Evidence map›Paper›PMID 25969463›Full record

ArticlePhysiological reports2015

Visualization and quantitation of GLUT4 translocation in human skeletal muscle following glucose ingestion and exercise.

Helen Bradley, Christopher S Shaw, Claus Bendtsen, Philip L Worthington, Oliver J Wilson, Juliette A Strauss, Gareth A Wallis, Alice M Turner, Anton J M Wagenmakers

Abstract read
In one paragraph

Article in Physiological reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

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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.

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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

9 authors.

Helen BradleySchool of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, UK.
Christopher S ShawSchool of Exercise and Nutrition Sciences, Deakin University, Geelong, Vic., Australia.
Claus BendtsenComputational Biology, Discovery Sciences, AstraZeneca R&D, Cambridge, UK.
Philip L WorthingtonComputational Biology, Discovery Sciences, AstraZeneca R&D, Alderley Park Macclesfield, UK.
Oliver J WilsonInstitute for Sport, Physical Activity and Leisure, Leeds Beckett University, Leeds, UK.
Juliette A StraussResearch Institute for Sport and Exercise Sciences, Liverpool John Moores University, Liverpool, UK.
Gareth A WallisSchool of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, UK.
Alice M TurnerSchool of Clinical and Experimental Medicine, University of Birmingham, Birmingham, UK Heart of England NHS Foundation Trust, Bordesley Green East Birmingham, UK.
Anton J M WagenmakersResearch Institute for Sport and Exercise Sciences, Liverpool John Moores University, Liverpool, UK a.j.wagenmakers@ljmu.ac.uk.

Funding

Medical Research Council MR/K00414X/1
6 · The paper itself

Abstract

Insulin- and contraction-stimulated increases in glucose uptake into skeletal muscle occur in part as a result of the translocation of glucose transporter 4 (GLUT4) from intracellular stores to the plasma membrane (PM). This study aimed to use immunofluorescence microscopy in human skeletal muscle to quantify GLUT4 redistribution from intracellular stores to the PM in response to glucose feeding and exercise. Percutaneous muscle biopsy samples were taken from the m. vastus lateralis of ten insulin-sensitive men in the basal state and following 30 min of cycling exercise (65% VO2 max). Muscle biopsy samples were also taken from a second cohort of ten age-, BMI- and VO2 max-matched insulin-sensitive men in the basal state and 30 and 60 min following glucose feeding (75 g glucose). GLUT4 and dystrophin colocalization, measured using the Pearson's correlation coefficient, was increased following 30 min of cycling exercise (baseline r = 0.47 ± 0.01; post exercise r = 0.58 ± 0.02; P < 0.001) and 30 min after glucose ingestion (baseline r = 0.42 ± 0.02; 30 min r = 0.46 ± 0.02; P < 0.05). Large and small GLUT4 clusters were partially depleted following 30 min cycling exercise, but not 30 min after glucose feeding. This study has, for the first time, used immunofluorescence microscopy in human skeletal muscle to quantify increases in GLUT4 and dystrophin colocalization and depletion of GLUT4 from large and smaller clusters as evidence of net GLUT4 translocation to the PM.

Indexed as

Exerciseglucose ingestionGLUT4 translocationskeletal muscle

Identifiers

PMID25969463
PMCPMC4463815

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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.