Evidence map›Paper›PMID 19245653›Full record

ReviewActa physiologica (Oxford, England)2009

AMP-activated protein kinase control of fat metabolism in skeletal muscle.

D M Thomson, W W Winder

Open access · greenAbstract readReview
In one paragraph

Review in Acta physiologica (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.1field-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

47 citing papers in PubMed, 111 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Nutrients · 2025
    Article
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  10. Microorganisms · 2022
    Review
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  12. Antioxidant Properties and Cytoprotective Effect ofAntioxidants (Basel, Switzerland) · 2021
    Article
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  15. Article
  16. Review
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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

2 authors at 1 institution in 1 country.

D M ThomsonDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84602, USA. david_thomson@byu.edu
W W Winder
Brigham Young University · US

Funding

Regulation of Skeletal Muscle LKB1R01AR051928 · NIAMS · BRIGHAM YOUNG UNIVERSITY · PI WINDER, WILLIAM · 2006 to 2010
$1.6M
PHYSIOLOGY OF MALONYL COA IN MUSCLE DURING EXERCISER01AR041438 · NIAMS · BRIGHAM YOUNG UNIVERSITY · PI WINDER, WILLIAM · 1992 to 2006
$1.4M
NIAMS NIH HHS AR 41438NIAMS NIH HHS AR 51928NIAMS NIH HHS R01 AR051928
6 · The paper itself

Abstract

AMP-activated protein kinase (AMPK) has emerged as a key regulator of skeletal muscle fat metabolism. Because abnormalities in skeletal muscle metabolism contribute to a variety of clinical diseases and disorders, understanding AMPK's role in the muscle is important. It was originally shown to stimulate fatty acid (FA) oxidation decades ago, and since then much research has been accomplished describing this role. In this brief review, we summarize much of these data, particularly in relation to changes in FA oxidation that occur during skeletal muscle exercise. Potential roles for AMPK exist in regulating FA transport into the mitochondria via interactions with acetyl-CoA carboxylase, malonyl-CoA decarboxylase, and perhaps FA transporter/CD36 (FAT/CD36). Likewise, AMPK may regulate transport of FAs into the cell through FAT/CD36. AMPK may also regulate capacity for FA oxidation by phosphorylation of transcription factors such as CREB or coactivators such as PGC-1alpha.

Indexed as

Lipid MetabolismAcetyl-CoA CarboxylaseAMP-Activated Protein KinasesAnimalsCarboxy-LyasesCell MembraneExerciseFatty AcidsHumansMitochondriaMuscle, SkeletalOxidation-ReductionAcetyl-CoA CarboxylaseAMP-Activated Protein KinasesCarboxy-LyasesFatty Acidsmalonyl-CoA decarboxylase

Identifiers

PMID19245653
PMCPMC2734509
OpenAlexW2091475986

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.