Evidence map›Paper›PMID 27184848›Full record

ArticleCell reports2016

Impaired Mitochondrial Fat Oxidation Induces FGF21 in Muscle.

Bolormaa Vandanmagsar, Jaycob D Warfel, Shawna E Wicks, Sujoy Ghosh, J Michael Salbaum, David Burk, Olga S Dubuisson, Tamra M Mendoza, Jingying Zhang, Robert C Noland and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

58 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Review
  7. Tissue specific roles of fatty acid oxidation.Advances in biological regulation · 2025
    Review
  8. Article
  9. Article
  10. Overexpression of CPT1A disrupts the maintenance and regenerative function of muscle stem cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  11. Article
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  13. Review
  14. Article
  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

11 authors at 2 institutions in 2 countries.

Bolormaa VandanmagsarGene Nutrient Interactions Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
Jaycob D WarfelGene Nutrient Interactions Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
Shawna E WicksGene Nutrient Interactions Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
Sujoy GhoshComputational Biology Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA; Centre for Computational Biology and Program in Cardiovascular and Metabolic Disorders, Duke-NUS Graduate Medical School, Singapore 169857, Singapore.
J Michael SalbaumGenomics Core Facility, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
David BurkCell Biology and Bioimaging Core Facility, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
Olga S DubuissonGene Nutrient Interactions Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
Tamra M MendozaGene Nutrient Interactions Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
Jingying ZhangTransgenic Core Facility, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
Robert C NolandSkeletal Muscle Metabolism Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA.
Randall L MynattGene Nutrient Interactions Laboratory, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA; Transgenic Core Facility, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USA. Electronic address: randall.mynatt@pbrc.edu.
Pennington Biomedical Research Center · USLouisiana State University · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI JUDD E SHELLITO · 2012 to 2026
$69.1M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Sujoy Ghosh · 2005 to 2026
$26.5M
THE ROLE OF PROTEIN MALNUTRITION ON CIRCADIAN PHYSIOLOGY OF C57BL/6J MOUSE DAMSP20RR021945 · NCRR · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2006 to 2011
$9.5M
Mentoring Obesity and Diabetes Research in LouisianaP20GM103528 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2012 to 2015
$8.8M
Transgenics CoreP30GM118430 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2016 to 2020
$5.8M
Training in Obesity ResearchT32DK064584 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI CORBY K MARTIN, Christopher D Morrison · 2003 to 2026
$5.3M
Defining the role of skeletal muscle peroxisomes in glucose homeostasisR01DK103860 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI NOLAND, ROBERT CHARLES · 2015 to 2019
$1.7M
Molecular Genetics of ThermogenesisR01DK089641 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MYNATT, RANDALL LEE, YOUNG, MARTIN E · 2010 to 2013
$1.6M
Inhibition of CPT-1b in muscle: effects on glucose homeostasisR01DK098687 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI MYNATT, RANDALL LEE · 2013 to 2017
$1.6M
NCRR NIH HHS P20 RR021945NIDDK NIH HHS P30 DK072476NIDDK NIH HHS R01 DK089641NIDDK NIH HHS R01 DK098687NIDDK NIH HHS R01 DK103860NIDDK NIH HHS T32 DK064584NIGMS NIH HHS P20 GM103528NIGMS NIH HHS P30 GM118430NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

Fatty acids are the primary fuel source for skeletal muscle during most of our daily activities, and impaired fatty acid oxidation (FAO) is associated with insulin resistance. We have developed a mouse model of impaired FAO by deleting carnitine palmitoyltransferase-1b specifically in skeletal muscle (Cpt1b(m-/-)). Cpt1b(m-/-) mice have increased glucose utilization and are resistant to diet-induced obesity. Here, we show that inhibition of mitochondrial FAO induces FGF21 expression specifically in skeletal muscle. The induction of FGF21 in Cpt1b-deficient muscle is dependent on AMPK and Akt1 signaling but independent of the stress signaling pathways. FGF21 appears to act in a paracrine manner to increase glucose uptake under low insulin conditions, but it does not contribute to the resistance to diet-induced obesity.

Indexed as

Lipid MetabolismAdenylate KinaseAdiponectinAdipose Tissue, BrownAdipose Tissue, WhiteAdiposityAnimalsCarnitine O-PalmitoyltransferaseEnergy MetabolismFibroblast Growth FactorsGlucoseHumansInsulinInsulin-Like Growth Factor IMiceMitochondriaAdenylate KinaseAdiponectinCarnitine O-PalmitoyltransferaseCPT1B protein, mousefibroblast growth factor 21Fibroblast Growth FactorsGlucoseInsulinInsulin-Like Growth Factor IProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID27184848
PMCPMC4880522
OpenAlexW2350983772

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.