Langridge-Smith J E
J Physiol. 1986 Jul;376:299-319. doi: 10.1113/jphysiol.1986.sp016155.
The active transport of Na and Cl across bovine tracheal epithelium was studied in vitro by measuring 22Na and 36Cl fluxes under short-circuit conditions. Under basal conditions, both net Cl secretion and net Na absorption were observed: the sum of these two net fluxes accounted for 85% of the measured short-circuit current. The rate of spontaneous Cl secretion exceeded that of Na absorption by a factor of 2. Indomethacin, an inhibitor of endogenous prostaglandin production, decreased Cl secretion and increased Na absorption, reversing the direction of net transepithelial ion flow from secretion to absorption. The ratio of the change in each net ion flux was about 1:1. 50% of the basal net flux of Na was inhibited by amiloride (10(-4) M). The indomethacin-induced increase in the lumen-to-serosa flux of Na was entirely amiloride sensitive. An amiloride-insensitive fraction of this flux, of constant magnitude, was apparent in both control and indomethacin-treated tissues. The Na transport inhibitor had no effect on unidirectional or net Cl fluxes. Cl secretion was abolished by 4-methyl-diphenylamine-2'-carboxylic acid (50B). The Cl transport inhibitor had no effect on unidirectional or net Na fluxes. The results suggest that the rates of Na and Cl transport may be modulated in a reciprocal fashion by certain agents, which probably act through cyclic AMP, but that the two transport processes are not mutually interdependent in any simple, direct fashion. The lack of evidence for direct interaction between Na and Cl transport raises the possibility that there are separate absorptive and secretory cells in the tracheal epithelium, rather than a single transporting cell.
通过在短路条件下测量(^{22}Na)和(^{36}Cl)通量,对牛气管上皮细胞中(Na)和(Cl)的主动转运进行了体外研究。在基础条件下,观察到了净(Cl)分泌和净(Na)吸收:这两种净通量之和占所测短路电流的(85%)。自发(Cl)分泌速率比(Na)吸收速率高(2)倍。吲哚美辛是一种内源性前列腺素生成抑制剂,它减少了(Cl)分泌并增加了(Na)吸收,使跨上皮离子流的净方向从分泌转变为吸收。每种净离子通量变化的比率约为(1:1)。(10^{-4}M)的氨氯地平抑制了(50%)的基础(Na)净通量。吲哚美辛诱导的(Na)从管腔到浆膜通量的增加完全对氨氯地平敏感。在对照组织和吲哚美辛处理的组织中,均明显存在该通量中恒定大小的氨氯地平不敏感部分。(Na)转运抑制剂对单向或净(Cl)通量没有影响。(4 - 甲基 - 二苯胺 - 2'- 羧酸(50B)消除了(Cl)分泌。(Cl)转运抑制剂对单向或净(Na)通量没有影响。结果表明,(Na)和(Cl)的转运速率可能会被某些可能通过环磷酸腺苷起作用的试剂以相互对应的方式调节,但这两个转运过程并非以任何简单、直接的方式相互依赖。缺乏(Na)和(Cl)转运之间直接相互作用的证据,增加了气管上皮中存在单独的吸收细胞和分泌细胞而非单个转运细胞的可能性。