# Combined Effects of Ketogenic Diet and Aerobic Exercise on Skeletal Muscle Fiber Remodeling and Metabolic Adaptation in Simulated Microgravity Mice

**Authors:** Jun Chen, Wenjiong Li, Liang Yu, Bowei Zhang, Zhili Li, Peng Zou, Bai Ding, Xiaoqian Dai, Qirong Wang

PMC · DOI: 10.3390/metabo15040270 · Metabolites · 2025-04-13

## TL;DR

A ketogenic diet and aerobic exercise together help reduce muscle atrophy and improve endurance in mice under simulated microgravity.

## Contribution

The study reveals the synergistic effects of a ketogenic diet and aerobic exercise in combating microgravity-induced muscle changes.

## Key findings

- The combination of a ketogenic diet and aerobic exercise increased oxidative muscle fibers and reduced glycolytic fibers.
- The intervention upregulated lipid metabolism genes like CPT-1b, HADH, and PGC-1α, improving exercise endurance.
- Mice showed improved muscle atrophy and metabolic adaptation compared to other hindlimb unloading groups.

## Abstract

Objective: Prolonged microgravity environments impair skeletal muscle homeostasis by triggering fiber-type transitions and metabolic dysregulation. Although exercise and nutritional interventions may alleviate disuse atrophy, their synergistic effects under microgravity conditions remain poorly characterized. This study investigated the effects of an 8-week ketogenic diet combined with aerobic exercise in hindlimb-unloaded mice on muscle fiber remodeling and metabolic adaptation. Methods: Seven-week-old male C57BL/6J mice were randomly divided into six groups: normal diet control (NC), normal diet with hindlimb unloading (NH), normal diet with hindlimb unloading and exercise (NHE), ketogenic diet control (KC), ketogenic diet with hindlimb unloading (KH), and ketogenic diet with hindlimb unloading and exercise (KHE). During the last two weeks of intervention, hindlimb unloading was applied to simulate microgravity. Aerobic exercise groups performed moderate-intensity treadmill running (12 m/min, 60 min/day, and 6 days/week) for 8 weeks. Body weight, blood ketone, and glucose levels were measured weekly. Post-intervention assessments included the respiratory exchange ratio (RER), exhaustive exercise performance tests, and biochemical analyses of blood metabolic parameters. The skeletal muscle fiber-type composition was evaluated via immunofluorescence staining, lipid deposition was assessed using Oil Red O staining, glycogen content was analyzed by Periodic Acid–Schiff (PAS) staining, and gene expression was quantified using quantitative real-time PCR (RT-qPCR). Results: Hindlimb unloading significantly decreased body weight, induced muscle atrophy, and reduced exercise endurance in mice. However, the combination of KD and aerobic exercise significantly attenuated these adverse effects, as evidenced by increased proportions of oxidative muscle fibers (MyHC-I) and decreased proportions of glycolytic fibers (MyHC-IIb). Additionally, this combined intervention upregulated the expression of lipid metabolism-associated genes, including CPT-1b, HADH, PGC-1α, and FGF21, enhancing lipid metabolism and ketone utilization. These metabolic adaptations corresponded with improved exercise performance, demonstrated by the increased time to exhaustion in the KHE group compared to other hindlimb unloading groups. Conclusions: The combination of a ketogenic diet and aerobic exercise effectively ameliorates simulated microgravity-induced skeletal muscle atrophy and endurance impairment, primarily by promoting a fiber-type transition from MyHC-IIb to MyHC-I and enhancing lipid metabolism gene expression (CPT-1b, HADH, and PGC-1α). These findings underscore the potential therapeutic value of combined dietary and exercise interventions for mitigating muscle atrophy under simulated microgravity conditions.

## Linked entities

- **Genes:** CPT1B (carnitine palmitoyltransferase 1B) [NCBI Gene 1375], HADH (hydroxyacyl-CoA dehydrogenase) [NCBI Gene 3033], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891], FGF21 (fibroblast growth factor 21) [NCBI Gene 26291]

## Full-text entities

- **Genes:** Hadh (hydroxyacyl-Coenzyme A dehydrogenase) [NCBI Gene 15107] {aka HCDH, Hadhsc, Schad}, Fgf21 (fibroblast growth factor 21) [NCBI Gene 56636] {aka Fgf8c}, Myh7 (myosin, heavy polypeptide 7, cardiac muscle, beta) [NCBI Gene 140781] {aka B-MHC, MYH-beta/slow, MyHC-I, Myhc-b, Myhcb, beta-MHC}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, Cpt1b (carnitine palmitoyltransferase 1b, muscle) [NCBI Gene 12895] {aka Cpt1, Cpt1-m, Cpti, Cpti-m, M-cpti}, Myh4 (myosin, heavy polypeptide 4, skeletal muscle) [NCBI Gene 17884] {aka MHC2B, MM, MYH-2B, Minimsc, Minmus, MyHC-IIb}
- **Diseases:** disuse atrophy (MESH:D020966), endurance impairment (MESH:D060825), muscle atrophy (MESH:D009133), metabolic dysregulation (MESH:D021081)
- **Chemicals:** glucose (MESH:D005947), lipid (MESH:D008055), Oil Red O (MESH:C011049), ketone (MESH:D007659), Periodic Acid (MESH:D010504), glycogen (MESH:D006003)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12029359/full.md

## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC12029359/full.md

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Source: https://tomesphere.com/paper/PMC12029359