# Caprylic Acid Restores Branched-Chain Amino Acid Metabolism in a Mouse Cachexia Model

**Authors:** Isao Kawahara, Rina Fujiwara-Tani, Takuya Mori, Shota Nukaga, Ryoichi Nishida, Yoshihiro Miyagawa, Kei Goto, Hitoshi Ohmori, Kiyomu Fujii, Yi Luo, Takamitsu Sasaki, Chie Nakashima, Ruiko Ogata, Hiroki Kuniyasu

PMC · DOI: 10.3390/cimb47050325 · Current Issues in Molecular Biology · 2025-05-01

## TL;DR

Caprylic acid helps restore amino acid metabolism in a mouse model of cancer-related muscle loss, potentially improving treatment outcomes.

## Contribution

Identifies caprylic acid as a novel agent to restore BCAA metabolism in cancer-induced sarcopenia.

## Key findings

- BCAAs failed to reduce oxidative stress or improve muscle growth in cancer models.
- Impaired BCAA catabolism was linked to elevated BCKD kinase and HMGB1 expression.
- Caprylic acid reversed BCAA metabolism impairments and restored BCAA efficacy.

## Abstract

Cancer-associated sarcopenia is closely linked to the prognosis of cancer patients, making its management a critical aspect of cancer treatment. Branched-chain amino acids (BCAAs) are known to promote skeletal muscle growth in healthy individuals; however, their efficacy in cancer patients remains controversial. In this study, we investigated the effects of BCAAs on cancer-associated sarcopenia to identify the underlying mechanisms that may suppress their effectiveness. In both a mouse cachexia model and an in vitro cachexia model, BCAAs did not significantly reduce oxidative stress, improve oxidative phosphorylation, suppress cytokine production, or enhance muscle mass and maturation, as observed in non-cancer-bearing models. Furthermore, treatment with 5-fluorouracil exacerbated sarcopenia in the mouse cachexia model, independent of tumor weight reduction, and this deterioration was not ameliorated by a BCAA-supplemented diet. The ineffectiveness of BCAAs was attributed to impaired BCAA catabolism, characterized by the decreased expression of branched-chain α-ketoacid dehydrogenase (BCKD) and increased levels of its inactive phosphorylated form, which were driven by elevated expression of BCKD kinase. These metabolic alterations were induced by high-mobility group box-1 (HMGB1). Notably, caprylic acid reversed these impairments in BCAA metabolism, thereby restoring BCAA efficacy. Our findings suggest that enhancing BCAA metabolism may improve their therapeutic potential in the treatment of cancer-associated sarcopenia.

## Linked entities

- **Genes:** LOC106567669 (branched-chain alpha-ketoacid dehydrogenase kinase) [NCBI Gene 106567669], HMGB1 (high mobility group box 1) [NCBI Gene 3146]
- **Chemicals:** caprylic acid (PubChem CID 379), 5-fluorouracil (PubChem CID 3385), branched-chain amino acids (PubChem CID 9886134)
- **Diseases:** cancer (MONDO:0004992)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Hmgb1 (high mobility group box 1) [NCBI Gene 15289] {aka HMG-1, Hmg1, SBP-1, p30}
- **Diseases:** Cachexia (MESH:D002100), Cancer (MESH:D009369), sarcopenia (MESH:D055948)
- **Chemicals:** 5-fluorouracil (MESH:D005472), BCAA (MESH:D000597), Amino Acid (MESH:D000596), Caprylic Acid (MESH:C031492)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12109939/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12109939/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12109939/full.md

---
Source: https://tomesphere.com/paper/PMC12109939