Abstract
Objectives
This study aims to analyze the expression of miR-324-3p in acute myocardial infarction (AMI), as well as its regulatory effects on inflammatory responses, oxidative stress, and cell viability in cardiomyocytes.Method
This study enrolled 77 AMI patients and 82 healthy controls. The serum miR-324-3p levels were detected using qRT-PCR, and their diagnostic efficacy was evaluated through ROC analysis. Then construct the H/R injury model to analyze the damage of inflammatory factors, oxidative stress, and cell viability to H9c2 cardiomyocytes. Through the combination of site prediction, luciferase reporter gene validation, and STAT3 gene rescue experiments, the critical role of STAT3 in the regulation of miR-324-3p was revealed.Results
In AMI patients, miR-324-3p is significantly upregulated and has high diagnostic value. Overexpression of miR-324-3p exacerbates H/R-induced inflammation, while its inhibition alleviates inflammation. Under H/R treatment, the expression of miR-324-3p increased while the expression of STAT3 decreased. Knocking down STAT3 can reverse the protective effect of the miR-324-3p inhibitor, further confirming the critical role of STAT3 in the miR-324-3p regulatory pathway.Conclusions
The abnormal elevation of miR-324-3p has a potential diagnostic value for AMI. miR-324-3p plays a significant role in H/R-injured cardiomyocytes by targeting and inhibiting the expression of STAT3.