Evidence map›Paper›PMID 23150693›Full record

ArticleThe Journal of clinical endocrinology and metabolism2013

Higher mitochondrial respiration and uncoupling with reduced electron transport chain content in vivo in muscle of sedentary versus active subjects.

Kevin E Conley, Catherine E Amara, Sudip Bajpeyi, Sheila R Costford, Kori Murray, Sharon A Jubrias, Lori Arakaki, David J Marcinek, Steven R Smith

Registry-linked trialOpen access · bronzeAbstract readControlled Clinical Trial
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01911091 (Identification of Novel Skeletal Muscle-derived Factors That Promote Lipid Oxidation in Both Skeletal Muscle and Adipose Tissue), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
8.7field-weighted citation impact, top 3% 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.

NCT01911091 naactive not recruitingnot on this map

Identification of Novel Skeletal Muscle-derived Factors That Promote Lipid Oxidation in Both Skeletal Muscle and Adipose Tissue

TypeinterventionalSponsorAdventHealth Translational Research InstituteRan2013 to 2026Enrolled56ConditionsObesity, Disorder of Lipid Storage and Metabolism, Lipid Metabolism Disorders, Metabolic DisorderArmsExercise
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Molecular correlates of MRS-basedNMR in biomedicine · 2021
    Trial
  2. Trial
  3. Trial
  4. Energy constraint on human health.Trends in endocrinology and metabolism: TEM · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Potential Causes of Elevated REE after High-Intensity Exercise.Medicine and science in sports and exercise · 2017
    Article
  14. Review
  15. Review
  16. CKD and Muscle Mitochondrial Energetics.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2016
    Article
  17. Article
  18. Review
  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

9 authors at 4 institutions in 1 country.

Kevin E ConleyDepartment of Radiology, University of Washington Medical Center, Box 357115, Seattle, Washington 98195-7115, USA. kconley@uw.edu
Catherine E Amara
Sudip Bajpeyi
Sheila R Costford
Kori Murray
Sharon A Jubrias
Lori Arakaki
David J Marcinek
Steven R Smith
Anna Needs Neuroblastoma Answers · USLouisiana State University System · USPennington Biomedical Research Center · USUniversity of Washington Medical Center · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 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
MR &Optical Diagnosis of Muscle Metabolism and FunctionR01AR041928 · NIAMS · UNIVERSITY OF WASHINGTON · PI CONLEY, KEVIN E · 1993 to 2011
$6.8M
Skeletal Muscle Mitochondrial Adaptations to a Two-Year Caloric RestictionR01AG030226 · NIA · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI SMITH, STEVEN RICHARD · 2008 to 2012
$1.6M
Translational Center for In Vivo Mitochondrial MedicineRC2AG036606 · NIA · UNIVERSITY OF WASHINGTON · PI CONLEY, KEVIN E, MARCINEK, DAVID J. · 2009 to 2010
$1.5M
Diet/Intramyocellular Lipid/Endurance PerformanceK01DK062018 · NIDDK · UNIVERSITY OF WYOMING · PI LARSON-MEYER, D ENETTE · 2003 to 2005
$271k
NCRR NIH HHS P20 RR021945NCRR NIH HHS P20-RR021945NIAMS NIH HHS R01 AR041928NIAMS NIH HHS R01-AR41928NIA NIH HHS R01 AG030226NIA NIH HHS R01-AG030226NIA NIH HHS RC2 AG036606NIA NIH HHS RC2-AG036606NIDDK NIH HHS K01 DK062018NIDDK NIH HHS P30 DK072476NIDDK NIH HHS P30-DK072476
6 · The paper itself

Abstract

objectiveThis study investigated the disparity between muscle metabolic rate and mitochondrial metabolism in human muscle of sedentary vs. active individuals. RESEARCH DESIGN AND

methodsChronic activity level was characterized by a physical activity questionnaire and a triaxial accelerometer as well as a maximal oxygen uptake test. The ATP and O(2) fluxes and mitochondrial coupling (ATP/O(2) or P/O) in resting muscle as well as mitochondrial capacity (ATP(max)) were determined in vivo in human vastus lateralis muscle using magnetic resonance and optical spectroscopy on 24 sedentary and seven active subjects. Muscle biopsies were analyzed for electron transport chain content (using complex III as a representative marker) and mitochondrial proteins associated with antioxidant protection.

resultsSedentary muscle had lower electron transport chain complex content (65% of the active group) in proportion to the reduction in ATP(max) (0.69 ± 0.07 vs. 1.07 ± 0.06 mM sec(-1)) as compared with active subjects. This lower ATP(max) paired with an unchanged O(2) flux in resting muscle between groups resulted in a doubling of O(2) flux per ATP(max) (3.3 ± 0.3 vs. 1.7 ± 0.2 μM O(2) per mM ATP) that reflected mitochondrial uncoupling (P/O = 1.41 ± 0.1 vs. 2.1 ± 0.3) and greater UCP3/complex III (6.0 ± 0.7 vs. 3.8 ± 0.3) in sedentary vs. active subjects.

conclusionA smaller mitochondrial pool serving the same O(2) flux resulted in elevated mitochondrial respiration in sedentary muscle. In addition, uncoupling contributed to this higher mitochondrial respiration. This finding resolves the paradox of stable muscle metabolism but greater mitochondrial respiration in muscle of inactive vs. active subjects.

Indexed as

Sedentary BehaviorAccelerometryAdultCell RespirationElectron TransportElectron Transport Chain Complex ProteinsEnergy MetabolismHumansMaleMitochondria, MuscleMotor ActivityMuscle, SkeletalOxygen ConsumptionRestSurveys and QuestionnairesUp-RegulationElectron Transport Chain Complex Proteins

Identifiers

PMID23150693
PMCPMC3537085
OpenAlexW2166877693

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.