# Research on the effect of Rosa roxburghii root in alleviating spleen and stomach damp–heat gastric ulcer by regulating the imbalance of oral–gut axis microbiota

**Authors:** Jiangsong Cao, Ziyu Zhang, Xiongwei Liu, Ying Zhou, Jiaxin Li, Xinyue Wang, Chang Liu

PMC · DOI: 10.3389/fmicb.2025.1701829 · Frontiers in Microbiology · 2025-11-07

## TL;DR

This study shows that Rosa roxburghii root may help treat gastric ulcers by balancing gut and oral bacteria and reducing inflammation.

## Contribution

The study is the first to investigate how Rosa roxburghii root alleviates gastric ulcers by modulating the oral–gut microbiota in a damp–heat syndrome model.

## Key findings

- Rosa roxburghii root reduced gastric ulcer severity and inflammation in rats.
- The herb reversed microbial dysbiosis in the oral and gut microbiota.
- RT increased beneficial bacteria like Lactobacillus and decreased harmful ones like Desulfovibrio.

## Abstract

Rosa roxburghii root (RT), a medicinal herb traditionally utilized by ethnic minorities in Guizhou Province, has demonstrated potential in managing gastrointestinal disorders. Nonetheless, its effectiveness in treating gastric ulcers (GU) accompanied by spleen–stomach damp–heat syndrome, especially through mechanisms that involve interactions with oral–gut microbiota, remains to be elucidated.

A rat model of GU with damp–heat syndrome was established. The rats were treated with various doses of RT, and gastric mucosal injury was assessed through ulcer index calculation and histopathological examination. Additionally, the levels of immunoglobulin 6 (IL-6), tumor necrosis factor alpha (TNF-α), nitric oxide (NO), inducible nitric oxide synthase (iNOS), motilin (MTL), prostaglandin E2 (PGE2), and malondialdehyde (MDA) were measured. A 16S ribosomal RNA (rRNA) sequencing was conducted on samples of tongue coating and intestinal contents to analyze the microbial composition and changes.

Compared to the control (CON) group, the gastric ulcer (GU) group exhibited significant pathological alterations in the gastric mucosa. The levels of IL-6, TNF-α, and MDA were significantly elevated (p < 0.01), whereas the levels of NO, iNOS, MTL, and PGE2 showed a notable reduction (p < 0.01). Compared to the GU group, the RT’s high-dose (RTH) groups exhibited statistically significant improvements in the ulcer index, reduced levels of TNF-α, IL-6, MDA, and increased levels of NO, MTL, iNOS, and PGE2 (p < 0.05). Moreover, RT reversed oral–gut microbial dysbiosis, increasing the relative abundance of oral bacteria Muribacter and Corynebacterium, as well as intestinal bacteria Lactobacillus, Romboutsia, and Limosilactobacillus, while decreasing the relative abundance of oral bacteria Rodentibacter, Rothia, and Streptococcus, and intestinal bacteria Ligilactobacillus and Desulfovibrio. Both oral and gut bacteria are closely associated with clinical inflammatory factors in GU. Following ulcer onset, decreased levels of NO, iNOS, PGE2, and MTL, alongside increased levels of TNF-α, IL-6, and MDA, directly induce a reduction in the abundance of bacteria, including Rothia, Streptococcus, Corynebacterium, Globicatella, Romboutsia, and Lactobacillus, with this effect being more pronounced in the oral cavity. However, treatment with RT may potentially increase the abundance of these bacteria within the intestine, which could directly regulate gastric ulcer-related inflammatory factor levels and ameliorate clinical symptoms. R. roxburghii root has therapeutic effects against the progression of gastric ulcers by promoting mucosal repair and suppressing the release of inflammatory mediators.

## Linked entities

- **Proteins:** IL6 (interleukin 6), TNF (tumor necrosis factor), Nos1 (nitric oxide synthase 1, neuronal), NOS2 (nitric oxide synthase 2), Mtl (Mig-2-like), ptges2.L (prostaglandin E synthase 2 L homeolog), so (sine oculis)
- **Diseases:** gastric ulcer (MONDO:0001126)
- **Species:** Rosa roxburghii (taxon 74654), Muribacter (taxon 1857532), Corynebacterium (taxon 1716), Lactobacillus (taxon 1578), Romboutsia (taxon 1501226), Limosilactobacillus (taxon 2742598), Rodentibacter (taxon 1960084), Rothia (taxon 32207), Streptococcus (taxon 1301), Ligilactobacillus (taxon 2767887), Desulfovibrio (taxon 872)

## Full-text entities

- **Diseases:** gastric mucosal injury (MESH:D013272), gastrointestinal disorders (MESH:D005767), GU (MESH:D013276), inflammatory (MESH:D007249), ulcer (MESH:D014456), heat (MESH:D018883)
- **Chemicals:** MDA (MESH:D008315), R. roxburghii root (-), NO (MESH:D009569), PGE2 (MESH:D015232)
- **Species:** Corynebacterium (genus) [taxon 1716], Globicatella (genus) [taxon 13075], Desulfovibrio (genus) [taxon 872], Rattus norvegicus (brown rat, species) [taxon 10116], Muribacter (genus) [taxon 1857532], Lactobacillus (genus) [taxon 1578], Streptococcus (genus) [taxon 1301], Rothia (genus) [taxon 508215]
- **Mutations:** A 16S

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12636000/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12636000/full.md

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Source: https://tomesphere.com/paper/PMC12636000