Molecular Mechanism Analysis of Jiangtang Xiaozhi Tablets in Treatment of NAFLD
10.13422/j.cnki.syfjx.20202349
- VernacularTitle:降糖消脂片治疗NAFLD的分子作用机制分析
- Author:
Min HOU
1
;
Wen-jing GAO
2
;
Yang DU
1
;
Pan WANG
2
;
Ju-qin PENG
2
;
Ya-dong LIN
2
;
Fu-zhi ZHANG
1
;
Jun-guo REN
2
;
Jian-xun LIU
2
Author Information
1. Beijing University of Chinese Medicine，Beijing 100029，China
2. Beijing Key Laboratory of Pharmacology of Traditional Chinese Medicine， Institute of Basic Medical Sciences，Xiyuan Hospital， China Academy of Chinese Medical Sciences，Beijing 100091，China
- Publication Type:Research Article
- Keywords:
network pharmacology;
molecular docking;
Jiangtang Xiaozhi tablets;
non-alcoholic fatty liver disease （NAFLD）;
quercetin;
mitogen-activated protein kinase （MAPK）;
phosphatidylinositol 3-kinase/protein kinase B （PI3K/Akt）
- From:
Chinese Journal of Experimental Traditional Medical Formulae
2021;27(5):147-157
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To explore the molecular mechanism of Jiangtang Xiaozhi tablets （JTXZT） in the treatment of non-alcoholic fatty liver disease （NAFLD） by means of network pharmacology and molecular docking. Method:With the help of traditional Chinese medicine （TCM） Systems Pharmacology Database and Analysis Platform （TCMSP）， TCMs Integrated Database （TCMID）， Encyclopedia of TCM （ETCM） and Bioinformatics Analysis Tool for Molecular Mechanism of TCM （BATMAN-TCM）， the chemical compositions of medicinal materials in JTXZT were obtained， the compound targets were predicted in SwissTargetPrediction database and STITCH database. The targets of NAFLD were searched by The Human Gene Database （GeneCards）， Online Mendelian Inheritance in Man （OMIM）， Therapeutic Target Database （TTD） and DisGeNET， and intersection analysis was performed with the targets of the active ingredients to obtain the targets of JTXZT for treatment of NAFLD. Based on STRING 11.0 database， the protein-protein interaction （PPI） network of therapeutic targets was constructed， and the enrichment analysis of therapeutic targets was carried out by DAVID 6.8. Finally， the interaction characteristics of key components and core therapeutic targets of JTXZT for treatment of NAFLD were verified based on molecular docking. Result:The key components of JTXZT for treatment of NAFLD were quercetin， luteolin， kaempferol， berberine， isorhamnetin， betulinic acid， oleanolic acid， ursolic acid. formononetin and hexitol， and the core targets of JTXZT for treatment of NAFLD were mitogen-activated protein kinase 1 （MAPK1）， Jun proto-oncogene， activator protein-1 （AP-1） transcription factor subunit （JUN）， MAPK3， protein kinase B1 （AKT1 or Akt1）， tumor protein p53 （TP53）， E1A binding protein p300 （EP300）， Fos proto-oncogene， AP-1 transcription factor subunit （FOS）， tumor necrosis factor （TNF），amyloid beta precursor protein （APP） and cytochrome P450 family 2 subfamily E member 1 （CYP2E1）. Biological function and pathway enrichment analysis showed that JTXZT mainly through xenobiotic metabolic process， oxidation-reduction process， cholesterol metabolic process and other biological processes， regulating phosphatidylinositol 3-kinase/protein kinase B （PI3K/Akt） signaling pathway， MAPK signaling pathway， NAFLD and insulin signaling pathway to play a role in the treatment of NAFLD. The results of molecular docking showed that the active components of JTXZT had a good affinity with the core targets of JTXZT for the treatment of NAFLD. Conclusion:JTXZT treats NAFLD through multiple active components， multiple key targets and multiple action pathways.
