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维拉帕米对出生后个体发育期间离体灌注大鼠心脏收缩功能的影响。

Effect of verapamil on contractile function of the isolated perfused rat heart during postnatal ontogeny.

作者信息

Kolár F, Ost'ádal B, Papousek F

机构信息

Institute of Physiology, Czechoslovak Academy of Sciences, Prague.

出版信息

Basic Res Cardiol. 1990 Sep-Oct;85(5):429-34. doi: 10.1007/BF01931488.

Abstract

The negative inotropic effect of the calcium antagonist, verapamil, was compared in isolated hearts from 15-, 30-, 45-, 60-, and 90-day-old rats. Electrically paced hearts were perfused in vitro according to Langendorff, either under constant pressure or under constant flow conditions. An intraventricular-pressure curve was measured isovolumetrically and analyzed on-line using a microcomputer. Changes in pressure amplitude and maximum rate of pressure development were evaluated during a stepwise increase of the verapamil concentration in the perfusion solution (10(-9) - 3.3 x 10(-7) mol.l-1). It was found that the sensitivity of cardiac contractile function to verapamil declines gradually in the course of postnatal ontogeny. The higher sensitivity of the developing heart to calcium channel blockade is probably a consequence of a higher functional dependence of the immature myocardium on trans-sarcolemmal calcium influx.

摘要

在15日龄、30日龄、45日龄、60日龄和90日龄大鼠的离体心脏中,比较了钙拮抗剂维拉帕米的负性肌力作用。按照Langendorff法,在恒压或恒流条件下对电起搏的心脏进行体外灌注。等容测量心室压力曲线,并使用微型计算机进行在线分析。在灌注液中维拉帕米浓度逐步增加(10^(-9) - 3.3 x 10^(-7) mol·l^(-1))的过程中,评估压力幅度和压力上升最大速率的变化。结果发现,在出生后的个体发育过程中,心脏收缩功能对维拉帕米的敏感性逐渐下降。发育中心脏对钙通道阻滞的较高敏感性可能是由于未成熟心肌对跨肌膜钙内流的功能依赖性较高所致。

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