Kobinger W, Pichler L
Clin Exp Hypertens (1978). 1978;1(2):229-49. doi: 10.3109/10641967809068606.
The response pattern of the autonomic nervous system was investigated after central administration (intra-cisternal, vertebral artery) of amphetamine, morphine, fentanyl, dextromoramide and the substance R 28935, chemically related to the neuroleptic agent pimozide. Effects on the sympathetic system were measured by recording electrical discharges of fibres of the (preganglionic) major splanchnic nerve in anaesthetized cats; those on the vagal system by recording the heart rate in anaesthetized dogs under beta-adrenoceptor blockade; the baroreceptor reflex was elicited by the blood pressure increase of i.v. injected angiotensin. All substances decreased the spontaneous discharge rate of the splanchnic nerve. Amphetamine facilitated the vagally mediated reflex bradycardia and this was antagonized by the alpha-adrenoceptor blocking agent piperoxan. Amphetamine did not affect the resting heart rate, as has already been shown for clonidine and related substances. The narcotic analgesics lowered the resting heart rate but did not facilitate the baroreceptor reflex response. R 28935 neither influenced resting heart rate nor the baroreceptor reflex response in beta-blocked dogs. On the basis of the vagal response pattern it was therefore possible to distinguish between 3 groups of central hypotensive drugs.
在向中枢(脑池内、椎动脉)注射苯丙胺、吗啡、芬太尼、右吗拉胺以及与抗精神病药物匹莫齐特化学相关的物质R 28935后,研究了自主神经系统的反应模式。通过记录麻醉猫的(节前)内脏大神经纤维的放电来测量对交感神经系统的影响;通过记录β-肾上腺素能受体阻断下麻醉犬的心率来测量对迷走神经系统的影响;静脉注射血管紧张素使血压升高来引发压力感受器反射。所有物质均降低了内脏神经的自发放电率。苯丙胺促进了迷走神经介导的反射性心动过缓,这被α-肾上腺素能受体阻断剂哌罗克生所拮抗。苯丙胺不影响静息心率,可乐定及相关物质也已被证明如此。麻醉性镇痛药降低了静息心率,但不促进压力感受器反射反应。在β受体阻断的犬中,R 28935既不影响静息心率,也不影响压力感受器反射反应。因此,根据迷走神经反应模式,可以区分出3类中枢性降压药物。