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On the mechanism of the amiloride-sodium entry site interaction in anuran skin epithelia

机译:关于无色皮肤上皮中阿米洛利钠进入位点相互作用的机制

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摘要

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.
机译:在孤立的无色皮肤上皮中研究了外部钠与利尿剂阿米洛利之间相互作用的稳态传输动力学。我们还研究了钙对这些上皮制剂中阿米洛利对短路电流(Isc)的抑制作用。这项研究的主要结论是:(a)阿米洛利是牛蛙和草蛙皮肤中Na进入的非竞争性抑制剂,但在R. temporaria和蟾蜍中却显示出混合的抑制作用。提出了一个假设,该假设指出在所有这些物种中阿米洛利和Na的相互作用位点在假定的进入蛋白上在空间上是不同的。 (b)阿米洛利和Na进入机制之间相互作用的化学计量不一定是一对一的。 (c)对于阿米洛利抑制作用的外部Ca需求不是绝对的。在所有浓度下,阿米洛利均有效地独立于是否存在外部Ca来抑制牛蛙皮的Isc。

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