Alihanka J, Lahdenperä A, Kaila T
Department of Physiology, University of Turku, Finland.
Eur J Clin Pharmacol. 1994;46(6):507-10. doi: 10.1007/BF00196106.
We studied the effect of transdermally applied scopolamine (scopolamine-TTS) on autonomic nervous activity during sleep. The double-blind, randomized, crossover study was carried out in six healthy male volunteers by applying 1.5 mg scopolamine-TTS or placebo patch on the retroauricular skin and by monitoring heart rate, cardiac ballistogram, respiration and body movements by using electrocardiogram and static charge sensitive bed. Scopolamine did not decrease the time the subjects desired to sleep (516 min after TTS, 511 min after placebo) or the number of body movements of 3-5 s duration the subjects spontaneously performed during sleep (47 after TTS, 58 after placebo). No adverse effects of scopolamine were reported spontaneously. Scopolamine-TTS slowed the mean heart rate during quiet sleep from 53.2 to 44.9 beats.min-1, and increased the duration of bradycardia in response to body movements (MIB-reflex) from 12.5 to 14.7 s with a significant difference between scopolamine and placebo effects. The bradycardias were not associated with disturbances in cardiorespiratory or central nervous system functions. The cardiac vagomimetic action of scopolamine-TTS could be explained by low plasma drug concentrations (175 pg/ml) primarily blocking only neuronal inhibitory prejunctional muscarinic receptors which regulate acetylcholine release from the autonomic ganglia and parasympathetic nerve-endings. Because of the central role of acetylcholine in the physiological regulation of sleep, the effect of scopolamine-TTS on sleep merits further investigations.
我们研究了经皮应用东莨菪碱(东莨菪碱透皮贴剂)对睡眠期间自主神经活动的影响。在六名健康男性志愿者中进行了双盲、随机、交叉研究,通过在耳后皮肤贴敷1.5毫克东莨菪碱透皮贴剂或安慰剂贴片,并使用心电图和静电敏感床监测心率、心冲击图、呼吸和身体运动。东莨菪碱并未减少受试者的期望睡眠时间(透皮贴剂后为516分钟,安慰剂后为511分钟),也未减少受试者睡眠期间自发进行的持续3 - 5秒的身体运动次数(透皮贴剂后为47次,安慰剂后为58次)。未自发报告东莨菪碱的不良反应。东莨菪碱透皮贴剂使安静睡眠期间的平均心率从53.2次/分钟减慢至44.9次/分钟,并使身体运动引起的心动过缓(MIB反射)持续时间从12.5秒增加至14.7秒,东莨菪碱和安慰剂的效果之间存在显著差异。心动过缓与心肺或中枢神经系统功能紊乱无关。东莨菪碱透皮贴剂的拟迷走神经作用可能是由于血浆药物浓度较低(175皮克/毫升),主要仅阻断调节自主神经节和副交感神经末梢乙酰胆碱释放的神经元抑制性节前毒蕈碱受体。由于乙酰胆碱在睡眠的生理调节中起核心作用,东莨菪碱透皮贴剂对睡眠的影响值得进一步研究。