Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27710, USA.
Neuron. 2019 Jun 5;102(5):1053-1065.e4. doi: 10.1016/j.neuron.2019.03.033. Epub 2019 Apr 18.
How general anesthesia (GA) induces loss of consciousness remains unclear, and whether diverse anesthetic drugs and sleep share a common neural pathway is unknown. Previous studies have revealed that many GA drugs inhibit neural activity through targeting GABA receptors. Here, using Fos staining, ex vivo brain slice recording, and in vivo multi-channel electrophysiology, we discovered a core ensemble of hypothalamic neurons in and near the supraoptic nucleus, consisting primarily of neuroendocrine cells, which are persistently and commonly activated by multiple classes of GA drugs. Remarkably, chemogenetic or brief optogenetic activations of these anesthesia-activated neurons (AANs) strongly promote slow-wave sleep and potentiates GA, whereas conditional ablation or inhibition of AANs led to diminished slow-wave oscillation, significant loss of sleep, and shortened durations of GA. These findings identify a common neural substrate underlying diverse GA drugs and natural sleep and reveal a crucial role of the neuroendocrine system in regulating global brain states. VIDEO ABSTRACT.
全麻(GA)如何引起意识丧失尚不清楚,不同的麻醉药物和睡眠是否共享共同的神经通路也不清楚。先前的研究表明,许多 GA 药物通过靶向 GABA 受体抑制神经活动。在这里,我们使用 Fos 染色、离体脑片记录和体内多通道电生理学,发现了一个位于视上核内和附近的下丘脑神经元核心集合,主要由神经内分泌细胞组成,这些细胞被多种 GA 药物持续且普遍激活。值得注意的是,这些麻醉激活神经元(AANs)的化学遗传学或短暂光遗传学激活强烈促进慢波睡眠并增强 GA,而 AANs 的条件性消融或抑制导致慢波振荡减少、显著的睡眠丧失和 GA 持续时间缩短。这些发现确定了不同 GA 药物和自然睡眠的共同神经基础,并揭示了神经内分泌系统在调节大脑整体状态中的关键作用。视频摘要。