Cheng Xingdong, Huang Tingting, Wang Chunhui, Hao Shuang, Shu Liliang, Wang Shixiong, Cheng Gao, Zhang Qiaoyun, Huang Jian, Chen Chen
Department of Anesthesiology, The Forth Affiliated Hospital of Anhui Medical University, Hefei, China.
Second Clinical Medical College, Lanzhou University, Lanzhou, China.
Front Pharmacol. 2022 May 12;13:894899. doi: 10.3389/fphar.2022.894899. eCollection 2022.
Myocardial ischemia/reperfusion injury (MI/RI) is a serious pathophysiological process relating to cardiovascular disease. Oroxin A (OA) is a natural flavonoid glycoside with various biological activities. However, its effect on the pathophysiological process of MI/RI has not yet been reported. The aim of this study was to determine whether OA could alleviate MI/RI induced inflammation and pyroptosis and , providing a novel therapeutic regimen for the treatment of MI/RI. A high-throughput drug screening strategy was employed to test 2,661 natural compound libraries that can alleviate MI/RI and . The rat model of MI/RI was established by ligating the left anterior descending (LAD) coronary artery. H9c2 cells were subjected to oxygen-glucose deprivation/reperfusion (OGD/R) to simulate MI/RI. The results show that OA is able to significantly inhibit apoptosis, pyroptosis and the inflammation response (TNF-α, IL-6, IL-8, IL-10, IL-1β, IL-18) and , and reduce the release of myocardial enzymes (cTnI, cTnT, CK-MB, LDH, AST). In the rat MI/RI model, OA can not only improve cardiac function and reduce inflammatory cell infiltration but also reduce myocardial infarct size. The results revealed that OA is an effective remedy against MI/RI as it reduces the inflammatory response and inhibits pyroptosis. This may provide a new therapeutic target for the clinical treatment of MI/RI.
心肌缺血/再灌注损伤(MI/RI)是一种与心血管疾病相关的严重病理生理过程。奥洛辛A(OA)是一种具有多种生物活性的天然黄酮糖苷。然而,其对MI/RI病理生理过程的影响尚未见报道。本研究的目的是确定OA是否能减轻MI/RI诱导的炎症和焦亡,并为MI/RI的治疗提供一种新的治疗方案。采用高通量药物筛选策略测试了2661种可减轻MI/RI的天然化合物库。通过结扎左冠状动脉前降支(LAD)建立MI/RI大鼠模型。对H9c2细胞进行氧糖剥夺/再灌注(OGD/R)以模拟MI/RI。结果表明,OA能够显著抑制细胞凋亡、焦亡和炎症反应(TNF-α、IL-6、IL-8、IL-10、IL-1β、IL-18),并减少心肌酶(cTnI、cTnT、CK-MB、LDH、AST)的释放。在大鼠MI/RI模型中,OA不仅可以改善心脏功能、减少炎性细胞浸润,还可以减小心肌梗死面积。结果显示,OA是一种有效的抗MI/RI药物,因为它可以减轻炎症反应并抑制焦亡。这可能为MI/RI的临床治疗提供一个新的治疗靶点。