Relative light sensitivities of four retinal hemi-fields for suppressing the synthesis of melatonin at night

Mark S. Rea, Rohan Nagare, Mariana G. Figueiro
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引用次数: 9

Abstract

The magnitude of the stimulus to the biological clock will depend upon the distribution of circadian phototransduction circuits across the retinae and the spatial distribution of luminous stimuli in the environment. The present study compared nocturnal melatonin suppression for light exposures to the superior, inferior, nasal, and temporal retina in one eye independent of shading from the brow and the nose. The stimulus was a 40° diameter luminous disc, half of which was blue light (LED, λpeak = 470 nm) and the other amber light (LED, λpeak = 590 nm). Experimentally, the orientation of the bipartite disc was rotated to each of the four cardinal points of the visual field. A full, 40° blue disc was also employed by replacing the amber half-disc with another blue half-disc. The blue full- and half-discs always produced 100 photopic lx at the cornea. As hypothesized, nocturnal melatonin suppression was statistically greatest when the blue half-disc was delivered to the nasal hemi-field (35%); the other three hemi-fields were equally affected by the blue half-disc (≈20%). Melatonin suppression for the full-disc was 24%, which was not statistically different than the average suppression for the four hemi-fields of 27%.

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夜间抑制褪黑激素合成的四种视网膜半场的相对光敏度
对生物钟的刺激程度将取决于视网膜上昼夜节律光导电路的分布以及环境中发光刺激的空间分布。本研究比较了夜间褪黑激素对一只眼睛的上、下、鼻和颞视网膜的抑制作用,与眉毛和鼻子的遮光无关。刺激为直径40°的发光盘,其中一半为蓝光(LED, λ峰= 470 nm),另一半为琥珀色光(LED, λ峰= 590 nm)。实验中,二分盘的方向被旋转到视野的四个基点中的每一个。用另一个蓝色半盘代替琥珀半盘,也采用了一个完整的40°蓝色半盘。蓝色的全圆盘和半圆盘在角膜处总是产生100视力克。正如假设的那样,夜间褪黑激素的抑制在统计上是最大的,当蓝色半盘被送到鼻半野时(35%);其他三个半场同样受到蓝色半盘的影响(≈20%)。褪黑素在全视场的抑制率为24%,与四个半视场的平均抑制率27%没有统计学差异。
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来源期刊
Neurobiology of Sleep and Circadian Rhythms
Neurobiology of Sleep and Circadian Rhythms Neuroscience-Behavioral Neuroscience
CiteScore
4.50
自引率
0.00%
发文量
9
审稿时长
69 days
期刊介绍: Neurobiology of Sleep and Circadian Rhythms is a multidisciplinary journal for the publication of original research and review articles on basic and translational research into sleep and circadian rhythms. The journal focuses on topics covering the mechanisms of sleep/wake and circadian regulation from molecular to systems level, and on the functional consequences of sleep and circadian disruption. A key aim of the journal is the translation of basic research findings to understand and treat sleep and circadian disorders. Topics include, but are not limited to: Basic and translational research, Molecular mechanisms, Genetics and epigenetics, Inflammation and immunology, Memory and learning, Neurological and neurodegenerative diseases, Neuropsychopharmacology and neuroendocrinology, Behavioral sleep and circadian disorders, Shiftwork, Social jetlag.
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