# Exercise has differential cardiometabolic effects in male and female mice on a high‐fat diet

**Authors:** L. E. Watson, M. Annandale, C. L. MacRae, J. Bai, J. Dayaram, N. Burgess, C. Puliuvea, C. P. Hedges, R. F. D'Souza, T. L. Merry, K. M. Mellor

PMC · DOI: 10.14814/phy2.70656 · Physiological Reports · 2026-01-28

## TL;DR

Exercise has different effects on heart and metabolism in male and female mice on a high-fat diet.

## Contribution

First evidence showing sex-specific cardiometabolic effects of exercise in a metabolic disease model.

## Key findings

- Exercise reduced body and fat mass in female but not male mice on a high-fat diet.
- Cardiac diastolic function improved in females but not males with exercise.
- Exercise had sex-specific anti-inflammatory effects in different tissues.

## Abstract

Sex differences in the metabolic and anti‐inflammatory effects of exercise have been reported, but whether males and females exhibit a differential response to exercise in a setting of cardiometabolic disease is unknown. The objective of this study was to investigate the glucose handling, adipose and cardiac effects of voluntary exercise in male and female mice in a cardiometabolic disease setting induced by a high‐fat diet (HFD). The extent of exercise tolerance improvement was similar between HFD male and HFD female mice with running wheel access, despite greater daily running distances in female HFD mice. Exercise attenuated HFD‐induced increased body and fat mass in females but had no effect in males. A slight improvement in insulin tolerance was observed in HFD males only. The anti‐inflammatory effects of exercise were evident in both HFD males and HFD females, but the inflammatory cell types and tissue depots involved were sex‐specific. Cardiac diastolic function was improved with exercise in HFD females but not HFD males. Surprisingly, cardiomyocyte dimensions increased with exercise in HFD females and decreased with exercise in HFD males. This study provides the first evidence that the cardiometabolic effects of exercise are differentially elicited in males and females in a metabolic disease setting.

## Linked entities

- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cd247 (CD247 antigen) [NCBI Gene 12503] {aka 4930549J05Rik, A430104F18Rik, Cd3, Cd3-eta, Cd3-zeta, Cd3h}, Il2ra (interleukin 2 receptor, alpha chain) [NCBI Gene 16184] {aka CD25, Il2r, Ly-43}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, Camk2d (calcium/calmodulin-dependent protein kinase II, delta) [NCBI Gene 108058] {aka 2810011D23Rik, 8030469K03Rik, CaMK II, [d]-CaMKII}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}
- **Diseases:** cardiac remodeling (MESH:D020257), hypertension (MESH:D006973), obese (MESH:D009765), body mass gain (MESH:C536030), cardiac hypertrophy (MESH:D006332), type 2 diabetes (MESH:D003924), cardiovascular disease (MESH:D002318), heart failure (MESH:D006333), diastolic dysfunction (MESH:D018487), weight loss (MESH:D015431), insulin (MESH:D007333), Cardiometabolic disease (MESH:D024821), glucose (MESH:D018149), cardiomyopathy (MESH:D009202), obese metabolic disease (MESH:D000067329), adipose inflammation (MESH:D007249), weight gain (MESH:D015430), metabolic abnormalities (MESH:D008659), excess (MESH:D006970), left ventricular physiological hypertrophy (MESH:D017379), impaired glucose homeostasis (MESH:D044882), cardiomyocyte hypertrophy (MESH:D006984), Chronic adipose tissue (MESH:D018205), myocardial infarction (MESH:D009203)
- **Chemicals:** D-Glucose (MESH:D005947), fatty acid (MESH:D005227), Lipid (MESH:D008055), fat (MESH:D005223), isopentane (MESH:C067038), MgSO4 (MESH:D008278), Alexa Fluor  594 (-), sucrose (MESH:D013395), O2 (MESH:D010100), carbohydrate (MESH:D002241), E (MESH:D004540), NH4Cl (MESH:D000643), EDTA (MESH:D004492), NaHCO3 (MESH:D017693), glycogen (MESH:D006003), paraformaldehyde (MESH:C003043), isoflurane (MESH:D007530), NaCl (MESH:D012965), water (MESH:D014867), KCl (MESH:D011189), oil (MESH:D009821), triglyceride (MESH:D014280), HEPES (MESH:D006531), insulin (MESH:D007328), Blood glucose (MESH:D001786), CO2 (MESH:D002245)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** -174 G/C

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12848585/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12848585/full.md

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Source: https://tomesphere.com/paper/PMC12848585