Benos D J, Mandel L J, Balaban R S
J Gen Physiol. 1979 Mar;73(3):307-26. doi: 10.1085/jgp.73.3.307.
The steady-state transport kinetics of the interaction between external sodium and the diuretic drug, amiloride, was studied in isolated anuran skin epithelia. We also investigated the effect of calcium on the amiloride-induced inhibition of short-circuit current (Isc) in these epithelial preparations. The major conclusions of this study are: (a) amiloride is a noncompetitive inhibitor of Na entry in bullfrog and grassfrog skin, but displays mixed inhibition in R. temporaria and the toad. A hypothesis which states that the interaction sites for amiloride and Na on the putative entry protein are spatially distinct in all of these species is proposed. (b) The stoichiometry of interaction between amiloride and the Na entry mechanism is not necessarily one-to-one. (c) The external Ca requirement for the inhibitory effect of amiloride is not absolute. Amiloride, at all concentrations, is equally effective in inhibiting Isc of bullfrog skin independently from the presence or absence of external Ca.
在离体无尾两栖类皮肤上皮中研究了外部钠离子与利尿药氨氯吡脒相互作用的稳态转运动力学。我们还研究了钙对这些上皮制剂中氨氯吡脒诱导的短路电流(Isc)抑制作用的影响。本研究的主要结论如下:(a)氨氯吡脒是牛蛙和林蛙皮肤中钠内流的非竞争性抑制剂,但在欧洲林蛙和蟾蜍中表现为混合抑制作用。提出了一种假说,即在所有这些物种中,氨氯吡脒和钠在假定的内流蛋白上的相互作用位点在空间上是不同的。(b)氨氯吡脒与钠内流机制之间相互作用的化学计量比不一定是一对一的。(c)氨氯吡脒产生抑制作用对外部钙的需求并非绝对。在所有浓度下,无论外部钙存在与否,氨氯吡脒对牛蛙皮肤Isc的抑制作用均同样有效。