Open Access
Open access

Chen’s peiyuan tang and premature ovarian failure: unveiling the mechanisms through network pharmacology

Xiao Yang 1
Yi-Ming Mao 2
Chong Yao 3, 4
Ding-ming Song 5
Yi-Bo He 6
Wei Shen 7
Publication typeJournal Article
Publication date2024-11-29
scimago Q1
wos Q1
SJR1.220
CiteScore8.9
Impact factor4.8
ISSN16639812
Abstract
Background

Chen’s Peiyuan Tang (CSPYT) is a compound herbal formula that has shown the potential to enhance ovarian function and reduce autophagy in ovarian granulosa cells, which plays a crucial role in follicular development and maturation. The application of Chinese herbal medicine offers a promising alternative to traditional hormone replacement therapy (HRT).

Methods

This study explores CSPYT’s therapeutic mechanisms in treating POF, focusing on its modulation of autophagy through network pharmacology and transcriptomics-based analysis, predicting potential interactions and pathways. KGN cell line and rat ovarian granulosa cells were used for in vitro experiment. 4-Hydroperoxy cyclophosphamide(4-HC) stimulation was carried out for establishing the POF cell model. Q-PCR, Western Blot, Transmission electron microscopy to detect the results.

Results

According to the drug and disease database, the common targets of Chen’s Peiyuan Tang and premature ovarian failure were screened, combined with autophagy gene targets and transcriptome analysis, and finally 8 intersection targets were obtained, namely CDKN1B, MAPK3, PRKCD, CDKN1A, MAPK1, RAF1, BIRC5, CTSB. Enrichment analysis of 8 genes found that they were closely related to the animal autophagy pathway. Construct PPI network diagram. CytoScape 3.9.1 builds CSPYT Drug Target-POF Disease Target-Autophagy Gene Network Diagram. Based on the PPI network diagram and CytoScape 3.9.1 analysis results, it is estimated that MAPK1 and MAPK3 are the key targets of CSPYT in the treatment of POF. The eight final intersection targets were docked with the corresponding active pharmaceutical ingredients. The one that docked most closely with the MAPK family was naringenin. In cell experiment verification, it was confirmed that Chen’s Peiyuan Tang can inhibit the MAPK signaling pathway, significantly reduce the number of autophagosomes, and reduce autophagy damage in ovarian granulosa cells.

Discussion

CSPYT can inhibit the MAPK signaling pathway, prevent autophagy overexpression and restore ovarian granulosa cell function, effectively alleviating the disease pressure of POF.

Found 
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Top-30

Journals

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1 publication, 20%
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1 publication, 20%
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Publishers

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Springer Nature
4 publications, 80%
Ovid Technologies (Wolters Kluwer Health)
1 publication, 20%
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GOST Copy
Yang X. et al. Chen’s peiyuan tang and premature ovarian failure: unveiling the mechanisms through network pharmacology // Frontiers in Pharmacology. 2024. Vol. 15.
GOST all authors (up to 50) Copy
Yang X., Mao Y., Yao C., Song D., He Y., Shen W. Chen’s peiyuan tang and premature ovarian failure: unveiling the mechanisms through network pharmacology // Frontiers in Pharmacology. 2024. Vol. 15.
RIS |
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TY - JOUR
DO - 10.3389/fphar.2024.1446707
UR - https://www.frontiersin.org/articles/10.3389/fphar.2024.1446707/full
TI - Chen’s peiyuan tang and premature ovarian failure: unveiling the mechanisms through network pharmacology
T2 - Frontiers in Pharmacology
AU - Yang, Xiao
AU - Mao, Yi-Ming
AU - Yao, Chong
AU - Song, Ding-ming
AU - He, Yi-Bo
AU - Shen, Wei
PY - 2024
DA - 2024/11/29
PB - Frontiers Media S.A.
VL - 15
PMID - 39679373
SN - 1663-9812
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2024_Yang,
author = {Xiao Yang and Yi-Ming Mao and Chong Yao and Ding-ming Song and Yi-Bo He and Wei Shen},
title = {Chen’s peiyuan tang and premature ovarian failure: unveiling the mechanisms through network pharmacology},
journal = {Frontiers in Pharmacology},
year = {2024},
volume = {15},
publisher = {Frontiers Media S.A.},
month = {nov},
url = {https://www.frontiersin.org/articles/10.3389/fphar.2024.1446707/full},
doi = {10.3389/fphar.2024.1446707}
}