Network Pharmacology and Experimental Validation of the Anti-Inflammatory Effect of Tingli Dazao Xiefei Decoction in Acute Lung Injury Treatment

被引:1
作者
Zhang, Chengxi [1 ,2 ]
Li, Xiaoqian [1 ,2 ]
Gao, Dan [1 ,2 ]
Zhu, Huahe [3 ]
Wang, Shun [1 ,2 ]
Tan, Bo [4 ]
Yang, Aidong [1 ,2 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Sch Tradit Chinese Med, Shanghai, Peoples R China
[2] Shanghai Inst Infect Dis & Biosecur, Ctr Tradit Chinese Med & Epidem Dis, Shanghai, Peoples R China
[3] Fudan Univ, Huashan Hosp, Dept Integrat Med, Shanghai, Peoples R China
[4] Shanghai Univ Tradit Chinese Med, Lab Clin Pharmacokinet, Shuguang Hosp, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
network pharmacology; molecular docking; lipopolysaccharide; PI3K/AKT/PTEN; JAK2/STAT3; RESPIRATORY-DISTRESS-SYNDROME; SEVERE ACUTE-PANCREATITIS; MORTALITY;
D O I
10.2147/JIR.S433840
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose: Tingli Dazao Xiefei Decoction (TDXD) is a Traditional Chinese Medicine (TCM) formula used to treat acute lung injury (ALI). However, the precise mechanism of TDXD in treating ALI remains unclear. We investigated the therapeutic mechanism of TDXD against ALI using a complementary approach combining network pharmacology, molecular docking, and in vitro and in vivo experiments.Material and Methods: Potential drug targets of TDXD and relevant target genes associated with ALI were retrieved from Chinese medicines and disease genes databases. Bioinformatics technology was employed to screen potential active ingredients and core targets. Validation experiments were conducted using a lipopolysaccharide (LPS)-induced ALI mouse (C57BL/6J) model, LPSinduced inflammatory RAW264.7 cells, and molecular docking between active compounds of TDXD and potential targets.Results: Network pharmacology suggested that the mechanism of TDXD against ALI involved phosphoinositide 3-kinase (PI3K) / protein kinase B (AKT) / phosphatase and tensin homolog (PTEN) and Janus kinase 2 (JAK2) / signal transducer and activator of transcription 3 (STAT3) pathways. Quercetin, beta-sitosterol, kaempferol, isorhamnetin, and L-stepholidine were identified as the main active compounds of TDXD that exerted anti-ALI effects. Molecular docking indicated that these compounds exhibited good binding capabilities (<= -5kcal/mol) to key targets in PI3K/AKT/PTEN and JAK2/STAT3 signaling pathways. In the animal model, TDXD alleviated injuries and inflammatory responses in lung tissues, accompanied by inhibition of expression of tumor necrosis factor-alpha (TNF-alpha), Interleukin-6 (IL-6), STAT3, and Suppressor of Cytokine Signaling 3 (SOCS3) mRNA, and key proteins in PI3K/AKT/ PTEN and JAK2/STAT3 pathways (all P values < 0.05). Cell based experiments showed that TDXD dose-dependently inhibited the expression of essential proteins in PI3K/AKT/PTEN and JAK2/STAT3 pathways (P < 0.05).Conclusion: This study revealed that the mechanism of TDXD in ALI treatment might involve simultaneous regulation of PI3K/ AKT/PTEN and JAK2/STAT3 pathways.
引用
收藏
页码:6195 / 6209
页数:15
相关论文
共 39 条
  • [1] Epidemiology, Patterns of Care, and Mortality for Patients With Acute Respiratory Distress Syndrome in Intensive Care Units in 50 Countries
    Bellani, Giacomo
    Laffey, John G.
    Pham, Tai
    Fan, Eddy
    Brochard, Laurent
    Esteban, Andres
    Gattinoni, Luciano
    van Haren, Frank
    Larsson, Anders
    McAuley, Daniel F.
    Ranieri, Marco
    Rubenfeld, Gordon
    Thompson, B. Taylor
    Wrigge, Hermann
    Slutsky, Arthur S.
    Pesenti, Antonio
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 315 (08): : 788 - 800
  • [2] Acute Lung Injury A Clinical and Molecular Review
    Butt, Yasmeen
    Kurdowska, Anna
    Allen, Timothy Craig
    [J]. ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2016, 140 (04) : 345 - 350
  • [3] Macrophage Sprouty4 deficiency diminishes sepsis-induced acute lung injury in mice
    Chen, Rong
    Cao, Chen
    Liu, Huimin
    Jiang, Wanli
    Pan, Rui
    He, He
    Ding, Ke
    Meng, Qingtao
    [J]. REDOX BIOLOGY, 2022, 58
  • [4] Recent trends in acute lung injury mortality: 1996-2005
    Erickson, Sara E.
    Martin, Greg S.
    Davis, J. Lucian
    Matthay, Michael A.
    Eisner, Mark D.
    [J]. CRITICAL CARE MEDICINE, 2009, 37 (05) : 1574 - 1579
  • [5] Fan Y, 2003, Medical Treasures of the Golden Chamber, P117
  • [6] Fu SQ, 2019, BIOSCIENCE REP, V39, DOI [10.1042/BSR20190789, 10.1042/bsr20190789]
  • [7] Enhancement of ICAM-1 via the JAK2/STAT3 signaling pathway in a rat model of severe acute pancreatitis-associated lung injury
    Han, Xiao
    Wang, Yuxi
    Chen, Hailong
    Zhang, Jingwen
    Xu, Caiming
    Li, Jian
    Li, Mingyue
    [J]. EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2016, 11 (03) : 788 - 796
  • [8] LXRs/ABCA1 activation contribute to the anti-inflammatory role of phytosterols on LPS-induced acute lung injury
    He, Daxue
    Wang, Shengquan
    Fang, Gaofeng
    Zhu, Qian
    Wu, Jingjing
    Li, Jianling
    Shi, Dan
    Lian, Xuemei
    [J]. JOURNAL OF FUNCTIONAL FOODS, 2022, 89
  • [9] Hongxia Z, 2021, Pract Clin J Integr Tradit Chin West Med., V21, P104, DOI [10.13638/j.issn.1671-4040.2021.13.051, DOI 10.13638/J.ISSN.1671-4040.2021.13.051]
  • [10] Jinghua L, 2020, Shandong Sci, V33, P1, DOI [10.3976/j.issn.1002-4026.2020.05.001, DOI 10.3976/J.ISSN.1002-4026.2020.05.001]