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选择性血栓素和前列腺素内过氧化物拮抗剂L655,240对缺血再灌注诱导的心律失常的影响。

The effects of L655,240, a selective thromboxane and prostaglandin endoperoxide antagonist, on ischemia- and reperfusion-induced cardiac arrhythmias.

作者信息

Wainwright C L, Parratt J R

机构信息

Department of Physiology and Pharmacology, Royal College, University of Strathclyde, Glasgow, Scotland.

出版信息

J Cardiovasc Pharmacol. 1988 Sep;12(3):264-71. doi: 10.1097/00005344-198809000-00002.

DOI:10.1097/00005344-198809000-00002
PMID:2464097
Abstract

The purpose of this investigation was to provide a detailed analysis of the effects of the thromboxane antagonist L655,240 (0.3 mg/kg i.v.) on early ischemia- and reperfusion-induced arrhythmias in a canine model of coronary artery occlusion. In a dose that abolished the pulmonary response to U46619, L655,240 attenuated markedly the severity of those arrhythmias that resulted from reperfusion of the myocardium; survival from the combined occlusion-reperfusion insult was increased from 10% in control animals to 70% in dogs administered L655,240. Drug intervention did not significantly alter the total number of arrhythmias during the period of ischemia, but a detailed analysis of the different types of arrhythmia that occurred during this period showed that L655,240 significantly reduced those arrhythmias in phase 1a (0-10 min of occlusion) without affecting the later phase 1b arrhythmias. This was particularly shown in the marked reduction in the number of salvos (couplets and triplets) during this period. Neither those arrhythmias occurring later in the ischaemia period (phase 1b) nor the total number of single ectopics and salvos or the incidence and duration of ventricular tachycardia was modified by L655,240. These results reveal that thromboxane antagonism protects especially against reperfusion-induced ventricular fibrillation and against early (phase 1a) ischemia-induced arrhythmias, possibly implicating a role for thromboxane in the genesis of these cardiac rhythm disturbances.

摘要

本研究的目的是详细分析血栓素拮抗剂L655,240(静脉注射0.3mg/kg)对犬冠状动脉闭塞模型中早期缺血和再灌注诱导的心律失常的影响。在消除肺对U46619反应的剂量下,L655,240显著减轻了心肌再灌注所致心律失常的严重程度;联合闭塞-再灌注损伤后的存活率从对照动物的10%提高到给予L655,240的犬的70%。药物干预并未显著改变缺血期间心律失常的总数,但对该期间发生的不同类型心律失常的详细分析表明,L655,240显著减少了1a期(闭塞0-10分钟)的心律失常,而不影响后期的1b期心律失常。这尤其表现为该期间连发(成对和三联律)数量的显著减少。L655,240对缺血后期(1b期)出现的心律失常、单个异位搏动和连发的总数或室性心动过速的发生率和持续时间均无影响。这些结果表明,血栓素拮抗作用尤其能预防再灌注诱导的心室颤动和早期(1a期)缺血诱导的心律失常,这可能意味着血栓素在这些心律失常的发生中起作用。

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1
The effects of L655,240, a selective thromboxane and prostaglandin endoperoxide antagonist, on ischemia- and reperfusion-induced cardiac arrhythmias.选择性血栓素和前列腺素内过氧化物拮抗剂L655,240对缺血再灌注诱导的心律失常的影响。
J Cardiovasc Pharmacol. 1988 Sep;12(3):264-71. doi: 10.1097/00005344-198809000-00002.
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