# Mechanisms of a Patented Chinese Herbal Medicine for Treating Hypothyroidism in In Vitro Fertilization-Embryo Transfer: A Combination of Network Pharmacology, Molecular Docking, and Molecular Dynamics Simulation

**Authors:** Chang Liu, Weihuan Hu, Tianyi Zhou, Jue Zhou, Fangfang Wang, Xiaoling Feng, Fan Qu

PMC · DOI: 10.2174/0113816128364578250212094405 · Current Pharmaceutical Design · 2025-04-15

## TL;DR

This study explores how a patented Chinese herbal medicine, QUF6, treats hypothyroidism during IVF-ET by identifying its active ingredients and molecular mechanisms.

## Contribution

The study combines network pharmacology, molecular docking, and dynamics simulations to reveal QUF6's mechanisms in treating hypothyroidism during IVF-ET.

## Key findings

- Quercetin and other compounds in QUF6 interact with key targets like TNF, IL-6, and BCL2.
- Molecular docking and simulations confirm stable binding between active components and disease-related targets.
- The treatment may modulate inflammation, oxidative stress, and apoptosis through these targets.

## Abstract

Qu’s formula 6 (QUF6), a patented Chinese herbal medicine, is used to treat hypothyroidism in the context of in vitro fertilization-embryo transfer (IVF-ET). This research aims to identify the potential bioactive components and elucidate the underlying molecular mechanisms by which QUF6 cures hypothyroidism during IVF-ET.

To find the active components of QUF6, the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) and relevant literature were searched. GeneCards and other resources were used to find the targets associated with hypothyroidism and IVF-ET. Using Cytoscape software, the network of interactions was created between the targets and components, the protein-protein interaction (PPI) network was built, and significant targets were verified. Afterward, Gene Ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed on crucial targets. Finally, molecular docking and dynamic modeling were carried out to analyze the essential components and core targets of QUF6.

By creating an interaction network, it was discovered that 92 active components in QUF6 can operate on 25 disease-related targets, with quercetin and other components playing important pharmacodynamic roles. Tumor necrosis factor (TNF), interleukin-6 (IL-6), interleukin-1B (IL-1B), apoptosis regulator Bcl-2 (BCL2), prostaglandin G/H synthase 2 (PTGS2), cellular tumor antigen p53 (TP53), and epidermal growth factor (EGF) were the main targets for the therapy of hypothyroidism. The KEGG pathway enrichment study identified 91 signaling pathways, whereas the GO enrichment analysis identified 1608 entries. Through molecular docking and MD simulations, stable binding was identified between the top five active constituents and the top seven potential targets.

Quercetin, beta-sitosterol, kaempferol, 7-ketocholesterol, and rehmapicrogenin were determined to be the active ingredients in QUF6. The potential mechanism of action for QUF6 may involve modulation of TNF, IL6, IL1B, BCL2, PTSG2, TP53, and EGF to regulate oxidative stress levels, inflammation responses, and apoptosis processes associated with hypothyroidism during IVF-ET.

## Linked entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124], IL6 (interleukin 6) [NCBI Gene 3569], IL1B (interleukin 1 beta) [NCBI Gene 3553], BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596], PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743], TP53 (tumor protein p53) [NCBI Gene 7157], EGF (epidermal growth factor) [NCBI Gene 1950]
- **Chemicals:** quercetin (PubChem CID 5280343), beta-sitosterol (PubChem CID 86821), kaempferol (PubChem CID 5280863), 7-ketocholesterol (PubChem CID 91474), rehmapicrogenin (PubChem CID 15693863)
- **Diseases:** hypothyroidism (MONDO:0005420)

## Full-text entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** Hypothyroidism (MESH:D007037), inflammation (MESH:D007249)
- **Chemicals:** 7-ketocholesterol (MESH:C003001), beta-sitosterol (MESH:C025473), Chinese Herbal Medicine (-), Quercetin (MESH:D011794), kaempferol (MESH:C006552)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12606615/full.md

## References

78 references — full list in the complete paper: https://tomesphere.com/paper/PMC12606615/full.md

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Source: https://tomesphere.com/paper/PMC12606615