Wolffenbuttel B H, Verdouw P D
Arch Int Pharmacodyn Ther. 1983 Nov;266(1):83-92.
The effects of intracoronary nifedipine on myocardial performance were studied in the absence and presence of beta-blockade with propranolol (0.5 mg X kg-1 i.v. bolus + infusion). In anaesthetized pigs nifedipine (0.025, 0.05 and 0.5 microgram X kg-1 X min-1) produced dose-dependent increases in coronary flow (up to 65% from base line, 39 +/- 4 ml X min-1) and decreases in myocardial O2-consumption (MO2-cons, up to 50%, base line 3.10 +/- 0.34 ml X min-1). The two lower doses caused a negligible depression of systemic haemodynamics (cardiac output, CO smaller than 8%, base line 2.70 +/- 0.14 l X min-1; mean arterial pressure, MAP smaller than 10%, base line 10.9 +/- 0.4 kPa), but after the highest dose MAP and CO decreased by 20%. Following pretreatment with propranolol, the effects of nifedipine on cardiac output and mean arterial pressure were additive for the two lower doses, but with 0.5 microgram X kg-1 X min-1 the superimposed effects were less pronounced. Nifedipine alone was able to increase cardiac efficiency, defined as (MAP X CO)/MO2-cons, by 10-20%, but failed to improve cardiac efficiency when this was previously reduced by administration of propranolol. Our data indicate that intracoronary infusion of nifedipine can be performed safely when beta-blockade is already instituted, but that nifedipine alone decreases MO2-consumption to the same level as the combination, with less depression of global myocardial function.
在使用普萘洛尔(0.5mg·kg⁻¹静脉推注+输注)进行β受体阻滞的情况下和未进行β受体阻滞时,研究了冠状动脉内硝苯地平对心肌功能的影响。在麻醉猪中,硝苯地平(0.025、0.05和0.5μg·kg⁻¹·min⁻¹)使冠状动脉血流量呈剂量依赖性增加(最高比基线增加65%,基线为39±4ml·min⁻¹),心肌耗氧量(MO₂-cons)降低(最高降低50%,基线为3.10±0.34ml·min⁻¹)。两个较低剂量对全身血流动力学的抑制作用可忽略不计(心输出量,CO降低小于8%,基线为2.70±0.14l·min⁻¹;平均动脉压,MAP降低小于10%,基线为10.9±0.4kPa),但最高剂量后MAP和CO降低了20%。用普萘洛尔预处理后,硝苯地平对心输出量和平均动脉压的影响在两个较低剂量时是相加的,但在0.5μg·kg⁻¹·min⁻¹时叠加效应不太明显。单独使用硝苯地平能够使心脏效率(定义为(MAP×CO)/MO₂-cons)提高10%-20%,但在预先因给予普萘洛尔而降低心脏效率时,未能改善心脏效率。我们的数据表明,当已经进行β受体阻滞时,冠状动脉内输注硝苯地平可以安全进行,但单独使用硝苯地平可将MO₂-cons降低到与联合使用时相同的水平,且对整体心肌功能的抑制作用较小。