乌巴因与钙通道阻滞剂对离体大鼠心脏收缩力的拮抗作用。

Journal de pharmacologie Pub Date : 1986-10-01
X Favereau, S Dunica, B Chevallier, C Mouas, B Swynghedauw
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引用次数: 0

摘要

钙通道阻滞剂和心脏糖苷的同时处方是心脏病学中常用的治疗组合,尽管其对肌力变性的影响尚未得到真正的评估。在恒定冠状动脉压灌注、恒定频率起搏和左心室球囊作用的离体大鼠心脏中,研究了这种关联。由于肌力作用取决于心肌收缩力的基本水平,控制了hypocontractile通过降低外部钙水平0.25毫米。同样的初始收缩压(45毫米汞柱)和+ dP / dTmax(150毫米汞柱X s - 1) 10(5)米乌本苷的影响肌肉收缩的效果大大减少明显的10 (6)M维拉帕米或10 (7)M硝苯地平在2.5毫米氯化钙比外部钙浓度低0.25毫米(增加+ dP / + / - 4 dTmax 35%, 29% + / - 6和110% + / - 18分别)。由于我们知道洋地黄的肌力特性可能是由于缓慢的钙向内电流的增加,我们得出结论,观察到的效果可能是由于钙阻滞剂阻断了这些通道。
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The antagonistic effects of ouabain and calcium channel blockers on the contractility of the isolated rat heart.

The simultaneous prescription of a calcium channel blocker and a cardiac glycoside is a frequently used therapeutic combination in cardiology, although its consequences on inotropism have not been really evaluated. This association is studied on isolated rat heart perfused at constant coronary pressure, paced at a constant frequency and working against a left intraventricular balloon. Since the inotropic effects are dependent on the basic level of myocardium contractility, controls were made hypocontractile by lowering external calcium level to 0.25 mM. For the same initial systolic pressure (45 mm Hg) and + dP/dTmax (150 mm Hg X s-1) the inotropic effect of 10(-5) M ouabain was significantly less pronounced in the presence of 10(-6) M verapamil or 10(-7) M nifedipine at 2.5 mM CaCl2 than at the low external calcium concentration of 0.25 mM (increasing the + dP/dtmax by 35% +/- 4, 29% +/- 6 and 110% +/- 18 respectively). Since we know that the inotropic properties of digitalis are probably due to an increase of the slow calcium inward current, we conclude that the observed effect would be due to a blockade of these channels by calcium blockers.

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