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Screening of antioxidant targets for the treatment of Alzheimer’s disease based on network pharmacology
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Jia-jia WANG1, 2, Long-tu LI2, Yu-meng ZHANG1, 2, Zhi-yan LIU2, Qian XIANG1, 2
Chinese Journal of Clinical Pharmacology | 2025, 41(20) : 2929 - 2933
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Chinese Journal of Clinical Pharmacology | 2025, 41(20): 2929-2933
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Screening of antioxidant targets for the treatment of Alzheimer’s disease based on network pharmacology
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Jia-jia WANG1, 2, Long-tu LI2, Yu-meng ZHANG1, 2, Zhi-yan LIU2, Qian XIANG1, 2
Affiliations
  • 1.School of Pharmacy, Xuzhou Medical University, Xuzhou 221004, Jiangsu Province, China
  • 2.Institute of Clinical Pharmacology, Peking University First Hospital, Beijing 100034, China
Published: 2025-10-28 doi: 10.13699/j.cnki.1001-6821.2025.20.014
Outline
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Objective

To systematically screen potential antioxidant targets for the treatment of Alzheimer’s disease (AD) based on network pharmacology strategy.

Methods

Firstly, the structure-data file (SDF) of the antioxidant compound library was converted into the standard simplified molecular input line entry system (SMILES) molecular structure format usingrational discovery kit (RDKit), and then the potential targets of antioxidant compounds were predicted using the SwissTargetPrediction platform. After the obtained targets were analyzed with the differentially expressed genes of AD, a protein interaction network (PPI network) was constructed, and the functional interaction relationship was mined based on the STRING database. Further, the "compound-disease target-signaling pathway" network diagram was established with the help of Cytoscape software to screen key therapeutic targets. Finally, the core targets were annotated with Gene Ontology (GO) function and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis using the DAVID database.

Results

Finally, 10 core targets with potential anti-Alzheimer’s disease effects were screened. Among them, the top three key nodes in degree value were heat shock protein 90α family class B member 1 (HSP90AB1), catenin β1 (CTNNB1) and proto-oncogene tyrosine protein kinase (SRC). Enrichment analysis suggested that these core targets may be mainly involved in the pathogenesis and intervention of Alzheimer’s disease through calcium signaling pathway and phosphatidyqinositol-3 kinase/protein kinase B (PI3K-Akt) signaling pathway, and had important therapeutic potential.

Conclusion

This study systematically identified the core antioxidant targets and key pathways for the treatment of Alzheimer’s disease from the perspective of network pharmacology, providing theoretical support for further research on antioxidant drugs.

Alzheimer’s disease  /  antioxidant drugs  /  network pharmacology
Jia-jia WANG, Long-tu LI, Yu-meng ZHANG, Zhi-yan LIU, Qian XIANG. Screening of antioxidant targets for the treatment of Alzheimer’s disease based on network pharmacology[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (20) : 2929 -2933 . DOI: 10.13699/j.cnki.1001-6821.2025.20.014
Year 2025 volume 41 Issue 20
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doi: 10.13699/j.cnki.1001-6821.2025.20.014
  • Receive Date:2025-09-15
  • Online Date:2026-08-05
  • Published:2025-10-28
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History
  • Received:2025-09-15
Funding
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    1.School of Pharmacy, Xuzhou Medical University, Xuzhou 221004, Jiangsu Province, China
    2.Institute of Clinical Pharmacology, Peking University First Hospital, Beijing 100034, 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
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Genus
种数
Number of
species
占总种数比例
Percentage of total
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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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