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Exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking

A large body of literature has shown that ginseng had a role in diabetes mellitus management. Ginsenosides are the main active components of ginseng. But what ginsenosides can manage in diabetic are not systematic. The targets of these ginsenosides are still incomplete. Our aim was to identify which...

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Autores principales: Li, Ming-han, Jin, Ming-hui, Hu, Rui-yi, Tang, Shan, Li, Ke-ke, Gong, Xiao-Jie, Sun, Yin-shi, Wang, Ying-ping, Wang, Zi, Li, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842641/
https://www.ncbi.nlm.nih.gov/pubmed/36646777
http://dx.doi.org/10.1038/s41598-023-27540-4
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author Li, Ming-han
Jin, Ming-hui
Hu, Rui-yi
Tang, Shan
Li, Ke-ke
Gong, Xiao-Jie
Sun, Yin-shi
Wang, Ying-ping
Wang, Zi
Li, Wei
author_facet Li, Ming-han
Jin, Ming-hui
Hu, Rui-yi
Tang, Shan
Li, Ke-ke
Gong, Xiao-Jie
Sun, Yin-shi
Wang, Ying-ping
Wang, Zi
Li, Wei
author_sort Li, Ming-han
collection PubMed
description A large body of literature has shown that ginseng had a role in diabetes mellitus management. Ginsenosides are the main active components of ginseng. But what ginsenosides can manage in diabetic are not systematic. The targets of these ginsenosides are still incomplete. Our aim was to identify which ginsenosides can manage diabetes mellitus through network pharmacology and molecular docking. To identify the targets of these ginsenosides. In this work, we retrieved and screened ginsenosides and corresponding diabetes mellitus targets across multiple databases. PPI networks of the genes were constructed using STRING, and the core targets were screened out through topological analysis. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were performed by using the R language. Finally, molecular docking was performed after bioinformatics analysis for verification. Our research results showed that 28 ginsenosides in ginseng might be against diabetes mellitus by modulating related proteins such as VEGFA, Caspase 3, and TNF-α. Among the 28 ginsenosides, 20(R)-Protopanaxatriol, 20(R)-Protopanaxadiol, and Ginsenoside Rg1 might play a significant role. Kyoto Encyclopedia of Genes and Genomes and Gene Ontology enrichment analysis showed that the management of diabetes mellitus by ginsenosides may be related to the positive regulation of reactive oxygen metabolic processes, associated with the insulin signaling pathway, TNF signaling pathway, and AMPK signaling pathway. Molecular docking results and molecular dynamics simulation showed that most ginsenosides could stably bind to the core target, mainly hydrogen bonding and hydrophobic bond. This study suggests the management of ginseng on diabetes mellitus. We believe that our results can contribute to the systematic study of the mechanism of ginsenosides for the management of diabetes mellitus. At the same time, it can provide a theoretical basis for subsequent studies on the management of ginsenosides in diabetes mellitus.
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spelling pubmed-98426412023-01-18 Exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking Li, Ming-han Jin, Ming-hui Hu, Rui-yi Tang, Shan Li, Ke-ke Gong, Xiao-Jie Sun, Yin-shi Wang, Ying-ping Wang, Zi Li, Wei Sci Rep Article A large body of literature has shown that ginseng had a role in diabetes mellitus management. Ginsenosides are the main active components of ginseng. But what ginsenosides can manage in diabetic are not systematic. The targets of these ginsenosides are still incomplete. Our aim was to identify which ginsenosides can manage diabetes mellitus through network pharmacology and molecular docking. To identify the targets of these ginsenosides. In this work, we retrieved and screened ginsenosides and corresponding diabetes mellitus targets across multiple databases. PPI networks of the genes were constructed using STRING, and the core targets were screened out through topological analysis. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were performed by using the R language. Finally, molecular docking was performed after bioinformatics analysis for verification. Our research results showed that 28 ginsenosides in ginseng might be against diabetes mellitus by modulating related proteins such as VEGFA, Caspase 3, and TNF-α. Among the 28 ginsenosides, 20(R)-Protopanaxatriol, 20(R)-Protopanaxadiol, and Ginsenoside Rg1 might play a significant role. Kyoto Encyclopedia of Genes and Genomes and Gene Ontology enrichment analysis showed that the management of diabetes mellitus by ginsenosides may be related to the positive regulation of reactive oxygen metabolic processes, associated with the insulin signaling pathway, TNF signaling pathway, and AMPK signaling pathway. Molecular docking results and molecular dynamics simulation showed that most ginsenosides could stably bind to the core target, mainly hydrogen bonding and hydrophobic bond. This study suggests the management of ginseng on diabetes mellitus. We believe that our results can contribute to the systematic study of the mechanism of ginsenosides for the management of diabetes mellitus. At the same time, it can provide a theoretical basis for subsequent studies on the management of ginsenosides in diabetes mellitus. Nature Publishing Group UK 2023-01-16 /pmc/articles/PMC9842641/ /pubmed/36646777 http://dx.doi.org/10.1038/s41598-023-27540-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Ming-han
Jin, Ming-hui
Hu, Rui-yi
Tang, Shan
Li, Ke-ke
Gong, Xiao-Jie
Sun, Yin-shi
Wang, Ying-ping
Wang, Zi
Li, Wei
Exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking
title Exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking
title_full Exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking
title_fullStr Exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking
title_full_unstemmed Exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking
title_short Exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking
title_sort exploring the mechanism of active components from ginseng to manage diabetes mellitus based on network pharmacology and molecular docking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842641/
https://www.ncbi.nlm.nih.gov/pubmed/36646777
http://dx.doi.org/10.1038/s41598-023-27540-4
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