Akrawi W P, Drummond J C, Kalkman C J, Patel P M
Department of Anesthesiology, University of California, San Diego, USA.
J Neurosurg Anesthesiol. 1996 Jan;8(1):40-6. doi: 10.1097/00008506-199601000-00010.
Electroencephalogram (EEG) burst-suppression can be produced with several anesthetic agents. Discussions of burst-suppression suggest that it has been viewed by many as a relatively uniform physiologic state independent of the agent used to produce it. This view may be an oversimplification. In this study, relatively deep EEG burst-suppression (suppression to burst time ratio, 4:1) was induced in rats with isoflurane (I), thiopental (T), etomidate (E), and propofol (P). Burst duration, maximum peak-to-peak voltage, area under the curve, and the ratio of power in high versus low frequencies of EEG recorded in both cortex and subcortex (thalamus) were determined. Analysis of the bursts revealed significant differences in duration [I, 1.4 +/- 0.4 (SD); T, 0.8 +/- 0.5; E, 0.3 +/- 0.1; P, 0.4 +/- 0.1 seconds], peak-to-peak voltage (I, 488 +/- 146; T, 285 +/- 106; E, 310 +/- 87; P, 249 +/- 50 muV), and area under the curve (I, 111 +/- 24; T, 35 +/- 31; E, 17 +/- 7; P, 21 +/- 4 muV-s) for all agent pairs except etomidate and propofol. Suppression phase analysis revealed considerable residual activity with all four agents, although peak-to-peak voltage (I, 129 +/- 29; T, 64 +/- 20; E, 62 +/- 11; P, 40 +/- 15 muV) and area under the curve (I, 73 +/- 17; T, 37 +/- 14; E, 30 +/- 5; P, 22 +/- 10 muV-s) were greatest with isoflurane. The cortical versus subcortical comparison revealed, for all agents, greater peak-to-peak voltage and area under the curve in the subcortex. The data indicate that the electrophysiologic characteristics of burst-suppression vary among the four agents, with the possible exception of etomidate and propofol. The data suggest that the neurophysiologic states associated with burst-suppression produced by various anesthetics should not be assumed to be uniform.
几种麻醉剂均可产生脑电图(EEG)爆发抑制。关于爆发抑制的讨论表明,许多人认为它是一种相对统一的生理状态,与用于产生它的药物无关。这种观点可能过于简单化。在本研究中,用异氟烷(I)、硫喷妥钠(T)、依托咪酯(E)和丙泊酚(P)诱导大鼠产生相对深度的EEG爆发抑制(抑制与爆发时间比为4:1)。测定了爆发持续时间、最大峰峰值电压、曲线下面积以及在皮层和皮层下(丘脑)记录的EEG高频与低频功率比。对爆发的分析显示,除依托咪酯和丙泊酚外,所有药物对的爆发持续时间[I,1.4±0.4(标准差);T,0.8±0.5;E,0.3±0.1;P,0.4±0.1秒]、峰峰值电压(I,488±146;T,285±106;E,310±87;P,249±50μV)和曲线下面积(I,111±24;T,35±31;E,17±7;P,21±4μV·秒)存在显著差异。抑制期分析显示,所有四种药物均有相当程度的残余活动,尽管异氟烷的峰峰值电压(I,129±29;T,64±20;E,62±11;P,40±15μV)和曲线下面积(I,73±17;T,37±14;E,30±5;P,22±10μV·秒)最大。皮层与皮层下的比较显示,对于所有药物,皮层下的峰峰值电压和曲线下面积更大。数据表明,除依托咪酯和丙泊酚外,四种药物的爆发抑制电生理特征各不相同。数据表明,不应假定由各种麻醉剂产生的与爆发抑制相关的神经生理状态是统一的。