The Multi-Target Action Mechanism for the Anti-Periodontitis Effect of Astragali radix Based on Bioinformatics Analysis and In Vitro Verification

<b>Background:</b><i>Astragali radix</i> is a traditional Chinese medicine with potential therapeutic effects on periodontitis; however, its underlying mechanisms require further investigation. <b>Methods:</b> We employed network pharmacology, molecular docking, molecular dynamics simulations, and in vitro experiments to explore the potential actions and mechanisms of <i>Astragali radix</i> in treating periodontitis. <b>Results:</b> A total of 17 compounds (including the most prevalent one, Kaempferol) from <i>Astragali radix</i> and 464 corresponding targets were identified, from which five major active ingredients were selected based on the drug-active ingredient and periodontitis gene network. Protein-protein interaction (PPI) network analysis identified the top ten core potential targets, seven of which possess suitable crystal structures for molecular docking. These include interleukin-6 (IL6), tumor necrosis factor (TNF), AKT serine/threonine kinase 1 (AKT1), interleukin-1β (IL1β), prostaglandin G/H synthase-2 (PTGS2), matrix metalloproteinase-9 (MMP9), and caspase-3 (CASP3). Additionally, 58 Gene Ontology (GO) terms and 146 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were identified. The five major active ingredients and seven core targets mentioned above were subjected to molecular docking analysis using Discovery Studio 2019 software. Molecular dynamic simulations confirmed a stable interaction between the CASP3 and the Kaempferol ligand system. In vitro experiments indicated that Kaempferol significantly inhibited lipopolysaccharide (LPS)-induced apoptosis in human periodontal ligament stem cells and reduced the expression levels of IL6, CASP3 and MMP9. <b>Conclusions:</b> This study systematically elucidates that the primary active ingredients derived from <i>Astragali radix</i> exert their pharmacological effects (including anti-inflammation and anti-apoptosis) primarily by interacting with multiple targets. These findings establish a promising foundation for the targeted application of <i>Astragali radix</i> in the treatment of periodontitis.

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Publication Details

Journal
Nutrients
Published
2025-02-10
DOI
https://doi.org/10.3390/nu17040627
Citations
1
Primary Topic
Plant-based Medicinal Research
Type
article
Field-Weighted Citation Impact
1.56
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The Multi-Target Action Mechanism for the Anti-Periodontitis Effect of Astragali radix Based on Bioinformatics Analysis and In Vitro Verification

Xiaoran Xu, Miaomiao Feng, Yuankun Zhai, Bowen Wang et al.
1 citations
Nutrients
Plant-based Medicinal Research
1.56
article

The Multi-Target Action Mechanism for the Anti-Periodontitis Effect of Astragali radix Based on Bioinformatics Analysis and In Vitro Verification

Xiaoran Xu, Miaomiao Feng, Yuankun Zhai, Bowen Wang, Ningli Li, Cory J. Xian, Tiejun Li, Mingzhen Yang
article en
1 citations

Abstract

<b>Background:</b><i>Astragali radix</i> is a traditional Chinese medicine with potential therapeutic effects on periodontitis; however, its underlying mechanisms require further investigation. <b>Methods:</b> We employed network pharmacology, molecular docking, molecular dynamics simulations, and in vitro experiments to explore the potential actions and mechanisms of <i>Astragali radix</i> in treating periodontitis. <b>Results:</b> A total of 17 compounds (including the most prevalent one, Kaempferol) from <i>Astragali radix</i> and 464 corresponding targets were identified, from which five major active ingredients were selected based on the drug-active ingredient and periodontitis gene network. Protein-protein interaction (PPI) network analysis identified the top ten core potential targets, seven of which possess suitable crystal structures for molecular docking. These include interleukin-6 (IL6), tumor necrosis factor (TNF), AKT serine/threonine kinase 1 (AKT1), interleukin-1β (IL1β), prostaglandin G/H synthase-2 (PTGS2), matrix metalloproteinase-9 (MMP9), and caspase-3 (CASP3). Additionally, 58 Gene Ontology (GO) terms and 146 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were identified. The five major active ingredients and seven core targets mentioned above were subjected to molecular docking analysis using Discovery Studio 2019 software. Molecular dynamic simulations confirmed a stable interaction between the CASP3 and the Kaempferol ligand system. In vitro experiments indicated that Kaempferol significantly inhibited lipopolysaccharide (LPS)-induced apoptosis in human periodontal ligament stem cells and reduced the expression levels of IL6, CASP3 and MMP9. <b>Conclusions:</b> This study systematically elucidates that the primary active ingredients derived from <i>Astragali radix</i> exert their pharmacological effects (including anti-inflammation and anti-apoptosis) primarily by interacting with multiple targets. These findings establish a promising foundation for the targeted application of <i>Astragali radix</i> in the treatment of periodontitis.

NutrientsVol. 17(4)
University of South Australia (AU), Henan University (CN), Peking University (CN), Kaifeng University (CN)
Openalex Percentile: Top 23%
Plant-based Medicinal Research
1.56
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