Computation and Neural Systems, California Institute of Technology, Pasadena, CA 91125, USA.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Neuron. 2017 Jun 21;94(6):1205-1219.e8. doi: 10.1016/j.neuron.2017.05.020. Epub 2017 Jun 8.
Ventral midbrain dopamine (DA) is unambiguously involved in motivation and behavioral arousal, yet the contributions of other DA populations to these processes are poorly understood. Here, we demonstrate that the dorsal raphe nucleus DA neurons are critical modulators of behavioral arousal and sleep-wake patterning. Using simultaneous fiber photometry and polysomnography, we observed time-delineated dorsal raphe nucleus dopaminergic (DRN) activity upon exposure to arousal-evoking salient cues, irrespective of their hedonic valence. We also observed broader fluctuations of DRN activity across sleep-wake cycles with highest activity during wakefulness. Both endogenous DRN activity and optogenetically driven DRN activity were associated with waking from sleep, with DA signal strength predictive of wake duration. Conversely, chemogenetic inhibition opposed wakefulness and promoted NREM sleep, even in the face of salient stimuli. Therefore, the DRN population is a critical contributor to wake-promoting pathways and is capable of modulating sleep-wake states according to the outside environment, wherein the perception of salient stimuli prompts vigilance and arousal.
腹侧中脑多巴胺(DA)明确参与动机和行为觉醒,但其他 DA 群体对这些过程的贡献了解甚少。在这里,我们证明了中缝背核 DA 神经元是行为觉醒和睡眠-觉醒模式的关键调节因子。使用同时进行的光纤光度测定法和多导睡眠描记术,我们观察到暴露于引起觉醒的明显线索时,中缝背核多巴胺能(DRN)活动有明确的时间划分,而与它们的享乐价值无关。我们还观察到 DRN 活动在睡眠-觉醒周期中更广泛的波动,在觉醒时活性最高。内源性 DRN 活性和光遗传学驱动的 DRN 活性都与从睡眠中醒来有关,DA 信号强度可预测觉醒持续时间。相反,化学遗传抑制则反对觉醒并促进 NREM 睡眠,即使面对明显的刺激也是如此。因此,DRN 群体是促进觉醒途径的关键贡献者,并且能够根据外部环境调节睡眠-觉醒状态,其中对明显刺激的感知会引起警觉和觉醒。