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新型III类抗心律失常药物RP 62719的正性肌力和变时性效应

[Positive inotropic and lusitropic effect of RP 62719, a new class III antiarrhythmia agent].

作者信息

Beregi J P, Escande D, Coudray N, Chemla D, Mestre M, Péry N, Lecarpentier Y

机构信息

Institut national de la santé et de la recherche médicale, Unité 275, LOA-ENSTA, Palaiseau.

出版信息

Arch Mal Coeur Vaiss. 1994 Feb;87(2):263-9.

PMID:7802535
Abstract

Antiarrhythmic drugs, especially the Class I family, exert a negative inotropic effect on the myocardium which is particularly undesirable in patients with depressed left ventricular function. Therefore, research has been directed to the development of new, more specific molecules of the Class III family. The authors studies the mechanical effects of RP 62719 on guinea pig left ventricular papillary muscle. This new molecule is a pure Class III antiarrhythmic, known to lengthen the duration of the cardiac action potential by selectively blocking the potassium current iK1 (inward rectifier K+ current). The mechanical parameters were determined during the phases of contraction and relaxation under isotonic and isometric conditions. At 0.2 and 2 microM concentrations, RP 62719 improved cardiac contraction under both isotonic and isometric conditions with an increase of about 30% of Vmax (p < 0.001), the maximum unloaded shortening velocity delta 1 (p < 0.001), the peak isometric active force normalized per cross-sectional area [AF/S (p < 0.001)]. At these two concentrations, a positive lusitropic effect (improved relaxation) was demonstrated by an increase in negative peak of derivative per mm2-dF/s and maximum lengthening velocity VR max (p < 0.01). At higher concentrations (20 microM), the inotropic and lusitropic effects were less marked with a bell-shaped form of the dose-effect curve. This study indicates that RP 62719 has moderate but significant positive inotropic and lusitropic effects. These actions could provide significant therapeutic advantages especially in patients cardiac failure.

摘要

抗心律失常药物,尤其是I类药物,对心肌有负性肌力作用,这在左心室功能降低的患者中尤为不利。因此,研究方向转向了开发III类家族新的、更具特异性的分子。作者研究了RP 62719对豚鼠左心室乳头肌的机械效应。这种新分子是一种纯III类抗心律失常药物,已知通过选择性阻断钾电流iK1(内向整流钾电流)来延长心脏动作电位的持续时间。在等张和等长条件下的收缩和舒张阶段测定机械参数。在0.2和2微摩尔浓度下,RP 62719在等张和等长条件下均改善了心脏收缩,Vmax(最大无负荷缩短速度)增加约30%(p<0.001),δ1(p<0.001),每横截面积归一化的峰值等长主动力[AF/S(p<0.001)]。在这两种浓度下,每平方毫米-dF/s导数的负峰值和最大延长速度VR max增加,证明了正性变时效应(改善舒张)(p<0.01)。在较高浓度(20微摩尔)下,变力和变时效应不那么明显,剂量-效应曲线呈钟形。这项研究表明,RP 62719具有中等但显著的正性变力和正性变时效应。这些作用可能具有显著的治疗优势,尤其是在心力衰竭患者中。

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