Saito Marina, Miyamoto Kentaro, Murakami Ikuya
Department of Psychology, the University of Tokyo, Tokyo 113-0033, Japan.
Japan Society for the Promotion of Science, Tokyo 102-0083, Japan.
iScience. 2024 Jul 30;27(9):110612. doi: 10.1016/j.isci.2024.110612. eCollection 2024 Sep 20.
Although the optic disk corresponding to the blind spot contains no classical photoreceptors, it contains photopigment melanopsin. To clarify whether melanopsin is involved in light detection, we conducted detection tasks for light stimuli presented in the normal visual field, with and without another illumination inside the blind spot. We found that a blue blind-spot illumination decreased the light detectability on a dark background. This effect was replicable when it was determined immediately after the blind-spot illumination was turned off, suggesting the contribution of a sluggish system rather than scattering. Moreover, the aforementioned effect was not observed when the blind-spot illumination was in red, indicating wavelength specificity in favor of melanopsin's sensitivity profile. These findings suggest that melanopsin is activated by the blind-spot illumination and thereby interferes with light detection near the absolute threshold. Light detection originating from conventional photoreceptors is modulated by melanopsin-based computation presumably estimating a baseline noise level.
尽管对应于盲点的视盘不包含经典的光感受器,但它含有光色素黑视蛋白。为了阐明黑视蛋白是否参与光检测,我们针对正常视野中呈现的光刺激进行了检测任务,同时在盲点内部有或没有另一种照明。我们发现,盲点处的蓝色照明降低了暗背景下的光检测能力。当在盲点照明关闭后立即进行测定时,这种效应是可重复的,这表明是一个反应迟缓的系统而非散射起了作用。此外,当盲点照明为红色时,未观察到上述效应,这表明存在有利于黑视蛋白敏感性特征的波长特异性。这些发现表明,黑视蛋白被盲点照明激活,从而干扰绝对阈值附近的光检测。源自传统光感受器的光检测可能通过基于黑视蛋白的计算进行调节,该计算大概是在估计基线噪声水平。