Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis

被引:12
作者
Guo, Jing-Yan [1 ]
Wang, Dong-Mei [1 ]
Wang, Meng-Jiao [1 ]
Zhou, Jun [2 ]
Pan, Ying-Ni [1 ]
Wang, Zheng-Zhong [2 ]
Xiao, Wei [3 ]
Liu, Xiao-Qiu [1 ]
机构
[1] Shenyang Pharmaceut Univ, Dept Tradit Chinese Med, 103 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
[2] Jiangsu Kan Pharmaceut Co Ltd, Lianyungang 222001, Peoples R China
[3] State Key Lab New Tech Chinese Med Pharmaceut Pro, Lianyungang 222001, Peoples R China
基金
中国国家自然科学基金;
关键词
Metabolic research; TCM; Network pharmacology; EXTRACT;
D O I
10.1016/j.jfda.2019.05.007
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Jinzhen oral liquid (JZ) is a classical traditional Chinese medicine formula used for the treatment of children lung disease. However, the effective substance of JZ is still unclear. In this study, we used lung injury rat model to study the protective effect of JZ, through UPLC-Q-TOF/MS detection coupled with metabolic research and network pharmacology analysis. Fortunately, 31 absorbed prototype constituents and 41 metabolites were identified or tentatively characterized based on UPLC-Q-TOF/MS analysis, and the possible metabolic pathways were hydroxylation, sulfation and glucuronidation. We optimized the data screening in the early stage of network pharmacology by collecting targets based on adsorbed constituents, and further analyzed the main biological processes and pathways. 24 selected core targets were frequently involved in reactive oxygen species metabolic process, dopaminergic synapse pathway and so on, which might play important roles in the mechanisms of JZ for the treatment of lung injury. Overall, the absorbed constituents and their possible metabolic pathways, as well as the absorbed constituent-target-disease network provided insights into the mechanisms of JZ for the treatment of lung injury. Further studies are needed to validate the biological processes and effect pathways of JZ. Copyright (C) 2019, Food and Drug Administration, Taiwan. Published by Elsevier Taiwan LLC.
引用
收藏
页码:793 / 804
页数:12
相关论文
共 30 条
[1]   Involvement of reactive oxygen species in the metabolic pathways triggered by diesel exhaust particles in human airway epithelial cells [J].
Baulig, A ;
Garlatti, M ;
Bonvallot, V ;
Marchand, A ;
Barouki, R ;
Marano, F ;
Baeza-Squiban, A .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2003, 285 (03) :L671-L679
[2]   Metabolic consequences of adenosine deaminase deficiency in mice are associated with defects in alveogenesis, pulmonary inflammation, and airway obstruction [J].
Blackburn, MR ;
Volmer, JB ;
Thrasher, JL ;
Zhong, HY ;
Crosby, JR ;
Lee, JJ ;
Kellems, RE .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :159-170
[3]  
Bolt RJ, 2010, PEDIAT PULMONOL, V32, P76
[4]   Extraction of relations between genes and diseases from text and large-scale data analysis: implications for translational research [J].
Bravo, Alex ;
Pinero, Janet ;
Queralt-Rosinach, Nuria ;
Rautschka, Michael ;
Furlong, Laura I. .
BMC BIOINFORMATICS, 2015, 16
[5]   TTD: Therapeutic Target Database [J].
Chen, X ;
Ji, ZL ;
Chen, YZ .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :412-415
[6]   Kinetic studies of AKR1B10, human aldose reductase-like protein: Endogenous substrates and inhibition by steroids [J].
Endo, Satoshi ;
Matsunaga, Toshiyuki ;
Mamiya, Hiroaki ;
Ohta, Chisato ;
Soda, Midori ;
Kitade, Yukio ;
Tajima, Kazuo ;
Zhao, Hai-Tao ;
El-Kabbani, Ossama ;
Hara, Akira .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2009, 487 (01) :1-9
[7]   SwissTargetPrediction: a web server for target prediction of bioactive small molecules [J].
Gfeller, David ;
Grosdidier, Aurelien ;
Wirth, Matthias ;
Daina, Antoine ;
Michielin, Olivier ;
Zoete, Vincent .
NUCLEIC ACIDS RESEARCH, 2014, 42 (W1) :W32-W38
[8]   Substrate Specificity, Inhibitor Selectivity and Structure-Function Relationships of Aldo-Keto Reductase 1B15: A Novel Human Retinaldehyde Reductase [J].
Gimenez-Dejoz, Joan ;
Kolar, Michal H. ;
Ruiz, Francesc X. ;
Crespo, Isidro ;
Cousido-Siah, Alexandra ;
Podjarny, Alberto ;
Barski, Oleg A. ;
Fanfrlik, Jindrich ;
Pares, Xavier ;
Farres, Jaume ;
Porte, Sergio .
PLOS ONE, 2015, 10 (07)
[9]  
Hamosh A, 2005, NUCLEIC ACIDS RES, V33, pD514
[10]   Adenosine A1 and A2 receptor agonists reduce endotoxin-induced cellular energy depletion and oedema formation in the lung [J].
Heller, A. R. ;
Rothermel, J. ;
Weigand, M. A. ;
Plaschke, K. ;
Schmeck, J. ;
Wendel, M. ;
Bardenheuer, H. J. ;
Koch, T. .
EUROPEAN JOURNAL OF ANAESTHESIOLOGY, 2007, 24 (03) :258-266