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Updated: Jan 28, 2026

Model of Ischemia and Reperfusion Injury in Rabbits
Published on: November 3, 2023
MicroRNA-144 attenuates cardiac ischemia/reperfusion injury by targeting FOXO1
Lusha E1,2, Hong Jiang1, Zhibing Lu1
1Department of Cardiology, Renmin Hospital of Wuhan University, Hubei General Hospital, Wuchang, Wuhan, Hubei 430060, P.R. China.
Abstract:
Cardiovascular ischemic disease refers to a large class of conditions that are harmful to human health. A number of previous studies have demonstrated that microRNAs (miRs) have notable roles in regulating cardiac injury. miR-144 is influential in the differentiation, growth, and metastatic processes of cells; however, the impact of miR-144 in cardiac ischemia/reperfusion (I/R) injury has not been thoroughly elucidated to date. In the present study, reverse transcription quantitative polymerase chain reaction was used to evaluate RNA expression. In addition, TTC staining was performed to detect the infarct area of the ischemic myocardia and a terminal deoxynucleotidyl-transferase-mediated dUTP nick end labeling assay was utilized to detect the apoptosis of the myocardia. It was observed that miR-144 expression is downregulated in an I/R model in rats and that overexpression of miR-144 significantly reduced myocardial ischemic injury and apoptosis. Consistent with this result, similar findings were demonstrated in H9c2 cells subjected to hypoxia/reoxygenation. Bioinformatic analysis using MiRanda and TargetScan, and luciferase assays confirmed that forkhead box protein O1was the target of miR-144. These findings suggest that miR-144 may be exploited as a novel molecular marker or therapeutic target for myocardial I/R injury.
Insights
MicroRNA-144 (miR-144) is downregulated in heart ischemia/reperfusion (I/R) injury. Overexpressing miR-144 reduces myocardial injury and apoptosis, suggesting its therapeutic potential.
Area of Science:
- Cardiovascular Biology
- Molecular Medicine
- Biochemistry
Background:
- Cardiovascular ischemic diseases pose significant health risks.
- MicroRNAs (miRs) play crucial roles in regulating cardiac injury.
- The specific role of miR-144 in cardiac ischemia/reperfusion (I/R) injury requires further investigation.
Purpose of the Study:
- To investigate the expression and function of miR-144 in myocardial I/R injury.
- To identify the molecular targets of miR-144 in the context of cardiac injury.
- To evaluate the potential of miR-144 as a therapeutic target for I/R injury.
Main Methods:
- Reverse transcription quantitative polymerase chain reaction (RT-qPCR) for RNA expression analysis.
- 2,3,5-triphenyltetrazolium chloride (TTC) staining to assess infarct size.
- Terminal deoxynucleotidyl-transferase-mediated dUTP nick end labeling (TUNEL) assay for apoptosis detection.
- Bioinformatic analysis (MiRanda, TargetScan) and luciferase assays to identify miR-144 targets.
Main Results:
- miR-144 expression was significantly downregulated in a rat model of I/R injury.
- Overexpression of miR-144 reduced myocardial infarct size and apoptosis in I/R conditions.
- Similar protective effects of miR-144 were observed in H9c2 cells under hypoxia/reoxygenation.
- Forkhead box protein O1 (FoxO1) was confirmed as a direct target of miR-144.
Conclusions:
- miR-144 plays a protective role against myocardial I/R injury.
- The miR-144/FoxO1 axis is involved in the regulation of cardiac I/R injury.
- miR-144 holds promise as a diagnostic marker and therapeutic agent for myocardial I/R injury.
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