Evidence map›Paper›PMID 27049667›Full record

ArticleEndocrinology2016

Chronic Hyperinsulinemia Increases Myoblast Proliferation in Fetal Sheep Skeletal Muscle.

Laura D Brown, Stephanie R Wesolowski, Jenai Kailey, Stephanie Bourque, Averi Wilson, Sasha E Andrews, William W Hay, Paul J Rozance

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Placental insufficiency disrupts cardiomyocyte ploidy and cell cycle fate in growth-restricted fetal sheep.American journal of physiology. Regulatory, integrative and comparative physiology · 2026
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  13. Effects of chronic hyperinsulinemia on metabolic pathways and insulin signaling in the fetal liver.American journal of physiology. Endocrinology and metabolism · 2020
    Article
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  16. Review
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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 1 institution in 1 country.

Laura D BrownPerinatal Research Center (L.D.B., S.R.W., J.K., S.B., A.W., W.W.H., P.J.R.), Department of Pediatrics, Center for Women's Health Research (L.D.B., S.R.W., P.J.R.), and Department of Obstetrics and Gynecology (S.E.A.), University of Colorado Denver School of Medicine, Aurora, Colorado 80045.
Stephanie R WesolowskiPerinatal Research Center (L.D.B., S.R.W., J.K., S.B., A.W., W.W.H., P.J.R.), Department of Pediatrics, Center for Women's Health Research (L.D.B., S.R.W., P.J.R.), and Department of Obstetrics and Gynecology (S.E.A.), University of Colorado Denver School of Medicine, Aurora, Colorado 80045.
Jenai KaileyPerinatal Research Center (L.D.B., S.R.W., J.K., S.B., A.W., W.W.H., P.J.R.), Department of Pediatrics, Center for Women's Health Research (L.D.B., S.R.W., P.J.R.), and Department of Obstetrics and Gynecology (S.E.A.), University of Colorado Denver School of Medicine, Aurora, Colorado 80045.
Stephanie BourquePerinatal Research Center (L.D.B., S.R.W., J.K., S.B., A.W., W.W.H., P.J.R.), Department of Pediatrics, Center for Women's Health Research (L.D.B., S.R.W., P.J.R.), and Department of Obstetrics and Gynecology (S.E.A.), University of Colorado Denver School of Medicine, Aurora, Colorado 80045.
Averi WilsonPerinatal Research Center (L.D.B., S.R.W., J.K., S.B., A.W., W.W.H., P.J.R.), Department of Pediatrics, Center for Women's Health Research (L.D.B., S.R.W., P.J.R.), and Department of Obstetrics and Gynecology (S.E.A.), University of Colorado Denver School of Medicine, Aurora, Colorado 80045.
Sasha E AndrewsPerinatal Research Center (L.D.B., S.R.W., J.K., S.B., A.W., W.W.H., P.J.R.), Department of Pediatrics, Center for Women's Health Research (L.D.B., S.R.W., P.J.R.), and Department of Obstetrics and Gynecology (S.E.A.), University of Colorado Denver School of Medicine, Aurora, Colorado 80045.
William W HayPerinatal Research Center (L.D.B., S.R.W., J.K., S.B., A.W., W.W.H., P.J.R.), Department of Pediatrics, Center for Women's Health Research (L.D.B., S.R.W., P.J.R.), and Department of Obstetrics and Gynecology (S.E.A.), University of Colorado Denver School of Medicine, Aurora, Colorado 80045.
Paul J RozancePerinatal Research Center (L.D.B., S.R.W., J.K., S.B., A.W., W.W.H., P.J.R.), Department of Pediatrics, Center for Women's Health Research (L.D.B., S.R.W., P.J.R.), and Department of Obstetrics and Gynecology (S.E.A.), University of Colorado Denver School of Medicine, Aurora, Colorado 80045.
University of Colorado Denver · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Edward L Melanson · 1995 to 2026
$32.6M
UCHSC: Building Interdisciplinary Research Careers in Women's HealthK12HD057022 · NICHD · UNIVERSITY OF COLORADO DENVER · PI REGENSTEINER, JUDITH G., SANTORO, NANETTE F. · 2007 to 2023
$8.5M
Nutrient Coordination of Pancreatic Vasculature and Beta-CellsR01DK088139 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI ROZANCE, PAUL JOSEPH · 2011 to 2020
$5.1M
Regulation of Fetal Skeletal Muscle Growth in IUGRR01HD079404 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Laura Davidson Brown · 2015 to 2026
$4.7M
Training in Basic and Translational Child Health ResearchK12HD068372 · NICHD · UNIVERSITY OF COLORADO DENVER · PI DANIELS, STEPHEN R · 2011 to 2020
$3.7M
Colorado Clinical and Translational Sciences InstituteKL2TR001080 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$2.6M
Colorado Clinical and Translational Sciences InstituteTL1TR001081 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$1.3M
TISSUE SPECIFIC REGULATION OF GLUCOSE METABOLISM AND INSULIN ACTION IN IUGR FETUSK01DK090199 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI WESOLOWSKI, STEPHANIE R · 2010 to 2014
$707k
Pancreatic beta-cell endothelial cell function and signaling in intrauterine growK08HD060688 · NICHD · UNIVERSITY OF COLORADO DENVER · PI ROZANCE, PAUL JOSEPH · 2009 to 2013
$591k
Effect of hypoxia on glucose metabolism in IUGR fetal liverR03DK102972 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI WESOLOWSKI, STEPHANIE R · 2014 to 2015
$155k
NCATS NIH HHS KL2 TR001080NCATS NIH HHS TL1 TR001081NCATS NIH HHS UL1 TR001082NICHD NIH HHS K08 HD060688NICHD NIH HHS K12 HD057022NICHD NIH HHS K12 HD068372NICHD NIH HHS R01 HD079404NIDDK NIH HHS K01 DK090199NIDDK NIH HHS R01 DK088139NIDDK NIH HHS R03 DK102972
6 · The paper itself

Abstract

Insulin is an important fetal growth factor. However, chronic experimental hyperinsulinemia in the fetus fails to accelerate linear and lean mass growth beyond normal rates. Mechanisms preventing accelerated lean mass accretion during hyperinsulinemia are unknown. To address potential mechanisms, late-gestation fetal sheep were infused with iv insulin and glucose to produce euglycemic hyperinsulinemia (INS) or saline for 7-9 days. Fetal substrate uptake and protein metabolic rates were measured. INS fetuses had 1.5-fold higher insulin concentrations (P < .0001) and equivalent glucose concentrations. INS fetuses had 20% more Pax7(+) nuclei in the biceps femoris, which indicates the potential for hyperinsulinemia to increase the number of myoblasts within late-gestation fetal skeletal muscle. Additionally, the percentage of Pax7(+) myoblasts that expressed Ki-67 was 1.3-fold higher and expression of myogenic regulatory factors was 50% lower in INS fetuses (MYF5 and MYOG [myogenin], P < .005), which indicates a shift toward myoblast proliferation over differentiation. There were no differences for fetal body, organ, or muscle weights, although INS placentas weighed 28% less (P < .05). Protein synthesis and accretion rates did not change in INS fetuses, nor did fiber muscle size. Essential amino acid concentrations were lower in the INS group (P < .05) except for tryptophan. Umbilical blood flow, net total amino acids, and O2 uptakes rates did not differ between groups. Arterial O2 content was 33% lower (P < .005) and norepinephrine was 100% higher in the INS fetuses (P < .01), all of which are factors that may counteract fetal protein accretion during hyperinsulinemia despite an increase in myoblast proliferation.

Indexed as

AnimalsCell ProliferationFemaleFetusHyperinsulinismInsulinIn Vitro TechniquesMuscle Fibers, SkeletalMuscle, SkeletalMyoblastsPregnancySheepInsulin

Identifiers

PMID27049667
PMCPMC4891788
OpenAlexW2313685424

What OpenQuestion holds

Textmetadata
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.