From the Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Department of Anaesthesia, Harvard Medical School, Boston, Massachusetts.
Anesth Analg. 2021 May 1;132(5):1254-1264. doi: 10.1213/ANE.0000000000005361.
General anesthesia is characterized by loss of consciousness, amnesia, analgesia, and immobility. Important molecular targets of general anesthetics have been identified, but the neural circuits underlying the discrete end points of general anesthesia remain incompletely understood. General anesthesia and natural sleep share the common feature of reversible unconsciousness, and recent developments in neuroscience have enabled elegant studies that investigate the brain nuclei and neural circuits underlying this important end point. A common approach to measure cortical activity across the brain is electroencephalogram (EEG), which can reflect local neuronal activity as well as connectivity among brain regions. The EEG oscillations observed during general anesthesia depend greatly on the anesthetic agent as well as dosing, and only some resemble those observed during sleep. For example, the EEG oscillations during dexmedetomidine sedation are similar to those of stage 2 nonrapid eye movement (NREM) sleep, but high doses of propofol and ether anesthetics produce burst suppression, a pattern that is never observed during natural sleep. Sleep is primarily driven by withdrawal of subcortical excitation to the cortex, but anesthetics can directly act at both subcortical and cortical targets. While some anesthetics appear to activate specific sleep-active regions to induce unconsciousness, not all sleep-active regions play a significant role in anesthesia. Anesthetics also inhibit cortical neurons, and it is likely that each class of anesthetic drugs produces a distinct combination of subcortical and cortical effects that lead to unconsciousness. Conversely, arousal circuits that promote wakefulness are involved in anesthetic emergence and activating them can induce emergence and accelerate recovery of consciousness. Modern neuroscience techniques that enable the manipulation of specific neural circuits have led to new insights into the neural circuitry underlying general anesthesia and sleep. In the coming years, we will continue to better understand the mechanisms that generate these distinct states of reversible unconsciousness.
全身麻醉的特点是意识丧失、遗忘、镇痛和不动。已经确定了全身麻醉的重要分子靶点,但全身麻醉离散终点背后的神经回路仍不完全清楚。全身麻醉和自然睡眠具有可逆性意识丧失的共同特征,神经科学的最新发展使人们能够进行优雅的研究,探讨大脑核和神经回路基础。一种常见的方法是通过脑电图 (EEG) 测量整个大脑的皮质活动,它可以反映局部神经元活动以及大脑区域之间的连接。全身麻醉期间观察到的 EEG 振荡在很大程度上取决于麻醉剂以及剂量,并且只有一些类似于睡眠期间观察到的振荡。例如,右美托咪定镇静期间的 EEG 振荡类似于 NREM 睡眠的第 2 阶段,但大剂量的丙泊酚和乙醚麻醉会产生爆发抑制,这是在自然睡眠中从未观察到的模式。睡眠主要是由皮质下对皮质的兴奋撤回驱动的,但麻醉剂可以直接作用于皮质下和皮质靶标。虽然一些麻醉剂似乎激活特定的睡眠活跃区域以诱导无意识,但并非所有睡眠活跃区域在麻醉中都发挥重要作用。麻醉剂还抑制皮质神经元,并且每种类别的麻醉药物可能产生导致无意识的独特的皮质下和皮质效应组合。相反,促进觉醒的唤醒回路参与麻醉苏醒,激活它们可以诱导苏醒并加速意识恢复。使特定神经回路能够操纵的现代神经科学技术为全身麻醉和睡眠的神经回路基础提供了新的见解。在未来几年,我们将继续更好地了解产生这些不同可逆无意识状态的机制。