Wang Guo-Qing, Du Yu-Zhen, Tong Jian
Department of Physiology, Medical School, Soochow University, Suzhou 215123, Jiangsu, China.
Chronobiol Int. 2007;24(1):9-20. doi: 10.1080/07420520601139821.
This study was conducted to investigate the circadian rhythms and light responses of Clock and arylalkylamine N-acetyltransferase (NAT) gene expressions in the rat pineal gland under the environmental conditions of a 12 h light (05:00-17:00 h): 12 h-dark (17:00-05:00 h) cycle (LD) and constant darkness (DD). The pineal gland of Sprague-Dawley rats housed under a LD regime (n=42) for four weeks and of a regime (n=42) for eight weeks were sampled at six different times, every 4 h (n=7 animals per time point), during a 24 h period. Total RNA was extracted from each sample, and the semiquantitative reverse transcription polymerase chain reaction (RT-PCR) was used to determine temporal changes in mRNA levels of Clock and NAT genes during different circadian or zeitgeber times. The data and parameters were analyzed by the cosine function software, Clock Lab software, and the amplitude F test was used to reveal the circadian rhythm. In the DD or LD condition, both the Clock and NAT mRNA levels in the pineal gland showed robust circadian oscillation (p<0.05) with the peak at the subjective night or at nighttime. In comparison with the DD regime, the amplitudes and mRNA levels at the peaks of Clock and NAT expressions in LD in the pineal gland were significantly reduced (p<0.05). In the DD or LD condition, the circadian expressions of NAT were similar in pattern to those of Clock in the pineal gland (p>0.05). These findings indicate that the transcriptions of Clock and NAT genes in the pineal gland not only show remarkably synchronous endogenous circadian rhythmic changes, but also respond to the ambient light signal in a reduced manner.
本研究旨在探讨在12小时光照(05:00 - 17:00):12小时黑暗(17:00 - 05:00)循环(LD)和持续黑暗(DD)的环境条件下,大鼠松果体中Clock基因和芳基烷基胺N - 乙酰基转移酶(NAT)基因表达的昼夜节律及光反应。将处于LD光照周期(n = 42)四周和八周的Sprague - Dawley大鼠的松果体在24小时内的六个不同时间点进行采样,每隔4小时采样一次(每个时间点n = 7只动物)。从每个样本中提取总RNA,并使用半定量逆转录聚合酶链反应(RT - PCR)来确定在不同昼夜或授时因子时间内Clock基因和NAT基因mRNA水平的时间变化。通过余弦函数软件、Clock Lab软件对数据和参数进行分析,并使用振幅F检验来揭示昼夜节律。在DD或LD条件下,松果体中Clock和NAT mRNA水平均呈现出强劲的昼夜振荡(p < 0.05),峰值出现在主观夜间或夜间。与DD光照周期相比,松果体中LD条件下Clock和NAT表达峰值的振幅和mRNA水平显著降低(p < 0.05)。在DD或LD条件下松果体中NAT的昼夜表达模式与Clock相似(p > 0.05)。这些发现表明,松果体中Clock基因和NAT基因不仅显示出显著同步的内源性昼夜节律变化,而且对环境光信号的反应有所减弱。