Kinoshita T, Strik W K, Michel C M, Yagyu T, Saito M, Lehmann D
Department of Neurology, University Hospital, Zurich, Switzerland.
Pharmacopsychiatry. 1995 Mar;28(2):51-5. doi: 10.1055/s-2007-979588.
Spontaneous multichannel brain electric field (EEG) map series of 20 seconds duration at 1, 15, 30, 45, and 60 minutes after the injection of a single dose of diazepam (13 ss) or sulpiride (6 ss) were segmented into microstates of quasi-constant landscape but varying durations. Post-minus-preinjection difference values were computed for the six microstate variables: specific window size, duration, orientation, distance between windows, and location of center of gravity on the anterior-posterior and left-right axis. Differences between drugs were explored with ANOVAs. Microstate duration increased after sulpiride, and the location of the microstate center of gravity on the anterior-posterior axis moved to a more anterior position after diazepam. The results are in agreement with expectations based on measurements of patients' EEG microstates and with results using estimates of EEG model source locations in the frequency domain. Microstate segmentation appears to be a useful method for physiologically meaningful reduction of multichannel brain electric field data in psychopharmacology.
在注射单剂量地西泮(13毫克)或舒必利(6毫克)后1、15、30、45和60分钟,记录时长为20秒的自发性多通道脑电场(脑电图)图谱系列,并将其分割为准恒定地形图但持续时间不同的微状态。计算六个微状态变量的注射后减去注射前的差值:特定窗口大小、持续时间、方向、窗口之间的距离以及前后轴和左右轴上重心的位置。通过方差分析探究药物之间的差异。舒必利注射后微状态持续时间增加,地西泮注射后微状态重心在前后轴上的位置向前移动。这些结果与基于患者脑电图微状态测量的预期一致,也与使用频域脑电图模型源位置估计的结果一致。微状态分割似乎是一种在精神药理学中对多通道脑电场数据进行生理意义上有效简化的有用方法。