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硝苯地平与维拉帕米对兔心脏窦房结和房室结电活动直接影响的比较。

Comparison of the direct effects of nifedipine and verapamil on the electrical activity of the sinoatrial and atrioventricular nodes of the rabbit heart.

作者信息

Ning W, Wit A L

出版信息

Am Heart J. 1983 Aug;106(2):345-55. doi: 10.1016/0002-8703(83)90202-8.

Abstract

We compared the effects of nifedipine and verapamil on the rabbit sinus and atrioventricular nodes. Both drugs slowed the rate of impulse initiation by sinus node cells. Verapamil exerted a greater negative chronotropic effect at low concentrations, but at higher concentrations verapamil and nifedipine were equipotent. Nifedipine also reduced the amplitude of sinus node action potentials and the Vmax of phase O, effects which are identical to those previously described for verapamil. Both drugs slowed AV nodal conduction and prolonged refractory periods, but verapamil was more potent than nifedipine. Nifedipine reduced the amplitude of AV nodal action potentials and Vmax of phase O the same as verapamil. Nifedipine and verapamil, therefore, have nearly identical direct effects on the nodes. The failure of nifedipine to depress AV nodal conduction in situ and abolish reentrant AV nodal tachycardia is probably a result of the decreased sensitivity of the AV node to nifedipine compared to verapamil.

摘要

我们比较了硝苯地平和维拉帕米对兔窦房结和房室结的作用。两种药物均减慢窦房结细胞的冲动起始速率。维拉帕米在低浓度时产生更大的负性变时作用,但在高浓度时维拉帕米和硝苯地平的作用相当。硝苯地平还降低窦房结动作电位的幅度和0期最大上升速率,这些作用与先前描述的维拉帕米的作用相同。两种药物均减慢房室结传导并延长不应期,但维拉帕米比硝苯地平更有效。硝苯地平与维拉帕米一样降低房室结动作电位的幅度和0期最大上升速率。因此,硝苯地平和维拉帕米对这些节点具有几乎相同的直接作用。硝苯地平在原位未能抑制房室结传导并消除折返性房室结性心动过速,可能是因为与维拉帕米相比,房室结对硝苯地平的敏感性降低。

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