Keifer J C, Baghdoyan H A, Lydic R
Department of Anesthesia, Pennsylvania State University, College of Medicine, Hershey 17033.
Anesthesiology. 1992 Nov;77(5):973-82. doi: 10.1097/00000542-199211000-00021.
The medial pontine reticular formation (mPRF) is a cholinoceptive brain stem region known to play a key role in regulating rapid eye movement (REM) sleep and state-dependent ventilatory depression. Numerous lines of evidence have shown that opioids inhibit both cholinergic neurotransmission and REM sleep. The present study examined the hypothesis that morphine applied to the cholinoceptive mPRF would inhibit REM sleep and alter ventilation. In six cats, guide cannulas were chronically implanted to permit pontine microinjection of morphine sulfate, naloxone, and the cholinergic agonist carbachol. After each mPRF microinjection, 2-h polygraphic recordings quantified respiratory frequency and the percent of time spent in states of wakefulness, non-REM sleep, and REM sleep. The results show that mPRF administration of morphine significantly inhibited REM sleep and that this REM sleep inhibitory effect was blocked by pretreating the mPRF with naloxone. Apneic episodes were increased after injection of morphine alone, and the apneas were decreased by the cholinergic agonist carbachol. The results also demonstrated that the ability of microinjected morphine to inhibit REM sleep was dose-dependent and site-dependent. Considered together, the site-localization, pharmacologic blocking, and dose-response data support the hypothesis that specific regions of the mPRF can contribute to the long-recognized ability of morphine to inhibit REM sleep and alter respiratory control.
脑桥内侧网状结构(mPRF)是一个对胆碱敏感的脑干区域,已知在调节快速眼动(REM)睡眠和状态依赖性通气抑制中起关键作用。大量证据表明,阿片类药物会抑制胆碱能神经传递和REM睡眠。本研究检验了以下假设:将吗啡应用于对胆碱敏感的mPRF会抑制REM睡眠并改变通气。在6只猫中,长期植入引导套管,以便对脑桥进行硫酸吗啡、纳洛酮和胆碱能激动剂卡巴胆碱的微量注射。每次mPRF微量注射后,进行2小时的多导记录,以量化呼吸频率以及在清醒、非REM睡眠和REM睡眠状态下所花费时间的百分比。结果表明,向mPRF注射吗啡可显著抑制REM睡眠,且这种REM睡眠抑制作用可被预先用纳洛酮处理mPRF所阻断。单独注射吗啡后呼吸暂停发作增加,而胆碱能激动剂卡巴胆碱可减少呼吸暂停。结果还表明,微量注射吗啡抑制REM睡眠的能力具有剂量依赖性和部位依赖性。综合来看,部位定位、药理学阻断和剂量反应数据支持以下假设:mPRF的特定区域可促成长期以来公认的吗啡抑制REM睡眠和改变呼吸控制的能力。