# Cereal Vinegar Sediment Modulates the Gut Microbiota–Metabolite Axis Associated with Hyperlipidemia in Apoe−/− Mice

**Authors:** Wenhui Duan, Qijie Guan, Yilin Ren, Jin-Song Shi, Zheng-Hong Xu, Yingyue Sheng, Yuzheng Xue, Chengcheng Zhang, Yan Geng

PMC · DOI: 10.3390/foods15030427 · Foods · 2026-01-24

## TL;DR

Cereal vinegar sediment (CVS) changes gut microbes and metabolites in mice with high cholesterol, suggesting potential health benefits.

## Contribution

This study reveals how different types of CVS reshape gut microbiota and metabolites in hyperlipidemic mice.

## Key findings

- CVS treatment altered gut microbial communities in Apoe−/− mice.
- Key metabolites like N1-acetylspermidine and 25-hydroxycholesterol were significantly affected by CVS.
- CVS modulated lipid-related pathways and showed partial lipid-lowering effects.

## Abstract

Cereal vinegar sediment (CVS), a byproduct of traditional vinegar fermentation, has been regarded as a health-promoting product. However, its role in genetically induced hyperlipidemia remains unclear. This study systematically evaluated the effects of Dade-CVS (DD-CVS) and Hengshun-CVS (HS-CVS) on apolipoprotein-E-deficient (Apoe−/−) mice. Both CVS varieties significantly improve certain serological parameters of Apoe−/− mice, although the overall impact on serum indicators remains limited. Nevertheless, 16S rRNA sequencing revealed that CVS treatment reshaped gut microbial communities to a notable extent. Compared with the Apoe−/− mice, the DD-CVS treatment significantly increased the relative abundance of Dubosiella while reducing the genus Desulfovibrio, whereas the HS-CVS treatment inhibited the growth of Bifidobacterium and Akkermansia. The pathways predicted in the KO-DD group included vitamin, amino acid, and energy metabolism, while HS-CVS treatment was associated with bile acid biosynthesis and energy pathways. Metabolomic analysis showed that several key metabolites, including N1-acetylspermidine, succinic acid, and 25-hydroxycholesterol, were significantly altered following CVS supplementation. Correlation analysis revealed significant associations between serum indicators and these metabolites. Alistipes, Enterorhabdus, and Romboutsia were also correlated with serum indicators. Overall, these findings indicate that CVS primarily modulated the gut microbiota–metabolite axis and partial lipid modulation in hyperlipidemic mice. The study provides a reference for studies on the beneficial functions of CVS in hyperlipidemia.

## Linked entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348]
- **Chemicals:** N1-acetylspermidine (PubChem CID 496), succinic acid (PubChem CID 1110), 25-hydroxycholesterol (PubChem CID 65094)
- **Diseases:** hyperlipidemia (MONDO:0021187)

## Full-text entities

- **Genes:** Apoe (apolipoprotein E) [NCBI Gene 11816] {aka Apo-E}
- **Diseases:** DD (MESH:C536170), Hyperlipidemia (MESH:D006949)
- **Chemicals:** N1-acetylspermidine (MESH:C017988), HS (MESH:D006859), DD (MESH:C007792), succinic acid (MESH:D019802), lipid (MESH:D008055), CVS (-), bile acid (MESH:D001647), 25-hydroxycholesterol (MESH:C007997)
- **Species:** Akkermansia (genus) [taxon 239934], Mus musculus (house mouse, species) [taxon 10090], Dubosiella (genus) [taxon 1937008], Bifidobacterium (genus) [taxon 1678], Desulfovibrio (genus) [taxon 872], Alistipes (genus) [taxon 239759]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12896822/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12896822/full.md

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Source: https://tomesphere.com/paper/PMC12896822