Exploring Mechanisms of Houshiheisan in Treating Ischemic Stroke with Network Pharmacology and Independent Cascade Model
- Authors: Cao B.1, Jin J.2, Tang Z.1, Luo Q.3, An J.1, Pang W.4
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Affiliations:
- Department of Health Informatics and Management, School of Health Humanities, Peking University
- School of Statistics, Beijing Normal University
- School of Nursing, Peking University
- Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University
- Issue: Vol 27, No 7 (2024)
- Pages: 959-968
- Section: Chemistry
- URL: https://vietnamjournal.ru/1386-2073/article/view/644913
- DOI: https://doi.org/10.2174/1386207326666230810094557
- ID: 644913
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Full Text
Abstract
Background:Houshiheisan (HSHS) has been effective in the treatment of ischemic stroke (IS) for centuries. However, its mechanisms are still underexplored.
Objective:The objective of this study is to identify the active ingredients and mechanisms of HSHS in treating IS.
Methods:We searched the main active compounds in HSHS and their potential targets, and key targets related to IS. Based on the common targets of HSHS and IS, we further expanded genes by KEGG database to obtain target genes and related genes, as well as gene interactions in the form of A→B, and then constructed a directed network including traditional Chinese medicines (TCMs), active compounds and genes. Finally, based on enrichment analysis, independent cascade (IC) model, and molecular docking, we explored the mechanisms of HSHS in treating IS.
Results:A directed network with 6,348 nodes and 64,996 edges was constructed. The enrichment analysis suggested that the AGE pathway, glucose metabolic pathway, lipid metabolic pathway, and inflammation pathway played critical roles in the treatment of IS by HSHS. Furthermore, the gene ontologies (GOs) of three monarch drugs in HSHS mainly involved cellular response to chemical stress, blood coagulation, hemostasis, positive regulation of MAPK cascade, and regulation of inflammatory response. Several candidate drug molecules were identified by molecular docking.
Conclusion:This study advocated potential drug development with targets in the AGE signaling pathway, with emphasis on neuroprotective, anti-inflammatory, and anti-apoptotic functions. The molecular docking simulation indicated that the ligand-target combination selection method based on the IC model was effective and reliable.
About the authors
Bo Cao
Department of Health Informatics and Management, School of Health Humanities, Peking University
Email: info@benthamscience.net
Jiao Jin
School of Statistics, Beijing Normal University
Email: info@benthamscience.net
Zhiyu Tang
Department of Health Informatics and Management, School of Health Humanities, Peking University
Email: info@benthamscience.net
Qiong Luo
School of Nursing, Peking University
Email: info@benthamscience.net
Jinbing An
Department of Health Informatics and Management, School of Health Humanities, Peking University
Author for correspondence.
Email: info@benthamscience.net
Wei Pang
Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University
Author for correspondence.
Email: info@benthamscience.net
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