# Crosstalk between skeletal muscle and the brain during physical activity - in search of epigenetic mechanisms

**Authors:** Cayla Boycott, Ewa Kilanczyk, Huiying A. Zhang, Jiaxi Zhang, Arian Abolhassani, Malgorzata Kubiak, Jan Celichowski, Katarzyna Kryściak, Dominika Gruszka, Joanna H. Sliwowska, Barbara Stefanska

PMC · DOI: 10.1080/15592294.2025.2590237 · 2025-11-24

## TL;DR

This review explores how physical activity improves brain function through communication between muscles and the brain, focusing on epigenetic changes.

## Contribution

The paper highlights novel epigenetic mechanisms in muscle-brain crosstalk during exercise and their implications for cognitive health.

## Key findings

- Myokines like cathepsin B and irisin mediate muscle-brain communication and influence cognitive functions.
- Exercise alters gene expression through epigenetic modifications, impacting metabolic and cognitive health.
- Obesity and diabetes are linked to cognitive decline, which may be mitigated by exercise-induced muscle-brain crosstalk.

## Abstract

Recent research highlights the crucial role of muscle-brain crosstalk in metabolic regulation, particularly in individuals with type 2 diabetes and obesity. Myokines, protein hormones secreted by skeletal muscle, play a crucial role in this communication, influencing brain functions such as neuroplasticity, memory, and mood. Specific myokines like cathepsin B, FNDC5/irisin and interleukin-6 have been identified as key players in this muscle-brain axis. Physical activity modulates the production of these molecular factors, enhancing muscle-brain crosstalk and influencing cellular interactions. Moreover, exercise training may lead to adaptive long-term changes in gene expression, mediated by epigenetic regulators. Metabolic pathways activated during exercise can directly impact epigenetic marks by modulating the availability of metabolic intermediates required for these modifications. In the present review, we summarize the latest findings on the association between obesity/diabetes and cognitive impairment due to hippocampal dysfunction, and elaborate on how exercise influences cognitive functions via the communication between skeletal muscle and the brain. We focus on the underlying mechanisms responsible for the muscle-brain crosstalk, emphasizing dynamic changes in the epigenome and epitranscriptome, which sheds light on novel preventive and therapeutic approaches to combat obesity and cognitive decline.

## Linked entities

- **Proteins:** IL6 (interleukin 6)
- **Diseases:** type 2 diabetes (MONDO:0005148), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** CTSB (cathepsin B) [NCBI Gene 1508] {aka APPS, CPSB, KWE, RECEUP}, FNDC5 (fibronectin type III domain containing 5) [NCBI Gene 252995] {aka FRCP2, irisin}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** obesity (MESH:D009765), hippocampal dysfunction (MESH:D001927), cognitive decline (MESH:D003072), diabetes (MESH:D003920), type 2 diabetes (MESH:D003924)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12645880/full.md

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Source: https://tomesphere.com/paper/PMC12645880