in this field will relate to the factors that alter transepithelial water permeability and the solute and water permeabilities of the junctional complexes. Investigation in this area is essential in understanding how changes in capillary and interstitial hydrostatic and colloid osmotic pressure may affect volume absorption.
目前的证据表明,近端小管具有较高的跨上皮渗透水通透性,范围在3500 - 6000微米/秒,这在很大程度上归因于细胞膜的高水通透性。水通过这些膜的移动可能通过特殊的蛋白质通道进行,这些通道可被巯基试剂阻断。水通道可能甚至排除最小的溶质,并且只允许水分子单排移动,就像先前在红细胞和抗利尿激素反应性上皮细胞中描述的水通道一样。如果相当一部分水流也通过连接复合体发生,那么这些连接很可能是溶质 - 溶剂偶联的位点,这将有助于通过溶剂拖曳进行溶质吸收,并导致一些溶质(如Na +和Cl -)的反射系数不为1。这种可能性仍然是激烈争论的话题。由于跨上皮水通透性很高,无论是在体内还是体外,驱动正常观察到的体积吸收速率只需要非常小的渗透压差异(1 - 10毫渗摩尔)。渗透压差异至少部分是由管腔液的稀释产生的,并且可能由于优先吸收的溶质的快速运输导致间质高渗而增大。未来,该领域最重要的工作可能与改变跨上皮水通透性以及连接复合体的溶质和水通透性的因素有关。在这个领域的研究对于理解毛细血管和间质静水压以及胶体渗透压的变化如何影响体积吸收至关重要。