Evidence map›Paper›PMID 26388784›Full record

ArticleFrontiers in physiology2015

The protective effects of oral low-dose quercetin on diabetic nephropathy in hypercholesterolemic mice.

Isabele B S Gomes, Marcella L Porto, Maria C L F S Santos, Bianca P Campagnaro, Agata L Gava, Silvana S Meyrelles, Thiago M C Pereira, Elisardo C Vasquez

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
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  16. Association between LXR-Journal of diabetes research · 2020
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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 2 institutions in 1 country.

Isabele B S GomesLaboratory of Translational Physiology, Health Sciences Center, Federal University of Espirito Santo Vitoria, Brazil.
Marcella L PortoLaboratory of Translational Physiology, Health Sciences Center, Federal University of Espirito Santo Vitoria, Brazil.
Maria C L F S SantosPharmaceutical Sciences Graduate Program, Vila Velha University Vila Velha, Brazil.
Bianca P CampagnaroLaboratory of Translational Physiology, Health Sciences Center, Federal University of Espirito Santo Vitoria, Brazil ; Pharmaceutical Sciences Graduate Program, Vila Velha University Vila Velha, Brazil.
Agata L GavaLaboratory of Translational Physiology, Health Sciences Center, Federal University of Espirito Santo Vitoria, Brazil.
Silvana S MeyrellesLaboratory of Translational Physiology, Health Sciences Center, Federal University of Espirito Santo Vitoria, Brazil.
Thiago M C PereiraPharmaceutical Sciences Graduate Program, Vila Velha University Vila Velha, Brazil ; Department of Biotechnology, Federal Institute of Education, Science and Technology (IFES) Vila Velha, Brazil.
Elisardo C VasquezLaboratory of Translational Physiology, Health Sciences Center, Federal University of Espirito Santo Vitoria, Brazil ; Pharmaceutical Sciences Graduate Program, Vila Velha University Vila Velha, Brazil ; Emescam School of Health Sciences Vitoria, Brazil.
Universidade Federal do Espírito Santo · BRUniversidade Vila Velha · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsDiabetic nephropathy (DN) is one of the most important causes of chronic renal disease, and the incidence of DN is increasing worldwide. Considering our previous report (Gomes et al., 2014) indicating that chronic treatment with oral low-dose quercetin (10 mg/Kg) demonstrated anti-oxidative, anti-apoptotic and renoprotective effects in the C57BL/6J model of DN, we investigated whether this flavonoid could also have beneficial effects in concurrent DN and spontaneous atherosclerosis using the apolipoprotein E-deficient mouse (apoE(-/-)).

methodsStreptozotocin was used to induce diabetes (100 mg/kg/day, 3 days) in male apoE(-/-) mice (8 week-old). After 6 weeks, the mice were randomly separated into DQ: diabetic apoE(-/-) mice treated with quercetin (10 mg/kg/day, 4 weeks, n = 8), DV: diabetic ApoE(-/-) mice treated with vehicle (n = 8) and ND: non-treated non-diabetic mice (n = 8).

resultsQuercetin treatment diminished polyuria (~30%; p < 0.05), glycemia (~25%, p < 0.05), normalized the hypertriglyceridemia. Moreover, this bioflavonoid diminished creatininemia (~30%, p < 0.01) and reduced proteinuria but not to normal levels. We also observed protective effects on the renal structural changes, including normalization of the index of glomerulosclerosis and kidney weight/body weight.

conclusionsOur data revealed that quercetin treatment significantly reduced DN in hypercholesterolemic mice by inducing biochemical changes (decrease in glucose and triglycerides serum levels) and reduction of glomerulosclerosis. Thus, this study highlights the relevance of quercetin as an alternative therapeutic option for DN, including in diabetes associated with dyslipidemia.

Indexed as

apoEatherosclerosisdiabetesnephropathyquercetinstreptozotocin

Identifiers

PMID26388784
PMCPMC4557109
OpenAlexW2170497918

What OpenQuestion holds

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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.