Lelkes Z, Obál F, Benedek G, Rubicsek G, Alföldi P, Obál F
Naunyn Schmiedebergs Arch Pharmacol. 1987 Feb;335(2):149-53. doi: 10.1007/BF00177716.
After the chronic administration of saline, rats were treated with nomifensine (0.1 or 1.0 mg/kg, twice a day, at light and dark onset) for 11 days. The sleep-wake activity was recorded for 24 h on the baseline day (saline), on nomifensine days 1, 5 and 11, and also on day 12, when saline was injected again (withdrawal day). Another group of rats was treated with saline throughout the experiment, without significant effect on the sleep-wake activity. The smaller dose of nomifensine increased non-REM sleep (NREMS) at the expense of wakefulness (W) in the light period. The effect persisted throughout the chronic treatment. A late increase in REM sleep (REMS) was noted on nomifensine days 5 and 11. Nomifensine failed to affect the sleep-wake activity in the dark period. On withdrawal, the baseline percentages of the vigilance states were recovered. As evaluated through spectral analysis of the EEG, the increase in NREMS was accompanied by an increase in slow wave activity. The higher dose of nomifensine elicited an increase in W and a reduction in both sleep states, followed by changes in W and NREMS in the opposite directions. These effects were evident in both the light and the dark periods of the day. Chronic treatment resulted in circadian variations in the effects. Withdrawal of the drug abolished the arousal reaction, but the late increase in NREMS persisted. The dose-dependent biphasic effects of nomifensine on sleep-wake activity can be explained by considering the proposed indirect dopamine and possibly noradrenaline agonist activity of the drug.(ABSTRACT TRUNCATED AT 250 WORDS)
在长期给予生理盐水后,大鼠接受诺米芬辛治疗(0.1或1.0毫克/千克,每天两次,在光照和黑暗开始时),持续11天。在基线日(生理盐水)、诺米芬辛治疗的第1、5和11天以及第12天(再次注射生理盐水的撤药日)记录24小时的睡眠-觉醒活动。另一组大鼠在整个实验过程中接受生理盐水治疗,对睡眠-觉醒活动无显著影响。较小剂量的诺米芬辛以牺牲光照期的觉醒(W)为代价增加了非快速眼动睡眠(NREMS)。这种效应在整个慢性治疗过程中持续存在。在诺米芬辛治疗的第5和11天观察到快速眼动睡眠(REMS)后期增加。诺米芬辛在黑暗期未影响睡眠-觉醒活动。撤药时,警觉状态的基线百分比恢复。通过脑电图频谱分析评估,NREMS的增加伴随着慢波活动的增加。较高剂量的诺米芬辛引起W增加和两种睡眠状态减少,随后W和NREMS朝相反方向变化。这些效应在白天的光照和黑暗期均明显。慢性治疗导致效应出现昼夜变化。药物撤药消除了唤醒反应,但NREMS后期增加持续存在。诺米芬辛对睡眠-觉醒活动的剂量依赖性双相效应可通过考虑该药物拟议的间接多巴胺及可能的去甲肾上腺素激动剂活性来解释。(摘要截断于250字)