Gonzáles E, Carpi-Medina P, Linares H, Whittembury G
Pflugers Arch. 1984 Nov;402(3):337-9. doi: 10.1007/BF00585520.
Osmotic steps, delta C, were produced across the apical cell membrane of isolated rabbit PST by perfusing their lumens with double barreled micropipettes at a rate of 0.5-0.8 nl/s. delta C = 15-46 mOsmolar were induced with mannitol. Changes in luminal diameter were recorded as a function of time with a TV camera and an integrator-processor system with space and time resolutions of 0.03 micron and 0.0167 s (3). The tubules were bathed with oil. Outer tubule diameter was time invariant. Pcaos, the apical cell osmotic permeability was therefore calculated from cell volume changes with time in units of 10(-4) cm3/cm2 X s. Osmolar. Pcaos was independent of delta C. The mean is 22.8 +/- 1.3 (n = 55). With a basolateral permeability of 50.4 (3,12), the transcellular permeability is 14 (same units) smaller than the transepithelial values available. This leads to the conclusion that a significant paracellular water osmotic permeability must exist.
通过用双管微量移液器以0.5 - 0.8 nl/s的速率灌注分离的兔近端小管(PST)的管腔,在其顶端细胞膜上产生渗透梯度(ΔC)。用甘露醇诱导出15 - 46毫摩尔渗透压浓度的ΔC。用电视摄像机和积分处理器系统记录管腔直径随时间的变化,其空间和时间分辨率分别为0.03微米和0.0167秒(3)。小管浸于油中。外管径不随时间变化。因此,顶端细胞渗透通透性(Pcaos)根据细胞体积随时间的变化以10⁻⁴ cm³/cm²×s·毫摩尔渗透压浓度为单位计算得出。Pcaos与ΔC无关。平均值为22.8±1.3(n = 55)。基底外侧通透性为50.4(3,12),跨细胞通透性比可得的跨上皮值小14(相同单位)。由此得出结论,必定存在显著的细胞旁水渗透通透性。