Oroxin B Resembles Bisoprolol in Attenuating Beta1-Adrenergic Receptor Autoantibody-Induced Atrial Remodelling via the PTEN/AKT/mTOR Signalling Pathway

被引:0
作者
Yang, Na [1 ,2 ]
Sun, Huaxin [3 ]
Xi, Linqiang [1 ,2 ]
Zhang, Ling [1 ]
Lu, Yanmei [1 ,2 ]
Wang, Qianhui [1 ,2 ]
Cao, Jiaru [1 ,2 ]
Song, Jie [1 ,2 ]
Tang, Baopeng [1 ,2 ]
Shang, Luxiang [4 ,5 ,6 ,7 ]
Zhou, Xianhui [1 ,2 ]
机构
[1] Xinjiang Med Univ, Affiliated Hosp 1, Xinjiang Key Lab Cardiac Electrophysiol & Remodell, Urumqi, Peoples R China
[2] Xinjiang Med Univ, Dept Pacing & Electrophysiol, Affiliated Hosp 1, Urumqi, Peoples R China
[3] Southwest Jiaotong Univ, Peoples Hosp Chengdu 3, Chengdu Cardiovasc Dis Res Inst, Dept Cardiol,Affiliated Hosp, Chengdu, Sichuan, Peoples R China
[4] Shandong First Med Univ, Affiliated Hosp 1, Dept Cardiol, Jinan, Peoples R China
[5] Shandong Prov Qianfoshan Hosp, Shandong Med & Hlth Key Lab Cardiac Electrophysiol, Jinan, Peoples R China
[6] Shandong First Med Univ, Med Sci & Technol Innovat Ctr, Jinan, Peoples R China
[7] Shandong Acad Med Sci, Jinan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
apoptosis; atrial fibrillation; autophagy; Oroxin B; beta; 1-AAbs; ARRHYTHMIAS; SUPPRESSES; DISEASE;
D O I
10.1111/1440-1681.70011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Beta1-adrenergic receptor autoantibodies (beta 1-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 beta 1-AAb-induced atrial fibrillation and to elucidate the underlying mechanisms involved. We established a rat model of beta 1-AAb-induced atrial fibrillation via active immunisation. The first stage was divided into three groups: the control group, the beta 1-AAb group and the beta 1-AAb + bisoprolol group. The second stage was divided into three groups: the control group, the beta 1-AAb group and the beta 1-AAb + Oroxin B group. Serum levels of beta 1-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 beta 1-blocker, improved beta 1-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 beta 1AAb-induced atrial fibrillation. In conclusion, our results demonstrate the potential therapeutic role of Oroxin B in beta 1AAb-induced atrial fibrillation and the underlying mechanisms, suggesting that Oroxin B may be an effective antiarrhythmic medication.
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页数:14
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