Yingst D R, Polasek P M, Kilgore P
Biochim Biophys Acta. 1985 Mar 14;813(2):277-81. doi: 10.1016/0005-2736(85)90242-1.
Ethanol in the range of 0.76-2.40 M caused an immediate increase in the Ca permeability of the plasma membrane of resealed human red blood cell ghosts in which intracellular free Ca could be continuously monitored by means of the Ca chromophore arsenazo III. At a given concentration of ethanol, the Ca permeability increased markedly a few minutes following the mixing of the ghosts and the ethanol, and continued to increase over at least the next 30 min. Preincubating the ghosts in ethanol for 15, 60 and 120 min before measuring the rate of free Ca accumulation, progressively increased the effect of a given concentration of ethanol. These results indicate that the effect of a given concentration of ethanol is a complex function of concentration and exposure time. The effects of ethanol in this concentration range were completely reversible. The resealed ghosts used in these experiments were depleted of ATP to avoid interference from the Ca pump and all experiments were carried out with 150 mM KCl on both sides of the membrane to minimize changes in either the volume or membrane potential associated with activation of the Ca-dependent K channel.
浓度在0.76 - 2.40 M范围内的乙醇会使重新封闭的人红细胞膜囊泡的质膜钙通透性立即增加,在这种膜囊泡中,细胞内游离钙可通过钙发色团偶氮胂III持续监测。在给定的乙醇浓度下,膜囊泡与乙醇混合后几分钟,钙通透性显著增加,并在至少接下来的30分钟内持续增加。在测量游离钙积累速率之前,将膜囊泡在乙醇中预孵育15、60和120分钟,会使给定浓度乙醇的作用逐渐增强。这些结果表明,给定浓度乙醇的作用是浓度和暴露时间的复杂函数。该浓度范围内乙醇的作用是完全可逆的。这些实验中使用的重新封闭的膜囊泡耗尽了ATP,以避免钙泵的干扰,并且所有实验均在膜两侧使用150 mM KCl进行,以尽量减少与钙依赖性钾通道激活相关的体积或膜电位变化。