# Aerobic Exercise Attenuates Epidermal Hyperplasia in an Obesity-Associated Psoriasiform Dermatitis Model

**Authors:** Yoshihiro Matsuda, Shin Morizane, Daiki Takezaki, Yuma Sakamoto, Nobuyasu Baba, Masanori Iseki, Yoshio Kawakami, Tatsushi Shiomi, Tomoyuki Mukai

PMC · DOI: 10.3390/ijms27052308 · 2026-02-28

## TL;DR

Aerobic exercise reduces skin thickening in an obesity-related skin disease model, even without reducing inflammation.

## Contribution

This study reveals that aerobic exercise can reduce epidermal hyperplasia in obesity-associated psoriasis without affecting inflammatory cytokines.

## Key findings

- Obesity worsens psoriasiform dermatitis in mice.
- Aerobic exercise reduces epidermal hyperplasia in obese mice.
- Exercise does not significantly alter inflammatory cytokine levels in the skin.

## Abstract

Obesity is an important risk factor for psoriasis, and clinical studies indicate that exercise interventions can improve disease severity. However, the mechanisms by which exercise influences psoriatic pathogenesis remain insufficiently understood. To investigate the effects of aerobic exercise on obesity-associated psoriasis, wild-type mice were fed a high-fat diet (HFD) for 7 weeks to induce obesity and subsequently underwent moderate-intensity treadmill running for 3 weeks. Psoriasiform dermatitis was induced by daily topical application of imiquimod (IMQ) to the skin for five consecutive days. HFD increased body weight, epididymal fat mass, and serum cholesterol. HFD-fed mice developed more severe IMQ-induced psoriatic skin changes compared with normal diet-fed mice. Treadmill exercise modestly reduced body weight gain and attenuated epidermal hyperplasia in HFD-fed mice. In contrast, inflammatory cytokine expression, including Tnfa, Il17a, and Il23a, showed modest increases in the skin of HFD-fed exercised mice, which did not parallel the improvement in epidermal hyperplasia. Overall, these findings indicate that while obesity exacerbates psoriasiform dermatitis, aerobic exercise ameliorates epidermal hyperplasia in obese mice without corresponding changes in inflammatory cytokine expression in the skin, suggesting that exercise may influence psoriatic skin changes through multiple metabolic and immunological pathways.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL17A (interleukin 17A), IL23A (interleukin 23 subunit alpha)
- **Chemicals:** imiquimod (PubChem CID 57469)
- **Diseases:** psoriasis (MONDO:0005083)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Il23a (interleukin 23, alpha subunit p19) [NCBI Gene 83430] {aka IL-23, p19}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** psoriasis (MESH:D011565), psoriatic (MESH:D015535), Obesity (MESH:D009765), Epidermal Hyperplasia (MESH:D006965), inflammatory (MESH:D007249), weight gain (MESH:D015430), Psoriasiform Dermatitis (OMIM:616834)
- **Chemicals:** fat (MESH:D005223), IMQ (MESH:D000077271), cholesterol (MESH:D002784)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12985546/full.md

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Source: https://tomesphere.com/paper/PMC12985546