# The Potential Effects of Exercise Training on Cortical Glutamatergic Synapse, Retrograde Endocannabinoid Signaling, and the Oxytocin Signaling Pathway in the Diabetic–Obesity Cortex: An In Silico Study

**Authors:** Yin-Yu Chiang, Michael Anekson Widjaya, Shin-Da Lee

PMC · DOI: 10.3390/ijms27010266 · International Journal of Molecular Sciences · 2025-12-26

## TL;DR

This study explores how exercise training affects brain pathways in diabetic-obese rats using in silico analysis of gene expression data.

## Contribution

The study identifies novel transcriptional pathways modulated by exercise in the diabetic–obese cortex.

## Key findings

- Exercise training reduced body weight and improved glucose control and blood pressure in diabetic–obese rats.
- RNA-seq analysis identified 814 differentially expressed genes linked to glutamatergic synapse and oxytocin signaling pathways.
- Pathway enrichment highlighted retrograde endocannabinoid signaling and calcium-dependent regulation in response to exercise.

## Abstract

Exercise training reduces metabolic dysfunction and improves neural function; however, its cortical molecular effects in diabetic–obese conditions remain unclear. Here, we aimed to identify transcriptional pathways by integrating physiological evaluation with an in silico analysis of cortical RNA-seq data from Zucker Fatty Diabetes Mellitus rats following a 12-week swimming training program. Exercise training reduced body weight and improved glucose control and blood pressure. RNA-seq analysis revealed 814 differentially expressed genes, with pathway enrichment highlighting glutamatergic synapse, retrograde endocannabinoid signaling, and oxytocin signaling pathways. These coordinated transcriptional shifts involved genes related to excitatory neurotransmission, neuromodulatory feedback, and calcium-dependent regulation. As hypothesis-generating models, these pathway-level patterns suggest that exercise training may modulate cortical signaling properties in diabetic–obese states and provide a conceptual framework for future mechanistic investigation.

## Full-text entities

- **Diseases:** metabolic dysfunction (MESH:D008659), Diabetic (MESH:D003920), Obesity (MESH:D009765)
- **Chemicals:** glucose (MESH:D005947), calcium (MESH:D002118), Endocannabinoid (MESH:D063388)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12786004/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786004/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786004/full.md

---
Source: https://tomesphere.com/paper/PMC12786004