Matthews G
J Physiol. 1985 Apr;361:205-17. doi: 10.1113/jphysiol.1985.sp015641.
Outer segment membrane current of single rod photoreceptors from toad retina was recorded with a suction electrode, and extracellular calcium concentration was manipulated by transferring the recorded cell from one pool of saline to another or by locally perfusing the outer segment. The large increase in dark current that resulted from exposure to low-calcium saline was accompanied by an increase in dark noise in the band 1-800 Hz. This noise was suppressed by bright light, and its power spectrum could be described by a single Lorentzian equation with average corner frequency of 40.1 +/- 9.5 Hz (mean +/- S.D., n = 11). In low-calcium saline, saturating flash responses were often followed by a transient increase in the dark current lasting 30-100 s. During this rebound period of increased dark current, increased dark noise similar to that described in 2 was observed. The power spectrum of this noise was also fitted by a single Lorentzian equation, with corner frequency averaging 29.7 +/- 6.6 Hz (mean +/- S.D., n = 27). To examine the possible role of intracellular voltage fluctuations in generating the noise, suction electrodes were filled with calcium-free saline and recordings were made from outer segments of rods attached to pieces of retina. In this recording configuration, the electrical coupling among the rods in the piece should attenuate voltage fluctuations associated with the post-light rebound period of increased dark current. In this situation, the rebound increase in dark current was still observed, but the noise was reduced or absent. Using the same recording configuration, isolated rods showed pronounced noise during the rebound. The result in 4 suggests that the noise resulted from fluctuations in intracellular voltage, not directly from fluctuations in the light-sensitive channels. In this view, the corner frequency of the noise power spectrum probably reflects the membrane time constant of the isolated rod.
用吸力电极记录蟾蜍视网膜单个视杆光感受器的外段膜电流,并通过将记录的细胞从一个盐溶液池转移到另一个盐溶液池或通过局部灌注外段来控制细胞外钙浓度。暴露于低钙盐溶液导致的暗电流大幅增加伴随着1-800Hz频段暗噪声的增加。这种噪声被强光抑制,其功率谱可用单个洛伦兹方程描述,平均转折频率为40.1±9.5Hz(平均值±标准差,n=11)。在低钙盐溶液中,饱和闪光反应后暗电流通常会有30-100秒的短暂增加。在暗电流增加的这个反弹期内,观察到类似于上述2中描述的暗噪声增加。这种噪声的功率谱也可用单个洛伦兹方程拟合,转折频率平均为29.7±6.6Hz(平均值±标准差,n=27)。为了研究细胞内电压波动在产生噪声中的可能作用,吸力电极充满无钙盐溶液,并从附着在视网膜片上的视杆外段进行记录。在这种记录配置下,视网膜片中视杆之间的电耦合应会减弱与暗电流增加的光后反弹期相关的电压波动。在这种情况下,仍观察到暗电流的反弹增加,但噪声减少或消失。使用相同的记录配置,分离的视杆在反弹期间显示出明显的噪声。4中的结果表明,噪声是由细胞内电压波动引起的,而不是直接由光敏感通道的波动引起的。按照这种观点,噪声功率谱的转折频率可能反映了分离视杆的膜时间常数。