Lin Yubi, Bian Ning, Li Hairui, Chen Jia, Xing Huijie, Li Hong, Huang Dandan, Lan Xianwu, Gong Bojun, Zhou Li, Liu Ruijie, Guan Min, Zhang Dongdong, Du Gang, Huang Zhengyi, Chen Xiaoming, Zhang Tao, Feng Jianyi, Wu Shaorong, Wang Liwei, Zhang Aidong, Li Zicheng
Department of Cardiology, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
ScientificWorldJournal. 2013 Jun 20;2013:781084. doi: 10.1155/2013/781084. Print 2013.
BACKGROUND: Rapid atrial pacing (RAP) can induce electrical and autonomic remodeling and facilitate atrial fibrillation (AF). Recent reports showed that low-level vagosympathetic nerve stimulation (LLVNS) can suppress AF, as an antiarrhythmic effect. We hypothesized that LLVNS can reverse substrate heterogeneity induced by RAP. METHODS AND RESULTS: Mongrel dogs were divided into (LLVNS+RAP) and RAP groups. Electrode catheters were sutured to multiple atrial sites, and LLVNS was applied to cervical vagosympathetic trunks with voltage 50% below the threshold slowing sinus rate by ≤ 30 msec. RAP induced a significant decrease in effective refractory period (ERP) and increase in the window of vulnerability at all sites, characterized by descending and elevated gradient differences towards the ganglionic plexi (GP) sites, respectively. The ERP dispersion was obviously enlarged by RAP and more significant when the ERP of GP-related sites was considered. Recovery time from AF was also prolonged significantly as a result of RAP. LLVNS could reverse all these changes induced by RAP and recover the heterogeneous substrate to baseline. Conclusions. LLVNS can reverse the electrical and autonomic remodeling and abolish the GP-central gradient differences induced by RAP, and thus it can recover the homogeneous substrate, which may be the underlying mechanism of its antiarrhythmic effect.
背景:快速心房起搏(RAP)可诱发电重构和自主神经重构,并促进心房颤动(AF)。最近的报告显示,低水平迷走交感神经刺激(LLVNS)可作为一种抗心律失常作用抑制AF。我们假设LLVNS可逆转由RAP诱导的基质异质性。 方法与结果:杂种犬分为(LLVNS+RAP)组和RAP组。将电极导管缝合至多个心房部位,并以低于使窦性心率减慢≤30毫秒阈值的50%的电压对颈迷走交感干施加LLVNS。RAP导致所有部位的有效不应期(ERP)显著降低,易损窗口增加,其特征分别为向神经节丛(GP)部位的梯度差异下降和升高。RAP明显扩大了ERP离散度,当考虑与GP相关部位的ERP时更为显著。RAP还导致AF的恢复时间显著延长。LLVNS可逆转RAP诱导的所有这些变化,并使异质基质恢复至基线水平。结论。LLVNS可逆转电重构和自主神经重构,消除由RAP诱导的GP中心梯度差异,从而恢复均匀基质,这可能是其抗心律失常作用的潜在机制。
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