Radulovacki M, Brodie M, Walovitch R, Yanik G
Gerontology. 1981;27(3):152-7. doi: 10.1159/000212464.
Bromocriptine mesylate (7.5 mg/kg, i.p.) and dihydroergotoxine mesylate (DHET); 3 mg/kg, i.p.) were administered 4 times at 9-hour intervals within a 27-hour period to rats polygraphically recorded for 84 h. Administration of bromocriptine resulted in increased wakefulness and reduced slow-wave sleep (SWS) and rapid eye movement sleep (REM) during the 0- to 36-hour period. Reduction of SWS or REM during this time period was not followed by a rebound of SWS or REM during the next 36- to 84-hour period. In addition, there was a significant reduction of SWS during the entire 0- to 84-hour period. Administration of DHET to rats did not significantly affect sleep although there was a tendency for wakefulness to increase and for SWS and REM to decrease. It appears that the effects of repeated administration of the two ergot compounds on the sleep-wakefulness cycle in rats may be indicative of the drugs' role in fulfillment of sleep 'need'.
在27小时内,以9小时间隔给大鼠腹腔注射甲磺酸溴隐亭(7.5毫克/千克)和甲磺酸二氢麦角隐亭(DHET,3毫克/千克),共4次,同时对大鼠进行84小时的多导睡眠图记录。注射溴隐亭导致在0至36小时期间清醒增加,慢波睡眠(SWS)和快速眼动睡眠(REM)减少。在此时间段内SWS或REM减少后,在接下来的36至84小时内SWS或REM并未出现反弹。此外,在整个0至84小时期间SWS显著减少。给大鼠注射DHET对睡眠没有显著影响,尽管有清醒增加、SWS和REM减少的趋势。看来,重复给予这两种麦角化合物对大鼠睡眠-清醒周期的影响可能表明这些药物在满足睡眠“需求”方面的作用。