# L-β-aminoisobutyric acid (L-BAIBA) in combination with voluntary wheel running exercise enhances musculoskeletal properties in middle-age male mice

**Authors:** Julian A. Vallejo, Yukiko Kitase, Thiagarajan Ganesh, Mark Dallas, Yixia Xie, David S. Moore, Mark L. Johnson, Lynda F. Bonewald, Michael J. Wacker

PMC · DOI: 10.18632/aging.206325 · Aging (Albany NY) · 2025-10-01

## TL;DR

This study shows that combining L-BAIBA with exercise improves muscle and bone health in middle-aged mice more than exercise alone.

## Contribution

The study reveals that L-BAIBA supplementation combined with exercise enhances musculoskeletal properties in middle-aged mice.

## Key findings

- Mice given L-BAIBA and exercise had larger, stronger soleus muscles with more slow-oxidative fibers.
- L-BAIBA plus exercise reduced bone marrow fat and improved bone quality in middle-aged mice.
- Combining L-BAIBA with exercise led to better musculoskeletal outcomes than either alone.

## Abstract

Contracting skeletal muscles secrete the metabolite L-β-aminoisobutyric acid (L-BAIBA), which when supplemented in the diet can mitigate disuse-induced musculoskeletal dysfunction. However, the effects of L-BAIBA supplementation alone and combined with exercise on cardiac and musculoskeletal properties are currently unknown. We hypothesized that exercise with L-BAIBA supplementation would promote greater cardiac and musculoskeletal benefits than exercise alone. To investigate this hypothesis, we subjected 12-month-old (as a model of middle-age) male C57BL6 mice to voluntary wheel running (VWR) with L-BAIBA (100mg/kg/day) (VWR+L-BAIBA), VWR alone, L-BAIBA alone, or none (CTRL) for three months. After the intervention, conscious electrocardiogram showed slightly prolonged QTc in VWR+L-BAIBA mice compared to CTRL (p<0.05). Soleus muscles from VWR+L-BAIBA, but not VWR, were larger, contracted more forcefully, and contained more slow-oxidative type I myofibers compared to CTRL (p<0.05). In EDL muscle, VWR but not VWR+L-BAIBA improved fatigue resistance and caffeine-induced recovery (p<0.05). In bone, VWR+L-BAIBA but not VWR showed lower bone marrow adiposity, higher trabecular thickness, and connectivity, smaller bone diameter and Moment of Inertia, but higher Modulus of Elasticity than CTRL (p<0.05), suggesting L-BAIBA delays aging-induced periosteal expansion due to better bone material qualities. These findings suggest a physiological interaction between exercise and L-BAIBA supplementation to improve soleus muscle and bone properties and reduce bone marrow adiposity.

## Linked entities

- **Chemicals:** L-β-aminoisobutyric acid (PubChem CID 439434), L-BAIBA (PubChem CID 439434)

## Full-text entities

- **Diseases:** prolonged QTc (MESH:D008133), fatigue (MESH:D005221), musculoskeletal dysfunction (MESH:D009140), marrow adiposity (MESH:D001855)
- **Chemicals:** L-BAIBA (-), caffeine (MESH:D002110)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12606963/full.md

## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12606963/full.md

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Source: https://tomesphere.com/paper/PMC12606963