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伊拉地平对陈旧性心肌梗死血流动力学参数及室性心动过速的影响。

Effects of isradipine on hemodynamic parameters and ventricular tachycardia in healed myocardial infarction.

作者信息

de Langen C D, van den Toren E W, Tio R A, Lie K I, Wesseling H

机构信息

Department of Clinical Pharmacology, University of Groningen, The Netherlands.

出版信息

J Cardiovasc Pharmacol. 1990 Feb;15(2):254-8. doi: 10.1097/00005344-199002000-00012.

Abstract

The calcium-entry blocker isradipine was tested in a closed-chest pig model for chronic myocardial infarction. Ischemia was evoked in anesthetized pigs (25-35 kg) by inflating a catheter balloon in the left anterior descending coronary artery for at least 45 min. Hemodynamic monitoring and signal averaging of X, Y, and Z electrocardiographic leads were performed (150 beats, filtered at 50 Hz). After reperfusion, all animals developed an accelerated idioventricular rhythm and high creatine kinase (CPK) plasma levels. Coronary venous purines and catecholamines increased transiently. Two hours after reperfusion, heart rate was elevated from the initial 87.5 +/- 6.3 to 126 +/- 6.4 beats/min (p less than 0.01) and the pressure-rate product (PRP, an index of oxygen demand) from 9,530 +/- 630 to 11,950 +/- 790 mm Hg/min (p less than 0.05). After 2 weeks, six surviving pigs had a decreased stroke volume (98 +/- 18 versus the initial 124 +/- 14 microliters/kg, p less than 0.05), a prolonged high-frequency signal-averaged QRS duration (81.2 +/- 6.5 versus 65.7 +/- 2.9 ms, initially; p less than 0.05), and ventricular tachycardias (VTs), inducible by programmed electrical stimulation (PES). After the infusion of isradipine (1 microgram/kg/min for 30 min), the cardiac index increased from 92 +/- 14 to 133 +/- 8.7 ml/min.kg (p less than 0.02). Even at a higher heart rate, the PRP dropped from 12,600 +/- 1,900 to 10,560 +/- 1,400 mm Hg/min (p less than 0.05). Sustained monomorphic tachycardias were inducible in five pigs before and in three pigs after isradipine, and no deterioration of the signal-averaged electrocardiogram parameters was found.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在慢性心肌梗死的闭胸猪模型中对钙通道阻滞剂伊拉地平进行了测试。通过在麻醉的猪(25 - 35千克)的左前降支冠状动脉中充盈导管球囊至少45分钟来诱发缺血。进行血流动力学监测以及对X、Y和Z心电图导联进行信号平均(150次搏动,以50赫兹滤波)。再灌注后,所有动物均出现加速性室性自主心律和高肌酸激酶(CPK)血浆水平。冠状静脉嘌呤和儿茶酚胺短暂升高。再灌注2小时后,心率从最初的87.5±6.3次/分钟升高至126±6.4次/分钟(p<0.01),压力 - 心率乘积(PRP,氧需求指标)从9530±630毫米汞柱/分钟升高至11950±790毫米汞柱/分钟(p<0.05)。2周后,6只存活的猪每搏输出量减少(98±18微升/千克,而最初为124±14微升/千克,p<0.05),高频信号平均QRS时限延长(最初为65.7±2.9毫秒,现为81.2±6.5毫秒;p<0.05),并且可通过程序电刺激(PES)诱发室性心动过速(VT)。输注伊拉地平(1微克/千克/分钟,持续30分钟)后,心脏指数从92±14升高至133±8.7毫升/分钟·千克(p<0.02)。即使在心率较高时,PRP也从12600±1900降至10560±1400毫米汞柱/分钟(p<0.05)。在伊拉地平给药前,5只猪可诱发持续性单形性心动过速,给药后3只猪可诱发,且未发现信号平均心电图参数恶化。(摘要截断于250字)

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