Gouzoulis E, Steiger A, Ensslin M, Kovar A, Hermle L
Department of Psychiatry, University of Freiburg, Germany.
Biol Psychiatry. 1992 Dec 15;32(12):1108-17. doi: 10.1016/0006-3223(92)90191-2.
3,4-methylenedioxyethamphetamine (MDE; "Eve") exerts similar psychotropic effects in humans as 3,4-methylenedioxymethamphetamine (MDMA; "Ecstasy") and is less toxic in animal studies. We conducted a double-blind, placebo-controlled, cross-over sleep electroencephalogram (EEG) study with healthy volunteers. One hundred forty milligrams of MDE or placebo were administered PO in six subjects at 11 PM. Sleep EEG was registered from 11 PM-7 AM the next morning. All subjects had a normal sleep onset latency. They all awoke 60 to 120 min after administration of MDE and stayed awake for at least 150 min (total sleep time, TST MDE < placebo and intermittent time awake MDE > placebo: p < 0.001). After again falling asleep rapid eye movement (REM) sleep was totally suppressed (REM during time in bed, TIB MDE < placebo: p < 0.001). A cyclic alternation of relatively long periods of slow wave sleep (SWS) with periods of light sleep occurred in three subjects during the second part of the night (stage 4 in second part of night MDE > placebo: p = 0.16). The effects of MDE on sleep variables largely demonstrate the stimulant, amphetamine-like properties of MDE.
3,4-亚甲二氧基乙胺(MDE;“伊芙”)对人类产生的精神作用与3,4-亚甲二氧基甲基苯丙胺(MDMA;“摇头丸”)相似,并且在动物研究中毒性较小。我们对健康志愿者进行了一项双盲、安慰剂对照的交叉睡眠脑电图(EEG)研究。晚上11点给6名受试者口服140毫克MDE或安慰剂。于次日凌晨11点至7点记录睡眠脑电图。所有受试者的入睡潜伏期均正常。服用MDE后,他们均在60至120分钟后醒来,并保持清醒至少150分钟(总睡眠时间,MDE组的TST < 安慰剂组,MDE组的间歇性清醒时间 > 安慰剂组:p < 0.001)。再次入睡后,快速眼动(REM)睡眠被完全抑制(床上时间的REM,MDE组的TIB < 安慰剂组:p < 0.001)。在夜间后半段,三名受试者出现了相对较长的慢波睡眠(SWS)期与浅睡眠期的周期性交替(夜间后半段的第4阶段,MDE组 > 安慰剂组:p = 0.16)。MDE对睡眠变量的影响在很大程度上证明了MDE具有兴奋剂、安非他明样特性。