Mechanisms of Quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validation

Abstract Atrial fibrillation (AF) is a common atrial arrhythmia for which there is no specific therapeutic drug. Quercetin (Que) has been used to treat cardiovascular diseases such as arrhythmias. In this study, we explored the mechanism of action of Que in AF using network pharmacology and molecula...

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Main Authors: Xin Tan, Wei Xian, Xiaorong Li, Yongfeng Chen, Jiayi Geng, Qiyi Wang, Qin Gao, Bi Tang, Hongju Wang, Pinfang Kang
Format: Article
Language:English
Published: Nature Portfolio 2022-06-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-13911-w
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author Xin Tan
Wei Xian
Xiaorong Li
Yongfeng Chen
Jiayi Geng
Qiyi Wang
Qin Gao
Bi Tang
Hongju Wang
Pinfang Kang
author_facet Xin Tan
Wei Xian
Xiaorong Li
Yongfeng Chen
Jiayi Geng
Qiyi Wang
Qin Gao
Bi Tang
Hongju Wang
Pinfang Kang
author_sort Xin Tan
collection DOAJ
description Abstract Atrial fibrillation (AF) is a common atrial arrhythmia for which there is no specific therapeutic drug. Quercetin (Que) has been used to treat cardiovascular diseases such as arrhythmias. In this study, we explored the mechanism of action of Que in AF using network pharmacology and molecular docking. The chemical structure of Que was obtained from Pubchem. TCMSP, Swiss Target Prediction, Drugbank, STITCH, Pharmmapper, CTD, GeneCards, DISGENET and TTD were used to obtain drug component targets and AF-related genes, and extract AF and normal tissue by GEO database differentially expressed genes by GEO database. The top targets were IL6, VEGFA, JUN, MMP9 and EGFR, and Que for AF treatment might involve the role of AGE-RAGE signaling pathway in diabetic complications, MAPK signaling pathway and IL-17 signaling pathway. Molecular docking showed that Que binds strongly to key targets and is differentially expressed in AF. In vivo results showed that Que significantly reduced the duration of AF fibrillation and improved atrial remodeling, reduced p-MAPK protein expression, and inhibited the progression of AF. Combining network pharmacology and molecular docking approaches with in vivo studies advance our understanding of the intensive mechanisms of Quercetin, and provide the targeted basis for clinical Atrial fibrillation treatment.
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spelling doaj.art-2b4a42e1084f478abdaa5906c0b74efc2022-12-22T03:31:10ZengNature PortfolioScientific Reports2045-23222022-06-0112111510.1038/s41598-022-13911-wMechanisms of Quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validationXin Tan0Wei Xian1Xiaorong Li2Yongfeng Chen3Jiayi Geng4Qiyi Wang5Qin Gao6Bi Tang7Hongju Wang8Pinfang Kang9Department of Cardiovascular Disease, the First Affiliated Hospital of Bengbu Medical CollegeDepartment of Cardiovascular Disease, the First Affiliated Hospital of Bengbu Medical CollegeDepartment of Cardiovascular Disease, the First Affiliated Hospital of Bengbu Medical CollegeDepartment of Cardiovascular Disease, the First Affiliated Hospital of Bengbu Medical CollegeDepartment of Psychiatry, Bengbu Medical CollegeDepartment of Physiology, Bengbu Medical CollegeDepartment of Physiology, Bengbu Medical CollegeDepartment of Cardiovascular Disease, the First Affiliated Hospital of Bengbu Medical CollegeDepartment of Cardiovascular Disease, the First Affiliated Hospital of Bengbu Medical CollegeDepartment of Cardiovascular Disease, the First Affiliated Hospital of Bengbu Medical CollegeAbstract Atrial fibrillation (AF) is a common atrial arrhythmia for which there is no specific therapeutic drug. Quercetin (Que) has been used to treat cardiovascular diseases such as arrhythmias. In this study, we explored the mechanism of action of Que in AF using network pharmacology and molecular docking. The chemical structure of Que was obtained from Pubchem. TCMSP, Swiss Target Prediction, Drugbank, STITCH, Pharmmapper, CTD, GeneCards, DISGENET and TTD were used to obtain drug component targets and AF-related genes, and extract AF and normal tissue by GEO database differentially expressed genes by GEO database. The top targets were IL6, VEGFA, JUN, MMP9 and EGFR, and Que for AF treatment might involve the role of AGE-RAGE signaling pathway in diabetic complications, MAPK signaling pathway and IL-17 signaling pathway. Molecular docking showed that Que binds strongly to key targets and is differentially expressed in AF. In vivo results showed that Que significantly reduced the duration of AF fibrillation and improved atrial remodeling, reduced p-MAPK protein expression, and inhibited the progression of AF. Combining network pharmacology and molecular docking approaches with in vivo studies advance our understanding of the intensive mechanisms of Quercetin, and provide the targeted basis for clinical Atrial fibrillation treatment.https://doi.org/10.1038/s41598-022-13911-w
spellingShingle Xin Tan
Wei Xian
Xiaorong Li
Yongfeng Chen
Jiayi Geng
Qiyi Wang
Qin Gao
Bi Tang
Hongju Wang
Pinfang Kang
Mechanisms of Quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validation
Scientific Reports
title Mechanisms of Quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validation
title_full Mechanisms of Quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validation
title_fullStr Mechanisms of Quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validation
title_full_unstemmed Mechanisms of Quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validation
title_short Mechanisms of Quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validation
title_sort mechanisms of quercetin against atrial fibrillation explored by network pharmacology combined with molecular docking and experimental validation
url https://doi.org/10.1038/s41598-022-13911-w
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