Ong B T, Chan S H
Exp Neurol. 1984 Oct;86(1):105-12. doi: 10.1016/0014-4886(84)90071-2.
In Sprague-Dawley rats anesthetized with pentobarbital sodium (40 mg/kg, i.p.), guanabenz and clonidine exhibited mutually interactive effects on the cardiovascular system. Pretreatment with either antihypertensive agent (5 or 10 micrograms/kg, i.v.) significantly potentiated both the degree and duration of the initial elevation in arterial pressure and cardiac contractility promoted by the other compound (10 micrograms/kg, i.v.). On the other hand, discernible antagonization existed mutually for their delayed hypotensive, as well as negative inotropic and chronotropic actions. Furthermore, these circulatory changes displayed comparable trends under parallel drug interaction schemes, as revealed by correlation coefficient evaluations. It is possible that guanabenz and clonidine may share a common mechanism(s) in their cardiovascular actions.
在戊巴比妥钠(40毫克/千克,腹腔注射)麻醉的Sprague-Dawley大鼠中,胍那苄和可乐定对心血管系统表现出相互作用。预先给予任何一种抗高血压药物(5或10微克/千克,静脉注射)均能显著增强另一种化合物(10微克/千克,静脉注射)所引起的动脉压初始升高程度和持续时间以及心脏收缩力。另一方面,它们延迟性降压作用以及负性肌力和变时作用之间存在明显的相互拮抗。此外,相关系数评估显示,在平行药物相互作用方案下,这些循环变化呈现出可比的趋势。胍那苄和可乐定在心血管作用中可能具有共同的机制。