Baruch H L, Kelwala S, Kapen S
Sleep. 1987 Jun;10(3):272-8. doi: 10.1093/sleep/10.3.272.
Nine narcoleptic and nine control subjects underwent 4 nights of sleep recordings. On nights 3 and 4, they received continuous intravenous infusions of saline. Additionally, on both nights they received 0.2 mg glycopyrrolate at the end of the first REM period (REM1) and 0.5 mg arecoline or placebo in random order 20 min after the end of REM1. Heart rates were counted for a 40-min period following the end of REM1. There was a significant and similar cardioacceleratory effect after arecoline in both narcoleptic and normal subjects, beginning at 5 min from the start of the infusion and peaking at 9 min. Placebo had no effect. Narcoleptic subjects had consistently higher baseline heart rates than controls on infusion and noninfusion nights, most likely owing to age differences between the two groups. The results suggest that narcoleptic persons do not have increased cholinergic sensitivity, or that the canine model of narcolepsy differs from the human model, or that the muscarinic receptors that play a role in the pathophysiology of narcolepsy differ in sensitivity from those that regulate heart rate.
9名发作性睡病患者和9名对照受试者进行了4晚的睡眠记录。在第3和第4晚,他们接受了生理盐水的持续静脉输注。此外,在这两晚,他们在第一个快速眼动期(REM1)结束时接受了0.2毫克格隆溴铵,并在REM1结束后20分钟以随机顺序接受了0.5毫克槟榔碱或安慰剂。在REM1结束后的40分钟内记录心率。在发作性睡病患者和正常受试者中,槟榔碱给药后均出现显著且相似的心动加速效应,从输注开始5分钟起,9分钟时达到峰值。安慰剂无此效应。在输注和非输注夜晚,发作性睡病患者的基线心率始终高于对照组,这很可能是由于两组之间的年龄差异。结果表明,发作性睡病患者没有更高的胆碱能敏感性,或者发作性睡病的犬类模型与人类模型不同,或者在发作性睡病病理生理学中起作用的毒蕈碱受体在敏感性上与调节心率的毒蕈碱受体不同。