Widdicombe J H, Nathanson I T, Highland E
Am J Physiol. 1983 Nov;245(5 Pt 1):C388-96. doi: 10.1152/ajpcell.1983.245.5.C388.
The "loop" diuretics MK-196, bumetanide, piretanide, and furosemide are all potent inhibitors of Cl transport by the dog's tracheal epithelium. In short-circuited tissues, the drugs caused significant decreases in both unidirectional Cl fluxes and in the net flux of Cl toward the lumen; the change in net Cl flux was not significantly different from the change in short-circuit current. The drugs had no effect on active Na absorption. All drugs caused a significant fall in tissue conductance. All drugs, except MK-196, were more potent from the serosal bath; MK-196 was equipotent from either side of the tissue. In experiments with isolated cells, the diuretics caused no significant changes in intracellular Na and K concentrations, a fall in intracellular Cl concentration, and approximately equal falls in Na and Cl influxes. These results suggest that the site of action of these drugs is on a basolateral linked Na-Cl entry process. Additional evidence for such a linked entry process was provided by experiments in which removal of Cl reduced Na influx and removal of Na reduced Cl influx.
“袢”利尿剂MK - 196、布美他尼、吡咯他尼和呋塞米都是犬气管上皮细胞氯离子转运的强效抑制剂。在短路组织中,这些药物可使单向氯离子通量以及氯离子向管腔的净通量显著降低;净氯离子通量的变化与短路电流的变化无显著差异。这些药物对主动钠吸收无影响。所有药物均导致组织电导显著下降。除MK - 196外,所有药物从浆膜浴给药时作用更强;MK - 196从组织两侧给药时效果相同。在分离细胞的实验中,利尿剂对细胞内钠和钾浓度无显著影响,细胞内氯离子浓度下降,钠和氯离子内流下降幅度大致相同。这些结果表明,这些药物的作用位点是在基底外侧相连的钠 - 氯进入过程。去除氯离子可减少钠内流,去除钠可减少氯离子内流的实验为这种相连的进入过程提供了额外证据。