# The therapeutic potential of Zuogui Wan in oligoasthenozoospermia: insights from network pharmacology, molecular docking, molecular dynamics simulation, and experimental validation

**Authors:** Mingzhao Zhang, Jisheng Wang, Junlong Feng, Baojun Ju, Jingxun Yang, Zhenfei Gao, Xiangyu Wang, Shuxi Zhou, Xiao Li

PMC · DOI: 10.1038/s41598-025-22348-w · Scientific Reports · 2025-11-04

## TL;DR

This study explores how Zuogui Wan, a traditional Chinese medicine, may treat male infertility by improving sperm quality through multiple scientific methods.

## Contribution

The study combines network pharmacology, molecular simulations, and experiments to reveal the molecular mechanisms of Zuogui Wan in treating oligoasthenozoospermia.

## Key findings

- Zuogui Wan promotes cell proliferation and reduces apoptosis in sperm-related cells.
- Key compounds like Cyasterone show strong binding to targets linked to male infertility.
- Zuogui Wan improves testicular structure and sperm quality in animal models.

## Abstract

Oligoasthenozoospermia (OAS) is a major cause of male infertility, with limited effective treatments. Chinese patent medicine Zuogui Wan (ZGW) has been traditionally used to improve sperm quality, but its molecular mechanisms remain unclear. This study integrates network pharmacology, molecular docking, molecular dynamics (MD) simulation, and in vivo and in vitro experiments to explore ZGW’s therapeutic effects in OAS. Active compounds and targets of ZGW were identified using network pharmacology, and intersecting OAS-related targets underwent enrichment and protein-protein interaction (PPI) analysis. Molecular docking and MD simulations assessed compound-target binding affinity and stability. In vitro, CCK-8 assays measured cell proliferation, while qPCR and Western blot analyzed key gene and protein expression. In vivo, a rat OAS model was used to evaluate ZGW’s therapeutic effects through transmission electron microscopy (TEM), hematoxylin & eosin (HE) staining, and TUNEL assays. The expression of key molecular targets was further validated by qPCR and Western blot. A total of 182 potential targets were identified, with TP53, NF-κB1, and PKC as key hub genes. KEGG pathway analysis highlighted the involvement of the PI3K-AKT and MAPK signaling pathways.Four core bioactive compounds—Cyasterone, Betavulgarin, Kaempferol, and Quercetin—were identified, with Cyasterone exhibiting the strongest binding affinity and highest stability.In vitro experiments demonstrated that ZGW significantly promoted cell proliferation and regulated apoptosis-related gene expression, indicating its potential in enhancing sperm function. In vivo, ZGW improved testicular structure, enhanced sperm quality, and reduced spermatogenic cell apoptosis, as evidenced by TEM, HE, and TUNEL assays. Molecular validation further confirmed ZGW’s modulation of key signaling pathways involved in OAS. ZGW modulates apoptosis, oxidative stress, and key pathways (PI3K-AKT, MAPK) while regulating TP53, NF-κB, and PKC expression. Cyasterone exhibits strong binding and stability with core targets. This study supports ZGW as a potential treatment for male infertility.

The online version contains supplementary material available at 10.1038/s41598-025-22348-w.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476]
- **Chemicals:** Cyasterone (PubChem CID 119444), Betavulgarin (PubChem CID 442668), Kaempferol (PubChem CID 5280863), Quercetin (PubChem CID 5280343)

## Full-text entities

- **Genes:** Tp53 (tumor protein p53) [NCBI Gene 24842] {aka Trp53, p53}, Prkcg (protein kinase C, gamma) [NCBI Gene 24681] {aka PKC, PKCI, Prkc, Prkcc, RATPKCI}, Akt1 (AKT serine/threonine kinase 1) [NCBI Gene 24185] {aka Akt}, Pik3cb (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta) [NCBI Gene 85243]
- **Diseases:** male infertility (MESH:D007248)
- **Chemicals:** Cyasterone (MESH:C002082), hematoxylin (MESH:D006416), Betavulgarin (MESH:C000715827), eosin (MESH:D004801), Kaempferol (MESH:C006552), CCK-8 (MESH:D012844), Quercetin (MESH:D011794)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12586514/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12586514/full.md

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Source: https://tomesphere.com/paper/PMC12586514