Modulation of the miR-122/Sirt-6/ACE2 axis on experimentally-induced myocardial infarction

被引:11
作者
Abdel-Nasser, Zeinab M. [1 ]
Zaafan, Mai A. [2 ]
Abdelhamid, Amr M. [1 ]
机构
[1] October Univ Modern Sci & Arts MSA, Fac Pharm, Biochem Dept, 6th Of October, Egypt
[2] October Univ Modern Sci & Arts MSA, Fac Pharm, Pharmacol & Toxicol Dept, 6th Of October, Egypt
关键词
Isoprenaline; Rats; Xanthenone; ACE2; miR-122; DISEASE; ATHEROSCLEROSIS; EPIDEMIOLOGY; EXPRESSION; PROTECTS; HEART; AMPK; MB;
D O I
10.1016/j.cbi.2022.110276
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Myocardial infarction (MI) is a progressive myocardial necrosis that can lead to a number of life-threatening complications. MiRNAs have a crucial role in the pathogenesis of many cardiovascular diseases. Remarkably, miR-122 targets the sirtuin-6 (Sirt-6) gene, which is an essential regulator of cardiovascular function and is considered a partial angiotensin converting enzyme 2 (ACE2) activator. Modulation of this axis is supposed to contribute to MI pathogenesis. The current study aims to investigate the cardioprotective effects of xanthenone through targeting the miR-122/Sirt-6/ACE2 axis on experimentally-induced MI in rats. Xanthenone was administered for 14 days and isoprenaline was injected in the last 2 days of the experiment. Xanthenone treatment resulted in a significant downregulation of miR-122, which further upregulated Sirt-6 and thus activated the adenosine monophosphate-activated protein kinase (AMPK). AMPK increases ACE2 levels and results in a decrease in the level of its substrate angiotensin II resulting in the normalization of the inflammatory cytokines and the cardiac biomarkers. Finally, by targeting the miR-122/Sirt-6/AMPK/ACE2 axis, xanthenone has the potential to be a promising cardioprotective agent against MI.
引用
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页数:7
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