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视杆细胞光反应动力学限制中间视觉的时间对比敏感度。

Rod Photoresponse Kinetics Limit Temporal Contrast Sensitivity in Mesopic Vision.

机构信息

Center for Vision Research, Department of Ophthalmology, SUNY Upstate Medical University, Syracuse, New York 13210, and.

Departments of Ophthalmology, Neuroscience, and Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

J Neurosci. 2019 Apr 17;39(16):3041-3056. doi: 10.1523/JNEUROSCI.1404-18.2019. Epub 2019 Feb 8.

Abstract

The mammalian visual system operates over an extended range of ambient light levels by switching between rod and cone photoreceptors. Rod-driven vision is sluggish, highly sensitive, and operates in dim or scotopic lights, whereas cone-driven vision is brisk, less sensitive, and operates in bright or photopic lights. At intermediate or mesopic lights, vision transitions seamlessly from rod-driven to cone-driven, despite the profound differences in rod and cone response dynamics. The neural mechanisms underlying such a smooth handoff are not understood. Using an operant behavior assay, electrophysiological recordings, and mathematical modeling we examined the neural underpinnings of the mesopic visual transition in mice of either sex. We found that rods, but not cones, drive visual sensitivity to temporal light variations over much of the mesopic range. Surprisingly, speeding up rod photoresponse recovery kinetics in transgenic mice improved visual sensitivity to slow temporal variations, in the range where perceptual sensitivity is governed by Weber's law of sensation. In contrast, physiological processes acting downstream from phototransduction limit sensitivity to high frequencies and temporal resolution. We traced the paradoxical control of visual temporal sensitivity to rod photoresponses themselves. A scenario emerges where perceptual sensitivity is limited by: (1) the kinetics of neural processes acting downstream from phototransduction in scotopic lights, (2) rod response kinetics in mesopic lights, and (3) cone response kinetics as light levels rise into the photopic range. Our ability to detect flickering lights is constrained by the dynamics of the slowest step in the visual pathway. Cone photoresponse kinetics limit visual temporal sensitivity in bright (photopic) lights, whereas mechanisms in the inner retina limit sensitivity in dim (scotopic) lights. The neural mechanisms underlying the transition between scotopic and photopic vision in mesopic lights, when both rods are cones are active, are unknown. This study provides a missing link in this mechanism by establishing that rod photoresponse kinetics limit temporal sensitivity during the mesopic transition. Surprisingly, this range is where Weber's Law of Sensation governs temporal contrast sensitivity in mouse. Our results will help guide future studies of complex and dynamic interactions between rod-cone signals in the mesopic retina.

摘要

哺乳动物视觉系统通过在视杆细胞和视锥细胞之间切换来适应广泛的环境光强度范围。视杆细胞驱动的视觉反应缓慢、高度敏感,在昏暗或暗视觉条件下工作,而视锥细胞驱动的视觉反应迅速、敏感度较低,在明亮或明视觉条件下工作。在中间或中光条件下,视觉从视杆细胞驱动无缝过渡到视锥细胞驱动,尽管视杆细胞和视锥细胞的反应动力学存在显著差异。这种平滑转换的神经机制尚不清楚。使用操作性行为测定、电生理记录和数学建模,我们研究了雌雄小鼠中从视杆细胞到视锥细胞的中光视觉转换的神经基础。我们发现,在中光范围内,视杆细胞而不是视锥细胞驱动对光强度变化的视觉敏感性。令人惊讶的是,在转基因小鼠中加速视杆细胞光反应恢复动力学可提高对慢时变光强度的视觉敏感性,而这种敏感性受威布尔感觉定律控制。相比之下,光转导下游的生理过程限制了对高频和时间分辨率的敏感性。我们将视觉时间敏感性的这种悖论控制归因于视杆细胞光反应本身。这种情况表明,感知敏感性受到以下三个因素的限制:(1)在暗视觉条件下,光转导下游的神经过程的动力学;(2)在中光条件下,视杆细胞的反应动力学;(3)随着光强度进入明视觉范围,视锥细胞的反应动力学。我们检测闪烁光的能力受到视觉通路中最慢步骤的动力学限制。在明亮(明视觉)光条件下,视锥细胞光反应动力学限制了视觉时间敏感性,而在昏暗(暗视觉)光条件下,内视网膜的机制限制了敏感性。在中光条件下,当视杆细胞和视锥细胞都活跃时,从暗视觉向明视觉转换的神经机制尚不清楚。本研究通过确定在中光转换期间视杆细胞光反应动力学限制了时间敏感性,为该机制提供了一个缺失的环节。令人惊讶的是,这个范围是威布尔感觉定律在小鼠中控制时间对比敏感度的范围。我们的研究结果将有助于指导在中光视网膜中视杆-视锥信号之间的复杂和动态相互作用的未来研究。

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