Departments of Physiology, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX, USA.
Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3825-34. doi: 10.1167/iovs.09-4806. Epub 2010 Mar 5.
PURPOSE. In Old World primates, the retina receives input from histaminergic neurons in the posterior hypothalamus. They are a subset of the neurons that project throughout the central nervous system and fire maximally during the day. The contribution of these neurons to vision, was examined by applying histamine to a dark-adapted, superfused baboon eye cup preparation while making extracellular recordings from peripheral retinal ganglion cells. METHODS. The stimuli were 5-ms, 560-nm, weak, full-field flashes in the low scotopic range. Ganglion cells with sustained and transient ON responses and two cell types with OFF responses were distinguished; their responses were recorded with a 16-channel microelectrode array. RESULTS. Low micromolar doses of histamine decreased the rate of maintained firing and the light sensitivity of ON ganglion cells. Both sustained and transient ON cells responded similarly to histamine. There were no statistically significant effects of histamine in a more limited study of OFF ganglion cells. The response latencies of ON cells were approximately 5 ms slower, on average, when histamine was present. Histamine also reduced the signal-to-noise ratio of ON cells, particularly in those cells with a histamine-induced increase in maintained activity. CONCLUSIONS. A major action of histamine released from retinopetal axons under dark-adapted conditions, when rod signals dominate the response, is to reduce the sensitivity of ON ganglion cells to light flashes. These findings may relate to reports that humans are less sensitive to light stimuli in the scotopic range during the day, when histamine release in the retina is expected to be at its maximum.
目的。在旧世界灵长类动物中,视网膜从前下丘脑的组胺能神经元接收输入。它们是投射到中枢神经系统的神经元的一个子集,在白天最大程度地发射。通过将组胺应用于暗适应的、超流的狒狒眼杯制剂,同时从周边视网膜神经节细胞进行细胞外记录,研究了这些神经元对视觉的贡献。
方法。刺激物是在低视敏度范围内的 5 毫秒、560nm、弱、全视野闪光。区分具有持续和瞬时 ON 反应的神经节细胞和具有 OFF 反应的两种细胞类型;使用 16 通道微电极阵列记录它们的反应。
结果。低微摩尔剂量的组胺降低了维持放电率和 ON 神经节细胞的光敏感性。持续和瞬时 ON 细胞对组胺的反应相似。在对 OFF 神经节细胞进行的更有限的研究中,组胺没有统计学上的显著影响。当组胺存在时,ON 细胞的反应潜伏期平均慢约 5 毫秒。组胺还降低了 ON 细胞的信噪比,尤其是在那些组胺诱导维持活动增加的细胞中。
结论。在暗适应条件下,从视回纤维轴突释放的组胺的主要作用是降低对光闪光的 ON 神经节细胞的敏感性。这些发现可能与以下报告有关,即当预期视网膜中组胺释放达到最大值时,人类在暗适应范围内对光刺激的敏感性在白天较低。