Evidence map›Paper›PMID 28587267›Full record

ArticleInternational journal of molecular sciences2017

Insulin Treatment May Alter Fatty Acid Carriers in Placentas from Gestational Diabetes Subjects.

Maria Ruiz-Palacios, Maria Teresa Prieto-Sánchez, Antonio José Ruiz-Alcaraz, José Eliseo Blanco-Carnero, Maria Sanchez-Campillo, Juan José Parrilla, Elvira Larqué

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  4. Characterization of human placental fetal vessels in gestational diabetes mellitus.Pflugers Archiv : European journal of physiology · 2025
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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

7 authors at 2 institutions in 1 country.

Maria Ruiz-PalaciosDepartment of Physiology, Faculty of Biology, Campus Mare Nostrum, University of Murcia, Murcia 30100, Spain. maria_coina_200@hotmail.com.
Maria Teresa Prieto-SánchezObstetrics and Gynecology Service, Virgen de la Arrixaca Clinical Hospital, University of Murcia, Murcia 30120, Spain. mariatemedicina@hotmail.com.
Antonio José Ruiz-AlcarazDepartment of Biochemistry, Molecular Biology B and Immunology, Campus Mare Nostrum, University of Murcia, Murcia 30100, Spain. ajruiz@um.es.
José Eliseo Blanco-CarneroObstetrics and Gynecology Service, Virgen de la Arrixaca Clinical Hospital, University of Murcia, Murcia 30120, Spain. jeblancoc@gmail.com.
Maria Sanchez-CampilloDepartment of Physiology, Faculty of Biology, Campus Mare Nostrum, University of Murcia, Murcia 30100, Spain. medit2011@gmail.com.
Juan José ParrillaObstetrics and Gynecology Service, Virgen de la Arrixaca Clinical Hospital, University of Murcia, Murcia 30120, Spain. jjparri@um.es.
Elvira LarquéDepartment of Physiology, Faculty of Biology, Campus Mare Nostrum, University of Murcia, Murcia 30100, Spain. elvirada@um.es.
Universidad de Murcia · ESHospital Universitario Virgen de la Arrixaca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is little information available on the effect of Gestational diabetes mellitus (GDM) treatment (diet or insulin) on placental lipid carriers, which may influence fetal fat accretion. Insulin may activate placental insulin receptors protein kinase (AKT) and extracellular signal regulated kinase ERK mediators, which might affect lipid metabolism. Placenta was collected from 25 control women, 23 GDM-Diet and 20 GDM-Insulin. Western blotting of insulin signaling mediators and lipid carriers was performed. The human choricarcinoma-derived cell line BeWo was preincubated with insulin inhibitors protein kinase (AKT) and extracellular signal regulated kinase (ERK) and ERK inhibitors to evaluate insulin regulation of lipid carriers. Maternal serum insulin at recruitment correlated to ultrasound fetal abdominal circumference in offspring of GDM and placental endothelial lipase (EL). Lipoprotein lipase in placenta was significantly reduced in both GDM, while most of the other lipid carriers tended to higher values, although not significantly. There was a significant increase in both phosphorylated-Akt and ERK in placentas from GDM-Insulin patients; both were associated to placental fatty acid translocase (FAT), fatty acid binding protein (A-FABP), and EL. BeWo cells treated with insulin pathway inhibitors significantly reduced A-FABP, fatty acid transport protein (FATP-1), and EL levels, confirming the role of insulin on these carriers. We conclude that insulin promotes the phosphorylation of placental insulin mediators contributing to higher levels of some specific fatty acid carriers in the placenta and fetal adiposity in GDM.

Indexed as

AdiposityCell LineDiabetes, GestationalFatty Acid-Binding ProteinsFatty AcidsFatty Acid Transport ProteinsFemaleFetusHumansHypoglycemic AgentsInsulinLipaseLipoprotein LipasePlacentaPregnancyFatty Acid-Binding ProteinsFatty AcidsFatty Acid Transport ProteinsHypoglycemic AgentsInsulinLipaseLIPG protein, humanLipoprotein Lipasefetal adipositygestational diabetesinsulin resistanceplacental lipid transport

Identifiers

PMID28587267
PMCPMC5486026
OpenAlexW2621612369

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.