Wilkins M R, Woods K L, Jack D B, Kendall M J, Laugher S J
Eur J Clin Pharmacol. 1985;28(2):113-7. doi: 10.1007/BF00609676.
In a placebo controlled exercise protocol using healthy volunteers the effects of nadolol 80 mg and 160 mg orally and of nadolol 80 mg during treatment with nifedipine 20 mg 8 hourly were compared. Resting systolic and diastolic blood pressures were reduced by both nifedipine (p less than 0.05) and nadolol (p less than 0.01) acting alone. An unexpected finding was that nifedipine alone significantly inhibited exercise tachycardia (p less than 0.01) (8 to 12 h post dose). Predictably both doses of nadolol produced significant reduction in exercise tachycardia which was still apparent at 24 h. There was a linear relationship between log10 plasma nadolol concentration and reduction in exercise heart rate. The combined inhibitory effects of nifedipine and nadolol 80 mg on exercise heart rate showed partial additivity but did not summate. There was no pharmacokinetic interaction between the 2 drugs. The inhibition of exercise tachycardia by nifedipine, not previously documented, is consistent with an effect of the drug on the sinus node, as has been reported in in-vitro studies, and may contribute to the drugs efficacy in angina.
在一项使用健康志愿者的安慰剂对照运动试验方案中,比较了口服80毫克和160毫克纳多洛尔的效果,以及在每8小时服用20毫克硝苯地平治疗期间服用80毫克纳多洛尔的效果。单独使用硝苯地平(p<0.05)和纳多洛尔(p<0.01)均可降低静息收缩压和舒张压。一个意外发现是,单独使用硝苯地平可显著抑制运动性心动过速(p<0.01)(给药后8至12小时)。可以预见,两种剂量的纳多洛尔均可显著降低运动性心动过速,在24小时时仍很明显。log10血浆纳多洛尔浓度与运动心率降低之间存在线性关系。硝苯地平和80毫克纳多洛尔对运动心率的联合抑制作用显示出部分相加性,但未达到总和。两种药物之间没有药代动力学相互作用。硝苯地平对运动性心动过速的抑制作用以前未被记录,这与该药物对窦房结的作用一致,如体外研究中所报道的,并且可能有助于该药物在心绞痛中的疗效。