Isabel Schöllhorn, Oliver Stefani, Robert J Lucas, Manuel Spitschan, Christian Epple, Christian Cajochen
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Therefore, we used a five-primary display prototype to generate light conditions that were matched in terms of L-, M-, and S-cone-opic irradiances, but with high and low melanopic irradiances (~3-fold difference). Seventy-two healthy, male participants completed a 2-week study protocol. The volunteers were assigned to one of the four groups that differed in luminance levels (27-285 cd/m<sup>2</sup>). Within the four groups, each volunteer was exposed to a low melanopic (LM) and a high melanopic (HM) condition. The two 17-h study protocols comprised 3.5 h of light exposure starting 4 h before habitual bedtime. Median pupil size was significantly smaller during HM than LM in all four light intensity groups. In addition, we observed a significant correlation between melanopic weighted corneal illuminance (melanopic equivalent daylight illuminance [mEDI]) and pupil size, such that higher mEDI values were associated with smaller pupil size. Using pupil size to estimate retinal irradiance showed a qualitatively similar goodness of fit as mEDI for predicting melatonin suppression. 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引用次数: 0
摘要
瞳孔调节到达视网膜的光量。决定瞳孔大小的不仅是亮度,还有光谱分布。先前的研究发现,稳态瞳孔大小和褪黑激素衰减主要由黑视蛋白驱动,而黑视蛋白是由对短波长光(约 480 纳米)敏感的内感光视网膜神经节细胞(ipRGCs)的独特亚群表达的。在这里,我们的目的是在傍晚选择性地靶向黑视蛋白系统,同时测量傍晚常见光照水平下的稳态瞳孔大小和褪黑激素浓度(2)。在四组志愿者中,每名志愿者分别暴露于低黑色素(LM)和高黑色素(HM)条件下。两个 17 小时的研究方案包括 3.5 小时的光照,从习惯就寝时间前 4 小时开始。在所有四个光照强度组中,HM 条件下的瞳孔中位数明显小于 LM 条件下的瞳孔中位数。此外,我们还观察到黑色素加权角膜照度(黑色素等效日光照度 [mEDI])与瞳孔大小之间存在明显的相关性,即 mEDI 值越高,瞳孔越小。在预测褪黑激素抑制时,使用瞳孔大小估算视网膜辐照度显示出与 mEDI 相似的质量拟合度。根据我们的研究结果,在比较光照对健康年轻人晚间褪黑激素浓度的影响时,使用在眼睛水平测量的黑色素辐照度仍然是合适的。
The Impact of Pupil Constriction on the Relationship Between Melanopic EDI and Melatonin Suppression in Young Adult Males.
The pupil modulates the amount of light that reaches the retina. Not only luminance but also the spectral distribution defines the pupil size. Previous research has identified steady-state pupil size and melatonin attenuation to be predominantly driven by melanopsin, which is expressed by a unique subgroup of intrinsically photosensitive retinal ganglion cells (ipRGCs) that are sensitive to short-wavelength light (~480 nm). Here, we aimed to selectively target the melanopsin system during the evening, while measuring steady-state pupil size and melatonin concentrations under commonly experienced evening light levels (<90 lx). Therefore, we used a five-primary display prototype to generate light conditions that were matched in terms of L-, M-, and S-cone-opic irradiances, but with high and low melanopic irradiances (~3-fold difference). Seventy-two healthy, male participants completed a 2-week study protocol. The volunteers were assigned to one of the four groups that differed in luminance levels (27-285 cd/m2). Within the four groups, each volunteer was exposed to a low melanopic (LM) and a high melanopic (HM) condition. The two 17-h study protocols comprised 3.5 h of light exposure starting 4 h before habitual bedtime. Median pupil size was significantly smaller during HM than LM in all four light intensity groups. In addition, we observed a significant correlation between melanopic weighted corneal illuminance (melanopic equivalent daylight illuminance [mEDI]) and pupil size, such that higher mEDI values were associated with smaller pupil size. Using pupil size to estimate retinal irradiance showed a qualitatively similar goodness of fit as mEDI for predicting melatonin suppression. Based on our results here, it remains appropriate to use melanopic irradiance measured at eye level when comparing light-dependent effects on evening melatonin concentrations in healthy young people at rather low light levels.
期刊介绍:
Journal of Biological Rhythms is the official journal of the Society for Research on Biological Rhythms and offers peer-reviewed original research in all aspects of biological rhythms, using genetic, biochemical, physiological, behavioral, epidemiological & modeling approaches, as well as clinical trials. Emphasis is on circadian and seasonal rhythms, but timely reviews and research on other periodicities are also considered. The journal is a member of the Committee on Publication Ethics (COPE).