Yang Na, Sun Huaxin, Xi Linqiang, Zhang Ling, Lu Yanmei, Wang Qianhui, Cao Jiaru, Song Jie, Tang Baopeng, Shang Luxiang, Zhou Xianhui
Xinjiang Key Laboratory of Cardiac Electrophysiology and Remodelling, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Department of Pacing and Electrophysiology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Clin Exp Pharmacol Physiol. 2025 Feb;52(2):e70011. doi: 10.1111/1440-1681.70011.
Beta1-adrenergic receptor autoantibodies (β1-AAbs) promote atrial remodelling and ultimately lead to the development of atrial fibrillation (AF). Oroxin B is a natural flavonoid glycoside with a variety of biological activities, including anti-inflammatory and autophagy-promoting effects, and has therapeutic benefits for a variety of diseases. The aim of this study was to investigate the potential therapeutic role of Oroxin B in the development of β1-AAb-induced atrial fibrillation and to elucidate the underlying mechanisms involved. We established a rat model of β1-AAb-induced atrial fibrillation via active immunisation. The first stage was divided into three groups: the control group, the β1-AAb group and the β1-AAb + bisoprolol group. The second stage was divided into three groups: the control group, the β1-AAb group and the β1-AAb + Oroxin B group. Serum levels of β1-AAbs, atrial tissue levels of cyclic monophosphate (cAMP), atrial electrophysiological parameters, cardiac structure and function, mitochondrial structure, autophagy levels, cardiomyocyte apoptosis and myocardial fibrosis were examined. The results showed that bisoprolol, a β1-blocker, improved β1-AAb-induced atrial electrical remodelling, reduced atrial collagen deposition, ameliorated the increase in LAD and regulated the balance of autophagy and apoptosis in atrial myocytes through the PTEN/AKT/mTOR signalling pathway. Oroxin B, a PTEN agonist, can improve the impairment of autophagy homeostasis and apoptosis in atrial tissue by activating the PTEN/AKT/mTOR signalling pathway, thereby improving atrial structure and electrical remodelling. Moreover, Oroxin B may play a therapeutic role in β1AAb-induced atrial fibrillation. In conclusion, our results demonstrate the potential therapeutic role of Oroxin B in β1AAb-induced atrial fibrillation and the underlying mechanisms, suggesting that Oroxin B may be an effective antiarrhythmic medication.
β1肾上腺素能受体自身抗体(β1-AAbs)可促进心房重构并最终导致心房颤动(AF)的发生。奥洛星B是一种具有多种生物活性的天然黄酮糖苷,包括抗炎和促进自噬作用,对多种疾病具有治疗作用。本研究旨在探讨奥洛星B在β1-AAb诱导的心房颤动发生中的潜在治疗作用,并阐明其潜在机制。我们通过主动免疫建立了β1-AAb诱导的大鼠心房颤动模型。第一阶段分为三组:对照组、β1-AAb组和β1-AAb+比索洛尔组。第二阶段分为三组:对照组、β1-AAb组和β1-AAb+奥洛星B组。检测血清β1-AAbs水平、心房组织环磷酸(cAMP)水平、心房电生理参数、心脏结构和功能、线粒体结构、自噬水平、心肌细胞凋亡和心肌纤维化。结果表明,β1受体阻滞剂比索洛尔可改善β1-AAb诱导的心房电重构,减少心房胶原沉积,改善左房内径增加,并通过PTEN/AKT/mTOR信号通路调节心房肌细胞自噬与凋亡平衡。PTEN激动剂奥洛星B可通过激活PTEN/AKT/mTOR信号通路改善心房组织自噬稳态和凋亡损伤,从而改善心房结构和电重构。此外,奥洛星B可能在β1AAb诱导的心房颤动中发挥治疗作用。总之,我们的结果证明了奥洛星B在β1AAb诱导的心房颤动中的潜在治疗作用及其潜在机制,提示奥洛星B可能是一种有效的抗心律失常药物。