Endocardial role in arrhythmias induced by acute ventricular stretch and the involvement of Purkinje fibres, in isolated rat hearts

IF 2.1 Q3 PHYSIOLOGY Current research in physiology Pub Date : 2023-01-01 DOI:10.1016/j.crphys.2023.100098
Miriam Hurley , Sarbjot Kaur , Richard Walton , Amelia Power , Michel Haïssaguerre , Olivier Bernus , Marie-Louise Ward , Ed White
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引用次数: 2

Abstract

Purkinje fibres (PFs) play an important role in some ventricular arrhythmias and acute ventricular stretch can evoke mechanically-induced arrhythmias. We tested whether PFs and specifically TRPM4 channels, play a role in these mechanically-induced arrhythmias. Pseudo-ECGs and left ventricular (LV) activation, measured by optical mapping, were recorded in isolated, Langendorff-perfused, rat hearts. The LV endocardial surface was irrigated with experimental agents, via an indwelling catheter. The number and period of ectopic activations was measured during LV lumen inflation via an indwelling fluid-filled balloon (100 μL added over 2 s, maintained for 38 s). Mechanically-induced arrhythmias occurred during balloon inflation: they were multifocal, maximal in the first 5 s and ceased within 20 s. Optical mapping revealed activation patterns indicating PF-mediated and ectopic focal sources. Irrigation of the LV lumen with Lugol solution (IK/I2) for 10s reduced ectopics by 93% (n = 16, P < 0.001); with ablation of endocardial PFs confirmed by histology. Five min irrigation of the LV lumen with 50 μM 9-Phenanthrol, a blocker of TRPM4 channels, reduced ectopics by 39% (n = 15, P < 0.01). Immunohistochemistry confirmed that TRPM4 was more abundant in PFs than myocardium. Our results show that the endocardial surface plays an important role in these mechanically-induced ectopic activations. Ectopic activation patterns indicate a participation of PFs in these arrhythmias, with a potential involvement of TRPM4 channels, shown by the reduction of arrhythmias by 9-Phenanthrol.

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心内膜在离体大鼠心脏急性心室拉伸和浦肯野纤维累及引起的心律失常中的作用
浦肯野纤维(PFs)在某些室性心律失常中起着重要作用,急性心室拉伸可引起机械性心律失常。我们测试了PFs,特别是TRPM4通道,是否在这些机械诱导的心律失常中发挥作用。在Langendorff灌注的离体大鼠心脏中记录通过光学标测测量的伪心电图和左心室(LV)激活。通过留置导管用实验药物冲洗左心室心内膜表面。在左心室管腔充气期间,通过留置充液球囊(在2 s内添加100μL,维持38 s)测量异位激活的次数和周期。机械性心律失常发生在球囊扩张期间:它们是多灶性的,在最初的5秒内达到最大值,并在20秒内停止。光学标测显示激活模式指示PF介导的和异位的局灶源。用Lugol溶液(IK/I2)冲洗左心室内腔10秒,异位减少93%(n=16,P<;0.001);组织学证实心内膜PFs消融。用50μM 9-菲罗醇(TRPM4通道阻断剂)冲洗左心室腔5分钟,异位减少39%(n=15,P<;0.01)。免疫组织化学证实TRPM4在PFs中比心肌中更丰富。我们的研究结果表明,心内膜表面在这些机械诱导的异位激活中起着重要作用。异位激活模式表明PFs参与了这些心律失常,TRPM4通道可能参与其中,9-菲罗可减少心律失常。
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