Ajayi A A, Campbell B C, Rubin P C, Reid J L
Clin Pharmacol Ther. 1985 Nov;38(5):560-5. doi: 10.1038/clpt.1985.224.
Captopril inhibits the metabolism of endogenous opioids in vitro and potentiates their effects in vivo. We examined the hypothesis that endogenous opioids contribute to the actions of captopril in man. The acute cardiovascular and autonomic effects of oral captopril, intravenous naloxone, and their combination were examined in eight healthy men with normotension in a double-blind, placebo-controlled study of a Latin squares design. Naloxone altered neither blood pressure nor heart rate. There were significant falls in systolic blood pressure during captopril dosing alone, but there was no fall in blood pressure during combination therapy. Heart rates were higher during the combination than during captopril alone. The combination caused sedation, but neither captopril nor naloxone alone had any behavioral effects. Modification of the acute circulatory effects of captopril by naloxone suggests a role for endogenous opioids in the responses to converting enzyme inhibition. The sedation caused by the combination raises the possibility that captopril may exert central nervous actions in man.
卡托普利在体外可抑制内源性阿片类物质的代谢,并在体内增强其作用。我们检验了内源性阿片类物质参与卡托普利对人体作用的假说。在一项采用拉丁方设计的双盲、安慰剂对照研究中,对8名血压正常的健康男性受试者,检测了口服卡托普利、静脉注射纳洛酮及其联合用药后的急性心血管和自主神经效应。纳洛酮既未改变血压,也未改变心率。单独服用卡托普利期间收缩压显著下降,但联合治疗期间血压未下降。联合用药时的心率高于单独服用卡托普利时。联合用药引起镇静作用,但单独使用卡托普利或纳洛酮均无任何行为学效应。纳洛酮对卡托普利急性循环效应的影响提示内源性阿片类物质在血管紧张素转换酶抑制反应中发挥作用。联合用药引起的镇静作用增加了卡托普利可能对人体产生中枢神经作用的可能性。