Benos D J, Hyde B A, Latorre R
J Gen Physiol. 1983 May;81(5):667-85. doi: 10.1085/jgp.81.5.667.
The sodium flux ratio of the amiloride-sensitive Na+ channel in the apical membrane of in vitro Rana catesbeiana skin has been evaluated at different sodium concentrations and membrane potentials in sulfate Ringer solution. Amiloride-sensitive unidirectional influxes and effluxes were determined as the difference between bidirectional 22Na and 24Na fluxes simultaneously measured in the absence and presence of 10(-4) M amiloride in the external bathing solution. Amiloride-sensitive Na+ effluxes were induced by incorporation of cation-selective ionophores (amphotericin B or nystatin) into the normally Na+-impermeable basolateral membrane. Apical membrane potentials (Va) were measured with intracellular microelectrodes. We conclude that since the flux ratio exponent, n', is very close to 1, sodium movement through this channel can be explained by a free-diffusion model in which ions move independently. This result, however, does not necessarily preclude the possibility that this transport channel may contain one or more ion binding sites.
在硫酸盐林格氏溶液中,于不同钠浓度和膜电位条件下,对体外牛蛙皮肤顶膜中阿米洛利敏感的Na⁺通道的钠通量比率进行了评估。阿米洛利敏感的单向流入和流出被确定为在外部浴液中不存在和存在10⁻⁴ M阿米洛利时同时测量的双向²²Na和²⁴Na通量之间的差异。通过将阳离子选择性离子载体(两性霉素B或制霉菌素)掺入通常对Na⁺不通透的基底外侧膜来诱导阿米洛利敏感的Na⁺流出。用细胞内微电极测量顶膜电位(Va)。我们得出结论,由于通量比率指数n'非常接近1,钠通过该通道的移动可以用自由扩散模型来解释,即离子独立移动。然而,这一结果并不一定排除该运输通道可能包含一个或多个离子结合位点的可能性。