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决奈达隆和胺碘酮对心肌梗死愈合动物的血流动力学及抗肾上腺素能作用

Hemodynamic and antiadrenergic effects of dronedarone and amiodarone in animals with a healed myocardial infarction.

作者信息

Djandjighian L, Planchenault J, Finance O, Pastor G, Gautier P, Nisato D

机构信息

Cardiovascular/Thrombosis Research Department, Sanofi-Synthelabo, Montpellier, France.

出版信息

J Cardiovasc Pharmacol. 2000 Sep;36(3):376-83. doi: 10.1097/00005344-200009000-00014.

Abstract

The hemodynamic and antiadrenergic effects of dronedarone, a noniodinated compound structurally related to amiodarone, were compared with those of amiodarone after prolonged oral administration, both at rest and during sympathetic stimulation in conscious dogs with a healed myocardial infarction. All dogs (n = 6) randomly received orally dronedarone (10 and 30 mg/kg), amiodarone (10 and 30 mg/kg), and placebo twice daily for 7 days, with a 3-week washout between consecutive treatments. Heart rate (HR), mean arterial pressure (MBP), positive rate of increase of left ventricular pressure (+LVdP/dt), echocardiographically assessed left ventricular ejection fraction (LVEF), and fractional shortening (FS), as well as chronotropic response to isoproterenol and exercise-induced sympathetic stimulation were evaluated under baseline and posttreatment conditions. Resting values of LVEF, FS, +LVdP/dt, and MBP remained unchanged whatever the drug and the dosing regimen, whereas resting HR was significantly and dose-dependently lowered after dronedarone and to a lesser extent after amiodarone. Both dronedarone and amiodarone significantly reduced the exercise-induced tachycardia and, at the highest dose, decreased the isoproterenol-induced tachycardia. Thus, dronedarone and amiodarone displayed a similar level of antiadrenergic effect and did not impair the resting left ventricular function. Consequently, dronedarone might be particularly suitable for the treatment and prevention of various clinical arrhythmias, without compromising the left ventricular function.

摘要

将结构上与胺碘酮相关的非碘化化合物决奈达隆的血流动力学和抗肾上腺素能作用,与胺碘酮在长期口服给药后,在患有陈旧性心肌梗死的清醒犬静息时和交感神经刺激期间的作用进行了比较。所有犬(n = 6)随机口服决奈达隆(10和30 mg/kg)、胺碘酮(10和30 mg/kg)和安慰剂,每日两次,共7天,连续治疗之间有3周的洗脱期。在基线和治疗后条件下评估心率(HR)、平均动脉压(MBP)、左心室压力上升阳性率(+LVdP/dt)、超声心动图评估的左心室射血分数(LVEF)和缩短分数(FS),以及对异丙肾上腺素的变时反应和运动诱发的交感神经刺激。无论药物和给药方案如何,LVEF、FS、+LVdP/dt和MBP的静息值均保持不变,而决奈达隆给药后静息HR显著且剂量依赖性降低,胺碘酮给药后降低程度较小。决奈达隆和胺碘酮均显著降低运动诱发的心动过速,且在最高剂量时降低异丙肾上腺素诱发的心动过速。因此,决奈达隆和胺碘酮显示出相似水平的抗肾上腺素能作用,且不损害静息左心室功能。因此,决奈达隆可能特别适合治疗和预防各种临床心律失常,而不影响左心室功能。

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