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七氟醚麻醉诱导和苏醒期反应迟钝与清醒α波振荡功率降低有关。

Lack of Responsiveness during the Onset and Offset of Sevoflurane Anesthesia Is Associated with Decreased Awake-Alpha Oscillation Power.

作者信息

Pavone Kara J, Su Lijuan, Gao Lei, Eromo Ersne, Vazquez Rafael, Rhee James, Hobbs Lauren E, Ibala Reine, Demircioglu Gizem, Purdon Patrick L, Brown Emery N, Akeju Oluwaseun

机构信息

Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical SchoolBoston, MA, United States.

School of Nursing, University of PennsylvaniaPhiladelphia, PA, United States.

出版信息

Front Syst Neurosci. 2017 May 30;11:38. doi: 10.3389/fnsys.2017.00038. eCollection 2017.

Abstract

Anesthetic drugs are typically administered to induce altered states of arousal that range from sedation to general anesthesia (GA). Systems neuroscience studies are currently being used to investigate the neural circuit mechanisms of anesthesia-induced altered arousal states. These studies suggest that by disrupting the oscillatory dynamics that are associated with arousal states, anesthesia-induced oscillations are a putative mechanism through which anesthetic drugs produce altered states of arousal. However, an empirical clinical observation is that even at relatively stable anesthetic doses, patients are sometimes intermittently responsive to verbal commands during states of light sedation. During these periods, prominent anesthesia-induced neural oscillations such as slow-delta (0.1-4 Hz) oscillations are notably absent. Neural correlates of intermittent responsiveness during light sedation have been insufficiently investigated. A principled understanding of the neural correlates of intermittent responsiveness may fundamentally advance our understanding of neural dynamics that are essential for maintaining arousal states, and how they are disrupted by anesthetics. Therefore, we performed a high-density (128 channels) electroencephalogram (EEG) study ( = 8) of sevoflurane-induced altered arousal in healthy volunteers. We administered temporally precise behavioral stimuli every 5 s to assess responsiveness. Here, we show that decreased eyes-closed, awake-alpha (8-12 Hz) oscillation power is associated with lack of responsiveness during sevoflurane effect-onset and -offset. We also show that anteriorization-the transition from occipitally dominant awake-alpha oscillations to frontally dominant anesthesia induced-alpha oscillations-is not a binary phenomenon. Rather, we suggest that periods, which were defined by lack of responsiveness, represent an intermediate brain state. We conclude that awake-alpha oscillation, previously thought to be an idling rhythm, is associated with responsiveness to behavioral stimuli.

摘要

麻醉药物通常用于诱导从镇静到全身麻醉(GA)的不同觉醒状态改变。目前,系统神经科学研究正用于探究麻醉诱导的觉醒状态改变的神经回路机制。这些研究表明,通过扰乱与觉醒状态相关的振荡动力学,麻醉诱导的振荡是麻醉药物产生觉醒状态改变的一种可能机制。然而,一项临床实证观察发现,即使在相对稳定的麻醉剂量下,患者在浅镇静状态下有时会对言语指令间歇性地产生反应。在这些时期,显著的麻醉诱导神经振荡,如慢δ(0.1 - 4赫兹)振荡明显不存在。浅镇静期间间歇性反应的神经关联尚未得到充分研究。对间歇性反应的神经关联有原则性的理解可能会从根本上推进我们对维持觉醒状态所必需的神经动力学以及它们如何被麻醉剂破坏的理解。因此,我们对健康志愿者进行了一项七氟醚诱导的觉醒改变的高密度(128通道)脑电图(EEG)研究(n = 8)。我们每隔5秒给予时间精确的行为刺激以评估反应性。在此,我们表明闭眼清醒时α(8 - 12赫兹)振荡功率降低与七氟醚起效和消退期间缺乏反应性有关。我们还表明,向前化——从枕叶主导的清醒α振荡到额叶主导的麻醉诱导α振荡的转变——不是一种二元现象。相反,我们认为由缺乏反应性定义的时期代表一种中间脑状态。我们得出结论,以前被认为是一种闲置节律的清醒α振荡与对行为刺激的反应性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e231/5447687/8da82b418a8e/fnsys-11-00038-g0001.jpg

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