# Dietary Glyceryl Monolaurate Supplementation During Pregnancy Enhances Fetal Intrauterine Development and Antioxidant Capacity in Sows via Microbiota Modulation

**Authors:** Zhichao Fu, Jun Wang, Yueqi Zhao, Tanyi Deng, Ziwei Ma, Wutai Guan, Xiangfang Zeng, Fang Chen

PMC · DOI: 10.3390/antiox14070783 · Antioxidants · 2025-06-25

## TL;DR

Adding glyceryl monolaurate to pregnant sows' diets improves fetal development and antioxidant capacity by changing gut bacteria.

## Contribution

This study shows how GML improves fetal development through microbiota modulation in sows.

## Key findings

- GML improved neonatal intestinal and muscle development in treated sows.
- GML enriched SCFA-producing bacteria like Lactobacillus and Akkermansia in maternal gut microbiota.
- GML increased SCFA levels and antioxidant capacity while inhibiting inflammatory pathways.

## Abstract

This study elucidates the mechanisms underlying the positive effect of glyceryl monolaurate (GML) on fetal intrauterine development via maternal gut-microbiota modulating effects using a sow model. Addition of GML (1000 mg/kg) improved neonatal intestinal conditions (jejunal villus height, VH/CD ratio and tight junctions) and dorsal longissimus muscle (MyoD, MyoG and MSTN) development in the GML-treated group. Furthermore, GML improved maternal gut microbiota composition by enriching short-chain fatty acid (SCFA)-producing bacteria Lactobacillus and Akkermansia. Meanwhile, SCFA concentrations in sow feces and newborn plasma, as well as their receptors (GPR41/43) in intestine and muscle were upregulated with GML, corresponding with enhanced antioxidative and anti-inflammatory capacity. Further correlation analysis revealed Akkermansia and Lactobacillus positively correlated with SCFAs, antioxidative indicators, and anti-inflammatory capacity markers. Moreover, GML inhibited the activation of the MAPK/NF-κB inflammatory signaling pathway. In summary, GML enhanced fetal intrauterine development by modulating sow intestinal SCFA-producing bacteria.

## Linked entities

- **Genes:** MYOD1 (myogenic differentiation 1) [NCBI Gene 4654], MYOG (myogenin) [NCBI Gene 4656], MSTN (myostatin) [NCBI Gene 2660], FFAR3 (free fatty acid receptor 3) [NCBI Gene 2865], FFAR2 (free fatty acid receptor 2) [NCBI Gene 2867], MAPK (mitogen activated kinase-like protein) [NCBI Gene 7446652], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790]
- **Chemicals:** glyceryl monolaurate (PubChem CID 14871)
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, MSTN (myostatin) [NCBI Gene 2660] {aka GDF8, MSLHP}, MYOD1 (myogenic differentiation 1) [NCBI Gene 4654] {aka CMYO17, CMYP17, MYF3, MYOD, MYODRIF, PUM}, MYOG (myogenin) [NCBI Gene 4656] {aka MYF4, bHLHc3, myf-4}
- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** GML (MESH:C020777), SCFA (MESH:D005232)
- **Species:** Akkermansia (genus) [taxon 239934], Lactobacillus (genus) [taxon 1578]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12291777/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12291777/full.md

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Source: https://tomesphere.com/paper/PMC12291777