Exploring the mechanism of Lingbao Huxin Dan in the treatment of bradycardia based on atrioventricular node electrical signal conduction

Jing Zhang , Guobin Zheng , Shangjing Liu , Yaodong Miao , Shu Yang , Sheng Li , Zhihui Yang , Danping Zhuo , Rui Guo , Yang Guo , Rongjiang Shao , Yunqing Hua , Chuanrui Ma
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Abstract

Background

Prolonged bradycardia leads to inadequate pumping of the heart, causing myocardial ischemia, which in turn affects cardiac function. Depending on its clinical features, improving the AV node conduction block may be an important tool to inhibit the progression of the disease. Lingbao Huxin Dan, which consists of several traditional Chinese medicines, is used for conditions similar to bradycardia and may be a potential therapeutic agent for bradycardia. In this experiment, we investigated its therapeutic significance and possible therapeutic targets for sinus bradycardia.

Methods

The bradycardia model of SD rats was prepared by using acetylcholine, propranolol, and verapamil respectively, and treated with Lingbao Huxin Dan for 3 weeks. At the end of treatment, the rats' ECG was recorded using a PV-LOOP heart rate recorder. The hearts and serum samples were collected to detect heart rate and related gene expression which were screened through network pharmacology analysis, as well as to evaluate the effect of Lingbao Huxin Dan on ion channels in the cardiac conduction system.

Results

Lingbao Huxin Dan improved the heart rate in the bradycardia model of SD rats and inhibited AV node conduction block by targeting ion channel proteins in the cardiac conduction system. The underlying molecular mechanism may be the activation of the β-adrenergic receptor-dependent cAMP/PKA signaling pathway targeted to enhance the expression of the pacing channel HCN4. In addition, Lingbao Huxin Dan prevented the deterioration of bradycardia by promoting the production of the oxygen radical scavenger SOD and inhibiting the upregulation of LDH due to cardiomyocyte damage.

Conclusions

Our study proved that Lingbao Huxin Dan alleviated bradycardia by downregulating CX45 and enhancing the expression of HCN4, ADRβ1, and TRPM7 to shorten the atrioventricular node induction period and improve sinoatrial node signaling. In addition, Lingbao Huxin Dan relieved myocardial injury induced by bradycardia by reducing the level of oxygen free radicals in the cardiac microenvironment.

Abstract Image

基于房室结电信号传导探讨灵宝护心丹治疗心动过缓的作用机制
背景:长期的心动过缓导致心脏供血不足,引起心肌缺血,进而影响心功能。根据其临床特点,改善房室结传导阻滞可能是抑制疾病进展的重要工具。灵宝护心丹由几种中药组成,用于治疗类似心动过缓的病症,可能是治疗心动过缓的潜在药物。本实验探讨其治疗窦性心动过缓的意义及可能的治疗靶点。方法分别用乙酰胆碱、心得安、维拉帕米制备SD大鼠心动过缓模型,并用灵宝护心丹治疗3周。在治疗结束时,使用PV-LOOP心率记录仪记录大鼠的心电图。采集心脏及血清样本,通过网络药理学分析筛选心率及相关基因表达,评价灵宝护心丹对心脏传导系统离子通道的影响。结果灵宝护心丹可提高SD大鼠心动过缓模型的心率,并通过靶向心脏传导系统的离子通道蛋白抑制房室结传导阻滞。其潜在的分子机制可能是激活β-肾上腺素能受体依赖的cAMP/PKA信号通路,以增强起搏通道HCN4的表达。此外,灵宝护心丹通过促进氧自由基清除剂SOD的产生,抑制心肌细胞损伤引起的LDH上调,从而防止心动过缓的恶化。结论灵宝护心丹通过下调CX45,提高HCN4、ADRβ1、TRPM7的表达,缩短房室结诱导期,改善窦房结信号传导,减轻心动过缓。此外,灵宝护心丹可通过降低心脏微环境中氧自由基水平减轻心动过缓所致心肌损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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