Holmes Andrew P, Yu Ting Y, Tull Samantha, Syeda Fahima, Kuhlmann Stefan M, O'Brien Sian-Marie, Patel Pushpa, Brain Keith L, Pavlovic Davor, Brown Nigel A, Fabritz Larissa, Kirchhof Paulus
Institute of Cardiovascular Science, University of Birmingham, Birmingham, United Kingdom.
Physical Sciences of Imaging in the Biomedical Sciences, School of Chemistry, College of Engineering Physical Sciences, University of Birmingham, Birmingham, United Kingdom.
PLoS One. 2016 May 5;11(5):e0154077. doi: 10.1371/journal.pone.0154077. eCollection 2016.
The left atrial posterior wall (LAPW) is potentially an important area for the development and maintenance of atrial fibrillation. We assessed whether there are regional electrical differences throughout the murine left atrial myocardium that could underlie regional differences in arrhythmia susceptibility.
We used high-resolution optical mapping and sharp microelectrode recordings to quantify regional differences in electrical activation and repolarisation within the intact, superfused murine left atrium and quantified regional ion channel mRNA expression by Taqman Low Density Array. We also performed selected cellular electrophysiology experiments to validate regional differences in ion channel function.
Spontaneous ectopic activity was observed during sustained 1Hz pacing in 10/19 intact LA and this was abolished following resection of LAPW (0/19 resected LA, P<0.001). The source of the ectopic activity was the LAPW myocardium, distinct from the pulmonary vein sleeve and LAA, determined by optical mapping. Overall, LAPW action potentials (APs) were ca. 40% longer than the LAA and this region displayed more APD heterogeneity. mRNA expression of Kcna4, Kcnj3 and Kcnj5 was lower in the LAPW myocardium than in the LAA. Cardiomyocytes isolated from the LAPW had decreased Ito and a reduced IKACh current density at both positive and negative test potentials.
The murine LAPW myocardium has a different electrical phenotype and ion channel mRNA expression profile compared with other regions of the LA, and this is associated with increased ectopic activity. If similar regional electrical differences are present in the human LA, then the LAPW may be a potential future target for treatment of atrial fibrillation.
左心房后壁(LAPW)可能是心房颤动发生和维持的重要区域。我们评估了整个小鼠左心房心肌是否存在区域电差异,这些差异可能是心律失常易感性区域差异的基础。
我们使用高分辨率光学标测和尖锐微电极记录来量化完整、灌注的小鼠左心房内电激活和复极化的区域差异,并通过Taqman低密度阵列量化区域离子通道mRNA表达。我们还进行了选定的细胞电生理实验,以验证离子通道功能的区域差异。
在19只完整左心房中,10只在持续1Hz起搏期间观察到自发性异位活动,切除LAPW后这种活动消失(19只切除LAPW的左心房中0只出现,P<0.001)。通过光学标测确定,异位活动的来源是LAPW心肌,与肺静脉袖套和左心耳不同。总体而言,LAPW动作电位(APs)比左心耳长约40%,且该区域显示出更多的动作电位时程(APD)异质性。LAPW心肌中Kcna4、Kcnj3和Kcnj5的mRNA表达低于左心耳。从LAPW分离的心肌细胞在正负测试电位下的Ito电流均降低,IKACh电流密度也降低。
与左心房的其他区域相比,小鼠LAPW心肌具有不同的电表型和离子通道mRNA表达谱,这与异位活动增加有关。如果人类左心房也存在类似的区域电差异,那么LAPW可能是未来治疗心房颤动的潜在靶点。