Biber T U, Mullen T L
Am J Physiol. 1977 Jan;232(1):C67-75. doi: 10.1152/ajpcell.1977.232.1.C67.
The transepithelial efflux of Na and several nonelectrolytes (mannitol, sucrose, and polyethylene glycol 900) were measured in the isolated frog skin under short-circuited conditions in chambers that had been specially designed to avoid edge damage. Ouabain (10(-3) and 10(-4) M) caused a dramatic increase in the efflux of Na, whereas the efflux of nonelectrolytes showed only a slight alteration. The efflux of Na increased after the application of dinitrophenol (10(-4) M), whereas the efflux of nonelectrolytes remained constant. Amiloride (10(-3) M) caused large variations in the efflux of Na, whereas the efflux of nonelectrolytes remained unchanged. The results provide evidence that these inhibitors do not alter the permeability of the paracellular pathway and that the total transepithelial efflux of Na or at least a very large portion of it, and possibly also the transepithelial efflux of Cl, proceeds via a transcellular pathway and not a paracellular pathway as has been widely accepted. The data further suggest that the Na proceeding via this pathway interacts directly or indirectly with the active transport step.
在经过特殊设计以避免边缘损伤的实验室内,在短路条件下,对分离的蛙皮中钠和几种非电解质(甘露醇、蔗糖和聚乙二醇900)的跨上皮外排进行了测量。哇巴因(10⁻³和10⁻⁴ M)使钠的外排显著增加,而非电解质的外排仅略有改变。应用二硝基酚(10⁻⁴ M)后,钠的外排增加,而非电解质的外排保持恒定。氨氯吡咪(10⁻³ M)使钠的外排发生很大变化,而非电解质的外排保持不变。结果表明,这些抑制剂不会改变细胞旁途径的通透性,并且钠的总跨上皮外排或至少其很大一部分,以及可能还有氯的跨上皮外排,是通过细胞内途径而非如广泛接受的细胞旁途径进行的。数据进一步表明,通过该途径进行的钠与主动转运步骤直接或间接相互作用。