Sleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, University of Oxford, OMPI-G, Oxford, UK.
Biomedical Sciences, Warwick Medical School, University of Warwick, Coventry, UK.
Nat Commun. 2021 Apr 9;12(1):2113. doi: 10.1038/s41467-021-22179-z.
The accumulation of adenosine is strongly correlated with the need for sleep and the detection of sleep pressure is antagonised by caffeine. Caffeine also affects the circadian timing system directly and independently of sleep physiology, but how caffeine mediates these effects upon the circadian clock is unclear. Here we identify an adenosine-based regulatory mechanism that allows sleep and circadian processes to interact for the optimisation of sleep/wake timing in mice. Adenosine encodes sleep history and this signal modulates circadian entrainment by light. Pharmacological and genetic approaches demonstrate that adenosine acts upon the circadian clockwork via adenosine A/A receptor signalling through the activation of the Ca -ERK-AP-1 and CREB/CRTC1-CRE pathways to regulate the clock genes Per1 and Per2. We show that these signalling pathways converge upon and inhibit the same pathways activated by light. Thus, circadian entrainment by light is systematically modulated on a daily basis by sleep history. These findings contribute to our understanding of how adenosine integrates signalling from both light and sleep to regulate circadian timing in mice.
腺苷的积累与睡眠需求密切相关,而咖啡因则拮抗睡眠压力的检测。咖啡因还直接且独立于睡眠生理学作用于昼夜节律计时系统,但咖啡因如何调节生物钟的这些影响尚不清楚。在这里,我们确定了一种基于腺苷的调节机制,该机制允许睡眠和昼夜节律过程相互作用,以优化小鼠的睡眠/觉醒时间。腺苷编码睡眠历史,该信号通过光的昼夜同步来调节生物钟。药理学和遗传学方法表明,腺苷通过激活 Ca-ERK-AP-1 和 CREB/CRTC1-CRE 途径来调节生物钟基因 Per1 和 Per2,通过腺苷 A/A 受体信号作用于生物钟。我们表明,这些信号通路汇聚并抑制光激活的相同通路。因此,睡眠历史会系统地调节光的昼夜同步。这些发现有助于我们理解腺苷如何整合来自光和睡眠的信号来调节小鼠的昼夜节律计时。