Integrated approach of network pharmacology, molecular docking, and clinical observations in evaluating the efficacy and safety of Bufei Huoxue capsules for pulmonary hypertension associated with chronic obstructive pulmonary disease

Author:

He Wenjun12ORCID,Liu Chunli1,Li Xuanyi1,Zhong Bihua1ORCID,Jiang Qian1,Lai Ning1,Xiong Yuanhui1,Feng Weici1,Chen Yilin1,Zhou Dansha1ORCID,Li Defu3,Lu Wenju1,Aman Jurjan2,Bogaard Harm Jan2,Wang Jian145ORCID,Chen Yuqin15ORCID

Affiliation:

1. State Key Laboratory of Respiratory Diseases, National Center for Respiratory Medicine, Guangdong Key Laboratory of Vascular Diseases, National Clinical Research Center for Respiratory Diseases, Guangzhou Institute of Respiratory Health The First Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong China

2. PHEniX laboratory, Department of Pulmonary Medicine, Amsterdam Cardiovascular Sciences, Pulmonary Hypertension and Thrombosis Amsterdam UMC location Vrije Universiteit Amsterdam Amsterdam The Netherlands

3. Department of Pulmonary and Critical Care Medicine The Fifth Affiliated Hospital of Guangzhou Medical University Guangzhou China

4. Guangzhou Laboratory Guangzhou International Bio Island Guangzhou Guangdong China

5. Section of Physiology, Department of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine University of California San Diego La Jolla California USA

Abstract

AbstractChronic obstructive pulmonary disease (COPD) is a persistent and progressive disorder characterized by airway or alveolar abnormalities, commonly leading to pulmonary hypertension (PH). This clinical observational study investigates the therapeutic mechanisms of Bufei Huoxue capsules (BHC) in treating PH in patients with COPD‐linked PH (COPD‐PH) using network pharmacology and molecular docking methods, and assesses the therapeutic efficacy and safety of BHCs. The active compounds and their target proteins in BHCs were sourced from the Traditional Chinese Medicine Systems Pharmacology database, with additional target proteins derived from the GeneCards and OMIM databases. An active network was constructed using Cytoscape 3.7.1, and interaction networks were established. Intersecting targets underwent Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis using the Metascape database. Network pharmacology and molecular docking studies demonstrated favorable binding affinities of BHC active ingredients, such as quercetin, bavachalcone, and isobavachin, for key targets including PTGS1, ESR1, and PTGS2. Gene Ontology enrichment analysis highlighted the involvement of these targets in processes such as the positive regulation of locomotion, the transmembrane receptor protein tyrosine kinase signaling pathway, and peptidyl‐tyrosine phosphorylation. KEGG pathway analysis indicated their roles in pathways related to cancer, AGE‐RAGE signaling in diabetic complications, and prostate cancer. BHCs exhibit therapeutic effects on COPD‐PH through multi‐component, multi‐target, and multi‐pathway interactions. This clinical observational study confirms the efficacy and safety of BHCs in improving cardiac and pulmonary functions, enhancing exercise tolerance, and elevating the quality of life in patients with COPD‐PH.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Reference30 articles.

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