Tamakawa Yuichi, Karashima Akihiro, Koyama Yoshimasa, Katayama Norihiro, Nakao Mitsuyuki
Graduate School of Information Sciences, Tohoku University, Sendai, Japan.
J Neurophysiol. 2006 Apr;95(4):2055-69. doi: 10.1152/jn.00575.2005. Epub 2005 Nov 9.
Physiological knowledge of the neural mechanisms regulating sleep and wakefulness has been advanced by the recent findings concerning sleep/wakefulness-related preoptic/anterior hypothalamic and perifornical (orexin-containing)/posterior hypothalamic neurons. In this paper, we propose a mathematical model of the mechanisms orchestrating a quartet neural system of sleep and wakefulness composed of the following: 1) sleep-active preoptic/anterior hypothalamic neurons (N-R group); 2) wake-active hypothalamic and brain stem neurons exhibiting the highest rate of discharge during wakefulness and the lowest rate of discharge during paradoxical or rapid eye movement (REM) sleep (WA group); 3) brain stem neurons exhibiting the highest rate of discharge during REM sleep (REM group); and 4) basal forebrain, hypothalamic, and brain stem neurons exhibiting a higher rate of discharge during both wakefulness and REM sleep than during nonrapid eye movement (NREM) sleep (W-R group). The WA neurons have mutual inhibitory couplings with the REM and N-R neurons. The W-R neurons have mutual excitatory couplings with the WA and REM neurons. The REM neurons receive unidirectional inhibition from the N-R neurons. In addition, the N-R neurons are activated by two types of sleep-promoting substances (SPS), which play different roles in the homeostatic regulation of sleep and wakefulness. The model well reproduces the actual sleep and wakefulness patterns of rats in addition to the sleep-related neuronal activities across state transitions. In addition, human sleep-wakefulness rhythms can be simulated by manipulating only a few model parameters: inhibitions from the N-R neurons to the REM and WA neurons are enhanced, and circadian regulation of the N-R and WA neurons is exaggerated. Our model could provide a novel framework for the quantitative understanding of the mechanisms regulating sleep and wakefulness.
近期关于与睡眠/觉醒相关的视前区/下丘脑前部以及穹窿周(含食欲素)/下丘脑后部神经元的研究发现,推动了对调节睡眠和觉醒的神经机制的生理学认识。在本文中,我们提出了一个数学模型,该模型描绘了一个由以下部分组成的睡眠和觉醒四重神经系统的协调机制:1)睡眠活跃的视前区/下丘脑前部神经元(N-R组);2)觉醒活跃的下丘脑和脑干神经元,在觉醒时放电率最高,在异相睡眠或快速眼动(REM)睡眠时放电率最低(WA组);3)在REM睡眠时放电率最高的脑干神经元(REM组);4)基底前脑、下丘脑和脑干神经元,在觉醒和REM睡眠时的放电率均高于非快速眼动(NREM)睡眠时(W-R组)。WA神经元与REM神经元和N-R神经元存在相互抑制性耦合。W-R神经元与WA神经元和REM神经元存在相互兴奋性耦合。REM神经元接受来自N-R神经元的单向抑制。此外,N-R神经元被两种促进睡眠的物质(SPS)激活,这两种物质在睡眠和觉醒的稳态调节中发挥着不同作用。该模型除了能很好地再现大鼠实际的睡眠和觉醒模式以及跨状态转换的与睡眠相关的神经元活动外,通过仅调整少数模型参数,还能模拟人类的睡眠-觉醒节律:增强N-R神经元对REM神经元和WA神经元的抑制,并夸大N-R神经元和WA神经元的昼夜节律调节。我们的模型可为定量理解调节睡眠和觉醒的机制提供一个新的框架。