Evidence map›Paper›PMID 25460361›Full record

ArticlePloS one2014

The flavonoid quercetin reverses pulmonary hypertension in rats.

Daniel Morales-Cano, Carmen Menendez, Enrique Moreno, Javier Moral-Sanz, Bianca Barreira, Pilar Galindo, Rachele Pandolfi, Rosario Jimenez, Laura Moreno, Angel Cogolludo and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. The right time, the right cell: the potential for precision senotherapy in pulmonary arterial hypertension.American journal of physiology. Lung cellular and molecular physiology · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Cellular senescence in adult pulmonary hypertension: current state and future challenges.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  7. Bioactive compound combinations fromFrontiers in pharmacology · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Flavonoids as Modulators of Potassium Channels.International journal of molecular sciences · 2023
    Review
  12. Article
  13. Article
  14. Review
  15. Antidepressant Potential of Quercetin and itsFrontiers in pharmacology · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Nutraceuticals in the Treatment of Pulmonary Arterial Hypertension.International journal of molecular sciences · 2020
    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

12 authors at 3 institutions in 2 countries.

Daniel Morales-CanoDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Carmen MenendezDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain; Faculty of Health Sciences, Universidad Autónoma de Chile, Santiago, Chile.
Enrique MorenoDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Javier Moral-SanzDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Bianca BarreiraDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Pilar GalindoDepartment of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain.
Rachele PandolfiDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Rosario JimenezDepartment of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain.
Laura MorenoDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Angel CogolludoDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Juan DuarteDepartment of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain.
Francisco Perez-VizcainoDepartment of Pharmacology, School of Medicine, University Complutense of Madrid, Madrid, Spain; Ciber Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESUniversidad Complutense de Madrid · ESUniversidad de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quercetin is a dietary flavonoid which exerts vasodilator, antiplatelet and antiproliferative effects and reduces blood pressure, oxidative status and end-organ damage in humans and animal models of systemic hypertension. We hypothesized that oral quercetin treatment might be protective in a rat model of pulmonary arterial hypertension. Three weeks after injection of monocrotaline, quercetin (10 mg/kg/d per os) or vehicle was administered for 10 days to adult Wistar rats. Quercetin significantly reduced mortality. In surviving animals, quercetin decreased pulmonary arterial pressure, right ventricular hypertrophy and muscularization of small pulmonary arteries. Classic biomarkers of pulmonary arterial hypertension such as the downregulated expression of lung BMPR2, Kv1.5, Kv2.1, upregulated survivin, endothelial dysfunction and hyperresponsiveness to 5-HT were unaffected by quercetin. Quercetin significantly restored the decrease in Kv currents, the upregulation of 5-HT2A receptors and reduced the Akt and S6 phosphorylation. In vitro, quercetin induced pulmonary artery vasodilator effects, inhibited pulmonary artery smooth muscle cell proliferation and induced apoptosis. In conclusion, quercetin is partially protective in this rat model of PAH. It delayed mortality by lowering PAP, RVH and vascular remodeling. Quercetin exerted effective vasodilator effects in isolated PA, inhibited cell proliferation and induced apoptosis in PASMCs. These effects were associated with decreased 5-HT2A receptor expression and Akt and S6 phosphorylation and partially restored Kv currents. Therefore, quercetin could be useful in the treatment of PAH.

Indexed as

AnimalsGene Expression ProfilingHypertension, PulmonaryHypertrophy, Right VentricularMaleMembrane PotentialsQuercetinRatsRats, WistarSurvival AnalysisQuercetin

Identifiers

PMID25460361
PMCPMC4252144
OpenAlexW2131264643

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.