Evidence map›Paper›PMID 30871106›Full record

ArticleNutrients2019

Offspring of Mice Exposed to a Low-Protein Diet in Utero Demonstrate Changes in mTOR Signaling in Pancreatic Islets of Langerhans, Associated with Altered Glucagon and Insulin Expression and a Lower β-Cell Mass.

Renee King, Jessica L Hill, Bibek Saha, Yuzhen Tong, Brenda J Strutt, Mark A Russell, Noel G Morgan, Sarah J Richardson, David J Hill

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2019. 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
3.3field-weighted citation impact, top 8% 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, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. A distinct role of STING in regulating glucose homeostasis through insulin sensitivity and insulin secretion.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
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 2 countries.

Renee KingLawson Health Research Institute, London, ON N6A 4V2, Canada. reneeking@rogers.com.
Jessica L HillLawson Health Research Institute, London, ON N6A 4V2, Canada. jh980@exeter.ac.uk.
Bibek SahaLawson Health Research Institute, London, ON N6A 4V2, Canada. bsaha2@uwo.ca.
Yuzhen TongLawson Health Research Institute, London, ON N6A 4V2, Canada. ytong33@uwo.ca.
Brenda J StruttLawson Health Research Institute, London, ON N6A 4V2, Canada. brenda.strutt@lawsonresearch.com.
Mark A RussellInstitute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter EX2 5DW, UK. M.Russell@exeter.ac.uk.
Noel G MorganInstitute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter EX2 5DW, UK. N.G.Morgan@exeter.ac.uk.ORCID 0000-0003-1537-8113
Sarah J RichardsonInstitute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter EX2 5DW, UK. S.Richardson@exeter.ac.uk.
David J HillLawson Health Research Institute, London, ON N6A 4V2, Canada. david.hill@lawsonresearch.com.
Lawson Health Research Institute · CAUniversity of Exeter · GBWestern University · CA

Funding

Alan Thicke Centre for Juvenile Diabetes Research NoneCIHR MOP-15263Diabetes UK 15/0005156Juvenile Diabetes Research Foundation United Kingdom 5-CDA-2014-221-A-N
6 · The paper itself

Abstract

Low birth weight is a risk factor for gestational and type 2 diabetes (T2D). Since mammalian target of rapamycin (mTOR) controls pancreatic β-cell mass and hormone release, we hypothesized that nutritional insult in utero might permanently alter mTOR signaling. Mice were fed a low-protein (LP, 8%) or control (C, 20%) diet throughout pregnancy, and offspring examined until 130 days age. Mice receiving LP were born 12% smaller and β-cell mass was significantly reduced throughout life. Islet mTOR levels were lower in LP-exposed mice and localized predominantly to α-rather than β-cells. Incubation of isolated mouse islets with rapamycin significantly reduced cell proliferation while increasing apoptosis. mRNA levels for mTORC complex genes mTOR, Rictor and Raptor were elevated at 7 days in LP mice, as were the mTOR and Raptor proteins. Proglucagon gene expression was similarly increased, but not insulin or the immune/metabolic defense protein STING. In human and mouse pancreas STING was strongly associated with islet β-cells. Results support long-term changes in islet mTOR signaling in response to nutritional insult in utero, with altered expression of glucagon and insulin and a reduced β-cell mass. This may contribute to an increased risk of gestational or type 2 diabetes.

Indexed as

Diet, Protein-RestrictedPrenatal Nutritional Physiological PhenomenaAnimalsCell LineDietary ProteinsFemaleGene Expression RegulationGlucagonInsulinIslets of LangerhansMiceMice, Inbred BALB CPregnancyRandom AllocationTOR Serine-Threonine KinasesDietary ProteinsGlucagonInsulinmTOR protein, mouseTOR Serine-Threonine Kinasesglucagoninsulinlow-proteinmousemTORpancreasSTINGβ-cell

Identifiers

PMID30871106
PMCPMC6471519
OpenAlexW2921261426

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.