Cianchetti C, Masala C, Olivari P, Giordano G
Psychopharmacology (Berl). 1984;83(2):179-82. doi: 10.1007/BF00429731.
A continuous intravenous infusion of the opiate receptor antagonist naloxone, at doses ranging from 0.7 to 1.0 micrograms/kg/min (total dose 8.8-13.2 mg), was performed in eight normal subjects during the first 240 min of night sleep. A significant reduction in stage REM and in stage 4 percent duration was observed. Pretreatment with the dopamine receptor blocking agent haloperidol (2 mg intramuscularly before sleep onset) partially prevented the naloxone effect, suggesting that it is due, at least in part, to the stimulation of dopamine receptors.
在8名正常受试者夜间睡眠的前240分钟内,以0.7至1.0微克/千克/分钟的剂量(总剂量8.8 - 13.2毫克)持续静脉输注阿片受体拮抗剂纳洛酮。观察到快速眼动睡眠期和4期睡眠时长百分比显著降低。在睡前肌肉注射多巴胺受体阻断剂氟哌啶醇(2毫克)进行预处理,部分地阻止了纳洛酮的作用,这表明该作用至少部分是由于多巴胺受体的刺激所致。