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Preliminary exploration of the effect and mechanism of verbascoside against acute lung injury by network pharmacology and molecular docking
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Hao Yin1, Tong-Tong Gao1, Yi Lei1, Wen-Yan Qin2, *, Jun-Bai Fan2, *
Medical Journal of Chinese People’s Liberation Army | 2024, 49(10) : 1174 - 1183
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Medical Journal of Chinese People’s Liberation Army | 2024, 49(10): 1174-1183
Basic Research
Preliminary exploration of the effect and mechanism of verbascoside against acute lung injury by network pharmacology and molecular docking
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Hao Yin1, Tong-Tong Gao1, Yi Lei1, Wen-Yan Qin2, *, Jun-Bai Fan2, *
Affiliations
  • 1College of Anesthesiology, Shanxi Medical University, Taiyuan, Shanxi 030001, China
  • 2Department of Anesthesiology, the Second Hospital of Shanxi Medical University, Taiyuan, Shanxi 030000, China
Published: 2024-10-28 doi: 10.11855/j.issn.0577-7402.1023.2024.0204
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Objective To investigate the molecular mechanism of verbascoside against acute lung injury (ALI) by network pharmacology and molecular docking methods, and to validate the findings experimentally. Methods The 2D structure of verbascoside was obtained from the Pubchem database. Active ingredient targets of verbascoside were acquired from Pharmmapper database and Swiss Target Prediction database. Active component targets of ALI were acquired from datebase such as Gene Cards, OMIM, and DisGeNET. Common targets between verbascoside and ALI were determined by overlapping these sets. PPI network for potential targets was constructed using String database and Cytoscape software. The intersection targets were imported into the DAVID database for enrichment analysis of GO biological processes, KEGG signaling pathway and the pathway target genes. Molecular docking between verbascoside and core targets was performed using Autodock vina software. The mRNA expression level of core genes was validated using real-time quantitative PCR (RT-qPCR), and the expression of related proteins was detected using Western blotting. Results A total of 150 target genes of verbascoside against ALI were screened, and the key targets of verbascoside against ALI mainly involve pathways such as Rap1 signaling pathway, PI3K-Akt signaling pathway and MAPK signaling pathway. Verbascoside docked well with the core target molecules. RT-qPCR results showed that, compared with the control group, the mRNA expression levels of HSP90AA1, ALB, TP53, TNF, INS, and HRAS were significantly decreased in cells after the effect of verbascoside (P<0.05); Western blotting indicated that, compared with the model group, verbascoside treatment significantly reduced the expression of p-Akt, p-p38, and p-ERK proteins (P<0.05). Conclusion Verbascoside could inhibit MAPK, Rap1 and PI3K/Akt signaling pathways to exert its anti-ALI effects.

acteoside  /  acute lung injury  /  network pharmacology  /  molecular docking  /  molecular mechanism
Hao Yin, Tong-Tong Gao, Yi Lei, Wen-Yan Qin, Jun-Bai Fan. Preliminary exploration of the effect and mechanism of verbascoside against acute lung injury by network pharmacology and molecular docking[J]. Medical Journal of Chinese People’s Liberation Army, 2024 , 49 (10) : 1174 -1183 . DOI: 10.11855/j.issn.0577-7402.1023.2024.0204
  • Physician Clinical Research Project of Shanxi Medical Doctor Association(YSXH-RF2022MZ004)
Year 2024 volume 49 Issue 10
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Article Info
doi: 10.11855/j.issn.0577-7402.1023.2024.0204
  • Receive Date:2023-08-02
  • Online Date:2025-11-20
  • Published:2024-10-28
Article Data
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History
  • Received:2023-08-02
  • Accepted:2023-10-07
Funding
Physician Clinical Research Project of Shanxi Medical Doctor Association(YSXH-RF2022MZ004)
Affiliations
    1College of Anesthesiology, Shanxi Medical University, Taiyuan, Shanxi 030001, China
    2Department of Anesthesiology, the Second Hospital of Shanxi Medical University, Taiyuan, Shanxi 030000, China

Corresponding:

Fan Jun-Bai, E-mail:
Qin Wen-Yan, E-mail:
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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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