Evidence map›Paper›PMID 34549711›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2021

[Exploring the therapeutic mechanism of quercetin for heart failure based on network pharmacology and molecular docking].

X Tan, W Xian, Y Chen, X Li, Q Wang, P Kang, H Wang

Open access · greenAbstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 47% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Quercetin improves heart failure by inhibiting cardiomyocyte apoptosisNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
  2. Research progress of quercetin in cardiovascular disease.Frontiers in cardiovascular medicine · 2023
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

X TanDepartment of Cardiology, First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College, Bengbu 233000, China.
W XianDepartment of Cardiology, First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College, Bengbu 233000, China.
Y ChenDepartment of Cardiology, First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College, Bengbu 233000, China.
X LiDepartment of Cardiology, First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College, Bengbu 233000, China.
Q WangDepartment of Physiology, Bengbu Medical College, Bengbu 233000, China.
P KangDepartment of Cardiology, First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College, Bengbu 233000, China.
H WangDepartment of Cardiology, First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College, Bengbu 233000, China.
Bengbu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the molecular mechanism of quercetin in the treatment of heart failure (HF) based on network pharmacology and molecular docking.

methodsQuercetin and HF-related targets were obtained using TCMSP, PharmMapper, CTD and GeneCards databases, and quercetin-HF intersection targets were obtained through the online website Venn; the protein interaction network was constructed and imported into Cytoscape 3.7.2 to identify the core targets of quercetin in the treatment of HF.GO and KEGG pathway enrichment analyses were performed using R package, and molecular docking was performed using Auto Dock Vina.The protein levels of AKT1, phospho-AKT(Ser473), eNOS, MMP9, and caspase-3 in quercetin-treated HF cell models were detected using protein immunoblotting.

resultsWe identified 80 quercetin-HF intersectional targets (AKT1, CASP3, MAPK1, MMP9, and MAPK8) and 5 core targets of quercetin for treatment of HF.GO analysis suggested that the therapeutic effect of quercetin for HF was mediated mainly by such biological processes as responses to peptide hormones, phosphatidylinositol-mediated signalling, responses to lipopolysaccharides, responses to molecules of bacterial origin and regulation of inflammatory responses.KEGG pathway enrichment analysis identified lipid and atherosclerosis pathway, proteoglycans in cancer, PI3K-AKT signaling pathway, diabetic cardiomyopathy and MAPK signaling pathway as the most significantly enriched signaling pathways.Molecular docking showed a good binding activity of quercetin to the 5 core targets.The results of protein immunoblotting showed that 100 μmol/L quercetin significantly reduced AKT1, phospho-AKT (Ser473), eNOS, MMP9 and caspase-3 levels in the cell models of HF (

conclusionQuercetin improves the pathological changes in HF possibly by regulating the AKT1-eNOS-MMP9 pathway to inhibit cell apoptosis.

Indexed as

Drugs, Chinese HerbalHeart FailureQuercetinHumansMolecular Docking SimulationDrugs, Chinese HerbalQuercetinheart failuremolecular dockingnetwork pharmacologyquercetin

Identifiers

PMID34549711
PMCPMC8527225
OpenAlexW3200813959

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.