Abramson L B, Brown A J, Sitaram N
Psychiatry Res. 1985 Nov;16(3):189-98. doi: 10.1016/0165-1781(85)90106-4.
We studied the cardiovascular effect of 0.5 mg of arecoline, a centrally active cholinergic muscarinic agonist, infused over a 3-minute period during the second non-REM (rapid-eye-movement) sleep cycle in 23 patients with major depression. A clear-cut cardioacceleratory response, beginning at the second minute of the 3-minute infusion, and reaching a peak about 5-6 minutes from the start of the infusion, was noted. Placebo infusion did not alter heart rate. There was a significant correlation between the magnitude of the heart rate increase and the latency to onset of the second REM period after arecoline infusion (-0.49). Neither baseline nor arecoline-induced heart rate increases were related to age, sex, or sleep stage changes during or following arecoline infusion. Our data suggest the use of the cardioacceleratory response to cholinomimetics as an additional research tool in assessing central cholinergic sensitivity in humans, especially in neuropsychiatric and stress-related states where cholinergic alterations may occur.
我们研究了0.5毫克槟榔碱(一种中枢活性胆碱能毒蕈碱激动剂)在23例重度抑郁症患者的第二个非快速眼动(REM)睡眠周期中3分钟内输注时的心血管效应。观察到一种明确的心动加速反应,从3分钟输注的第二分钟开始,从输注开始约5 - 6分钟达到峰值。安慰剂输注未改变心率。心率增加幅度与槟榔碱输注后第二个REM期开始的潜伏期之间存在显著相关性(-0.49)。基线心率及槟榔碱诱导的心率增加均与年龄、性别或槟榔碱输注期间或之后的睡眠阶段变化无关。我们的数据表明,使用拟胆碱药引起的心动加速反应作为评估人类中枢胆碱能敏感性的额外研究工具,特别是在可能发生胆碱能改变的神经精神和应激相关状态中。