Analysis of anti-fatigue mechanism and potential targets of ginseng.
10.19540/j.cnki.cjcmm.20190805.401
- Author:
Fei-Xiang LIU
1
;
Zi-Xuan LIN
2
;
Huai-Liang ZHANG
1
;
Zhen-Qiang ZHANG
2
;
Ke-Qin YANG
1
;
Xiao-Fei FAN
1
;
Jin XU
1
;
Yong-Tao WANG
1
;
Yu-Nan ZHAO
3
Author Information
1. the First Affiliated Hospital of Henan University of Traditional Chinese Medicine Zhengzhou 450000,China.
2. Henan University of Traditional Chinese Medicine Zhengzhou 450000,China.
3. School of Medicine and Life Sciences,Nanjing University of Traditional Medicine Nanjing 210023,China.
- Publication Type:Journal Article
- Keywords:
fatigue;
fatigue syndrome;
ginseng;
ginsenoside;
network pharmacology
- MeSH:
Animals;
Fatigue/prevention & control*;
Gene Expression Regulation;
Gene Ontology;
Ginsenosides/pharmacology*;
Male;
Mice;
Panax/chemistry*;
Plant Extracts/pharmacology*;
Random Allocation
- From:
China Journal of Chinese Materia Medica
2019;44(24):5479-5487
- CountryChina
- Language:Chinese
-
Abstract:
Ginseng has effects in reinforcing vital energy,invigorating health effectively and relieving fatigue symptoms,and ginsenoside( GS) is the main component of its anti-fatigue effect. Totally 17 active components and 92 drug targets of ginseng compounds were screened from Traditional Chinese Medicine Systems Pharmacology; and 78 intersecting genes of diseases and drug targets were obtained based on R Language Technology. The protein-protein interaction( PPI) network was constructed by STRING 11. 0 software,and Matthews Correlation Coefficient( MCC) algorithm was used to screen core target genes. Gene ontology enrichment analysis and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis were used to analyze the major genes and their roles in regulatory networks. The results indicated that ginseng could regulate the core target genes,including AKT serine/threonine kinase( AKT1),interleukin-1β,Toll-like receptor binding molecule 1( ICAM1),mitogen-activated protein kinase 8( MAPK8),AP-1 transcription factor subunit( JUN),transducer and activator of transcription 1( STAT1) and prostaglandin peroxidase synthase 2( PTGS2). It could participate in the functions of cytokine receptor binding,cell adhesion molecule binding and tumor necrosis factor receptor superfamily binding,and also regulate the signal pathways of tumor necrosis factor,interleukin 17 and c-type lectin receptor,so as to exert an anti-fatigue effect. Based on the results of network analysis,32 four-week-old male SPFACR mice were randomly divided into control group,low-dose ginsenoside group,middle-dose ginsenoside group and high-dose ginsenoside group. The corresponding drugs were administrated for 3 weeks. The results showed that GS could significantly up-regulate the expressions of STAT1 and AKT1( P<0. 01,P<0. 05),and downregulate the expressions of PTGS2 and JUN( P<0. 01). However,there was no significant effect on MAPK8,IL-1β and ICAM1. Ginseng's anti-fatigue regulation network was constructed through network pharmacology,and the results were verified by experiments,in order to reveal the anti-fatigue mechanism of ginseng and provide scientific basis for its clinical application.
