Sannita W G, Balbi A, Giacchino F, Rosadini G
Center for Neuropsychoactive Drugs, University, Genoa, Italy.
Neuropsychobiology. 1990;23(4):205-12. doi: 10.1159/000119453.
Single, 50- and 100-mg oral doses of phenobarbital and a matching placebo were administered double-blind to 8 young, healthy male subjects. Multilead electroencephalographic (EEG) samples were recorded prior to, and at regular intervals within the 2 h following administration. The EEG signal was processed by power spectral analysis; the drug plasma concentration was assessed concomitantly. Plasma peaks after the 50- and 100-mg dose were, respectively, 3.38 +/- 1.29 and 4.09 +/- 1.24 micrograms/ml. Despite the low drug plasma concentration, a systematic power increment of the EEG fast frequency spectral segments occurred at either dose on the anterior scalp areas from the 30- or 60-min postdrug control onward, and was preponderant on central electrodes; a significant correlation (Kendal's coefficient for ranked data) with the drug plasma concentration was observed limitedly to the anterior scalp areas. No correlation with plasma levels was observed for unsystematic EEG variations.
对8名年轻健康男性受试者进行双盲试验,分别给予单次口服50毫克和100毫克苯巴比妥及匹配的安慰剂。在给药前以及给药后2小时内定期记录多导联脑电图(EEG)样本。通过功率谱分析处理EEG信号;同时评估药物血浆浓度。50毫克和100毫克剂量后的血浆峰值分别为3.38±1.29和4.09±1.24微克/毫升。尽管药物血浆浓度较低,但从给药后30分钟或60分钟起,在前额头皮区域,两种剂量均出现EEG快频率谱段的系统性功率增加,且在中央电极上更为明显;仅在前额头皮区域观察到与药物血浆浓度有显著相关性(肯德尔等级数据系数)。未观察到EEG非系统性变化与血浆水平的相关性。