Baylor D A, Matthews G, Nunn B J
J Physiol. 1984 Sep;354:203-23. doi: 10.1113/jphysiol.1984.sp015372.
The functional role and spatial location of voltage-sensitive conductances that modify the light-evoked electrical signals were studied in retinal rods of the tiger salamander. An isolated rod was drawn into a suction electrode for recording membrane current and impaled with an intracellular electrode for recording membrane potential and passing current. A bright flash gave a rapid initial hyperpolarization that relaxed to a smaller plateau. Simultaneously the dark current of the outer segment was shut off with the time course of a rounded step function. This characteristic difference between the wave forms demonstrates that the voltage relaxation does not result from reopening of light-sensitive channels. The voltage relaxation in (2) did not require light or interruption of the dark current, as the wave form was duplicated by suddenly switching off a depolarizing current injected during steady saturating light. This is explained if the relaxation depends purely on voltage-sensitive conductances. The voltage response to a dim flash reached its peak value before the current response. The voltage wave form was predicted assuming that the recorded photo-current drove a linear high-pass filter with parameters derived from analysis of the voltage response to injection of a current step. When the intracellular voltage was changed by current injection the slope resistance of the outer segment slowly declined to a lower level, indicating that the outer segment contains a voltage-sensitive conductance. When a current step was injected in bright steady light, the current recorded from the outer segment consisted of a capacity component proportional to dV/dt and a small extracellular leakage current but no detectable ionic current. This supports other evidence indicating that light-sensitive channels comprise the main or exclusive ionic conductance of the outer segment. The behaviour in (5) is explained if the light-sensitive channels themselves are slowly opened by hyperpolarization and closed by depolarization. Analysis of the current-injection experiments suggests that most of the high-pass filtering in a rod results from the action of voltage-sensitive conductances located in the inner segment. Addition of 10 mM-CsCl to the Ringer solution abolished the relaxation in the voltage response to a bright flash but left intact the high-pass filtering of small signals. This would be explained by a selective block of one of two sets of voltage-sensitive channels in the inner segment or by a voltage-sensitive block of one kind of channel.
在虎螈的视网膜视杆细胞中,研究了改变光诱发电信号的电压敏感电导的功能作用和空间位置。将一个分离的视杆细胞吸入吸力电极以记录膜电流,并用细胞内电极刺入以记录膜电位和通过电流。一个明亮的闪光会产生一个快速的初始超极化,然后松弛到一个较小的平台期。同时,外段的暗电流以圆形阶跃函数的时间进程被关闭。波形之间的这种特征差异表明,电压松弛不是由光敏感通道的重新开放引起的。(2)中的电压松弛不需要光或暗电流的中断,因为通过突然关闭在稳定饱和光期间注入的去极化电流可以复制波形。如果松弛纯粹取决于电压敏感电导,这就可以得到解释。对暗淡闪光的电压响应在电流响应之前达到峰值。假设记录的光电流驱动一个线性高通滤波器,其参数来自对电流阶跃注入的电压响应分析,从而预测了电压波形。当通过电流注入改变细胞内电压时,外段的斜率电阻会缓慢下降到较低水平,这表明外段包含一个电压敏感电导。当在明亮的稳定光下注入电流阶跃时,从外段记录的电流由与dV/dt成比例的电容成分和小的细胞外泄漏电流组成,但没有可检测到的离子电流。这支持了其他证据,表明光敏感通道构成了外段的主要或唯一离子电导。如果光敏感通道本身通过超极化缓慢打开并通过去极化关闭,那么(5)中的行为就可以得到解释。对电流注入实验的分析表明,视杆细胞中的大部分高通滤波是由位于内段的电压敏感电导的作用引起的。向林格溶液中添加10 mM - CsCl消除了对明亮闪光的电压响应中的松弛,但保留了小信号的高通滤波。这可以通过对内段两组电压敏感通道之一的选择性阻断或一种通道的电压敏感阻断来解释。