Wang Yang, Sun Zhe, Yin Zong-Tao, Zhang Jian, Xin Fang-Ran, Xu Yin-Li, Lan Huai
General Hospital of Northern Theater Command, Department of Cardiovascular Surgery, Shenyang, Liaoning, China.
J Appl Biomed. 2025 Jun;23(2):63-79. doi: 10.32725/jab.2025.007. Epub 2025 May 27.
Atrial fibrillation (AF) is a common arrhythmia encountered in clinical practice, characterized by myocardial fibrosis and atrial remodeling as its primary pathological features, and associated with significantly high mortality and disability rates. Currently, there are no specific pharmacological treatments for AF, and traditional anti-arrhythmic drugs have not achieved the desired efficacy, often resulting in a high incidence of adverse drug reactions. Thus, there is an urgent need for the development of novel anti-AF medications. Berberine, the main active component of Coptis chinensis, has been shown to have antiarrhythmic and anti-heart failure effects. However, its potential to improve atrial fibrosis and remodeling resulting from AF remains largely unexplored. In this study, we used a rapid atrial pacing (RAP) procedure to establish a rabbit model of AF associated with atrial fibrosis. Our objective was to assess the inhibitory effects of berberine on myocardial fibrosis, evaluate its impact on atrial remodeling, and investigate its underlying molecular mechanisms. Our findings indicate that berberine reduces left atrial weight and the area of myocardial fibrosis, inhibits the expression of α-SMA protein in atrial tissue, and decreases the levels of inflammation and oxidative stress. In addition, berberine effectively inhibits atrial remodeling, which may contribute to the prevention of AF. Through transcriptomics, molecular docking, and molecular dynamics simulations, we have tentatively confirmed that berberine may activate the AMPK-PPARα signaling pathway by directly binding to AMPK and PPARα, thereby improving atrial fibrillation.
心房颤动(AF)是临床实践中常见的心律失常,其主要病理特征为心肌纤维化和心房重构,且与显著较高的死亡率和致残率相关。目前,AF尚无特异性药物治疗方法,传统抗心律失常药物未达到预期疗效,常常导致药物不良反应发生率较高。因此,迫切需要研发新型抗AF药物。黄连素是黄连的主要活性成分,已被证明具有抗心律失常和抗心力衰竭作用。然而,其改善AF所致心房纤维化和重构的潜力在很大程度上仍未得到探索。在本研究中,我们采用快速心房起搏(RAP)方法建立了与心房纤维化相关的兔AF模型。我们的目的是评估黄连素对心肌纤维化的抑制作用,评价其对心房重构的影响,并研究其潜在分子机制。我们的研究结果表明,黄连素可减轻左心房重量和心肌纤维化面积,抑制心房组织中α-SMA蛋白的表达,并降低炎症和氧化应激水平。此外,黄连素可有效抑制心房重构,这可能有助于预防AF。通过转录组学、分子对接和分子动力学模拟,我们初步证实黄连素可能通过直接结合AMPK和PPARα激活AMPK-PPARα信号通路,从而改善心房颤动。