Lee B B, Smith V C, Pokorny J, Kremers J
Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Vision Res. 1997 Oct;37(20):2813-28. doi: 10.1016/s0042-6989(97)00108-9.
The strength of rod inputs to ganglion cells was assessed in the macaque retina at retinal positions within 3-15 deg eccentricity. The experimental paradigm used temporally modulated heterochromatic lights whose relative phase was varied. This paradigm provided a sensitive test to detect rod input. In parvocellular (PC) pathway cells, the gain of the cone-driven signal decreased with decrease in luminance. At 2 td a weak rod response, of a few impulses per second for 100% rod modulation, was revealed in about 60% of cells. For blue-on cells, the cone-driven response also decreased with retinal illuminance, but no rod response could be found. In magnocellular (MC) pathway cells, rod input was much more apparent. Responses became rod dominated at and below 20 td; we cannot exclude rod intrusion at higher retinal illuminances. Responsivity was maintained even at low retinal illuminances. Temporal-frequency dependent rod-cone interactions were observed in MC-pathway cells. Rod responses were of longer latency than cone responses, but there was no evidence of any difference in rod latency between parvocellular and magnocellular pathways.
在猕猴视网膜中,于离心率3 - 15度范围内的视网膜位置评估了视杆细胞输入到神经节细胞的强度。所采用的实验范式使用了相对相位可变的时间调制异色光。该范式为检测视杆细胞输入提供了一种灵敏的测试方法。在小细胞(PC)通路细胞中,锥体细胞驱动信号的增益随亮度降低而减小。在2 td时,约60%的细胞中显示出微弱的视杆细胞反应,对于100%视杆细胞调制,每秒有几个脉冲。对于蓝光开启细胞,锥体细胞驱动反应也随视网膜照度降低,但未发现视杆细胞反应。在大细胞(MC)通路细胞中,视杆细胞输入更为明显。在20 td及以下,反应变得以视杆细胞为主;我们不能排除在较高视网膜照度下视杆细胞的干扰。即使在低视网膜照度下,反应性仍得以维持。在大细胞通路细胞中观察到了时间频率依赖性的视杆 - 锥体细胞相互作用。视杆细胞反应的潜伏期比锥体细胞反应长,但没有证据表明小细胞通路和大细胞通路在视杆细胞潜伏期上存在任何差异。