# Black ginseng under forest as a natural antidepressant: insights into its active components and mechanisms

**Authors:** Yixuan Sui, Yiying Tan, Yajing Li, Xiaochen Gao, Han Lu, Jiaming Shen, Xuesheng Hu, Lei Wang, Liting Zhao, Jiaming Sun, Chunnan Li

PMC · DOI: 10.3389/fchem.2025.1619060 · Frontiers in Chemistry · 2025-05-30

## TL;DR

Black Ginseng under forest may act as a natural antidepressant by reducing neuroinflammation through specific compounds like Ginsenoside F1.

## Contribution

The study identifies Ginsenoside F1 as a key active component in Black Ginseng with potent anti-neuroinflammatory effects.

## Key findings

- Black Ginseng showed stronger anti-neuroinflammatory effects than Ginseng under forest.
- Ginsenoside F1 was found to be the most effective component in reducing cell migration and apoptosis.
- BG modulates the PI3K-Akt pathway, reducing mRNA levels of AKT1, MAPK1, PIK3CA, and EGFR.

## Abstract

Depression is a psychological disorder with significant global impact. It is widely hypothesized that this disorder is associated with neuroinflammation, which disrupts neural homeostasis through various pathways. This study aims to investigate the effective compounds and mechanisms of Black Ginseng under forest (BG) in combating neuroinflammation. Utilizing methods such as UPLC-QE Orbitrap-MS, network pharmacology, molecular docking, and cell biology, the efficacy of BG was demonstrated, and its active components were identified. Cell viability and apoptosis were assessed using Trans well migration assays and flow cytometry. The mRNA expression of target genes was confirmed through real-time quantitative PCR (RT-qPCR), elucidating the anti-neuroinflammatory mechanism. The results indicated that BG exhibited a more pronounced effect on ameliorating neuroinflammatory conditions compared to Ginseng under forest (FG). The main active components were found through research and development, including Ginsenoside F1, Ginsenoside Rk1, Ginsenoside Rg3, etc. Among these, Ginsenoside F1 emerged as the most potent active component for treating neuroinflammation, as evidenced by reduced cell migration and apoptosis. The study demonstrates that BG can modulate the PI3K-Akt signaling pathway, leading to a reduction in the expression levels of AKT1, MAPK1, PIK3CA, EGFR, and other mRNAs. These findings suggest that BG is a promising natural antidepressant, providing both theoretical and experimental foundations for the development of new antidepressants based on BG and its active components.

## Linked entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], EGFR (epidermal growth factor receptor) [NCBI Gene 1956]
- **Chemicals:** Ginsenoside F1 (PubChem CID 9809542), Ginsenoside Rk1 (PubChem CID 10232023), Ginsenoside Rg3 (PubChem CID 9918693)
- **Diseases:** depression (MONDO:0002050)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12162673/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12162673/full.md

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Source: https://tomesphere.com/paper/PMC12162673