Educational Physiology Laboratory, Graduate School of Education, The University of Tokyo, Tokyo, Japan.
Sleep. 2011 Oct 1;34(10):1423-32. doi: 10.5665/SLEEP.1292.
The cyclic sequence of NREM and REM sleep, the so-called ultradian rhythm, is a highly characteristic feature of sleep. However, the mechanisms responsible for the ultradian REM sleep rhythm, particularly in humans, have not to date been fully elucidated. We hypothesize that a stage transition mechanism is involved in the determination of the ultradian REM sleep rhythm.
Ten healthy young male volunteers (AGE: 22 ± 4 years, range 19-31 years) spent 3 nights in a sleep laboratory. The first was the adaptation night, and the second was the baseline night. On the third night, the subjects received risperidone (1 mg tablet), a central serotonergic and dopaminergic antagonist, 30 min before the polysomnography recording.
We measured and investigated transition probabilities between waking, REM, and NREM sleep stages (N1, N2, and N3) within the REM-onset intervals, defined as the intervals between the onset of one REM period and the beginning of the next, altered by risperidone. We also calculated the transition intensity (i.e., instantaneous transition rate) and examined the temporal pattern of transitions within the altered REM-onset intervals. We found that when the REM-onset interval was prolonged by risperidone, the probability of transitions from N2 to N3 was significantly increased within the same prolonged interval, with a significant delay and/or recurrences of the peak intensity of transitions from N2 to N3.
These results suggest that the mechanism governing NREM sleep stage transitions (from light to deep sleep) plays an important role in determining ultradian REM sleep rhythms.
非快速眼动(NREM)和快速眼动(REM)睡眠的周期性序列,即所谓的超日周期节律,是睡眠的一个高度特征性特征。然而,负责超日周期 REM 睡眠节律的机制,特别是在人类中,尚未得到充分阐明。我们假设存在一个阶段转换机制参与了超日周期 REM 睡眠节律的确定。
10 名健康的年轻男性志愿者(年龄:22±4 岁,范围 19-31 岁)在睡眠实验室度过了 3 个晚上。第一晚是适应期,第二晚是基线期。第三晚,受试者在多导睡眠图记录前 30 分钟接受利培酮(1 毫克片剂),一种中枢血清素能和多巴胺能拮抗剂。
我们测量并研究了在 REM 起始间隔内(定义为一个 REM 期结束和下一个 REM 期开始之间的间隔),从觉醒、REM 和 NREM 睡眠阶段(N1、N2 和 N3)之间的转换概率,这些间隔被利培酮改变。我们还计算了转换强度(即瞬时转换率),并检查了在改变的 REM 起始间隔内的转换的时间模式。我们发现,当 REM 起始间隔被利培酮延长时,N2 到 N3 的转换概率在相同延长的间隔内显著增加,同时 N2 到 N3 的转换强度峰值出现明显延迟和/或复发。
这些结果表明,控制 NREM 睡眠阶段转换(从浅睡到深睡)的机制在确定超日周期 REM 睡眠节律中起着重要作用。