Department of Cardiology, Shenzhen People's Hospital, The Second Clinical Medical College of Jinan University, The First Affiliated Hospital of Southern University of Science and Technology, Shenzhen, 518020, Guangdong, China.
Emergency Department, Shenzhen People's Hospital, The Second Clinical Medical College of Jinan University, The First Affiliated Hospital of Southern University of Science and Technology, 1017 Dongmen North Road, Luohu District, Shenzhen, 518020, Guangdong, China.
J Cardiovasc Transl Res. 2024 Apr;17(2):376-387. doi: 10.1007/s12265-023-10426-1. Epub 2023 Aug 14.
Myocardial ischemia/reperfusion (I/R) injury after the onset of acute myocardial infarction (AMI) can be life-threatening, and there is no effective strategy for therapeutic intervention. Here, we studied the potential of protectin D1 in protecting from I/R-induced cardiac damages and investigated the underlying mechanisms. An in vivo rat model of I/R after AMI induction was established through the ligation of the left anterior descending (LAD) artery to assess the cardiac functions and evaluate the protective effect of protectin D1. Protectin D1 protected against I/R-induced oxidative stress and inflammation in the rat model, improved the cardiac function, and reduced the infarct size in myocardial tissues. The beneficial effect of protectin D1 was associated with the up-regulation of miRNA-210 and the effects on PI3K/AKT signaling and HIF-1α expression. Together, our data suggest that protectin D1 could serve as a potential cardioprotective agent against I/R-associated cardiac defects.
心肌缺血/再灌注(I/R)损伤是急性心肌梗死(AMI)发病后的致命因素,目前尚无有效的治疗干预策略。在这里,我们研究了保护素 D1 对保护 I/R 诱导的心脏损伤的潜力,并探讨了其潜在机制。通过结扎左前降支(LAD)动脉建立 AMI 诱导后的体内大鼠 I/R 模型,评估心脏功能并评估保护素 D1 的保护作用。保护素 D1 可防止大鼠模型发生 I/R 诱导的氧化应激和炎症,改善心脏功能,并减少心肌组织中的梗死面积。保护素 D1 的有益作用与 miRNA-210 的上调以及对 PI3K/AKT 信号和 HIF-1α表达的影响有关。总之,我们的数据表明,保护素 D1 可能成为一种潜在的针对与 I/R 相关的心脏缺陷的心脏保护剂。