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Light-induced melatonin suppression in humans with polychromatic and monochromatic light

机译:用多色和单色光抑制人体内的褪黑素

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The relative contribution of rods, cones, and melanopsin to non-image-forming (NIF) responses under light conditions differing in irradiance, duration, and spectral composition remains to be determined in humans. NIF responses to a polychromatic light source may be very different to that predicted from the published human action spectra data, which have utilized narrow band monochromatic light and demonstrated short wavelength sensitivity. To test the hypothesis that only melanopsin is driving NIF responses in humans, monochromatic blue light (lambda(max) 479 nm) was matched with polychromatic white light for total melanopsin-stimulating photons at three light intensities. The ability of these light conditions to suppress nocturnal melatonin production was assessed. A within-subject crossover design was used to investigate the suppressive effect of nocturnal light on melatonin production in a group of diurnally active young male subjects aged 18-35 yrs (24.9 +/- 3.8 yrs; mean +/- SD; n = 11). A 30 min light pulse, individually timed to occur on the rising phase of the melatonin rhythm, was administered between 23:30 and 01:30 h. Regularly timed blood samples were taken for measurement of plasma melatonin. Repeated measures two-way ANOVA, with irradiance and light condition as factors, was used for statistical analysis (n = 9 analyzed). There was a significant effect of both light intensity (p < 0.001) and light condition (p < 0.01). Polychromatic light was more effective at suppressing nocturnal melatonin than monochromatic blue light matched for melanopsin stimulation, implying that the melatonin suppression response is not solely driven by melanopsin. The findings suggest a stimulatory effect of the additional wavelengths of light present in the polychromatic light, which could be mediated via the stimulation of cone photopigments and/or melanopsin regeneration. The results of this study may be relevant to designing the spectral composition of polychromatic lights for use in the home and workplace, as well as in the treatment of circadian rhythm disorders. (Author correspondence: v.revell@surrey.ac.uk).
机译:在光照,持续时间和光谱组成不同的光照条件下,杆,视锥细胞和黑色素对非图像形成(NIF)反应的相对贡献仍有待人类确定。 NIF对多色光源的响应可能与根据已发布的人类动作光谱数据预测的响应大不相同,后者已利用窄带单色光并显示出短波长灵敏度。为了测试仅黑色素在人类中驱动NIF反应的假设,将单色蓝光(λ(最大)479 nm)与多色白光相匹配,以激发三种光强度的总黑色素。评估了这些光照条件抑制夜间褪黑激素产生的能力。受试者内部交叉设计用于研究夜间光对一组年龄在18-35岁(24.9 +/- 3.8岁;平均+/- SD;平均+/- SD; n = 11)的昼夜活跃年轻男性受试者中褪黑激素产生的抑制作用)。在23:30至01:30 h之间分别给予30分钟的光脉冲,分别定时发生在褪黑激素节律的上升阶段。定期采集血样以测定血浆褪黑激素。以辐照度和光照条件为因素的重复测量两次方差分析用于统计分析(分析的n = 9)。光照强度(p <0.001)和光照条件(p <0.01)都有显着影响。多色光在抑制夜间褪黑激素方面比单色光对蓝黑素刺激更有效,这意味着褪黑素抑制反应并非仅由黑素所驱动。这些发现表明存在于多色光中的其他波长的光具有刺激作用,这可以通过刺激锥体色素和/或黑色素再生来介导。这项研究的结果可能与设计用于家庭和工作场所以及用于昼夜节律障碍的多色光的光谱组成有关。 (作者通讯:v.revell@surrey.ac.uk)。

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