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首页> 外文期刊>Life sciences >Cardioprotection without cardiosuppression by SEA0400, a novel inhibitor of Na+-Ca2+ exchanger, during ischemia and reperfusion in guinea-pig myocardium
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Cardioprotection without cardiosuppression by SEA0400, a novel inhibitor of Na+-Ca2+ exchanger, during ischemia and reperfusion in guinea-pig myocardium

机译:SEA0400(一种新型的Na + -Ca2 +交换抑制剂)在豚鼠心肌缺血和再灌注过程中的心脏保护作用而无心脏抑制作用

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摘要

The effect of SEA0400, a novel Na+-Ca2+ exchanger inhibitor, on mechanical and electrophysiological parameters of coronary-perfused guinea-pig right ventricular tissue preparation was examined during no-flow ischemia and reperfusion. Contractile force and action potential duration were decreased during no-flow ischemia, while the resting tension was increased. Upon reperfusion, transient arrhythmias were observed and contractile force returned to less than 50% of preischemic values. SEA0400 (1 mu M) had no effect on the decline in contractile force during the no-flow ischemia, but abolished the rise in resting tension. SEA0400 significantly improved the recovery of contractile force after reperfusion to about 80% of the preischemic value. SEA0400 had no effect on the action potential under normal conditions and during ischemia, but significantly improved the recovery of action potential duration after reperfusion. Enhancement of the recovery of contractile force during reperfusion by SEA0400 was also observed when the drug was applied only before and during the ischemic period and when the drug was applied only during reperfusion. The present results indicate that inhibition of Na+-Ca2+ exchanger either during ischemia or during reperfusion exerts cardioprotective effects and enhances the recovery of myocardial contractile function. (c) 2005 Elsevier Inc. All rights reserved.
机译:在无血流缺血和再灌注期间,检查了SEA0400(一种新型的Na + -Ca2 +交换抑制剂)对冠状动脉灌注的豚鼠右心室组织制剂的机械和电生理参数的影响。无血流缺血期间收缩力和动作电位持续时间减少,而静息张力增加。再灌注后,观察到短暂性心律不齐,收缩力恢复到缺血前值的不到50%。 SEA0400(1μM)对无血流缺血期间的收缩力下降没有影响,但消除了静息张力的上升。 SEA0400将再灌注后的收缩力恢复显着提高至缺血前值的80%。 SEA0400在正常情况下和缺血期间对动作电位没有影响,但显着提高了再灌注后动作电位持续时间的恢复。当仅在缺血期之前和期间以及在仅在再灌注期间施用药物时,也观察到通过SEA0400增强了在再灌注期间收缩力的恢复。本结果表明,在局部缺血或再灌注期间抑制Na + -Ca 2+交换体发挥心脏保护作用,并增强心肌收缩功能的恢复。 (c)2005 Elsevier Inc.保留所有权利。

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