Background
Chronic obstructive pulmonary disease (COPD) is a common respiratory disorder in pulmonology. Chuanbeimu (CBM) is a traditional Chinese medicinal herb for treating COPD and has been widely utilized in clinical practice. However, the mechanism of CBM in the treatment of COPD remains incompletely understood. This study aims to investigate the underlying therapeutic mechanism of CBM for COPD using network pharmacology and experimental approaches.
Methods
Active ingredients and their targets were obtained from the Traditional Chinese Medicine Systems Pharmacology database. COPD-associated targets were retrieved from the GeneCards database. The common targets for CBM and COPD were identified through Venn diagram analysis. Protein-protein interaction (PPI) networks and disease-herb-ingredient-target networks were constructed. Subsequently, the results of the network pharmacology were validated by molecular docking and in vitro experiments.
Results
Seven active ingredients and 32 potential targets for CBM were identified as closely associated with COPD. The results of the disease-herb-ingredient-target network and PPI network showed that peimisine emerged as the core ingredient, and
SRC, ADRB2, MMP2
, and
NOS3
were the potential targets for CBM in treating COPD. Molecular docking analysis confirmed that peimisine exhibited high binding affinity with
SRC, ADRB2, MMP2
, and
NOS3
. In vitro experiments demonstrated that peimisine significantly upregulated the expression of
ADRB2
and
NOS3
and downregulated the expression of
SRC
and
MMP2
.
Conclusion
These findings indicate that CBM may modulate the expression of
SRC, ADRB2, MMP2
, and
NOS3
, thereby exerting a protective effect against COPD.