Pellejero T, Monti J M, Baglietto J, Jantos H, Pazos S, Cichevski V, Hawkins M
Sleep. 1984;7(4):365-72. doi: 10.1093/sleep/7.4.365.
A study was carried out on the effects of methoxamine, prazosin, and yohimbine on the sleep-wake cycle in rats prepared for chronic sleep recordings. Methoxamine (4-8 mg/kg), an alpha 1-adrenoceptor agonist, induced a dose-related increase in wakefulness (W) and a decrease in slow-wave sleep (SWS) and REM sleep (REMS). Prazosin (0.125-1 mg/kg), which selectively blocks alpha 1-adrenoceptors, modified only slightly the amount of time spent in W and SWS, and consistently decreased REMS values. Prazosin (0.5 mg/kg) reversed the effects of methoxamine, decreasing W and increasing sleep. Yohimbine (3 mg/kg), which blocks alpha 2-adrenoceptors, augmented W and diminished sleep. Methoxamine (4 mg/kg) in animals pretreated with yohimbine (3 mg/kg) induced a further decrease of SWS and REMS and an increase of W. Thus, pharmacological activation of alpha 1- or blocking of alpha 2-adrenoceptors appears to decrease sleep and increase W. Further, blocking of alpha 1-adrenoceptors decreases REMS. Rapid eye movement sleep depression by the alpha 1-agonist or the alpha 1-antagonist is tentatively ascribed to a critical change in noradrenergic transmission in the brain.
对甲氧明、哌唑嗪和育亨宾对准备进行慢性睡眠记录的大鼠睡眠-觉醒周期的影响进行了一项研究。α1肾上腺素能受体激动剂甲氧明(4-8毫克/千克)引起觉醒(W)呈剂量相关增加,慢波睡眠(SWS)和快速眼动睡眠(REMS)减少。选择性阻断α1肾上腺素能受体的哌唑嗪(0.125-1毫克/千克)仅轻微改变W和SWS的时间量,并持续降低REMS值。哌唑嗪(0.5毫克/千克)逆转了甲氧明的作用,减少W并增加睡眠。阻断α2肾上腺素能受体的育亨宾(3毫克/千克)增加W并减少睡眠。在预先用育亨宾(3毫克/千克)处理的动物中,甲氧明(4毫克/千克)导致SWS和REMS进一步减少以及W增加。因此,α1肾上腺素能受体的药理激活或α2肾上腺素能受体的阻断似乎会减少睡眠并增加W。此外,α1肾上腺素能受体的阻断会降低REMS。α1激动剂或α1拮抗剂引起的快速眼动睡眠抑制初步归因于大脑中去甲肾上腺素能传递的关键变化。