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关于美金刚促醒作用的大鼠研究。

Studies on wakefulness-promoting effect of memantine in rats.

机构信息

Department of Medicinal Pharmacology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 1-1-1 Tsushima-Naka, Kita-Ku, 700-8530, Okayama, Japan.

出版信息

Behav Brain Res. 2010 Jan 20;206(2):274-8. doi: 10.1016/j.bbr.2009.09.025. Epub 2009 Sep 23.

Abstract

We hypothesized that memantine, an anti-dementia drug, may be useful for the treatment of excessive daytime sleepiness. The effect of memantine on excessive sleepiness after 6 h sleep deprivation was studied in comparison with that of methylphenidate, and the involvement of the dopaminergic system in the wakefulness-promoting effect of memantine was also evaluated. Electrodes for electroencephalogram (EEG) and electromyogram (EMG) were chronically implanted into the cortex and dorsal neck muscle, respectively, of adult male rats. EEG and EMG were recorded with an electroencephalograph for 6 h (19:00-01:00). After sleep deprivation (13:00-19:00), compensatory excessive sleepiness (19:00-01:00) was observed in rats. Memantine (10 mg/kg, p.o.) and methylphenidate (10-30 mg/kg, p.o.) caused a significant increase of sleep latency compared with the control group. Furthermore, a significant increase in total awake time and significant decreases in total non-rapid eye movement (NREM) sleep and REM sleep times were observed by administration of memantine (3-10 mg/kg) and methylphenidate (3-30 mg/kg) compared with control in sleep deprivation rats. Although the effect of memantine was significantly suppressed by D1 receptor antagonist SCH 23390 (0.1 mg/kg, i.p.), D2 receptor antagonist raclopride had no antagonistic effect (1 mg/kg, i.p.). From these results, the effect of memantine on sleepiness after sleep deprivation was similar to that of methylphenidate, and D1 receptor may be involved in the effect of memantine.

摘要

我们假设美金刚,一种抗痴呆药物,可能对治疗日间过度嗜睡有用。研究了美金刚对 6 小时睡眠剥夺后过度嗜睡的影响,并与哌甲酯进行了比较,还评估了多巴胺能系统在美金刚促醒作用中的参与情况。将用于脑电图(EEG)和肌电图(EMG)的电极分别慢性植入成年雄性大鼠的皮质和颈部背侧肌肉。使用脑电图记录 EEG 和 EMG 长达 6 小时(19:00-01:00)。睡眠剥夺后(13:00-19:00),大鼠观察到补偿性过度嗜睡(19:00-01:00)。与对照组相比,美金刚(10mg/kg,po)和哌甲酯(10-30mg/kg,po)可显著延长睡眠潜伏期。此外,与对照组相比,美金刚(3-10mg/kg)和哌甲酯(3-30mg/kg)给药可显著增加总清醒时间,并显著减少总非快速眼动(NREM)睡眠时间和 REM 睡眠时间。虽然 D1 受体拮抗剂 SCH 23390(0.1mg/kg,ip)显著抑制了美金刚的作用,但 D2 受体拮抗剂氯丙嗪(1mg/kg,ip)没有拮抗作用。从这些结果来看,美金刚对睡眠剥夺后嗜睡的作用类似于哌甲酯,D1 受体可能参与了美金刚的作用。

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