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Characterisation of dark adaptation in human cone pathways: an application of the equivalent background hypothesis

机译:人类锥体途径中暗适应的表征:等效背景假说的应用

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摘要

It is well accepted that in rod photoreceptors the photoproducts generated by a bleach cause desensitisation during dark adaptation. We examine whether this notion holds for cones.A model of cone dark adaptation is developed based on the equivalent background concept. The underlying theory of the model relies on a series of assumptions that link psychophysically determined detection thresholds to cone phototransduction. Correction of thresholds for the reduced quantum-catching ability of the cones (due to the depletion of photopigment caused by a bleaching light) is an important aspect of the model.Foveal detection thresholds were measured for a small test flash presented on a large steady background field or presented alone after adapting to the background field. Test and background fields were monochromatic, with wavelengths closely matched to promote detection by the luminance mechanism.The model provided a good description of the data collected under these conditions. Parameters of the model were similar for all wavelengths and each observer, as were the derived equivalent background relationships. Analysis of previously published data for Stiles’ π5 mechanism gave analogous results.The model is made up of two components. The early (fast) component is likely to be due to the direct action of the cone equivalent of inactivated Rh* on the G-protein cascade and/or the reverse reaction of the cone equivalent of inactivated Rh* to Rh*. The later (slow) component may be due to the direct action of cone opsin on the G-protein cascade.
机译:公认的是,在棒状感光体中,由漂白剂产生的光产物在暗适应期间引起脱敏。我们研究了这一概念是否适用于视锥细胞。基于等效背景概念,开发了视锥细胞暗适应模型。该模型的基础理论依赖于一系列假设,这些假设将心理上确定的检测阈值与锥体光电导联系起来。该模型的一个重要方面是校正视锥细胞量子捕获能力降低的阈值(由于漂白光引起的光致色素的耗尽)。针对在较大的稳定背景下呈现的小型测试闪光,测量了人眼检测阈值。字段或适应背景字段后单独显示。测试和背景场是单色的,波长紧密匹配以促进通过亮度机制进行检测。该模型很好地描述了在这些条件下收集的数据。对于所有波长和每个观察者,模型的参数都是相似的,导出的等效背景关系也是如此。对Stiles的π5机制先前发布的数据进行分析得出的结果相似。该模型由两个部分组成。早期(快速)成分很可能是由于灭活的Rh *的视锥当量对G蛋白级联的直接作用和/或灭活的Rh *的视锥当量与Rh *的逆反应。较晚的(缓慢的)成分可能是视锥蛋白对G蛋白级联反应的直接作用。

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