# Effects of Galacto-Oligosaccharide Supplementation on Cecal Microbiota, Phospholipid and Aromatic Amino Acid Metabolism in Mice

**Authors:** Zisong Gao, Jue Wang, Zhiheng Cheng, Ziyang Zha, Ting Xu, Ke Yang, Tiantian Zhao, Jinglun Jiang, Pengchao Zheng, Yu Pi, Shiyi Tian

PMC · DOI: 10.3390/microorganisms14030652 · Microorganisms · 2026-03-13

## TL;DR

This study shows how adding galacto-oligosaccharides to mice diets changes gut bacteria and affects metabolism, potentially improving intestinal health.

## Contribution

The study reveals novel metabolic and microbial effects of GOS supplementation in mice cecum.

## Key findings

- GOS increased cecal bacterial diversity and specific bacterial groups like [Eubacterium] brachy and Clostridium.
- Low-dose GOS reduced phospholipid metabolites, suggesting improved intestinal integrity.
- High-dose GOS altered aromatic amino acid metabolism and increased indole-3-acetic acid production.

## Abstract

Galacto-oligosaccharides (GOSs) are well-recognized for their beneficial effects on intestinal health, yet their regulatory impacts on the metabolic dynamics of other intestinal metabolites remain elusive. In this study, 24 male C57BL/6 mice were assigned to three groups: control (CON), low-dose GOS (L-GOS; 500 mg/kg body weight), and high-dose GOS (H-GOS; 800 mg/kg body weight). Following a 4-week intervention, the cecal contents were analyzed to characterize the bacterial community structure and metabolic profiles. Results indicated that GOS supplementation significantly increased the ACE and Chao1 indices of cecal bacteria. Specifically, L-GOS led to notable enrichment of the [Eubacterium] brachy group, Coriobacteriaceae UCG-002, Faecalimonas, and the [Eubacterium] siraeum group, whereas H-GOS significantly increased the abundance of Clostridium, Ruminiclostridium, Thomasclavelia, Adlercreutzia, and Faecalimonas. Metabolomic profiling revealed that L-GOS profoundly reduced levels of phosphatidylethanolamine, phosphatidylcholine and their downstream metabolites, while inhibiting the conversion of sphingolipids to ceramides. The changes in phospholipid derivatives imply enhanced intestinal epithelial integrity, supporting intestinal homeostasis. GOS intervention also decreased phenylacetic acid content. L-GOS increased the 4-hydroxyphenylpyruvic acid content, whereas H-GOS reduced 4-hydroxyphenyllactic acid levels. Notably, H-GOS significantly up-regulated the production of indole-3-acetic acid, a tryptophan-derived microbial metabolite with multiple biological activities. Collectively, these findings provide insights and potential targets for future research on GOS application in intestinal health interventions.

## Linked entities

- **Chemicals:** galacto-oligosaccharides (PubChem CID 871), phosphatidylethanolamine (PubChem CID 5327011), phenylacetic acid (PubChem CID 999), 4-hydroxyphenylpyruvic acid (PubChem CID 979), 4-hydroxyphenyllactic acid (PubChem CID 9378), indole-3-acetic acid (PubChem CID 802)
- **Species:** Eubacterium (taxon 1730), Faecalimonas (taxon 2005355), Clostridium (taxon 1485), Ruminiclostridium (taxon 1508657), Thomasclavelia (taxon 3025755), Adlercreutzia (taxon 447020)

## Full-text entities

- **Chemicals:** 4-hydroxyphenylpyruvic acid (MESH:C010590), GOS (-), 4-hydroxyphenyllactic acid (MESH:C001418), tryptophan (MESH:D014364), phenylacetic acid (MESH:C025136), Phospholipid (MESH:D010743), sphingolipids (MESH:D013107), phosphatidylcholine (MESH:D010713), ceramides (MESH:D002518), indole-3-acetic acid (MESH:C030737), Aromatic Amino Acid (MESH:D024322), phosphatidylethanolamine (MESH:C483858)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Eubacterium (genus) [taxon 1730], Clostridium (genus) [taxon 1485], Ruminiclostridium (genus) [taxon 1508657]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13029313/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029313/full.md

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Source: https://tomesphere.com/paper/PMC13029313