...
首页> 外文期刊>Fundamental & clinical pharmacology. >Sparfloxacin but not levofloxacin or ofloxacin prolongs cardiac repolarization in rabbit Purkinje fibers.
【24h】

Sparfloxacin but not levofloxacin or ofloxacin prolongs cardiac repolarization in rabbit Purkinje fibers.

机译:司帕沙星(而非左氧氟沙星或氧氟沙星)可延长兔Purkinje纤维的心脏复极化。

获取原文
获取原文并翻译 | 示例
           

摘要

Sparfloxacin, a fluoroquinolone antibacterial, has been reported to prolong cardiac repolarization in some patients. In this study, we have investigated the in vitro cardiac electrophysiological effects of two other fluoroquinolones, levofloxacin and ofloxacin, and compared them with those exerted by sparfloxacin. Cardiac action potentials have been recorded from rabbit Purkinje fibers using conventional glass microelectrodes. The influence of a sudden decrease in stimulation rate on repolarization is examined. It is found that ofloxacin and levofloxacin (1-100 microM) do not alter the action potential parameters even at a concentration as high as 100 microM. The stimulation rate is without effect on repolarization. On the contrary, sparfloxacin (1-100 microM) lengthens concentration-dependently the duration of action potential, this effect being significant from the concentration of 10 microM. A non significant decrease in maximal rate of rise of phase 0 depolarization was observed at the concentration of 100 microM. Under low stimulation rate, the sparfloxacin-induced prolonging effect was magnified and early afterdepolarizations occurred in one of seven fibers from the concentration of 30 microM and in four other fibers at the concentration of 100 microM. These results suggest that levofloxacin and ofloxacin had no effect on cardiac cellular electrophysiology whereas sparfloxacin exerts pure class III electrophysiological effects, which can explain the prolongation of QT interval observed clinically in some patients and might become arrhythmogenic in the presence of other predisposing factors.
机译:据报道,氟喹诺酮类抗菌药司帕沙星可延长某些患者的心脏复极。在这项研究中,我们研究了另外两种氟喹诺酮类药物左氧氟沙星和氧氟沙星的体外心脏电生理作用,并将它们与司帕沙星的作用进行了比较。已经使用常规玻璃微电极从兔浦肯野纤维记录了心脏动作电位。检查了刺激速率突然降低对复极化的影响。发现氧氟沙星和左氧氟沙星(1-100 microM)即使在高达100 microM的浓度下也不会改变动作电位参数。刺激速率对复极没有影响。相反,司帕沙星(1-100 microM)浓度依赖地延长了动作电位的持续时间,这种作用从10 microM的浓度开始就很明显。在浓度为100 microM时,观察到0相去极化的最大上升速率没有明显降低。在低刺激速率下,司帕沙星诱导的延长作用被放大,并且从浓度为30 microM的七种纤维之一和浓度为100 microM的其他四种纤维中发生了早期的去极化作用。这些结果表明,左氧氟沙星和氧氟沙星对心脏细胞的电生理没有影响,而司帕沙星具有纯的III类电生理作用,这可以解释某些患者在临床上观察到的QT间隔延长,并且在存在其他诱发因素的情况下可能会导致心律失常。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号