Title:Identifying the Mechanisms and Molecular Targets of Guchang Zhixie
Pills on Ulcerative Colitis: Coupling Network Pharmacology with GEO
Database and Experiment Verification
Volume: 26
Issue: 11
Author(s): Weihao Wang, Xujiao Song, Shanshan Ding, Chunlin Chen and Hao Ma*
Affiliation:
- Aesthetic Medical
School, Yichun University, Yichun 336000, Jiangxi, China
Keywords:
Network pharmacology, Guchang Zhixie pills, molecular docking, ulcerative colitis, inflammation, immune infiltration
Abstract:
Objective: This research investigates the mechanisms and molecular targets of the
Guchang Zhixie pill (GCZXP) against ulcerative colitis (UC) in silico and in vivo.
Methods: The compounds and related targets of GCZXP were collected from the traditional Chinese
medicine systems pharmacology database. UC targets were from Gene Expression Omnibus
and GeneCards databases. Hub genes were acquired through Cytoscape. Gene ontology and Kyoto
Encyclopedia of Genes and Genomes enrichment were performed in the David database. R packages
were used to investigate the relationship between immune cells and hub genes and the diagnostic
model. AutoDock was used to verify the molecular docking of the core compounds and hub genes,
as well as nuclear factor-kappa B (NF-κB) p65 and IκBα. The hub genes and NF-κB pathway were
verified via experiment.
Results: In GCZXP, a total of 51 active compounds were discovered. Enrichment analysis was used
to study inflammation, chemokine activity, NF-κB signalling pathway, etc. Thirteen key therapeutic
targets were involved, of which included three hub genes PTGS2, IL-1β and CXCL8. Immune infiltration
revealed that all of the 3 hub genes were positively correlated with M1 macrophages, neutrophils,
and activated memory CD4 cells, and negatively correlated with plasma cells. In the training
and validation sets, the area under the curve (AUC) of the diagnostic model developed by hub genes
reached 0.929 and 0.905, respectively, indicating a good forecasting potential. The rat experiment
proved that GCZXP significantly reduced the expressions of IL-1β, CXCL8, COX-2, and NF-κB
p65 while increasing IκBα and Bcl-2, alleviated colonic inflammatory injury and promoted ulcer
healing.
Conclusion: GCZXP reduced the release of cytokines and regulated Bcl-2 in the treatment of UC
by inhibiting the NF-κB signalling pathway.