Evidence map›Paper›PMID 22396201›Full record

ArticleDiabetes2012

A novel method to measure glucose uptake and myosin heavy chain isoform expression of single fibers from rat skeletal muscle.

James G Mackrell, Gregory D Cartee

Abstract read
In one paragraph

Article in Diabetes, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

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

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Skeletal muscle cell-specific differences in type 2 diabetes.Cellular and molecular life sciences : CMLS · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Fiber type-selective exercise effects on AS160 phosphorylation.American journal of physiology. Endocrinology and metabolism · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors.

James G MackrellMuscle Biology Laboratory, School of Kinesiology, University of Michigan, Ann Arbor, Michigan, USA.
Gregory D Cartee

Funding

Aging, Calorie Restriction, Exercise and Insulin SensitivityR01AG010026 · NIA · UNIVERSITY OF WISCONSIN MADISON · PI CARTEE, GREGORY D. · 1998 to 2023
$6.8M
Skeletal Muscle Glucose Uptake: Exercise and InsulinR01DK071771 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CARTEE, GREGORY D. · 2006 to 2020
$4.5M
AGE EFFECTS ON EXERCISE-STIMULATION OF GLUCOSE TRANSPORTR29AG010026 · NIA · UNIVERSITY OF WISCONSIN MADISON · PI CARTEE, GREGORY D. · 1992 to 1996
–
NIA NIH HHS AG-10026NIA NIH HHS R01 AG010026NIDDK NIH HHS DK-071771NIDDK NIH HHS R01 DK071771
6 · The paper itself

Abstract

Skeletal muscle includes many individual fibers with diverse phenotypes. A barrier to understanding muscle glucose uptake at the cellular level has been the absence of a method to measure glucose uptake by single fibers from mammalian skeletal muscle. This study's primary objective was to develop a procedure to measure glucose uptake by single fibers from rat skeletal muscle. Rat epitrochlearis muscles were incubated ex vivo with [(3)H]-2-deoxy-d-glucose, with or without insulin or AICAR, before isolation of ~10-30 single fibers from each muscle. Fiber type (myosin heavy chain [MHC] isoform) and glucose uptake were determined for each single fiber. Insulin-stimulated glucose uptake (which was cytochalasin B inhibitable) varied according to MHC isoform expression, with ~2-fold greater values for IIA versus IIB or IIX fibers and ~1.3-fold greater for hybrid (IIB/X) versus IIB fibers. In contrast, AICAR-stimulated glucose uptake was ~1.5-fold greater for IIB versus IIA fibers. A secondary objective was to assess insulin resistance of single fibers from obese versus lean Zucker rats. Genotype differences were observed for insulin-stimulated glucose uptake and inhibitor κB (IκB)-β abundance in single fibers (obese less than lean), with decrements for glucose uptake (44-58%) and IκB-β (25-32%) in each fiber type. This novel method creates a unique opportunity for future research focused on understanding muscle glucose uptake at the cellular level.

Indexed as

Adaptor Proteins, Signal TransducingAminoimidazole CarboxamideAnimalsDeoxyglucoseGene Expression RegulationGenotypeGlucoseI-kappa B KinaseInsulinInsulin ResistanceMaleMuscle Fibers, SkeletalMyosin Heavy ChainsNerve Tissue ProteinsProtein IsoformsRatsAdaptor Proteins, Signal TransducingAICA ribonucleotideAminoimidazole CarboxamideAppl1 protein, ratDeoxyglucoseGlucoseI-kappa B KinaseInsulinMyosin Heavy ChainsNerve Tissue ProteinsProtein IsoformsRibonucleotides

Identifiers

PMID22396201
PMCPMC3331778

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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.