Suppr超能文献

低钾血症致心律失常性的发生机制。

Mechanisms of hypokalemia-induced ventricular arrhythmogenicity.

机构信息

Department of Biomedical Sciences, The Danish National Research Foundation Centre for Cardiac Arrhythmia, The Panum Institute, University of Copenhagen, Blegdamsvej 3, 2200 Copenhagen N, Denmark.

出版信息

Fundam Clin Pharmacol. 2010 Oct;24(5):547-59. doi: 10.1111/j.1472-8206.2010.00835.x.

Abstract

Hypokalemia is a common biochemical finding in cardiac patients and may represent a side effect of diuretic therapy or result from endogenous activation of renin-angiotensin system and high adrenergic tone. Hypokalemia is independent risk factor contributing to reduced survival of cardiac patients and increased incidence of arrhythmic death. Animal studies demonstrate that hypokalemia-induced arrhythmogenicity is attributed to prolonged ventricular repolarization, slowed conduction, and abnormal pacemaker activity. The prolongation of ventricular repolarization in hypokalemic setting is caused by inhibition of outward potassium currents and often associated with increased propensity for early afterdepolarizations. Slowed conduction is attributed to membrane hyperpolarization and increased excitation threshold. Abnormal pacemaker activity is attributed to increased slope of diastolic depolarization in Purkinje fibers, as well as delayed afterdepolarizations caused by Ca2+ overload secondary to inhibition of Na+--K+ pump and stimulation of the reverse mode of the Na+--Ca2+ exchange. Hypokalemia effect on repolarization is not uniform at distinct ventricular sites thereby contributing to amplified spatial repolarization gradients which promote unidirectional conduction block. In hypokalemic heart preparations, the prolongation of action potential may be associated with shortening of effective refractory period, thus increasing the propensity for ventricular re-excitation over late phase of repolarization. Shortened refractoriness and slowed conduction contribute to reduced excitation wavelength thereby facilitating re-entry. The interplay of triggering factors (early and delayed afterdepolarizations, oscillatory prepotentials in Purkinje fibers) and a favorable electrophysiological substrate (unidirectional conduction block, reduced excitation wavelength, increased critical interval for ventricular re-excitation) may account for the mechanism of life-threatening tachyarrhythmias in hypokalemic patients.

摘要

低血钾症是心脏病人常见的生化异常,可能是利尿剂治疗的副作用,也可能是肾素-血管紧张素系统的内源性激活和高肾上腺素能张力的结果。低血钾症是导致心脏病人存活率降低和心律失常性死亡发生率增加的独立危险因素。动物研究表明,低血钾引起的心律失常性是由于心室复极延长、传导减慢和异常起搏活动。低血钾状态下心室复极的延长是由于外向钾电流的抑制,并且常伴有早期后除极的增加倾向。传导减慢归因于膜超极化和兴奋阈值增加。异常起搏活动归因于浦肯野纤维舒张期去极化斜率增加,以及由于 Na+-K+泵抑制和 Na+-Ca2+交换反向模式刺激引起的 Ca2+超载导致的延迟后除极。低血钾对不同心室部位复极的影响并不一致,从而导致空间复极梯度放大,促进单向传导阻滞。在低钾心脏标本中,动作电位的延长可能与有效不应期缩短有关,从而增加了在复极晚期心室再次兴奋的倾向。缩短的不应期和传导减慢导致兴奋波长减少,从而促进折返。触发因素(早期和延迟后除极、浦肯野纤维中的振荡预潜能)和有利的电生理基质(单向传导阻滞、兴奋波长减少、心室再次兴奋的临界间隔增加)的相互作用可能解释了低钾血症患者危及生命的心动过速性心律失常的机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验