Farnell Yuhua Z, West James R, Chen Wei-Jung A, Allen Gregg C, Earnest David J
Department of Human Anatomy and Medical Neurobiology, Texas A&M University System Health Science Center, College of Medicine, College Station, Texas 77843-1114, USA.
Alcohol Clin Exp Res. 2004 Jul;28(7):1020-7. doi: 10.1097/01.alc.0000130807.21020.1b.
Developmental alcohol (EtOH) exposure produces long-term changes in the photic regulation of rat circadian behavior. Because entrainment of circadian rhythms to 24-hr light/dark cycles is mediated by phase shifting or resetting the clock mechanism, we examined whether developmental EtOH exposure also alters the phase-shifting effects of light pulses on the rat activity rhythm.
Artificially reared Sprague-Dawley rat pups were exposed to EtOH (4.5 g/kg/day) or an isocaloric milk formula (gastrostomy control; GC) on postnatal days 4 to 9. At 2 months of age, rats from the EtOH, GC, and suckle control groups were housed individually, and wheel-running behavior was continuously recorded first in a 12-hr light/12-hr dark photoperiod for 10 to 14 days and thereafter in constant darkness (DD). Once the activity rhythm was observed to stably free-run in DD for at least 14 days, animals were exposed to a 15-min light pulse at either 2 or 10 hr after the onset of activity [i.e., circadian time (CT) 14 or 22, respectively], because light exposure at these times induces maximal phase delays or advances of the rat activity rhythm.
EtOH-treated rats were distinguished by robust increases in their phase-shifting responses to light. In the suckle control and GC groups, light pulses shifted the activity rhythm as expected, inducing phase delays of approximately 2 hr at CT 14 and advances of similar amplitude at CT 22. In contrast, the same light stimulus produced phase delays at CT 14 and advances at CT 22 of longer than 3 hr in EtOH-treated rats. The mean phase delay at CT 14 and advance at CT 22 in EtOH rats were significantly greater (p < 0.05) than the light-induced shifts observed in control animals.
The data indicate that developmental EtOH exposure alters the phase-shifting responses of the rat activity rhythm to light. This finding, coupled with changes in the circadian period and light/dark entrainment observed in EtOH-treated rats, suggests that developmental EtOH exposure may permanently alter the clock mechanism in the suprachiasmatic nucleus and its regulation of circadian behavior.
发育期酒精(乙醇)暴露会对大鼠昼夜节律行为的光调节产生长期影响。由于昼夜节律与24小时明暗周期的同步是通过时钟机制的相位移动或重置来介导的,我们研究了发育期乙醇暴露是否也会改变光脉冲对大鼠活动节律的相位移动效应。
将人工饲养的斯普拉格-道利大鼠幼崽在出生后第4至9天暴露于乙醇(4.5克/千克/天)或等热量的牛奶配方奶(胃造口对照;GC)中。在2个月大时,将乙醇组、GC组和哺乳对照组的大鼠单独饲养,并首先在12小时光照/12小时黑暗的光周期中连续记录10至14天的轮转行为,之后在持续黑暗(DD)环境中记录。一旦观察到活动节律在DD环境中稳定地自由运行至少14天,动物在活动开始后2小时或10小时(即分别为昼夜时间(CT)14或22)接受15分钟的光脉冲照射,因为在这些时间点进行光照会诱导大鼠活动节律出现最大相位延迟或提前。
乙醇处理的大鼠对光的相位移动反应显著增强。在哺乳对照组和GC组中,光脉冲按预期改变了活动节律,在CT 14时诱导约2小时的相位延迟,在CT 22时诱导相似幅度的提前。相比之下,相同的光刺激在乙醇处理的大鼠中在CT 14时产生超过3小时的相位延迟,在CT 22时产生提前。乙醇处理大鼠在CT 14时的平均相位延迟和CT 22时的提前幅度显著大于(p < 0.05)对照组动物中光诱导的相位移动。
数据表明发育期乙醇暴露会改变大鼠活动节律对光的相位移动反应。这一发现,再加上在乙醇处理的大鼠中观察到的昼夜周期和明暗同步的变化,表明发育期乙醇暴露可能会永久性地改变视交叉上核中的时钟机制及其对昼夜节律行为的调节。