| Literature DB >> 30993760 |
Jinzhu Zhang1, Jingjing Niu1, Baoqing Tian1, Meng Zhao1.
Abstract
The current study aimed to explore the functions and roles of microRNA-193b (miR-193b) in the myocardium with ischemia-reperfusion (I/R) injury and a potential therapeutic method for myocardial I/R injury. The mice were subjected to myocardial I/R with or without miR-193b pretreatment. The infarct size and myocardial enzymes were detected. The terminal deoxynucleotidyl transferase dUTP nick-end labeling assay was conducted to investigate the effect of miR-193b on cardiomyocyte apoptosis. The expression levels of miR-193b and mastermind-like 1 (MAML1) were validated by quantitative real-time polymerase chain reaction and Western blot analysis. The results suggested that the miR-193b expression level was significantly downregulated in the myocardium with I/R injury compared with control group. miR-193b overexpression is able to reduce infarct size and myocardial enzymes after myocardial I/R injury. Furthermore, overexpression of miR-193b could alleviate the apoptosis level after myocardial I/R injury. Taken together, the present study demonstrated that upregulated miRNA-193b alleviated myocardial I/R injury via targeting MAML1.Entities:
Keywords: ischemic heart disease; mastermind-like 1; microRNA-193b; myocardial enzymes; myocardial ischemia-reperfusion injury
Year: 2019 PMID: 30993760 DOI: 10.1002/jcb.28684
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429