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March 29, 2026Frontiers in Cell and Developmental Biology0 citationsOpen Access

MicroRNA, MicroRNA-lncRNA and MicroRNA-Circular RNA axes, and exosomal MicroRNAs: driving exercise-induced cardioprotection in heart failure

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YLYang LiJWJunmin WangDMDe Ma

Key Points

  • To investigate the role of non-coding RNAs like microRNAs in exercise-induced cardioprotection in heart failure.
  • Reviewed literature on the role of microRNAs in cardiovascular diseases especially related to exercise.
  • Explored interactions of microRNA with lncRNA and circRNA in physiological conditions.
  • Analyzed effects of exosomal microRNAs derived from different tissues and their pathways.
  • Identified specific microRNAs linked to cardiac remodeling and exercise benefits such as miR-1, miR-21, and miR-126.
  • Demonstrated that microRNAs can differentiate between beneficial and pathological heart conditions.
  • Highlighted the role of exosomal microRNAs in activating protective signaling pathways.

Abstract

Regular physical activity is a powerful non-pharmacological strategy for preventing and managing cardiovascular diseases (CVDs), including heart failure, by promoting cardioprotective adaptations through molecular mechanisms that remain incompletely elucidated. This review explores the central role of non-coding RNAs (ncRNAs), particularly microRNAs (miRNAs), in exercise-induced cardioprotection, highlighting their interactions within miRNA-lncRNA and miRNA-circRNA axes, as well as the function of exosomal miRNAs as key exerkines facilitating inter-organ crosstalk. Synthesizing current literature, we examine ncRNA biogenesis, canonical functions, and exercise-responsive profiles, focusing on pivotal miRNAs such as miR-1, miR-133, miR-21, miR-126, miR-29, miR-208a, and miR-499; lncRNA-miRNA networks including MALAT1/miR-150-5p, H19/miR-139, and GAS5/miR-217; circRNA-miRNA interactions like circUtrn/miR-132/212; and exosomal miRNAs derived from skeletal muscle (e.g., miR-130a, miR-1), brown adipose tissue (e.g., miR-17-3p), endothelium (e.g., miR-126), and cardiomyocytes (e.g., miR-21-3p). These elements are evaluated in models of physiological cardiac remodeling, myocardial infarction, ischemia-reperfusion injury, diabetic cardiomyopathy, and heart failure, with consideration of influencing factors such as sex, age, and training modality. Exercise-modulated miRNAs differentiate benign “athlete’s heart” from pathological hypertrophy by governing angiogenesis, fibrosis, metabolic shifts, and arrhythmia risk, while lncRNA-miRNA and circRNA-miRNA axes regulate apoptosis, inflammation, mitochondrial dynamics, and extracellular matrix remodeling in CVD contexts. Exosomal miRNAs enable remote protection by activating survival, angiogenic, and anti-fibrotic pathways via signaling cascades like PI3K/AKT and NF-κB. Responses exhibit variability based on demographic and exercise variables, underscoring ncRNAs' promise as diagnostic biomarkers, therapeutic targets, or mimics of exercise benefits for heart failure management.

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Cite This Study

Li et al. (2026) studied this question.

synapsesocial.com/papers/69c8c115de0f0f753b39b9d1https://doi.org/10.3389/fcell.2026.1767057
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