Evidence map›Paper›PMID 21048074›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2011

Exercise training reverses impaired skeletal muscle metabolism induced by artificial selection for low aerobic capacity.

Sarah J Lessard, Donato A Rivas, Erin J Stephenson, Ben B Yaspelkis, Lauren G Koch, Steven L Britton, John A Hawley

Abstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

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  16. Role of intrinsic aerobic capacity and ventilator-induced diaphragm dysfunction.Journal of applied physiology (Bethesda, Md. : 1985) · 2015
    Article
  17. Review
  18. Article
  19. Differential skeletal muscle proteome of high- and low-active mice.Journal of applied physiology (Bethesda, Md. : 1985) · 2014
    Article
  20. Leanness and heightened nonresting energy expenditure: role of skeletal muscle activity thermogenesis.American journal of physiology. Endocrinology and metabolism · 2014
    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

7 authors at 2 institutions in 1 country.

Sarah J LessardRoyal Melbourne Institute of Technology, Bundoora, Victoria, Australia.
Donato A Rivas
Erin J Stephenson
Ben B Yaspelkis
Lauren G Koch
Steven L Britton
John A Hawley
University of Michigan–Ann Arbor · USCalifornia State University, Northridge · US

Funding

RESOURCE FOR RAT GENETIC MODELS OF AEROBIC CAPACITYR24RR017718 · NCRR · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI BRITTON, STEVEN LOYAL · 2003 to 2011
$4.0M
NCRR NIH HHS R24 RR017718
6 · The paper itself

Abstract

We have used a novel model of genetically imparted endurance exercise capacity and metabolic health to study the genetic and environmental contributions to skeletal muscle glucose and lipid metabolism. We hypothesized that metabolic abnormalities associated with low intrinsic running capacity would be ameliorated by exercise training. Selective breeding for 22 generations resulted in rat models with a fivefold difference in intrinsic aerobic capacity. Low (LCR)- and high (HCR)-capacity runners remained sedentary (SED) or underwent 6 wk of exercise training (EXT). Insulin-stimulated glucose transport, insulin signal transduction, and rates of palmitate oxidation were lower in LCR SED vs. HCR SED (P < 0.05). Decreases in glucose and lipid metabolism were associated with decreased β₂-adrenergic receptor (β₂-AR), and reduced expression of Nur77 target proteins that are critical regulators of muscle glucose and lipid metabolism [uncoupling protein-3 (UCP3), fatty acid transporter (FAT)/CD36; P < 0.01 and P < 0.05, respectively]. EXT reversed the impairments to glucose and lipid metabolism observed in the skeletal muscle of LCR, while increasing the expression of β₂-AR, Nur77, GLUT4, UCP3, and FAT/CD36 (P < 0.05) in this tissue. However, no metabolic improvements were observed following exercise training in HCR. Our results demonstrate that metabolic impairments resulting from genetic factors (low intrinsic aerobic capacity) can be overcome by an environmental intervention (exercise training). Furthermore, we identify Nur77 as a potential mechanism for improved skeletal muscle metabolism in response to EXT.

Indexed as

AnimalsCarbohydrate MetabolismLipid MetabolismModels, AnimalMuscle, SkeletalNuclear Receptor Subfamily 4, Group A, Member 1Physical Conditioning, AnimalPhysical EnduranceRatsRats, Inbred StrainsReceptors, Adrenergic, betaSignal TransductionNr4a1 protein, ratNuclear Receptor Subfamily 4, Group A, Member 1Receptors, Adrenergic, beta

Identifiers

PMID21048074
PMCPMC3023282
OpenAlexW2151347850

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.