Evidence map›Paper›PMID 26106459›Full record

ArticleOxidative medicine and cellular longevity2015

Quercetin Affects Erythropoiesis and Heart Mitochondrial Function in Mice.

Lina M Ruiz, Celia Salazar, Erik Jensen, Paula A Ruiz, William Tiznado, Rodrigo A Quintanilla, Marlen Barreto, Alvaro A Elorza

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

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  10. Effects ofBiology · 2018
    Article
  11. Natural Compounds as Occult Ototoxins? Ginkgo biloba Flavonoids Moderately Damage Lateral Line Hair Cells.Journal of the Association for Research in Otolaryngology : JARO · 2017
    Article
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

8 authors at 3 institutions in 2 countries.

Lina M RuizCenter of Biomedical Research, Faculty of Health Sciences, Universidad Autónoma de Chile, Ricardo Morales 3369, 8910132 Santiago, Chile.ORCID 0000-0002-9363-2730
Celia SalazarCenter of Biomedical Research, Faculty of Health Sciences, Universidad Autónoma de Chile, Ricardo Morales 3369, 8910132 Santiago, Chile.ORCID 0000-0002-8558-5444
Erik JensenCenter for Biomedical Research, Faculty of Biological Sciences and Faculty of Medicine, Universidad Andres Bello, República 217, 8370146 Santiago, Chile.ORCID 0000-0002-2538-4093
Paula A RuiziEng Solutions Ltd., London N12 0DR, UK.
William TiznadoDepartment of Chemical Sciences, Faculty of Exact Sciences, Universidad Andres Bello, República 275, 8370146 Santiago, Chile.ORCID 0000-0002-6061-8879
Rodrigo A QuintanillaCenter of Biomedical Research, Faculty of Health Sciences, Universidad Autónoma de Chile, Ricardo Morales 3369, 8910132 Santiago, Chile.ORCID 0000-0002-9582-6379
Marlen BarretoCenter of Biomedical Research, Faculty of Health Sciences, Universidad Autónoma de Chile, Ricardo Morales 3369, 8910132 Santiago, Chile.
Alvaro A ElorzaCenter for Biomedical Research, Faculty of Biological Sciences and Faculty of Medicine, Universidad Andres Bello, República 217, 8370146 Santiago, Chile ; Millennium Institute of Immunology and Immunotherapy, Santiago, Chile.
Universidad Autónoma de Chile · CLUniversidad Andrés Bello · CLIntegrated Environmental Solutions (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quercetin, a dietary flavonoid used as a food supplement, showed powerful antioxidant effects in different cellular models. However, recent in vitro and in vivo studies in mammals have suggested a prooxidant effect of quercetin and described an interaction with mitochondria causing an increase in O2 (∙-) production, a decrease in ATP levels, and impairment of respiratory chain in liver tissue. Therefore, because of its dual actions, we studied the effect of quercetin in vivo to analyze heart mitochondrial function and erythropoiesis. Mice were injected with 50 mg/kg of quercetin for 15 days. Treatment with quercetin decreased body weight, serum insulin, and ceruloplasmin levels as compared with untreated mice. Along with an impaired antioxidant capacity in plasma, quercetin-treated mice showed a significant delay on erythropoiesis progression. Heart mitochondrial function was also impaired displaying more protein oxidation and less activity for IV, respectively, than no-treated mice. In addition, a significant reduction in the protein expression levels of Mitofusin 2 and Voltage-Dependent Anion Carrier was observed. All these results suggest that quercetin affects erythropoiesis and mitochondrial function and then its potential use as a dietary supplement should be reexamined.

Indexed as

AnimalsAntioxidantsBody WeightBone Marrow CellsCeruloplasminErythropoiesisFerritinsGTP PhosphohydrolasesInsulinMaleMiceMice, Inbred C57BLMitochondriaMyocardiumPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaQuercetinAntioxidantsCeruloplasminFerritinsGTP PhosphohydrolasesInsulinMfn2 protein, mousePeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mouseQuercetinTranscription Factors

Identifiers

PMID26106459
PMCPMC4464588
OpenAlexW1524041536

What OpenQuestion holds

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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.