Lancel M, Mathias S, Faulhaber J, Schiffelholz T
Max-Planck Institute of Psychiatry, Department of Neuroendocrinology, Munich, Germany.
Am J Physiol. 1996 Apr;270(4 Pt 2):R830-7. doi: 10.1152/ajpregu.1996.270.4.R830.
The cytokine interleukin (IL)-1 is a key mediator of the somnogenic response to immune challenge. In this vehicle-controlled study we evaluated circadian interference with the sleep-promoting effects of IL-1 beta. In two randomized experiments, rats were injected intracerebroventricularly with 5 ng IL-1 beta either at the beginning of the rest phase or at the beginning of the activity phase. Recordings were made during the 24 h preceding the injections (baseline) and during the first 12 postinjection hours. To avoid masking effects of light, the rats were maintained under a skeleton photoperiod during recording. During both the rest and activity phase, IL-1 beta induced fever and initially promoted non-rapid eye movement sleep (REMS). The effect of IL-1 beta on the duration of non-REMS and electroencephalogram (EEG) power densities within non-REMS was related to circadian phase. During the rest phase, IL-1 beta resulted in a minor increase in non-REMS duration but a prominent enhancement in EEG activity in the delta (0.5-4 Hz) and most other frequency bands. During the activity phase, IL-1 beta evoked a larger increase in the duration of non-REMS but hardly affected EEG activity within this state. Thus the effects of IL-1 beta on non-REMS are strongly influenced by diurnal phase. The alterations in EEG power density are in contrast to those elicited by sleep deprivation, which are largely independent of time of day. It is concluded that IL-1 beta activates EEG regulatory mechanisms mediated by processes that depend on circadian phase.
细胞因子白细胞介素(IL)-1是免疫应激诱导睡眠反应的关键介质。在这项以溶媒为对照的研究中,我们评估了昼夜节律对IL-1β促睡眠作用的干扰。在两项随机实验中,分别于大鼠休息期开始时或活动期开始时脑室内注射5 ng IL-1β。在注射前24小时(基线期)及注射后前12小时进行记录。为避免光照的掩盖效应,记录期间大鼠饲养于骨架光周期条件下。在休息期和活动期,IL-1β均诱导发热并最初促进非快速眼动睡眠(REMS)。IL-1β对非快速眼动睡眠持续时间及非快速眼动睡眠期脑电图(EEG)功率密度的影响与昼夜节律相位有关。在休息期,IL-1β导致非快速眼动睡眠持续时间略有增加,但δ波(0.5 - 4 Hz)及大多数其他频段的EEG活动显著增强。在活动期,IL-1β引起非快速眼动睡眠持续时间大幅增加,但在此状态下对EEG活动影响不大。因此,IL-1β对非快速眼动睡眠的影响受昼夜相位强烈影响。EEG功率密度的改变与睡眠剥夺引起的改变相反,睡眠剥夺引起的改变在很大程度上与一天中的时间无关。结论是,IL-1β激活了由依赖昼夜节律相位的过程介导的EEG调节机制。