Department of Anesthesiology, University of Wisconsin, Madison, WI, USA.
Department of Anesthesiology, University of Wisconsin, Madison, WI, USA.
Br J Anaesth. 2018 Nov;121(5):1084-1096. doi: 10.1016/j.bja.2018.07.006. Epub 2018 Aug 21.
Impaired consciousness has been associated with impaired cortical signal propagation after transcranial magnetic stimulation (TMS). We hypothesised that the reduced current propagation under propofol-induced unresponsiveness is associated with changes in both feedforward and feedback connectivity across the cortical hierarchy.
Eight subjects underwent left occipital TMS coupled with high-density EEG recordings during wakefulness and propofol-induced unconsciousness. Spectral analysis was applied to responses recorded from sensors overlying six hierarchical cortical sources involved in visual processing. Dynamic causal modelling (DCM) of induced time-frequency responses and evoked response potentials were used to investigate propofol's effects on connectivity between regions.
Sensor space analysis demonstrated that propofol reduced both induced and evoked power after TMS in occipital, parietal, and frontal electrodes. Bayesian model selection supported a DCM with hierarchical feedforward and feedback connections. DCM of induced EEG responses revealed that the primary effect of propofol was impaired feedforward responses in cross-frequency theta/alpha-gamma coupling and within frequency theta coupling (F contrast, family-wise error corrected P<0.05). An exploratory analysis (thresholded at uncorrected P<0.001) also suggested that propofol impaired feedforward and feedback beta band coupling. Post hoc analyses showed impairments in all feedforward connections and one feedback connection from parietal to occipital cortex. DCM of the evoked response potential showed impaired feedforward connectivity between left-sided occipital and parietal cortex (T contrast P=0.004, Bonferroni corrected).
Propofol-induced loss of consciousness is associated with impaired hierarchical feedforward connectivity assessed by EEG after occipital TMS.
经颅磁刺激(TMS)后,意识障碍与皮质信号传播受损有关。我们假设异丙酚诱导的无反应状态下电流传播减少与皮质层次结构中前馈和反馈连接的变化有关。
8 名受试者在清醒和异丙酚诱导的无意识期间接受左侧枕叶 TMS 联合高密度 EEG 记录。对来自参与视觉处理的六个分层皮质源上方传感器记录的响应进行频谱分析。应用诱导时频响应和诱发反应电位的动态因果建模(DCM)来研究异丙酚对区域间连接的影响。
传感器空间分析表明,异丙酚降低了枕叶、顶叶和额叶电极 TMS 后诱导和诱发的功率。贝叶斯模型选择支持具有分层前馈和反馈连接的 DCM。诱导 EEG 响应的 DCM 表明,异丙酚的主要影响是在交叉频域θ/α-γ耦合和频域内θ耦合中受损的前馈响应(F 对比,经家族错误校正 P<0.05)。一项探索性分析(未校正 P<0.001 阈值)还表明,异丙酚损害了前馈和反馈β带耦合。事后分析显示所有前馈连接和一个从顶叶到枕叶的反馈连接受损。诱发反应电位的 DCM 显示左侧枕叶和顶叶皮质之间的前馈连接受损(T 对比 P=0.004,Bonferroni 校正)。
枕叶 TMS 后,异丙酚诱导的意识丧失与 EEG 评估的分层前馈连接受损有关。