Evidence map›Paper›PMID 30811418›Full record

ArticlePloS one2019

Pharmacological AMPK activation induces transcriptional responses congruent to exercise in skeletal and cardiac muscle, adipose tissues and liver.

Eric S Muise, Hong-Ping Guan, Jinqi Liu, Andrea R Nawrocki, Xiaodong Yang, Chuanlin Wang, Carlos G Rodríguez, Dan Zhou, Judith N Gorski, Marc M Kurtz and 21 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. The AMPK Pathway: Molecular Rejuvenation of Metabolism and Mitochondria.Annual review of cell and developmental biology · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Repurposing Metformin for Vascular Disease.Current medicinal chemistry · 2023
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Downregulation of theAntioxidants (Basel, Switzerland) · 2020
    Article
  19. Article
  20. Review
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

31 authors at 2 institutions in 1 country.

Eric S MuiseGenetics and Pharmacogenomics Department, MRL, Kenilworth, NJ, United States of America.ORCID 0000-0002-1238-5118
Hong-Ping GuanBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Jinqi LiuBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Andrea R NawrockiIn Vivo Pharmacology Department, MRL, Kenilworth, NJ, United States of America.
Xiaodong YangBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Chuanlin WangBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Carlos G RodríguezIn Vivo Pharmacology Department, MRL, Kenilworth, NJ, United States of America.
Dan ZhouIn Vivo Pharmacology Department, MRL, Kenilworth, NJ, United States of America.
Judith N GorskiIn Vivo Pharmacology Department, MRL, Kenilworth, NJ, United States of America.
Marc M KurtzIn Vitro PharmacologyDepartment, MRL, NJ, United States of America.
Danqing FengMedicinal ChemistryDepartment, MRL, Kenilworth, NJ, United States of America.
Kenneth J LeavittMedicinal ChemistryDepartment, MRL, Kenilworth, NJ, United States of America.
Lan WeiMedicinal ChemistryDepartment, MRL, Kenilworth, NJ, United States of America.
Robert R WilkeningMedicinal ChemistryDepartment, MRL, Kenilworth, NJ, United States of America.
James M ApgarMedicinal ChemistryDepartment, MRL, Kenilworth, NJ, United States of America.
Shiyao XuPPDM Preclinical ADME Department, MRL, Kenilworth, NJ, United States of America.
Ku LuBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Wen FengBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Ying LiBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Huaibing HePPDM Preclinical ADME Department, MRL, Kenilworth, NJ, United States of America.
Stephen F PrevisBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Xiaolan ShenSALAR Department, MRL, Kenilworth, NJ, United States of America.
Margaret van HeekIn Vivo Pharmacology Department, MRL, Kenilworth, NJ, United States of America.
Sandra C SouzaBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Mark J RosenbachBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Tesfaye BiftuMedicinal ChemistryDepartment, MRL, Kenilworth, NJ, United States of America.
Mark D ErionBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
David E KelleyBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Daniel M KempBiology-Discovery Department, MRL, Kenilworth, NJ, United States of America.
Robert W MyersIn Vitro PharmacologyDepartment, MRL, NJ, United States of America.
Iyassu K SebhatMedicinal ChemistryDepartment, MRL, Kenilworth, NJ, United States of America.
Massanutten Regional Library · USInstitute for In Vitro Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Physical activity promotes metabolic and cardiovascular health benefits that derive in part from the transcriptional responses to exercise that occur within skeletal muscle and other organs. There is interest in discovering a pharmacologic exercise mimetic that could imbue wellness and alleviate disease burden. However, the molecular physiology by which exercise signals the transcriptional response is highly complex, making it challenging to identify a single target for pharmacological mimicry. The current studies evaluated the transcriptome responses in skeletal muscle, heart, liver, and white and brown adipose to novel small molecule activators of AMPK (pan-activators for all AMPK isoforms) compared to that of exercise. A striking level of congruence between exercise and pharmacological AMPK activation was observed across the induced transcriptome of these five tissues. However, differences in acute metabolic response between exercise and pharmacologic AMPK activation were observed, notably for acute glycogen balances and related to the energy expenditure induced by exercise but not pharmacologic AMPK activation. Nevertheless, intervention with repeated daily administration of short-acting activation of AMPK was found to mitigate hyperglycemia and hyperinsulinemia in four rodent models of metabolic disease and without the cardiac glycogen accretion noted with sustained pharmacologic AMPK activation. These findings affirm that activation of AMPK is a key node governing exercise mediated transcription and is an attractive target as an exercise mimetic.

Indexed as

Adipose TissueAMP-Activated Protein KinasesAnimalsEnergy MetabolismEnzyme ActivationFatty AcidsGene Expression RegulationGlucoseHomeostasisLiverMice, Inbred C57BLMuscle, SkeletalMyocardiumOxidation-ReductionPhysical Conditioning, AnimalAMP-Activated Protein KinasesFatty AcidsGlucose

Identifiers

PMID30811418
PMCPMC6392219
OpenAlexW2918013817

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.