Helman S I, Nagel W, Fisher R S
J Gen Physiol. 1979 Jul;74(1):105-27. doi: 10.1085/jgp.74.1.105.
Studies were done with isolated frog skin to determine the effects of 10(-4) M ouabain on the electrophysiological parameters of outer and inner barriers of the Na-transporting cells. Microelectrodes were used to impale the skins from the outer surface to determine the intracellular voltages (Vsco) under conditions of short-circuiting and under conditions where a voltage clamp was used to vary the transepithelial voltage, VT. From this, the electrical resistances of outer (Rfo) and inner (RI) barriers were estimated. In addition, the driving force for active transepithelial Na transport (ENa = E'1) was estimated from the values of VT when the Vo = 0 mV (Helman and Fisher. 1977. J. Gen. Physiol. 69: 571-604). Studies were done with skins bathed with the usual 2.4 meq/liter [K]i in the inner solution as well as with reduced [K]i of 0.5 and 0 meq/liter. Characteristically, the responses to ouabain could be described by an initial rapid phase (5-10 min) during which time the Ri was increased markedly and the E'1 was decreased from control values. Thereafter, during the slow phases of the response, the resistances of both outer and inner barriers increased continuously and markedly with time leading ultimately to essentially complete inhibition of the short-circuit current. Similar studies were done with skins exposed to 10(-4) M amiloride in the outer solution. Although estimates of Ri could not be obtained under these conditions, the effects on the Vsco and E'1 were similar to those observed for the Na-transporting skins. However, the magnitudes of the effects were less and relatively slower than observed for the Na-transporting skins. The results of these studies were analyzed within the context of a proposed electrical model that takes into account the observation that the magnitude of the voltage at the inner barrier appears to exceed the equilibrium potential for K especially when transepithelial Na transport is inhibited at the apical barrier of the cells.
利用离体蛙皮进行研究,以确定10⁻⁴ M哇巴因对钠转运细胞外屏障和内屏障电生理参数的影响。使用微电极从外表面刺入皮肤,以确定在短路条件下以及使用电压钳改变跨上皮电压VT时的细胞内电压(Vsco)。据此,估算外屏障(Rfo)和内屏障(RI)的电阻。此外,当Vo = 0 mV时,根据VT值估算主动跨上皮钠转运的驱动力(ENa = E'1)(Helman和Fisher,1977年,《普通生理学杂志》69: 571 - 604)。研究使用内溶液中含有通常的2.4 meq/升[K]i以及[K]i降低至0.5和0 meq/升的皮肤进行。典型地,对哇巴因的反应可分为初始快速阶段(5 - 10分钟),在此期间RI显著增加,E'1从对照值降低。此后,在反应的缓慢阶段,外屏障和内屏障的电阻均随时间持续且显著增加,最终导致短路电流基本完全被抑制。对置于外溶液中含10⁻⁴ M氨氯吡咪的皮肤进行了类似研究。尽管在这些条件下无法获得RI的估算值,但对Vsco和E'1的影响与钠转运皮肤所观察到的相似。然而,其影响程度较小且比钠转运皮肤观察到的相对较慢。这些研究结果在一个提出的电模型背景下进行了分析,该模型考虑到以下观察结果:内屏障处的电压幅度似乎超过钾的平衡电位,尤其是当细胞顶端屏障处的跨上皮钠转运受到抑制时。