Evidence map›Paper›PMID 24747582›Full record

ArticleExperimental gerontology2014

The effects of age and muscle contraction on AMPK activity and heterotrimer composition.

Shalene E Hardman, Derrick E Hall, Alyssa J Cabrera, Chad R Hancock, David M Thomson

Open access · greenAbstract read
In one paragraph

Article in Experimental gerontology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Physiological Systems in Promoting Frailty.Comprehensive Physiology · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Mitochondria-localized AMPK responds to local energetics and contributes to exercise and energetic stress-induced mitophagy.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Article
  17. Article
  18. Review
  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

5 authors at 1 institution in 1 country.

Shalene E HardmanDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, UT, 84602, USA.
Derrick E HallDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, UT, 84602, USA.
Alyssa J CabreraDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, UT, 84602, USA.
Chad R HancockDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, UT, 84602, USA.
David M ThomsonDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, UT, 84602, USA. Electronic address: david_thomson@byu.edu.
Brigham Young University · US

Funding

Regulation of Skeletal Muscle LKB1R01AR051928 · NIAMS · BRIGHAM YOUNG UNIVERSITY · PI WINDER, WILLIAM · 2006 to 2010
$1.6M
NIAMS NIH HHS R01 AR-051928NIAMS NIH HHS R01 AR051928
6 · The paper itself

Abstract

Sarcopenia is characterized by increased skeletal muscle atrophy due in part to alterations in muscle metabolism. AMP-activated protein kinase (AMPK) is a master regulator of skeletal muscle metabolic pathways which regulate many cellular processes that are disrupted in old-age. Functional AMPK is a heterotrimer composed of α, β and γ subunits, and each subunit can be represented in the heterotrimer by one of two (α1/α2, β1/β2) or three (γ1/γ2/γ3) isoforms. Altered isoform composition affects AMPK localization and function. Previous work has shown that overall AMPK activation with endurance-type exercise is blunted in old vs. young skeletal muscle. However, details regarding the activation of the specific isoforms of AMPK, as well as the heterotrimeric composition of AMPK in old skeletal muscle, are unknown. Our purpose here, therefore, was to determine the effect of old-age on 1) the activation of the α1 and α2 catalytic subunits of AMPK in skeletal muscle by a continuous contraction bout, and 2) the heterotrimeric composition of skeletal muscle AMPK. We studied gastrocnemius (GAST) and tibialis anterior (TA) muscles from young adult (YA; 8months old) and old (O; 30months old) male Fischer344×Brown Norway F1 hybrid rats after an in situ bout of endurance-type contractions produced via electrical stimulation of the sciatic nerve (STIM). AMPKα phosphorylation and AMPKα1 and α2 activities were unaffected by age at rest. However, AMPKα phosphorylation and AMPKα2 protein content and activity were lower in O vs. YA after STIM. Conversely, AMPKα1 content was greater in O vs. YA muscle, and α1 activity increased with STIM in O but not YA muscles. AMPKγ3 overall concentration and its association with AMPKα1 and α2 were lower in O vs. YA GAST. We conclude that activation of AMPKα1 is enhanced, while activation of α2 is suppressed immediately after repeated skeletal muscle contractions in O vs. YA skeletal muscle. These changes are associated with changes in the AMPK heterotrimer composition. Given the known roles of AMPK α1, α2 and γ3, this may contribute to sarcopenia and associated muscle metabolic dysfunction.

Indexed as

Acetyl-CoA CarboxylaseAgingAMP-Activated Protein Kinase KinasesAMP-Activated Protein KinasesAnimalsElectric StimulationEnzyme ActivationIsoenzymesMaleMuscle ContractionMuscle, SkeletalPhosphorylationPhysical Conditioning, AnimalProtein Serine-Threonine KinasesRatsRats, Inbred F344Acetyl-CoA CarboxylaseAMP-Activated Protein Kinase KinasesAMP-Activated Protein KinasesIsoenzymesProtein Serine-Threonine KinasesStk11 protein, ratAgingAMPKExerciseSarcopeniaSkeletal muscle

Identifiers

PMID24747582
PMCPMC4081450
OpenAlexW2135407336

What OpenQuestion holds

Textmetadata
LicenceTDM
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.