Evidence map›Paper›PMID 26680597›Full record

ArticleEuropean journal of nutrition2017

Metabolic syndrome and selenium during gestation and lactation.

Fátima Nogales, M Luisa Ojeda, Paulina Muñoz Del Valle, Alejandra Serrano, M Luisa Murillo, Olimpia Carreras Sánchez

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Article in European journal of nutrition, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 17 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.

Fátima NogalesDepartment of Physiology, Faculty of Pharmacy, Seville University, C/Profesor García González, No 2, 41012, Seville, Spain.
M Luisa OjedaDepartment of Physiology, Faculty of Pharmacy, Seville University, C/Profesor García González, No 2, 41012, Seville, Spain.
Paulina Muñoz Del ValleDepartment of Physiology, Faculty of Pharmacy, Seville University, C/Profesor García González, No 2, 41012, Seville, Spain.
Alejandra SerranoDepartment of Physiology, Faculty of Pharmacy, Seville University, C/Profesor García González, No 2, 41012, Seville, Spain.
M Luisa MurilloDepartment of Physiology, Faculty of Pharmacy, Seville University, C/Profesor García González, No 2, 41012, Seville, Spain.
Olimpia Carreras SánchezDepartment of Physiology, Faculty of Pharmacy, Seville University, C/Profesor García González, No 2, 41012, Seville, Spain. olimpia@us.es.
Universidad de Sevilla · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSelenium (Se) has a dual role in metabolic syndrome (MS) development as it has an antioxidant action against both "good" and "bad" reactive oxygen species. This study evaluates Se body profile in dams which present MS during gestation and lactation, in order to elucidate a normal dietary Se's implication in this pathology.

methodRats were randomized into control (C) and fructose (F) groups. The rich fructose diet (65 %) during gestation and lactation periods induced MS in dams. Se body distribution was determined by atomic absorption spectrophotometry, and the hepatic activity of the four antioxidant enzymes and the bimolecular oxidation were determined by spectrophotometry. The cardiac activity was monitored using the indirect tail occlusion method. Lipid and glucidic profile was also analyzed.

resultsDespite the fact that the diet supplied has 0.1 ppm of Se, the minimal dietary requirement for rats, F dams ate less amount of food, and therefore, they had lower Se retention. However, they had normal levels of Se in serum and milk. Dams with MS had Se depletion in heart and muscle joint to hypertension and a lower heart rate, and Se repletion in liver and kidney. Despite the increase in hepatic glutathione peroxidase (GPx) and catalase activity found, lipid oxidation occurred-probably because superoxide dismutase activity was diminished. In heart, the activity and expression of the selenoprotein GPx1 were decreased.

conclusionWith these results, it is not possible to elucidate whether a dietary Se supplementation or a Se-restricted diet are good for MS; because despite the fact that GPx activity is increased in liver, it is also found, for the first time, that heart Se deposits are significantly decreased during MS.

Indexed as

LactationOxidative StressAnimalsBiomarkersBradycardiaDiet, Carbohydrate LoadingDyslipidemiasFemaleFructoseHypertensionLipid PeroxidationLiverMaleMaternal Nutritional Physiological PhenomenaMetabolic SyndromeMilkBiomarkersFructoseOxidoreductasesSeleniumGestationLactationMetabolic syndromeSelenium

Identifiers

PMID26680597
OpenAlexW2203858659

What Socratic 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 Socratic graph.