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硝苯地平与尼群地平急性血流动力学效应的比较及尼群地平对人体电生理效应的研究。

Comparison of the acute hemodynamic effects of nifedipine with nitrendipine and a study of the electrophysiological effects of nitrendipine in man.

作者信息

Rutsch W, Schmutzler H

出版信息

J Cardiovasc Pharmacol. 1984;6 Suppl 7:S1011-5.

PMID:6085358
Abstract

Calcium antagonists are known to have an inhibitory effect on the contractile status of the smooth muscle of the arterioles, the muscle fibers of the heart, and the cardiac conduction system, especially the atrioventricular node. The vasodilatation that is produced may be observed in the coronary arteries but predominates in the peripheral resistance vessels. Nifedipine and its 1,4-dihydropyridine derivative, nitrendipine, are not only useful in coronary artery disease but also have potential as antihypertensive agents. The acute hemodynamic effects of both nifedipine and nitrendipine, administered in a 1.0 mg intravenous dose, were studied. The compounds were randomly allocated to six patients, where each served as his own control. In addition, the effect of 1 mg of nitrendipine intravenously on the electrophysiological impulse formation and conduction was investigated in a second group of six patients. There were substantial differences in the intensity and duration of the hemodynamic effects of both drugs. The total peripheral resistance (TPR) fell after nifedipine from 1,730 +/- 240 to 1,280 +/- 120 and after nitrendipine from 1,960 +/- 420 to 1,200 +/- 150 dynes-s-cm-5. There was a concurrent significant reduction in the systolic aortic and left ventricular pressure after nifedipine and nitrendipine from 152 +/- 8 to 128 +/- 13 and 161 +/- 19 to 122 +/- 18 mm Hg, respectively. Heart rate increased due to baroreceptor stimulation by 21% with nifedipine and by 32% with nitrendipine. From the results of the electrophysiological study, nitrendipine did not have any significant effect on the sinus or atrioventricular node function. The substance may be safely used in patients with conduction disturbances.

摘要

已知钙拮抗剂对小动脉平滑肌、心肌纤维及心脏传导系统,尤其是房室结的收缩状态有抑制作用。所产生的血管扩张在冠状动脉中可见,但在外周阻力血管中更为明显。硝苯地平及其1,4 - 二氢吡啶衍生物尼群地平不仅对冠状动脉疾病有用,而且有作为抗高血压药物的潜力。研究了静脉注射1.0毫克剂量的硝苯地平和尼群地平的急性血流动力学效应。将这些化合物随机分配给6名患者,每名患者均作为自身对照。此外,在另一组6名患者中研究了静脉注射1毫克尼群地平对电生理冲动形成和传导的影响。两种药物的血流动力学效应在强度和持续时间上存在显著差异。硝苯地平给药后总外周阻力(TPR)从1730±240降至1280±120,尼群地平给药后从1960±420降至1200±150达因·秒·厘米⁻⁵。硝苯地平和尼群地平给药后,收缩期主动脉压和左心室压同时显著降低,分别从152±8降至128±13毫米汞柱和从161±19降至122±18毫米汞柱。由于压力感受器刺激,心率在硝苯地平作用下增加21%,在尼群地平作用下增加32%。从电生理研究结果来看,尼群地平对窦房结或房室结功能没有任何显著影响。该物质可安全用于有传导障碍的患者。

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