• 中国核心期刊数据库收录期刊
  • 中文科技期刊数据库收录期刊
  • 中国期刊全文数据库收录期刊
  • 中国学术期刊综合评价数据库统计源期刊等

快速检索引用检索图表检索高级检索

中国医药导刊 ›› 2025, Vol. 27 ›› Issue (3): 239-246.

• 医药信息学 • 上一篇    下一篇

基于HPLC-Q-TOF-MS/MS结合网络药理学的补肺丸肺分布成分及其干预肺结节的作用机制研究

王榆鑫1a, 翁小刚1b, 杨丽1a, 聂颖兰1a, 彭娟1a, 胡文青1a2, 程浩洁1a
杨司宇1a3, 张美玉1a, 孙健1a*   

  1. 1.中国中医科学院医学实验中心a,中药研究所b,北京 100700;

    2.沈阳药科大学,辽宁 本溪 117004; 3.黑龙江中医药大学,黑龙江 哈尔滨 150040

  • 收稿日期:2025-03-13 修回日期:2025-02-21 出版日期:2025-03-28 发布日期:2025-03-28
  • 基金资助:

    中央级公益性科研院所基本科研业务费专项资金(XTCX2021003);北京市自然科学基金项目(M23012)

Study on the lung distribution components of Bufei Wan and its mechanism of action in intervention of pulmonary nodules based on HPLC-Q-TOF-MS/MS combined with network pharmacology

  1. 1.Experimental Research Centera Institute of Chinese Materia Medicab China Academy of Chinese Medical Sciences
    Beijing 100700, China  2.Shenyang Pharmaceutical University Liaoning Benxi 117004, China; 3.Heilongjiang University of Chinese Medicine Heilongjiang Harbin 150040, China
  • Received:2025-03-13 Revised:2025-02-21 Online:2025-03-28 Published:2025-03-28
  • Contact: Jian Sun jianSun

摘要:

目的:探讨补肺丸干预肺结节的潜在活性成分及作用机制。方法:采用HPLC-Q-TOF-MS/MS对大鼠口服补肺丸后的肺分布成分进行分析,使用Swiss Target PredictionGeneCards等数据库筛选补肺丸关联靶点与肺结节相关靶点,并通过Venny筛选补肺丸干预肺结节的潜在靶点;应用String数据库与Cytoscape软件构建并分析蛋白质-蛋白质相互作用(PPI)网络,筛选核心靶点;通过基因本体论(GO)和京都基因与基因组百科全书(KEGG)进行富集分析。结果:共检测出44个补肺丸入肺成分,获得737个药物潜在靶点、1 689个肺结节治疗潜在靶点和172个交集靶点,筛选出70个核心靶点。经网络药理学GOKEGG富集分析,发现补肺丸可能通过kaempferolvanillic acidononin等多成分调控EGFRNFKB1SRCFGF2等多靶点,进而调节MAPKPI3K-AktNF-κB等信号通路发挥干预肺结节的作用。结论:该研究对补肺丸入肺成分进行了全面解析,为进一步开展补肺丸干预肺结节的药效物质基础研究提供参考依据,为补肺丸的临床应用提供理论基础。


关键词:  , 补肺丸;肺结节;入肺成分;HPLC-Q-TOF-MS/MS;作用机制

Abstract:

Objective: To investigate the potential active ingredients and mechanism of action of Bufei Wan in the intervention of pulmonary nodules.Methods: HPLC-Q-TOF-MS/MS was used to analyze the lung distribution components of rats after oral administration of Bufei Wan. Databases such as SwissTargetPrediction and GeneCards were used to screen Bufei Wan-related targets and pulmonary nodules-related targets and Venny was used to screen Bufei Wan' potential targets for the intervention of pulmonary nodules. String database and Cytoscape software were used to construct and analyze protein-protein interaction PPI networks and screen core targets. Finally enrichment analysis was performed using Gene Ontology GO and Kyoto Encyclopedia of Genes and Genomes KEGG.Results: A total of 44 Bufei Wan' lung components were detected 737 potential drug targets 1 689 potential targets for the treatment of pulmonary nodules and 172 intersection targets were obtained and 70 core targets were screened. Through network pharmacology GO and KEGG enrichment analysis it was found that Bufei Wan may regulate multiple targets such as EGFR NFKB1 SRC FGF2 etc. through multiple components such as kaempferol vanillic acid ononin and then regulate signaling pathways such as MAPK PI3K-Akt and NF-κB to play a role in intervening in pulmonary nodules.Conclusion: This study comprehensively analyzed the components of Bufei Wan that enter the lungs providing a reference for further research on the pharmacological material basis of Bufei Wan in intervening in pulmonary nodules and providing a theoretical basis for the clinical application of Bufei Wan.


Key words:  , Bufei wan , Pulmonary nodules , Lung distribution components , HPLC-Q-TOF-MS/MS , Mechanism

中图分类号: