Salín-Pascual R J, García-Ferreiro R, Moro-López M L, Blanco-Centurión C, Drucker-Colín R
Departamento de Fisiologia, Facultad de Medicina, UNAM, Mexico, DF.
Psychopharmacology (Berl). 1997 Jun;131(3):216-9. doi: 10.1007/s002130050286.
Repeated haloperidol administration produces up-regulation of dopamine (DA) receptors. REM sleep deprivation (REMSD) does also, but in addition, has been shown to produce REM sleep rebound. Should DA receptor up-regulation play a role in REM sleep rebound, haloperidol could conceivably have effects similar to those observed following REMSD. This is the central question investigated in this study. Male Wistar rats were prepared for sleep recordings. They were randomly assigned to the following groups: group 1, REMSD by small platforms (40 h REMSD + 8 h recording); group 2, was the large platform control group (40 h in large platforms + 8 h of recording); group 3, received 2-week daily administration of haloperidol (3 mg/kg, i.p.) plus REMSD (40 h REMSD + 8 h of recording); group 4, 2-week administration of haloperidol (3 mg/kg) without sleep manipulation and at the end 40 h were allowed to elapse, following which 8 h of sleep recordings was carried out. In each group the sleep manipulation and/or sleep recordings were repeated five consecutive times. Repeated REMSD produced increases of REM sleep time after each recovery in group 1. Large platforms did not produce increases of REM sleep during the recovery trials. The 2-week administration of haloperidol plus REMSD prevented REM sleep rebound (group 3). The 2-week administration of haloperidol without sleep manipulation (group 4) produced a REM sleep reduction. Dopamine modulation seems not to be important for REM sleep rebound. Hypersensitivity of DA receptors developed after REMSD may be an epiphenomenon associated with this sleep manipulation, but seems not to participate in REM sleep enhancement after REMSD.
重复给予氟哌啶醇会导致多巴胺(DA)受体上调。快速眼动睡眠剥夺(REMSD)也会如此,但除此之外,还会导致快速眼动睡眠反弹。如果DA受体上调在快速眼动睡眠反弹中起作用,那么可以想象氟哌啶醇可能会产生与快速眼动睡眠剥夺后观察到的类似效果。这是本研究中探讨的核心问题。雄性Wistar大鼠准备用于睡眠记录。它们被随机分为以下几组:第1组,通过小平台进行快速眼动睡眠剥夺(40小时快速眼动睡眠剥夺 + 8小时记录);第2组,是大平台对照组(在大平台中40小时 + 8小时记录);第3组,接受为期2周的每日氟哌啶醇给药(3毫克/千克,腹腔注射)加快速眼动睡眠剥夺(40小时快速眼动睡眠剥夺 + 8小时记录);第4组,为期2周的氟哌啶醇给药(3毫克/千克),无睡眠操作,在最后40小时过去后,进行8小时的睡眠记录。每组中睡眠操作和/或睡眠记录连续重复5次。重复的快速眼动睡眠剥夺在第1组每次恢复后导致快速眼动睡眠时间增加。大平台在恢复试验期间未导致快速眼动睡眠增加。为期2周的氟哌啶醇给药加快速眼动睡眠剥夺可防止快速眼动睡眠反弹(第3组)。为期2周的无睡眠操作的氟哌啶醇给药(第4组)导致快速眼动睡眠减少。多巴胺调节似乎对快速眼动睡眠反弹不重要。快速眼动睡眠剥夺后出现的DA受体超敏反应可能是与这种睡眠操作相关的一种附带现象,但似乎不参与快速眼动睡眠剥夺后的快速眼动睡眠增强。