Mayeda A, Mannon S, Hofstetter J, Adkins M, Baker R, Hu K, Nurnberger J
Department of Veterans Affairs Medical Center and Department of Psychiatry, Indiana University School of Medicine, Indianapolis 46202-4887, USA.
Psychiatry Res. 1998 Oct 19;81(1):9-17. doi: 10.1016/s0165-1781(98)00069-9.
An indirect lighting protocol was developed to measure nocturnal melatonin suppression by light in normal human subjects. Goals were to minimize both discomfort due to staring intensely at a bright light source, and behavioral variation due to wandering gaze. Subjects sat with a bank of five full-spectrum light sources placed behind them. Lights reflecting off the surfaces before each subject produced a hemisphere of light that measured 500 lx +/- 5%. Subjects retired to bed in darkness by midnight and then sat in the hemisphere of light from 02.00 h to 04.00 h. Blood for melatonin was drawn at 20-30-min intervals from midnight to 06.00 h. Plasma melatonin was measured by radioimmunoassay. The indirect lighting protocol was used to compare the effects of 500 lx light to dark (21 subjects) and to study varying light intensities from 300 to 2000 lx (7 subjects). We studied the effects of the sitting posture in very dim light of 20-30 lx (6 subjects). We also studied the effects of propranolol plus dark and propranolol plus 500 lx light on melatonin levels. Subjects received placebo, 10 mg propranolol or 40 mg propranolol orally at 23.00 h, and were then exposed to either the dark or light condition. Melatonin levels obtained with the indirect lighting protocol were consistent with studies using direct lighting; light of 500 lx significantly suppressed nocturnal melatonin and suppression was dose related between 300 and 2000 lx. Sitting in dim light had no significant effect on melatonin suppression when compared with the supine posture in the dark in six subjects. Propranolol caused a dose-dependent decrease in melatonin levels in both the dark and the light. There was no relationship between suppression of melatonin by propranolol and suppression by light.
我们开发了一种间接照明方案,用于测量正常人类受试者中光照对夜间褪黑素分泌的抑制作用。目标是尽量减少因长时间直视明亮光源而产生的不适,以及因目光游移而导致的行为差异。受试者坐在五组全光谱光源组成的灯组后面,这些光源反射到每个受试者面前的表面上,产生一个照度为500勒克斯±5%的半球形光照区域。受试者在午夜前进入黑暗环境睡觉,然后在凌晨2点至4点坐在这个半球形光照区域内。从午夜到凌晨6点,每隔20 - 30分钟采集一次血液样本用于检测褪黑素。通过放射免疫分析法测定血浆褪黑素水平。使用间接照明方案比较了500勒克斯光照与黑暗环境的影响(21名受试者),并研究了300至2000勒克斯不同光照强度的影响(7名受试者)。我们研究了在20 - 30勒克斯的极暗光线下坐姿的影响(6名受试者)。我们还研究了普萘洛尔加黑暗环境以及普萘洛尔加500勒克斯光照对褪黑素水平的影响。受试者在23点口服安慰剂、10毫克普萘洛尔或40毫克普萘洛尔,然后暴露于黑暗或光照条件下。通过间接照明方案获得的褪黑素水平与使用直接照明的研究结果一致;500勒克斯的光照显著抑制夜间褪黑素分泌,且在300至2000勒克斯之间抑制作用与剂量相关。与6名受试者在黑暗中仰卧姿势相比,在暗光线下坐姿对褪黑素抑制没有显著影响。普萘洛尔在黑暗和光照条件下均导致褪黑素水平呈剂量依赖性下降。普萘洛尔对褪黑素的抑制作用与光照对褪黑素的抑制作用之间没有关联。