Dorigo P, Maragno I
Arch Int Pharmacodyn Ther. 1985 Mar;274(1):80-8.
The nature of the digoxin-verapamil interaction was explored "in vitro" by determining the effect of verapamil on digoxin-induced inotropism in isolated guinea-pig atria. Verapamil, at concentrations (2.10(-8)-3.10(-8)M) too low to have any significant effect on the amplitude or frequency of the basal contractile activity, reduced the inotropic action of digoxin in all experimental circumstances, i.e. in spontaneously beating atria from reserpine-treated or untreated animals, in electrically driven (at 1 Hz frequency stimulation) left atria. The results obtained suggest that a competitive antagonism exists between verapamil and digoxin. In spontaneously beating atria an apparently competitive antagonism was also observed between verapamil and ouabain. The interaction observed between cardiac glycosides and the Ca++ channel blocker suggests that Ca++ movements across the sarcolemma may influence the inotropic effect of digitalis or its toxicity.
通过测定维拉帕米对豚鼠离体心房中地高辛诱导的变力作用的影响,在“体外”研究了地高辛与维拉帕米相互作用的性质。维拉帕米浓度(2×10⁻⁸ - 3×10⁻⁸M)过低,对基础收缩活动的幅度或频率无任何显著影响,但在所有实验条件下均降低了地高辛的变力作用,即在利血平处理或未处理动物的自发搏动心房中,以及在电驱动(1Hz频率刺激)的左心房中。所得结果表明维拉帕米与地高辛之间存在竞争性拮抗作用。在自发搏动心房中,维拉帕米与哇巴因之间也观察到明显的竞争性拮抗作用。强心苷与钙通道阻滞剂之间观察到的相互作用表明,钙离子跨肌膜的移动可能会影响洋地黄的变力作用或其毒性。