Uncovering the Mechanism of Chinese Hawthorn Leaf on Myocardial Ischemia Based on Network Pharmacology, Molecular Docking Verification, and In Vitro Studies

Hawthorn leaf has shown therapeutic effects in the patients with myocardial ischemia. Our study combines network pharmacology, molecular docking techniques, and in vitro experiment with the aim of revealing the mechanism of hawthorn leaves in the treatment of myocardial ischemia. The active ingredie...

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Veröffentlicht in:Cardiovascular toxicology 2024-02, Vol.24 (2), p.171-183
Hauptverfasser: Gao, Jingyun, Wang, Yueyue, Xiong, Hui, Zhao, Shengnan, He, Mingmei, He, Meiting, Pan, Haifeng
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container_issue 2
container_start_page 171
container_title Cardiovascular toxicology
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creator Gao, Jingyun
Wang, Yueyue
Xiong, Hui
Zhao, Shengnan
He, Mingmei
He, Meiting
Pan, Haifeng
description Hawthorn leaf has shown therapeutic effects in the patients with myocardial ischemia. Our study combines network pharmacology, molecular docking techniques, and in vitro experiment with the aim of revealing the mechanism of hawthorn leaves in the treatment of myocardial ischemia. The active ingredients and corresponding targets of hawthorn leaf through Traditional Chinese Medicine System Pharmacology and Swiss Target Prediction databases. Targets related to myocardial ischemia were retrieved by Gene Card, Online Mendelian Inheritance in Man, Disgenet, and Therapeutic Targets Database databases. Cytoscape software was used to construct an ingredient–target–organ network and enrichment analysis of common targets was analyzed. Molecular docking verification of the core compound and target interactions was performed using MOE software. In vitro cell experiment was performed to verify the findings from bioinformatics analysis. Six active components and 107 potential therapeutic targets were screened. The protein–protein interaction network analysis indicated that 10 targets, including AKT1 and EGFR, were hub genes. Quercetin, kaempferol and isorhamnetin were taken as core active components. Through pathway enrichment analysis, nearly 455 Gene Ontology entries and 77 Kyoto Encyclopedia of Genes and Genomes pathways were obtained, mainly including PI3K/Akt, estrogen and other signaling pathways. Molecular docking prediction showed that three main active ingredients were firmly combined with the core targets. Cellular experiments showed that quercetin alleviated oxidative damage in cells and regulated the expression of PI3K, P-AKT/AKT and Bax/Bcl-2 proteins. This study identified the potential targets of Hawthorn leaf against myocardial ischemia using network pharmacology and in vitro verification, which provided a new understanding of the pharmacological mechanisms of Hawthorn leaf in treatment of myocardial ischemia.
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Our study combines network pharmacology, molecular docking techniques, and in vitro experiment with the aim of revealing the mechanism of hawthorn leaves in the treatment of myocardial ischemia. The active ingredients and corresponding targets of hawthorn leaf through Traditional Chinese Medicine System Pharmacology and Swiss Target Prediction databases. Targets related to myocardial ischemia were retrieved by Gene Card, Online Mendelian Inheritance in Man, Disgenet, and Therapeutic Targets Database databases. Cytoscape software was used to construct an ingredient–target–organ network and enrichment analysis of common targets was analyzed. Molecular docking verification of the core compound and target interactions was performed using MOE software. In vitro cell experiment was performed to verify the findings from bioinformatics analysis. Six active components and 107 potential therapeutic targets were screened. The protein–protein interaction network analysis indicated that 10 targets, including AKT1 and EGFR, were hub genes. Quercetin, kaempferol and isorhamnetin were taken as core active components. Through pathway enrichment analysis, nearly 455 Gene Ontology entries and 77 Kyoto Encyclopedia of Genes and Genomes pathways were obtained, mainly including PI3K/Akt, estrogen and other signaling pathways. Molecular docking prediction showed that three main active ingredients were firmly combined with the core targets. Cellular experiments showed that quercetin alleviated oxidative damage in cells and regulated the expression of PI3K, P-AKT/AKT and Bax/Bcl-2 proteins. This study identified the potential targets of Hawthorn leaf against myocardial ischemia using network pharmacology and in vitro verification, which provided a new understanding of the pharmacological mechanisms of Hawthorn leaf in treatment of myocardial ischemia.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>38376772</pmid><doi>10.1007/s12012-024-09825-w</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-1791-5827</orcidid></addata></record>
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subjects 1-Phosphatidylinositol 3-kinase
AKT protein
AKT1 protein
BAX protein
Bcl-2 protein
Bioinformatics
Biomedical and Life Sciences
Biomedicine
Cardiology
Coronary Artery Disease
Crataegus
Databases, Genetic
Drugs, Chinese Herbal - pharmacology
Encyclopedias
Estrogens
Genes
Genomes
Herbal medicine
Humans
Ingredients
Ischemia
Kaempferol
Leaves
Molecular docking
Molecular Docking Simulation
Myocardial ischemia
Myocardial Ischemia - drug therapy
Myocardial Ischemia - genetics
Network analysis
Network Pharmacology
Pharmacology
Pharmacology/Toxicology
Phosphatidylinositol 3-Kinases
Proteins
Proto-Oncogene Proteins c-akt
Quercetin
Quercetin - pharmacology
Software
Therapeutic targets
Traditional Chinese medicine
Verification
title Uncovering the Mechanism of Chinese Hawthorn Leaf on Myocardial Ischemia Based on Network Pharmacology, Molecular Docking Verification, and In Vitro Studies
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