Canton Jillian L, Smith Mark R, Choi Ho-Sun, Eastman Charmane I
Biological Rhythms Research Laboratory, Department of Behavioral Sciences, Rush University Medical Center, Chicago, IL, USA.
J Circadian Rhythms. 2009 Jul 17;7:8. doi: 10.1186/1740-3391-7-8.
Light exposure in the late evening and nighttime and a delay of the sleep/dark episode can phase delay the circadian clock. This study assessed the size of the phase delay produced by a single light pulse combined with a moderate delay of the sleep/dark episode for one day. Because iris color or race has been reported to influence light-induced melatonin suppression, and we have recently reported racial differences in free-running circadian period and circadian phase shifting in response to light pulses, we also tested for differences in the magnitude of the phase delay in subjects with blue and brown irises.
Subjects (blue-eyed n = 7; brown eyed n = 6) maintained a regular sleep schedule for 1 week before coming to the laboratory for a baseline phase assessment, during which saliva was collected every 30 minutes to determine the time of the dim light melatonin onset (DLMO). Immediately following the baseline phase assessment, which ended 2 hours after baseline bedtime, subjects received a 2-hour bright light pulse (~4,000 lux). An 8-hour sleep episode followed the light pulse (i.e. was delayed 4 hours from baseline). A final phase assessment was conducted the subsequent night to determine the phase shift of the DLMO from the baseline to final phase assessment.Phase delays of the DLMO were compared in subjects with blue and brown irises. Iris color was also quantified from photographs using the three dimensions of red-green-blue color axes, as well as a lightness scale. These variables were correlated with phase shift of the DLMO, with the hypothesis that subjects with lighter irises would have larger phase delays.
The average phase delay of the DLMO was -1.3 +/- 0.6 h, with a maximum delay of ~2 hours, and was similar for subjects with blue and brown irises. There were no significant correlations between any of the iris color variables and the magnitude of the phase delay.
A single 2-hour bright light pulse combined with a moderate delay of the sleep/dark episode delayed the circadian clock an average of ~1.5 hours. There was no evidence that iris color influenced the magnitude of the phase shift. Future studies are needed to replicate our findings that iris color does not impact the magnitude of light-induced circadian phase shifts, and that the previously reported differences may be due to race.
傍晚和夜间的光照以及睡眠/黑暗时段的延迟会使昼夜节律时钟发生相位延迟。本研究评估了单次光脉冲与睡眠/黑暗时段适度延迟一天所产生的相位延迟大小。由于据报道虹膜颜色或种族会影响光诱导的褪黑素抑制,并且我们最近报道了自由运行的昼夜节律周期和对光脉冲的昼夜节律相移存在种族差异,因此我们还测试了蓝眼睛和棕眼睛受试者的相位延迟幅度差异。
受试者(蓝眼睛n = 7;棕眼睛n = 6)在进入实验室进行基线相位评估前保持1周的规律睡眠时间表,在此期间每30分钟收集一次唾液以确定暗光褪黑素开始时间(DLMO)。在基线相位评估结束后立即(基线就寝时间后2小时),受试者接受2小时的强光脉冲(约4000勒克斯)。光脉冲后紧接着是8小时的睡眠时段(即比基线延迟4小时)。在随后的夜晚进行最终相位评估,以确定从基线到最终相位评估的DLMO相移。比较蓝眼睛和棕眼睛受试者的DLMO相位延迟。还使用红-绿-蓝颜色轴的三个维度以及亮度标度从照片中量化虹膜颜色。这些变量与DLMO的相移相关,假设虹膜颜色较浅的受试者相位延迟更大。
DLMO的平均相位延迟为-1.3±0.6小时,最大延迟约为2小时,蓝眼睛和棕眼睛受试者相似。虹膜颜色变量与相位延迟幅度之间均无显著相关性。
单次2小时的强光脉冲与睡眠/黑暗时段的适度延迟使昼夜节律时钟平均延迟约1.5小时。没有证据表明虹膜颜色会影响相移幅度。需要进一步的研究来重复我们的发现,即虹膜颜色不会影响光诱导的昼夜节律相移幅度,并且先前报道的差异可能归因于种族。