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Possible mechanisms by which Polygonati rhizoma opposes atherosclerosis based on network pharmacology and molecular docking analyses
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Feng-feng GAO1, Yan-ling PEI2, Yue REN1, Zi-jun CHEN1, Jian-qiu LU1, *, Yan-ling ZHANG1, *
Acta Pharmaceutica Sinica | 2020, 55(11) : 2642 - 2650
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Acta Pharmaceutica Sinica | 2020, 55(11): 2642-2650
Original Articles
Possible mechanisms by which Polygonati rhizoma opposes atherosclerosis based on network pharmacology and molecular docking analyses
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Feng-feng GAO1, Yan-ling PEI2, Yue REN1, Zi-jun CHEN1, Jian-qiu LU1, *, Yan-ling ZHANG1, *
Affiliations
  • 1. School of Chinese Material Medica, Beijing University of Chinese Medicine, Beijing 100102, China
  • 2. XinMinHe Testing(HeBei) Co. Ltd., Anguo 071200, China
Published: 2020-11-12 doi: 10.16438/j.0513-4870.2020-0299
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Possible mechanisms by which Polygonati rhizoma opposes atherosclerosis (AS) were identified by network pharmacology and molecular docking analyses. The Traditional Chinese Medicine Database (TCMD) and the Traditional Chinese Medicine Systems Pharmacology Database (TCMSP) were utilized to identify the likely active components of Polygonati rhizoma. The potential targets set of Polygonati rhizoma were predicted with the PharmaDB database and the Swiss TargetPrediction database. The targets set for AS was retrieved by OMIM, DisGeNET and NCBI Gene database. We used the STRING platform to construct a protein-protein interaction network of the intersectional targets and performed visual analysis in Cytoscape. The key targets of Polygonati rhizoma in AS were searched by network topology and the resulting GO and KEGG enrichment was analyzed by Clue GO. In addition, the key targets were verified by molecular docking in Discovery Studio 4.0. A total of 45 active ingredients and 51 potential targets were obtained in the treatment of AS. The results of the topology analysis included five key targets:serum albumin, mitogen-activated protein kinase 3, mitogen-activated protein kinase 1, proto-oncogene tyrosine-protein kinase Src and matrix metalloproteinase-9. The 131 GO items showed that the biological process mainly involved the steroid receptor, cell response to steroid stimulation, the phosphatidylinositol-3 kinase signal pathway, and others. The KEGG pathway analysis included 37 pathways, which were closely related to peroxisome proliferation activated receptor signaling pathway, platelet activation pathway, vascular endothelial growth factor pathway, hypoxia inducible factor pathway and adhesion connection pathway. The results of molecular docking proved that the combined activity of the components with potential key targets is excellent. This study proposes mechanisms by which Polygonati rhizoma might act to reverse or minimize AS and provides a scientific basis for clinical research on Polygonati rhizoma.

Polygonati rhizoma  /  atherosclerosis  /  network pharmacology  /  molecular docking technology  /  mechanism of action
Feng-feng GAO, Yan-ling PEI, Yue REN, Zi-jun CHEN, Jian-qiu LU, Yan-ling ZHANG. Possible mechanisms by which Polygonati rhizoma opposes atherosclerosis based on network pharmacology and molecular docking analyses[J]. Acta Pharmaceutica Sinica, 2020 , 55 (11) : 2642 -2650 . DOI: 10.16438/j.0513-4870.2020-0299
Year 2020 volume 55 Issue 11
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Article Info
doi: 10.16438/j.0513-4870.2020-0299
  • Receive Date:2020-03-11
  • Online Date:2026-01-23
  • Published:2020-11-12
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  • Received:2020-03-11
  • Revised:2020-05-08
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    1. School of Chinese Material Medica, Beijing University of Chinese Medicine, Beijing 100102, China
    2. XinMinHe Testing(HeBei) Co. Ltd., Anguo 071200, 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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