Evidence map›Paper›PMID 24511298›Full record

ArticleTheScientificWorldJournal2014

Changes in iron metabolism and oxidative status in STZ-induced diabetic rats treated with bis(maltolato) oxovanadium (IV) as an antidiabetic agent.

Cristina Sánchez-González, Carlos López-Chaves, Cristina E Trenzado, Pilar Aranda, María López-Jurado, Jorge Gómez-Aracena, María Montes-Bayón, Alfredo Sanz-Medel, Juan Llopis

Open access · goldAbstract read
In one paragraph

Article in TheScientificWorldJournal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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  5. Article
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  7. 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

9 authors at 3 institutions in 1 country.

Cristina Sánchez-GonzálezDepartment of Physiology, Faculty of Pharmacy, University of Granada, 18071 Granada, Spain.
Carlos López-ChavesDepartment of Physiology, Faculty of Pharmacy, University of Granada, 18071 Granada, Spain.
Cristina E TrenzadoDepartment of Cellular Biology, Faculty of Sciences, University of Granada, 18071 Granada, Spain.
Pilar ArandaDepartment of Physiology, Faculty of Pharmacy, University of Granada, 18071 Granada, Spain.
María López-JuradoDepartment of Physiology, Faculty of Pharmacy, University of Granada, 18071 Granada, Spain.
Jorge Gómez-AracenaDepartment of Analytical Chemistry, Faculty of Chemistry, University of Oviedo, 33007 Oviedo, Spain.
María Montes-BayónDepartment of Preventive Medicine and Public Health, Faculty of Medicine, University of Málaga, 29071 Málaga, Spain.
Alfredo Sanz-MedelDepartment of Preventive Medicine and Public Health, Faculty of Medicine, University of Málaga, 29071 Málaga, Spain.
Juan LlopisDepartment of Physiology, Faculty of Pharmacy, University of Granada, 18071 Granada, Spain.
Universidad de Granada · ESUniversidad de Málaga · ESUniversidad de Oviedo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of vanadium as a micronutrient and hypoglycaemic agent has yet to be fully clarified. The present study was undertaken to investigate changes in the metabolism of iron and in antioxidant defences of diabetic STZ rats following treatment with vanadium. Four groups were examined: control; diabetic; diabetic treated with 1 mgV/day; and Diabetic treated with 3 mgV/day. The vanadium was supplied in drinking water as bis(maltolato) oxovanadium (IV) (BMOV). The experiment had a duration of five weeks. Iron was measured in food, faeces, urine, serum, muscle, kidney, liver, spleen, and femur. Superoxide dismutase, catalase, NAD(P)H: quinone-oxidoreductase-1 (NQO1) activity, and protein carbonyl group levels in the liver were determined. In the diabetic rats, higher levels of Fe absorbed, Fe content in kidney, muscle, and femur, and NQO1 activity were recorded, together with decreased catalase activity, in comparison with the control rats. In the rats treated with 3 mgV/day, there was a significant decrease in fasting glycaemia, Fe content in the liver, spleen, and heart, catalase activity, and levels of protein carbonyl groups in comparison with the diabetic group. In conclusion BMOV was a dose-dependent hypoglycaemic agent. Treatment with 3 mgV/day provoked increased Fe deposits in the tissues, which promoted a protein oxidative damage in the liver.

Indexed as

AnimalsCatalaseDiabetes Mellitus, ExperimentalHypoglycemic AgentsIronKidneyLiverMaleMuscle, SkeletalMyocardiumNAD(P)H Dehydrogenase (Quinone)Oxidation-ReductionPyronesRatsSpleenSuperoxide Dismutasebis(maltolato)oxovanadium(IV)CatalaseHypoglycemic AgentsIronNAD(P)H Dehydrogenase (Quinone)PyronesSuperoxide DismutaseVanadates

Identifiers

PMID24511298
PMCPMC3913100
OpenAlexW2021738333

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.