Evidence map›Paper›PMID 27496880›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2016

Comprehensive metabolic modeling of multiple 13C-isotopomer data sets to study metabolism in perfused working hearts.

Scott B Crown, Joanne K Kelleher, Rosanne Rouf, Deborah M Muoio, Maciek R Antoniewicz

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Sarco/Endoplasmic Reticulum CaJournal of the American Heart Association · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Stable Isotopes for Tracing Cardiac Metabolism in Diseases.Frontiers in cardiovascular medicine · 2021
    Review
  10. Article
  11. Article
  12. A model for determining cardiac mitochondrial substrate utilisation using stableMetabolomics : Official journal of the Metabolomic Society · 2019
    Article
  13. Article
  14. p13CMFA: Parsimonious 13C metabolic flux analysis.PLoS computational biology · 2019
    Article
  15. Cardiovascular Metabolomics.Circulation research · 2018
    Review
  16. Article
  17. Review
  18. 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 4 institutions in 1 country.

Scott B CrownSarah W. Stedman Nutrition and Metabolism Center, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina; scott.crown@duke.edu.
Joanne K KelleherDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Rosanne RoufDivision of Cardiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Deborah M MuoioSarah W. Stedman Nutrition and Metabolism Center, Duke Molecular Physiology Institute, Duke University, Durham, North Carolina; Department of Medicine, Duke University, Durham, North Carolina; Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina; and.
Maciek R AntoniewiczDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delware.
Duke University · USJohns Hopkins University · USMassachusetts Institute of Technology · USUniversity of Delaware · US

Funding

TARGETED RESPONSIVE MR AND PET AGENTS FOR B-CELL IMAGINGP01DK058398 · NIDDK · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MUOIO, DEBORAH M · 2000 to 2016
$26.1M
Role of Carnitine Acetyltransferase in Mitochondrial and Metabolic FunctionR01DK089312 · NIDDK · DUKE UNIVERSITY · PI DEBORAH M MUOIO · 2010 to 2026
$7.8M
Probing the Role of Mitochondrial Short-chain Carbon Homeostasis in the Hypertrophied and Failing HeartR01HL128349 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MUOIO, DEBORAH M · 2016 to 2024
$6.1M
NHLBI NIH HHS R01 HL128349NIDDK NIH HHS P01 DK058398NIDDK NIH HHS R01 DK089312
6 · The paper itself

Abstract

In many forms of cardiomyopathy, alterations in energy substrate metabolism play a key role in disease pathogenesis. Stable isotope tracing in rodent heart perfusion systems can be used to determine cardiac metabolic fluxes, namely those relative fluxes that contribute to pyruvate, the acetyl-CoA pool, and pyruvate anaplerosis, which are critical to cardiac homeostasis. Methods have previously been developed to interrogate these relative fluxes using isotopomer enrichments of measured metabolites and algebraic equations to determine a predefined metabolic flux model. However, this approach is exquisitely sensitive to measurement error, thus precluding accurate relative flux parameter determination. In this study, we applied a novel mathematical approach to determine relative cardiac metabolic fluxes using

Indexed as

Metabolic Flux AnalysisAcetyl Coenzyme AAnimalsCarbon IsotopesEnergy MetabolismGlucoseIsolated Heart PreparationLactic AcidMaleMetabolic Networks and PathwaysMiceModels, BiologicalModels, CardiovascularMyocardiumOleic AcidPyruvic AcidAcetyl Coenzyme ACarbon IsotopesGlucoseLactic AcidOleic AcidPyruvic Acid13C-MFAheart metabolismmetabolic fluxparallel labeling experimentsperfusion

Identifiers

PMID27496880
PMCPMC5114467
OpenAlexW2498850419

What OpenQuestion holds

Textmetadata
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.