Zak R, Radulovacki M
Brain Res Bull. 1982 Mar;8(3):329-31. doi: 10.1016/0361-9230(82)90067-3.
Rats implanted with electrodes for polygraphic recording were deprived of REM sleep for 24 hr. Following REM sleep deprivation animals were injected with quipazine maleate (7.5 mg/kg IP) and were polygraphically recorded for 48 hr. The results show that quipazine reduces REM sleep rebound and that it has a biphasic effect on slow-wave sleep: initial 6 hr suppression is followed by a delayed increase in the second 24 hr recording period. The initial suppression of slow-wave sleep we attribute to the stimulation of central serotonergic receptors while the effect on REM sleep rebound may result from quipazine's action on central catecholamines.
将电极植入大鼠用于多导睡眠图记录,剥夺其快速眼动睡眠24小时。快速眼动睡眠剥夺后,给动物注射马来酸喹哌嗪(7.5毫克/千克,腹腔注射),并进行48小时的多导睡眠图记录。结果表明,喹哌嗪可减少快速眼动睡眠反弹,并且对慢波睡眠有双相作用:最初6小时抑制,随后在第二个24小时记录期延迟增加。我们将慢波睡眠的最初抑制归因于中枢5-羟色胺能受体的刺激,而对快速眼动睡眠反弹的影响可能是由于喹哌嗪对中枢儿茶酚胺的作用。