Pinto L H, Pak W L
J Gen Physiol. 1974 Jul;64(1):26-48. doi: 10.1085/jgp.64.1.26.
The time-course of the light-induced changes in membrane voltage and resistance were measured for single photoreceptors in the retina of Gekko gekko. In the surgically isolated retina, small stimuli directed toward the impaled receptor produced a membrane hyperpolarization the time-course of which was identical to that of the increase in membrane resistance. In the eyecup preparation nearly identical time-courses were evoked only after perfusion of the vitreous surface with solution having high (Mg(++)). Disparate time-courses were obtained in (a) the isolated retina when large or displaced stimuli were used, and (b) the eyecup preparation when it was treated normally (see Pinto and Pak. 1974. J. Gen. Physiol. 64:49) and when it was exposed to aspartate ions or hypoxia. These results are consistent with the hypothesis that the receptor potential (elicited in the impaled receptor as a result of quanta only it captures) is generated by a single ionic process that decreases membrane conductance. These measurements provide a means to distinguish the receptor potential from interactions. From direct measurements of membrane time constant and total resistance in darkness, total membrane capacitance was calculated. The mean capacitance was 7.1 x 10(-5) microF. This high value is consistent with anatomical observations of membrane infoldings at the base of gecko photoreceptors.
对gekko gekko视网膜中的单个光感受器,测量了光诱导的膜电压和电阻变化的时间进程。在手术分离的视网膜中,指向被刺穿感受器的小刺激会产生膜超极化,其时间进程与膜电阻增加的时间进程相同。在眼杯标本中,只有在用高(Mg(++))溶液灌注玻璃体表面后,才会诱发几乎相同的时间进程。在以下情况下会得到不同的时间进程:(a)在分离的视网膜中使用大的或移位的刺激时;(b)在正常处理的眼杯标本中(见Pinto和Pak,1974年,《普通生理学杂志》64:49),以及当它暴露于天冬氨酸离子或缺氧时。这些结果与以下假设一致:感受器电位(仅由被刺穿感受器捕获的量子引发)是由一个降低膜电导的单一离子过程产生的。这些测量提供了一种区分感受器电位与相互作用的方法。通过在黑暗中直接测量膜时间常数和总电阻,计算出了总膜电容。平均电容为7.1×10(-5)微法。这个高值与对壁虎光感受器基部膜褶皱的解剖学观察结果一致。