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基于网络药理学分析及香烟烟雾与脂多糖诱导的慢性阻塞性肺疾病大鼠模型对降气定喘丸疗效的评价
Authors Zhou J, Song J, Peng D, Zheng Y, Ning N, Chen G, Huang Q, Li Y
Received 6 September 2024
Accepted for publication 21 March 2025
Published 2 April 2025 Volume 2025:20 Pages 929—941
DOI http://doi.org/10.2147/COPD.S489696
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Richard Russell
Jiewen Zhou,1,* Jinbin Song,2,* Danting Peng,3 Yanqiu Zheng,2 Na Ning,4 Guirong Chen,2 Qiuling Huang,4 Yanwu Li2
1The First Clinical College, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, People’s Republic of China; 2Science and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, People’s Republic of China; 3Clinical Research Center, Guangzhou Baiyunshan Qixing Pharmaceutical Co. Ltd, Guangzhou, Guangdong, People’s Republic of China; 4Clinical Research Center, Guangzhou Baiyunshan Zhongyi Pharmaceutical Co. Ltd, Guangzhou, Guangdong, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Qiuling Huang, Email huangqiuling1982@163.com Yanwu Li, Email liyanwu@gzucm.edu.cn
Background: Jiangqi Dingchuan Pill (JDP) is a patent Chinese medicine in the treatment of asthma. JDP consists of six herbal drugs, namely, Ephedrae Herba, Mori Cortex, Citri Reticulatae Pericarpium, Perillae Fructus, Descurainiae Semen, Sinapis Semen.
Objective: To employ the tools of network pharmacology and in vivo experiments, exploring the possible mechanism of JDP in treating chronic obstructive pulmonary disease (COPD).
Materials and Methods: Chemical constituents of JDP, collection of targets of COPD, target prediction were conducted, and then network pharmacological analysis was performed based on protein–protein interaction (PPI). The cigarette smoke and lipopolysaccharide-induced COPD model was applied to assess the effects of JDP. Rats were randomly divided into five groups (n = 8), ie, a sham group, a COPD-control group, two COPD groups treated with different doses of JDP (1.26 and 2.52 g/kg/d, respectively), and one COPD group treated with aminophylline (54 mg/kg/d). Pulmonary functions were assessed. The inflammatory cytokines in bronchial alveolar lavage fluid (BALF) were quantified using enzyme-linked immunosorbent assay (ELISA). The expression of matrix metalloprotein-9 (MMP-9) was quantified using Western blot.
Results: A total of 108 genes were found to be the main target genes regulated by JDP in the treatment of COPD, according to PPI analysis. Compared with the COPD-control group, rats in the JDP group exhibited amelioration in lung function, including 20 ms forced expiratory volume/forced vital capacity, maximal mid-expiratory flow curve, and airway resistance (all p < 0.05). A reduction of IL-1β and TNF-α expressions in BALF was also observed (both p < 0.05). Compared with the COPD-control group, the expression of MMP-9 in lung tissue was down-regulated in the JDP group (p < 0.05).
Conclusion: This study explored the effects and its mechanisms of JDP in COPD treatment. JDP exhibited therapeutic potential as a COPD intervention drug.
Keywords: Traditional Chinese Medicine, network pharmacology, chronic obstructive pulmonary disease, Jiangqi Dingchuan Pill