Amlie J P, Refsum H, Landmark K
Acta Pharmacol Toxicol (Copenh). 1979 Mar;44(3):185-90. doi: 10.1111/j.1600-0773.1979.tb02315.x.
The effect of nifedipine, a calcium-antagonistic drug, was studied on the electrophysiology of the right ventricle in the dog heart in situ. Monophasic action potential recordings were obtained by the suction electrode technique and refractoriness was measured by means of programmed electrical stimulation. Pentobarbital anaesthesia was used. As the basic cardiac effects of nifedipine can be altered by the release of catecholamines from sympathetic nerves of the heart and vessels, the dogs were pretreated with the beta-adrenergic receptor blocking agent acebutolol which increased the action potential duration and the refractoriness. Intravenous injection of nifedipine 30 microgram/kg body weight decreased the times for 50 and 90 per cent repolarization of the monophasic action potential and to a smaller extent the effective and functional refractory period. It is suggested that nifedipine decreases the action potential duration and the refractoriness of the right ventricle of the dog heart in situ due to a direct effect of the drug on the myocardium.
研究了钙拮抗剂硝苯地平对犬原位心脏右心室电生理的影响。采用吸引电极技术记录单相动作电位,并通过程控电刺激测量不应期。采用戊巴比妥麻醉。由于硝苯地平的基本心脏效应可因心脏和血管交感神经释放儿茶酚胺而改变,因此先用β-肾上腺素能受体阻滞剂醋丁洛尔对犬进行预处理,该药物可延长动作电位时程和不应期。静脉注射硝苯地平30微克/千克体重可缩短单相动作电位50%和90%复极化的时间,并在较小程度上缩短有效不应期和功能不应期。提示硝苯地平对犬原位心脏右心室动作电位时程和不应期的缩短作用是由于药物对心肌的直接作用。