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在山羊模型中,随着房颤持续存在,在无纤维化的情况下,局部传导阻滞和连接蛋白紊乱会导致电信号碎裂。

Fractionation of electrograms is caused by colocalized conduction block and connexin disorganization in the absence of fibrosis as AF becomes persistent in the goat model.

作者信息

Kirubakaran Senthil, Chowdhury Rasheda A, Hall Mark C S, Patel Pravina M, Garratt Clifford J, Peters Nicholas S

机构信息

Manchester Heart Centre, Manchester Royal Infirmary, Manchester, M13 9WL, United Kingdom.

Imperial College London, London, SW7 2AZ, United Kingdom.

出版信息

Heart Rhythm. 2015 Feb;12(2):397-408. doi: 10.1016/j.hrthm.2014.10.027. Epub 2014 Oct 27.

Abstract

BACKGROUND

Electrogram fractionation and atrial fibrosis are both thought to be pathophysiological hallmarks of evolving persistence of atrial fibrillation (AF), but recent studies in humans have shown that they do not colocalize. The interrelationship and relative roles of fractionation and fibrotic change in AF persistence therefore remain unclear.

OBJECTIVE

The aim of the study was to examine the hypothesis that electrogram fractionation with increasing persistence of AF results from localized conduction slowing or block due to changes in atrial connexin distribution in the absence of fibrotic change.

METHODS

Of 12 goats, atrial burst pacemakers maintained AF in 9 goats for up to 3 consecutive 4-week periods. After each 4-week period, 3 goats underwent epicardial mapping studies of the right atrium and examination of the atrial myocardium for immunodetection of connexins 43 and 40 (Cx43 and Cx40) and quantification of connective tissue.

RESULTS

Despite refractoriness returning to normal in between each 4-week period of AF, there was a cumulative increase in the prevalence of fractionated atrial electrograms during both atrial pacing (control and 1, 2, and 3 months period of AF 0.3%, 1.3% ± 1.5%, 10.6% ± 2%, and 17% ± 5%, respectively; analysis of variance, P < .05) and AF (0.3% ± 0.1%, 2.3% ± 1.2%, 14% ± 2%, and 23% ± 3%; P < .05) caused by colocalized areas of conduction block during both pacing (local conduction velocity <10 cm/s: 0.1% ± 0.1%, 0.3% ± 0.6%, 6.5% ± 3%, and 6.9% ± 4%; P < .05) and AF (1.5% ± 0.5%, 2.7% ± 1.1%, 10.1% ± 1.2%, and 13.6% ± 0.4%; P < .05), associated with an increase in the heterogeneity of Cx40 and lateralization of Cx43 (lateralization scores: 1.75 ± 0.89, 1.44 ± 0.31, 2.85 ± 0.96, and 2.94 ± 0.31; P < .02), but not associated with change in connective tissue content or net conduction velocity.

CONCLUSION

Electrogram fractionation with increasing persistence of AF results from slow localized conduction or block associated with changes in atrial connexin distribution in the absence of fibrotic change.

摘要

背景

心电图碎裂和心房纤维化均被认为是房颤(AF)持续进展的病理生理特征,但最近在人体中的研究表明它们并非共定位。因此,碎裂和纤维化改变在房颤持续中的相互关系及相对作用仍不明确。

目的

本研究旨在检验这一假说,即随着房颤持续时间增加,心电图碎裂是由于在无纤维化改变的情况下,心房连接蛋白分布变化导致局部传导减慢或阻滞所致。

方法

在12只山羊中,心房猝发起搏器使9只山羊维持房颤状态长达3个连续的4周周期。在每个4周周期后,3只山羊接受右心房的心外膜标测研究,并检查心房心肌,以免疫检测连接蛋白43和40(Cx43和Cx40)并定量结缔组织。

结果

尽管在每个4周的房颤周期之间不应期恢复正常,但在心房起搏期间(对照组以及房颤1、2和3个月时,分别为0.3%、1.3%±1.5%、10.6%±2%和17%±5%;方差分析,P<.05)和房颤期间(0.3%±0.1%、2.3%±1.2%、14%±2%和23%±3%;P<.05),碎裂心房电图的患病率均有累积增加,这是由起搏期间(局部传导速度<10 cm/s:0.1%±0.1%、0.3%±0.6%、6.5%±3%和6.9%±4%;P<.05)和房颤期间(1.5%±0.5%、2.7%±1.1%、10.1%±1.2%和13.6%±0.4%;P<.05)共定位的传导阻滞区域引起的,与Cx40异质性增加和Cx43侧向化(侧向化评分:1.75±0.89、1.44±0.31、2.85±0.96和2.94±0.31;P<.02)相关,但与结缔组织含量或净传导速度变化无关。

结论

随着房颤持续时间增加,心电图碎裂是由于在无纤维化改变的情况下,与心房连接蛋白分布变化相关的局部传导减慢或阻滞所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dbf/4315883/068d5662cb71/gr1.jpg

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