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Exploration of the molecular mechanism of Lishi-Kuijie decoction in the treatment of ulcerative colitis based on network pharmacology
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Rui TIAN1, Yu-fei LI2, Ying-qian LI2, Ji-wen ZHENG1, Hua-shan LI2, *
Acta Pharmaceutica Sinica | 2020, 55(11) : 2657 - 2664
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Acta Pharmaceutica Sinica | 2020, 55(11): 2657-2664
Original Articles
Exploration of the molecular mechanism of Lishi-Kuijie decoction in the treatment of ulcerative colitis based on network pharmacology
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Rui TIAN1, Yu-fei LI2, Ying-qian LI2, Ji-wen ZHENG1, Hua-shan LI2, *
Affiliations
  • 1. Beijing University of Traditional Chinese Medicine, Beijing 100029, China
  • 2. Guang'anmen Hospital of the China Academy of Traditional Chinese Medicine, Beijing 100053, China
Published: 2020-11-12 doi: 10.16438/j.0513-4870.2020-0556
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We used network pharmacology and molecular docking to investigate the molecular mechanism of Lishi-Kuijie decoction (KJF) in the treatment of ulcerative colitis (UC). Chemical components and targets related to the 13 herbs of Chinese Materia Medical in KJF were searched through the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP). The UC-related targets were identified through OMIM, DisGeNet and GeneCards databases. Using Cytoscape 3.7.2 software a drug-compound-disease-target network was established. The target interaction network and core target for KJF against UC was built and selected based on the String database and topological parameters. Using the R package clusterprofile in Bioconductor, the intersection genes and the disease-drug intersection targets were transformed to Entrez gene ID, followed by gene ontology biological process enrichment analysis and KEGG pathway annotation analysis. The KJF compound-UC target network contained 149 compounds, 108 corresponding targets and 12 core targets (including signal transducer and activator of transcription 3, interleukin 6, tumor necrosis factor, c-x-c motif chemokine ligand 8, interleukin 2, etc.). We identified 2 371 GO terms and 155 pathways (mainly involving IBD, PI3K-ATK, NF-kappa B, TNF, Toll-like receptor signaling pathway) as determined by enrichment analysis. Molecular docking, used with the key molecular factors and the core targets, revealed stable binding for IL2, TNF-α, MAPK1 and RELA. These results suggest the possible molecular mechanism of KJF in treatment of UC and lay the foundation for further characterization of the components and their mechanisms.

network pharmacology  /  molecular docking  /  ulcerative colitis  /  mechanism  /  target
Rui TIAN, Yu-fei LI, Ying-qian LI, Ji-wen ZHENG, Hua-shan LI. Exploration of the molecular mechanism of Lishi-Kuijie decoction in the treatment of ulcerative colitis based on network pharmacology[J]. Acta Pharmaceutica Sinica, 2020 , 55 (11) : 2657 -2664 . DOI: 10.16438/j.0513-4870.2020-0556
Year 2020 volume 55 Issue 11
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doi: 10.16438/j.0513-4870.2020-0556
  • Receive Date:2020-04-15
  • Online Date:2026-01-23
  • Published:2020-11-12
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  • Received:2020-04-15
  • Revised:2020-05-17
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    1. Beijing University of Traditional Chinese Medicine, Beijing 100029, China
    2. Guang'anmen Hospital of the China Academy of Traditional Chinese Medicine, Beijing 100053, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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