# The anti-depressive role of the Pei Yuan Kai Yu formula in cerebral small vessel disease based on gut microbiota

**Authors:** Lixuan Yang, Yutian Ao, Yannan Li, Baoan Dai, Junnan Li, Wenzhe Duan, Kaiqiang Dong, Zhenyun Han, Rongjuan Guo

PMC · DOI: 10.3389/fphar.2025.1510250 · Frontiers in Pharmacology · 2025-06-13

## TL;DR

A traditional formula called Pei Yuan Kai Yu (PY) may help treat depression in cerebral small vessel disease by improving gut microbiota and reducing brain inflammation.

## Contribution

This study demonstrates that PY alleviates depression in CSVD by modulating gut microbiota and reducing hippocampal inflammation and endothelial dysfunction.

## Key findings

- PY reduced inflammatory cytokines (TNF-α, IL-1β, IL-6) in both serum and hippocampus.
- PY improved gut microbiota diversity and reversed hippocampal nerve damage and microglial overexpression.
- PY enhanced microbiota-mediated metabolism linked to inflammation, endothelial dysfunction, and depressive behaviors.

## Abstract

Cerebral small vessel disease (CSVD), characterized by pathological changes in brain vessels, is a common cause of death in the elderly and often accompanied by depression, which significantly affects patients’ quality of life and rehabilitation; understanding its pathogenesis and developing innovative therapies are urgently needed, especially considering the role of the blood - brain barrier impairment and the gut - microbiota - gut - brain axis in this complex condition.

Dahl/SS rats were fed a diet containing 8% NaCl and were subjected to chronic unpredictable mild stress (CUMS) stimulation for 4 weeks. PY (1.407 g/kg/day) was administered intragastrically to evaluate its role in CSVD with depression. Pseudo germ-free rats were colonized with gut microbiota from high-salt-fed rats exposed to CUMS, followed by PY administration.

In rats with CSVD and depression, PY significantly increased body weight; alleviated depression-like behaviors; and decreased the levels of inflammatory cytokines such as TNF-α, IL-1β, and IL-6 in both serum and hippocampus. Additionally, PY reversed inflammation-induced nerve damage; reduced the overexpression of microglia in the hippocampus; decreased the levels of hippocampal VEGF and MMP-9, and increased the levels of hippocampal occludin, ZO-1, and claudin-5. Moreover, PY improved the composition of gut microbiota and enhanced microbial diversity. PY induced characteristic changes in the microbiome, which were associated with inflammation, endothelial dysfunction, and depressive-like behaviors. These significant metabolites were identified and were found closely related to inflammation, endothelial cell dysfunction, and depression-like behaviors.

In conclusion, PY acts as an antidepressant to slow down the progression of CSVD by inhibiting microglial activation, reducing inflammation and ameliorating endothelial dysfunction. It exerts its effect, at least in part, by enhancing microbiota-mediated metabolism in vivo.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL1B (interleukin 1 beta), IL6 (interleukin 6), VEGFA (vascular endothelial growth factor A), MMP9 (matrix metallopeptidase 9), si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3), TJP1 (tight junction protein 1), cldn5.L (claudin 5 (transmembrane protein deleted in velocardiofacial syndrome) L homeolog)
- **Chemicals:** NaCl (PubChem CID 5234)
- **Diseases:** depression (MONDO:0002050)

## Full-text entities

- **Genes:** Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 81687], Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, Ocln (occludin) [NCBI Gene 83497], Vegfa (vascular endothelial growth factor A) [NCBI Gene 83785] {aka VEGF-A, VEGF111, VEGF164, VPF, Vegf}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Tjp1 (tight junction protein 1) [NCBI Gene 292994] {aka ZO-1}, Cldn5 (claudin 5) [NCBI Gene 65131]
- **Diseases:** inflammation (MESH:D007249), endothelial dysfunction (MESH:D014652), nerve damage (MESH:D000080902), depression (MESH:D003866), death (MESH:D003643), endothelial cell dysfunction (MESH:D055954), CSVD (MESH:D059345)
- **Chemicals:** NaCl (MESH:D012965), salt (MESH:D012492)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12202353/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12202353/full.md

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Source: https://tomesphere.com/paper/PMC12202353