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黑视蛋白增强图像持久度。

Melanopsin enhances image persistence.

机构信息

Division of Neuroscience and Centre for Biological Timing, School of Biology, Faculty of Biology Medicine and Health, University of Manchester, Upper Brook Street, M13 9PT Manchester, UK.

Division of Neuroscience and Centre for Biological Timing, School of Biology, Faculty of Biology Medicine and Health, University of Manchester, Upper Brook Street, M13 9PT Manchester, UK.

出版信息

Curr Biol. 2023 Dec 4;33(23):5048-5056.e4. doi: 10.1016/j.cub.2023.10.039. Epub 2023 Nov 14.

Abstract

Contributions of the inner retinal photopigment melanopsin to human visual perception are incompletely understood. Here, we use a four-primary display to produce stimuli differing in melanopsin versus cone contrast in psychophysical paradigms in eight subjects with normal color vision. We address two predictions from electrophysiological recordings of the melanopsin system in non-human mammals: melanopsin influences color and/or supports image persistence under visual fixation. We first construct chromatic contrast sensitivity contours for stimuli differing in melanopsin excitation presented as a central annulus (10°) or peripheral (22.5°) spot. We find that although including melanopsin contrast produces modest changes in the average chromatic coordinates in both eccentricities, this occurs equally at low (0.5 Hz) and higher (3.75 Hz) temporal frequencies, arguing that it reflects divergence in cone spectral sensitivity in our participants from that captured in standardized cone fundamentals rather than a melanopsin contribution to color. We continue to ask whether the established ability of melanopsin to sustain firing of visual neurons under extended light exposure has a visual correlate, using the optical illusion of Troxler fading in which blurred spots in periphery disappear during visual fixation. We find that introducing additional melanopsin contrast (+28% Michelson contrast) to either bright or dark spots increases fading latency by 35% ± 8.8% and 41% ± 13.6%, respectively. Our data argue that the primary contribution of melanopsin to perception under these conditions is not to provide a color percept but rather to enhance persistence of low spatial frequency patterns during visual fixation.

摘要

内视网膜光色素黑素细胞在人类视觉感知中的作用尚未完全了解。在这里,我们使用四原色显示器在八位具有正常色觉的受试者的心理物理范式中产生了不同的黑素细胞与视锥细胞对比度的刺激。我们解决了非人类哺乳动物中黑素细胞系统的电生理记录所提出的两个预测:黑素细胞影响颜色和/或支持视觉固定下的图像持久性。我们首先构建了不同黑素细胞兴奋的刺激的色觉对比灵敏度轮廓,这些刺激呈现为中央环(10°)或外围(22.5°)点。我们发现,尽管包括黑素细胞对比度会在两个偏心度下的平均色坐标产生适度变化,但在低(0.5 Hz)和高(3.75 Hz)时间频率下都会发生这种情况,这表明这反映了我们参与者的视锥光谱灵敏度与标准化视锥基本原理所捕获的灵敏度之间的差异,而不是黑素细胞对颜色的贡献。我们继续询问在扩展的光照下持续激发视觉神经元的黑素细胞的既定能力是否具有视觉相关性,使用 Troxler 褪色的光学错觉,在该错觉中,外围的模糊斑点在视觉固定时消失。我们发现,向亮或暗点引入额外的黑素细胞对比度(+28%Michelson 对比度)分别将褪色潜伏期增加了 35%±8.8%和 41%±13.6%。我们的数据表明,在这些条件下,黑素细胞对感知的主要贡献不是提供颜色感知,而是增强视觉固定期间低空间频率模式的持久性。

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