Crumb W J
Department of Pediatrics, Tulane University School of Medicine, New Orleans, Louisiana 70112-2699, USA.
Br J Pharmacol. 1999 Feb;126(3):575-80. doi: 10.1038/sj.bjp.0702273.
The antihistamine loratadine is widely prescribed for the treatment of symptoms associated with allergies. Although generally believed to be free of adverse cardiac effects, there are a number of recent reports suggesting that loratadine use may be associated with arrhythmias, in particular atrial arrhythmias. Nothing is known regarding the potassium channel blocking properties of loratadine in human cardiac cells. Using the whole-cell patch clamp technique, the effects of loratadine on the transient outward K current (Ito), sustained current (Isus), and current measured at -100 mV (IK1 and Ins), the major inward and outward potassium currents present in human atrial myocytes, were examined in order to provide a possible molecular mechanism for the observed atrial arrhythmias reported with loratadine use. Loratadine rate-dependently inhibited Ito at therapeutic concentrations with 10 nM loratadine reducing Ito amplitude at a pacing rate of 2 Hz by 34.9+/-6.0%. In contrast, loratadine had no effect on either Isus or current measured at -100 mV. These results may provide a possible mechanism for the incidences of supraventricular arrhythmias reported with the use of loratadine.
抗组胺药氯雷他定被广泛用于治疗与过敏相关的症状。尽管一般认为其无不良心脏影响,但最近有许多报告表明,使用氯雷他定可能与心律失常有关,尤其是房性心律失常。关于氯雷他定在人心脏细胞中的钾通道阻断特性尚不清楚。为了为使用氯雷他定后观察到的房性心律失常提供一种可能的分子机制,采用全细胞膜片钳技术,研究了氯雷他定对人心房肌细胞中主要的内向和外向钾电流,即瞬时外向钾电流(Ito)、持续电流(Isus)以及在-100 mV处测量的电流(IK1和Ins)的影响。氯雷他定在治疗浓度下呈速率依赖性抑制Ito,10 nM氯雷他定在2 Hz起搏频率下使Ito幅度降低34.9±6.0%。相比之下,氯雷他定对Isus或在-100 mV处测量的电流均无影响。这些结果可能为使用氯雷他定后报告的室上性心律失常的发生提供一种可能的机制。