Downregulation of OIP5-AS1 inhibits apoptosis in myocardial ischemia/reperfusion injury via modulating the MiR-145-5p/ROCK1 axis
Jingyan Yang, Jing Liu, Xiaobo Liu, Dongling Xu, Juan Zhang, Alexis Carrasco, Alexis Carrasco, Alexis Carrasco, Alexis Carrasco

TL;DR
This study shows that reducing OIP5-AS1 can protect heart cells from injury during reperfusion by regulating miR-145-5p and ROCK1.
Contribution
The study identifies a novel regulatory axis involving OIP5-AS1, miR-145-5p, and ROCK1 in myocardial I/R injury.
Findings
OIP5-AS1 levels are elevated in I/R injury and linked to increased apoptosis.
Silencing OIP5-AS1 reduces apoptosis and modulates miR-145-5p and ROCK1 expression.
miR-145-5p suppression reverses the protective effects of OIP5-AS1 depletion.
Abstract
The role of Long noncoding RNA OIP5-AS1 in myocardial ischemia/reperfusion (I/R) injury-induced apoptosis remains to be fully elucidated. The present study was conducted with the objective of investigating the function of OIP5-AS1 in myocardial I/R injury and exploring its potential mechanisms. In order to simulate the conditions of I/R, H9c2 cells were cultured in hypoxic/reoxygenated environments. Induction of I/R in Sprague-Dawley rats was achieved by ligating the left anterior descending coronary artery for 30 minutes followed by 180 minutes of reperfusion. OIP5-AS1 expression levels were assessed, and the degree of apoptosis was evaluated by TUNEL staining. Bioinformatic analysis was conducted to predict the interaction between microRNA-145-5p (miR-145-5p) and OIP5-AS1, and the expression levels of miR-145-5p and ROCK1 were determined. Elevated levels of OIP5-AS1 were observed in…
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Taxonomy
TopicsCancer-related molecular mechanisms research · Cardiac Ischemia and Reperfusion · Traditional Chinese Medicine Analysis
