Evans M H, Sutton M R, Williamson N M
Neuropharmacology. 1983 Jan;22(1):35-43. doi: 10.1016/0028-3908(83)90258-7.
The heart rate of the anaesthetized rabbit was slowed by electrical stimulation of the hypothalamus with 7-9 sec trains of 250-330 microA pulses, duration 1 msec, frequency 60 Hz. This vagally-mediated cardio-decelerator response was attenuated in a dose-dependent manner after intravenous administration of phenoxybenzamine (0.01-5 mg/kg), phentolamine (0.01-3 mg/kg) or yohimbine (0.1-5 mg/kg). The attenuation of the cardio-decelerator response was not due to any vagolytic action of these drugs nor to block of the baroreceptor reflex, but appeared to be due to a central block of pathways descending from the hypothalamus. Propranolol, haloperidol, pimozide and spiperone did not show this central blocking action except in very large doses when there was evidence of some alpha-adrenoceptor blockade.
用250 - 330微安脉冲、持续时间1毫秒、频率60赫兹的7 - 9秒串刺激麻醉兔的下丘脑,可使其心率减慢。静脉注射酚苄明(0.01 - 5毫克/千克)、酚妥拉明(0.01 - 3毫克/千克)或育亨宾(0.1 - 5毫克/千克)后,这种由迷走神经介导的心脏减速反应以剂量依赖的方式减弱。心脏减速反应的减弱并非由于这些药物的任何迷走神经阻滞作用,也不是由于压力感受器反射的阻断,而是似乎由于下丘脑下行通路的中枢性阻断。普萘洛尔、氟哌啶醇、匹莫齐特和螺哌隆没有表现出这种中枢性阻断作用,除非在非常大的剂量下,此时有一些α - 肾上腺素能受体阻断的证据。