Laboratory of Sleep Medicine and Chronobiology, Research Service, Ralph H. Johnson Veterans Healthcare System Charleston, SC, USA.
Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Sleep. 2024 May 10;47(5). doi: 10.1093/sleep/zsae065.
Dynorphin is an endogenous opiate localized in many brain regions and spinal cord, but the activity of dynorphin neurons during sleep is unknown. Dynorphin is an inhibitory neuropeptide that is coreleased with orexin, an excitatory neuropeptide. We used microendoscopy to test the hypothesis that, like orexin, the dynorphin neurons are wake-active. Dynorphin-cre mice (n = 3) were administered rAAV8-Ef1a-Con/Foff 2.0-GCaMP6M into the zona incerta-perifornical area, implanted with a GRIN lens (gradient reflective index), and electrodes to the skull that recorded sleep. One month later, a miniscope imaged calcium fluorescence in dynorphin neurons during multiple bouts of wake, non-rapid-eye movement (NREM), and rapid-eye movement (REM) sleep. Unbiased data analysis identified changes in calcium fluorescence in 64 dynorphin neurons. Most of the dynorphin neurons (72%) had the highest fluorescence during bouts of active and quiet waking compared to NREM or REM sleep; a subset (20%) were REM-max. Our results are consistent with the emerging evidence that the activity of orexin neurons can be classified as wake-max or REM-max. Since the two neuropeptides are coexpressed and coreleased, we suggest that dynorphin-cre-driven calcium sensors could increase understanding of the role of this endogenous opiate in pain and sleep.
脑啡肽是一种内源性阿片肽,存在于许多脑区和脊髓中,但睡眠期间脑啡肽神经元的活动尚不清楚。脑啡肽是一种抑制性神经肽,与兴奋性神经肽食欲素一起被释放。我们使用微内窥镜测试了这样一个假设,即与食欲素一样,脑啡肽神经元在觉醒时活跃。在zona incerta-perifornical area 中给予 dynorphin-cre 小鼠 (n = 3) rAAV8-Ef1a-Con/Foff 2.0-GCaMP6M,植入 GRIN 透镜(梯度反射指数)和记录睡眠的颅骨电极。一个月后,微型内窥镜在多次觉醒、非快速眼动 (NREM) 和快速眼动 (REM) 睡眠期间对 dynorphin 神经元中的钙荧光进行成像。无偏数据分析确定了 64 个 dynorphin 神经元中钙荧光的变化。与 NREM 或 REM 睡眠相比,大多数 dynorphin 神经元 (72%) 在活跃和安静觉醒期间的荧光最强;一部分 (20%) 是 REM 最大。我们的结果与越来越多的证据一致,即食欲素神经元的活动可以分为觉醒最大或 REM 最大。由于这两种神经肽共同表达和共同释放,我们认为 dynorphin-cre 驱动的钙传感器可以增加对这种内源性阿片肽在疼痛和睡眠中的作用的理解。