Pieprzyk A R, Weiner W W, Chamberlain S C
Department of Bioengineering and Neuroscience, Institute for Sensory Research, Syracuse University, Syracuse, NY 13244-5290, USA.
J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2003 Aug;189(8):643-53. doi: 10.1007/s00359-003-0437-8. Epub 2003 Jun 26.
Electroretinograms were recorded from the horseshoe crab compound eye using a high-intensity light-emitting diode and a whole-eye seawater electrode. Recordings were made from both lateral eyes in natural daylight or in continuous darkness with the optic nerve intact or cut. Recordings from two eyes of the same animal in different conditions facilitated direct comparisons of the effects of diurnal lighting and circadian efferent activity on the daily patterns of sensitivity of the eye. Structural changes appear to account for about half of the total electroretinogram excursion. Circadian input begins about 45 min in advance of sunset and the nighttime sensitivity returns to the daytime values 20 min after sunrise. When the optic nerve is cut, the nighttime sensitivity shows exponential decay over the next 5 or 6 days, consistent with a light-triggered structural light adaptation process unopposed by efferent input. Our results suggest that two mechanisms mediate the increase in lateral eye sensitivity at night-physiological dark adaptation and circadian efferent input. Three mechanisms appear to be involved in mediating the decrease in lateral eye sensitivity during daylight-physiological light adaptation, a continuous structural light adaptation process, and a separate light-triggered, efferent-primed structural light adaptation process.
使用高强度发光二极管和全眼海水电极,从鲎的复眼中记录视网膜电图。在自然日光下或持续黑暗中,在视神经完整或切断的情况下,对两只侧眼进行记录。在不同条件下对同一只动物的两只眼睛进行记录,便于直接比较昼夜光照和昼夜传出活动对眼睛每日敏感度模式的影响。结构变化似乎占视网膜电图总偏移量的一半左右。昼夜节律输入在日落前约45分钟开始,夜间敏感度在日出后20分钟恢复到白天的值。当视神经被切断时,夜间敏感度在接下来的5或6天内呈指数衰减,这与一个不受传出输入反对的光触发结构光适应过程一致。我们的结果表明,有两种机制介导夜间侧眼敏感度的增加——生理暗适应和昼夜传出输入。在白天,似乎有三种机制参与介导侧眼敏感度的降低——生理光适应、持续的结构光适应过程以及一个单独的光触发、传出启动的结构光适应过程。