Evidence map›Paper›PMID 25685776›Full record

ArticleBioMed research international2015

Iron dextran increases hepatic oxidative stress and alters expression of genes related to lipid metabolism contributing to hyperlipidaemia in murine model.

Maísa Silva, Joyce Ferreira da Costa Guerra, Ana Flávia Santos Sampaio, Wanderson Geraldo de Lima, Marcelo Eustáquio Silva, Maria Lucia Pedrosa

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Maísa SilvaBasic Department-Health Area, Federal University of Juiz de Fora, Campus Universitário s/n, 36036-900 Juiz de Fora, MG, Brazil.
Joyce Ferreira da Costa GuerraResearch Center in Biological Sciences (NUPEB), Federal University of Ouro Preto, Campus Morro do Cruzeiro s/n, 35400-000 Ouro Preto, MG, Brazil.
Ana Flávia Santos SampaioProgram of Health and Nutrition, Federal University of Ouro Preto, Campus Morro do Cruzeiro s/n, 35400-000 Ouro Preto, MG, Brazil.
Wanderson Geraldo de LimaResearch Center in Biological Sciences (NUPEB), Federal University of Ouro Preto, Campus Morro do Cruzeiro s/n, 35400-000 Ouro Preto, MG, Brazil ; Department of Biological Sciences, Federal University of Ouro Preto, Campus Morro do Cruzeiro s/n, 35400-000 Ouro Preto, MG, Brazil.
Marcelo Eustáquio SilvaResearch Center in Biological Sciences (NUPEB), Federal University of Ouro Preto, Campus Morro do Cruzeiro s/n, 35400-000 Ouro Preto, MG, Brazil ; Department of Foods, Federal University of Ouro Preto, Campus Morro do Cruzeiro s/n, 35400-000 Ouro Preto, MG, Brazil.
Maria Lucia PedrosaResearch Center in Biological Sciences (NUPEB), Federal University of Ouro Preto, Campus Morro do Cruzeiro s/n, 35400-000 Ouro Preto, MG, Brazil ; Department of Biological Sciences, Federal University of Ouro Preto, Campus Morro do Cruzeiro s/n, 35400-000 Ouro Preto, MG, Brazil.ORCID 0000-0002-6128-1745
Universidade Federal de Ouro Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study was to investigate the effects of iron dextran on lipid metabolism and to determine the involvement of oxidative stress. Fischer rats were divided into two groups: the standard group (S), which was fed the AIN-93M diet, and the standard plus iron group (SI), which was fed the same diet but also received iron dextran injections. Serum cholesterol and triacylglycerol levels were higher in the SI group than in the S group. Iron dextran was associated with decreased mRNA levels of pparα, and its downstream gene cpt1a, which is involved in lipid oxidation. Iron dextran also increased mRNA levels of apoB-100, MTP, and L-FABP indicating alterations in lipid secretion. Carbonyl protein and TBARS were consistently higher in the liver of the iron-treated rats. Moreover, a significant positive correlation was found between oxidative stress products, lfabp expression, and iron stores. In addition, a negative correlation was found between pparα expression, TBARS, carbonyl protein, and iron stores. In conclusion, our results suggest that the increase observed in the transport of lipids in the bloodstream and the decreased fatty acid oxidation in rats, which was promoted by iron dextran, might be attributed to increased oxidative stress.

Indexed as

AnimalsApolipoprotein B-100Carrier ProteinsFatty Acid-Binding ProteinsGene Expression RegulationHematinicsHyperlipidemiasIron-Dextran ComplexLipid MetabolismLiverMaleOxidative StressRatsRats, Inbred F344Apolipoprotein B-100Carrier ProteinsFabp1 protein, mouseFatty Acid-Binding ProteinsHematinicsIron-Dextran Complexmicrosomal triglyceride transfer protein

Identifiers

PMID25685776
PMCPMC4313725
OpenAlexW2083174831

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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.