Ajayi A A, Rubin P C, Reid J L
Br J Clin Pharmacol. 1986 May;21(5):543-5. doi: 10.1111/j.1365-2125.1986.tb02840.x.
Six patients maintained on 50-100 mg captopril, for 2-25 months, were administered captopril 50 mg orally, together with either naloxone or 0.9% saline vehicle (placebo) given intravenously, in a double-blind crossover study. Naloxone did not appear to modify the circulatory effects of captopril in these patients, in contrast to earlier findings after acute captopril administration in normotensives. The results do not support an important endogenous opioid role in the chronic antihypertensive effect of captopril, but provide evidence that different mechanisms may contribute to the early short term falls in blood pressure, compared to the later long term effects.
在一项双盲交叉研究中,对6名服用50 - 100毫克卡托普利持续2 - 25个月的患者,口服50毫克卡托普利,并静脉注射纳洛酮或0.9%生理盐水载体(安慰剂)。与正常血压者急性服用卡托普利后的早期发现相反,纳洛酮似乎并未改变这些患者中卡托普利的循环效应。结果不支持内源性阿片类物质在卡托普利的慢性降压作用中起重要作用,但提供了证据表明,与后期长期效应相比,不同机制可能导致早期短期血压下降。