Gordon J, Shapley R M, Kaplan E
J Gen Physiol. 1978 Feb;71(2):123-38. doi: 10.1085/jgp.71.2.123.
Light and electron microscopy revealed that there are both rods and cones in the retina of the eel Anguilla rostrata. The rods predominate with a rod to cone ratio of 150:1. The spectral sensitivity of the dark-adapted eyecup ERG had a peak at about 520 nm and was well fit by a vitamin A2 nomogram pigment with a lambdamax = 520 nm. This agrees with the eel photopigment measurements of other investigators. This result implies that a single spectral mechanism--the rods--provides the input for the dark-adapted ERG. The spectral sensitivity of the ERG to flicker in the light-adapted eyecup preparation was shifted to longer wavelengths; it peaked at around 550 nm. However, there was evidence that this technique might not have completely eliminated rod intrusion. Rod responses were abolished in a bleached isolated retina preparation, in which it was shown that there were two classes of cone-like mechanisms, one with lambdamax of 550 nm and the other with lambdamax of less than 450 nm. Ganglion cell recording provided preliminary evidence for opponent-color processing. Horizontal cells were only of the L type with both rod and cone inputs.
光学显微镜和电子显微镜检查显示,美洲鳗鲡视网膜中既有视杆细胞又有视锥细胞。视杆细胞占主导,视杆细胞与视锥细胞的比例为150:1。暗适应眼杯视网膜电图的光谱敏感性在约520纳米处有一个峰值,并且与λmax = 520纳米的维生素A2列线图色素拟合良好。这与其他研究者对鳗鱼光色素的测量结果一致。该结果表明,单一的光谱机制——视杆细胞——为暗适应视网膜电图提供输入。在明适应眼杯标本中,视网膜电图对闪烁的光谱敏感性向更长波长偏移;它在约550纳米处达到峰值。然而,有证据表明该技术可能没有完全消除视杆细胞的干扰。在漂白的离体视网膜标本中,视杆细胞反应被消除,在该标本中显示有两类视锥样机制,一类λmax为550纳米,另一类λmax小于450纳米。神经节细胞记录为对立色处理提供了初步证据。水平细胞仅为L型,同时接受视杆细胞和视锥细胞的输入。