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Combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of Shengyu Decoction for treating anemia
Anemia is a common clinical hematological disease with a high incidence, which seriously affects human health. Shengyu Decoction is often used in the treatment of anemia. However, the pharmacodynamic substance basis and therapeutic mechanism are still unclear, which hinders the comprehensive develop...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107194/ https://www.ncbi.nlm.nih.gov/pubmed/36437813 http://dx.doi.org/10.1002/jssc.202200678 |
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author | Hu, Yu Sun, Hui Yan, Guangli Zhang, Xiwu Guan, Yu Li, Dan Wang, Xijun |
author_facet | Hu, Yu Sun, Hui Yan, Guangli Zhang, Xiwu Guan, Yu Li, Dan Wang, Xijun |
author_sort | Hu, Yu |
collection | PubMed |
description | Anemia is a common clinical hematological disease with a high incidence, which seriously affects human health. Shengyu Decoction is often used in the treatment of anemia. However, the pharmacodynamic substance basis and therapeutic mechanism are still unclear, which hinders the comprehensive development and utilization of Shengyu Decoction. In this study, 143 compounds were identified in Shengyu Decoction using high‐throughput ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry, 24 of which were absorbed into the blood. Taking these blood‐entering ingredients as the research object, we found through network pharmacology research that ferulic acid, calycosin, and astragaloside A can act on AKT1, MAPK1, and MAPK14, and play a role in treating anemia through PI3K‐Akt signaling pathway and Pathways in anemia. Finally, it was demonstrated that the active compound could bind to the core target with good affinity by molecular docking. The research shows that Shengyu Decoction has multi‐component, multi‐target, and multi‐channel effects in the treatment of anemia, which provides a basis for the development and clinical application of Shengyu Decoction. |
format | Online Article Text |
id | pubmed-10107194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101071942023-04-18 Combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of Shengyu Decoction for treating anemia Hu, Yu Sun, Hui Yan, Guangli Zhang, Xiwu Guan, Yu Li, Dan Wang, Xijun J Sep Sci Liquid Chromatography Anemia is a common clinical hematological disease with a high incidence, which seriously affects human health. Shengyu Decoction is often used in the treatment of anemia. However, the pharmacodynamic substance basis and therapeutic mechanism are still unclear, which hinders the comprehensive development and utilization of Shengyu Decoction. In this study, 143 compounds were identified in Shengyu Decoction using high‐throughput ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry, 24 of which were absorbed into the blood. Taking these blood‐entering ingredients as the research object, we found through network pharmacology research that ferulic acid, calycosin, and astragaloside A can act on AKT1, MAPK1, and MAPK14, and play a role in treating anemia through PI3K‐Akt signaling pathway and Pathways in anemia. Finally, it was demonstrated that the active compound could bind to the core target with good affinity by molecular docking. The research shows that Shengyu Decoction has multi‐component, multi‐target, and multi‐channel effects in the treatment of anemia, which provides a basis for the development and clinical application of Shengyu Decoction. John Wiley and Sons Inc. 2022-12-11 2023-02 /pmc/articles/PMC10107194/ /pubmed/36437813 http://dx.doi.org/10.1002/jssc.202200678 Text en © 2022 The Authors. Journal of Separation Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Liquid Chromatography Hu, Yu Sun, Hui Yan, Guangli Zhang, Xiwu Guan, Yu Li, Dan Wang, Xijun Combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of Shengyu Decoction for treating anemia |
title | Combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of Shengyu Decoction for treating anemia |
title_full | Combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of Shengyu Decoction for treating anemia |
title_fullStr | Combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of Shengyu Decoction for treating anemia |
title_full_unstemmed | Combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of Shengyu Decoction for treating anemia |
title_short | Combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of Shengyu Decoction for treating anemia |
title_sort | combination of ultra‐performance liquid chromatography‐quadrupole time‐of‐flight mass spectrometry and network pharmacology to reveal the mechanism of shengyu decoction for treating anemia |
topic | Liquid Chromatography |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107194/ https://www.ncbi.nlm.nih.gov/pubmed/36437813 http://dx.doi.org/10.1002/jssc.202200678 |
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