Evidence map›Paper›PMID 24995939›Full record

ArticleJournal of molecular and cellular cardiology2014

Cardiac mitochondrial proteome dynamics with heavy water reveals stable rate of mitochondrial protein synthesis in heart failure despite decline in mitochondrial oxidative capacity.

Kadambari Chandra Shekar, Ling Li, Erinne R Dabkowski, Wenhong Xu, Rogerio Faustino Ribeiro, Peter A Hecker, Fabio A Recchia, Rovshan G Sadygov, Belinda Willard, Takhar Kasumov and 1 more

Abstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Kinetic Lipidomics: QuantifyingbioRxiv : the preprint server for biology · 2026
    Article
  2. Blueprint of the distinct metabolite profiles of healthy pig heart chambers.Journal of molecular and cellular cardiology plus · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Intimate Relations-Mitochondria and Ageing.International journal of molecular sciences · 2020
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Gaussian Process Modeling of Protein Turnover.Journal of proteome research · 2016
    Article
  17. Review
  18. Review
  19. Review
  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

11 authors at 5 institutions in 3 countries.

Kadambari Chandra ShekarDivision of Cardiology and Department of Medicine, University of Maryland, Baltimore, MD, USA.
Ling LiProteomics Core, Department of Research Core Services, Cleveland Clinic, Cleveland, OH, USA.
Erinne R DabkowskiDivision of Cardiology and Department of Medicine, University of Maryland, Baltimore, MD, USA.
Wenhong XuDivision of Cardiology and Department of Medicine, University of Maryland, Baltimore, MD, USA.
Rogerio Faustino RibeiroDivision of Cardiology and Department of Medicine, University of Maryland, Baltimore, MD, USA.
Peter A HeckerDivision of Cardiology and Department of Medicine, University of Maryland, Baltimore, MD, USA.
Fabio A RecchiaDepartment of Physiology, Temple University School of Medicine, Philadelphia, PA, USA; Institute of Life Sciences, Scuola Superiore Sant'Anna, Pisa, Italy.
Rovshan G SadygovDepartment of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, TX, USA.
Belinda WillardProteomics Core, Department of Research Core Services, Cleveland Clinic, Cleveland, OH, USA.
Takhar KasumovDepartment of Gastroenterology & Hepatology, Cleveland Clinic, Cleveland, OH, USA. Electronic address: kasumot@ccf.org.
William C StanleyDivision of Cardiology and Department of Medicine, University of Maryland, Baltimore, MD, USA; Discipline of Physiology, University of Sydney, Anderson Stuart Building (F13) Sydney, NSW 2006 Australia.
University of Maryland, Baltimore · USCleveland Clinic · USScuola Superiore Sant'Anna · ITThe University of Texas Medical Branch at Galveston · USUniversity of Sydney · AU

Funding

Substrate Selection and Oxidative Stress in Heart FailureP01HL074237 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI STANLEY, WILLIAM C · 2003 to 2013
$19.9M
VEGF receptor-1-mediated protection in dilated cardiomyopathyR01HL108213 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI RECCHIA, FABIO A · 2012 to 2015
$1.6M
LTQ-Orbitrap Velos instrumentS10RR031537 · NCRR · CLEVELAND CLINIC LERNER COM-CWRU · PI WILLARD, BELINDA BELLE · 2011 to 2011
$600k
Mitochondrial Proteome Dynamics in Heart Failure Assessed with Heavy WaterR21HL114407 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KASUMOV, TAKHAR · 2012 to 2013
$394k
NCRR NIH HHS S10 RR031537NHLBI NIH HHS HHSN268201000037CNHLBI NIH HHS HL-074237NHLBI NIH HHS HL-114407NHLBI NIH HHS P01 HL074237NHLBI NIH HHS P01 HL-74237NHLBI NIH HHS R01 HL108213NHLBI NIH HHS R21 HL114407
6 · The paper itself

Abstract

We recently developed a method to measure mitochondrial proteome dynamics with heavy water ((2)H2O)-based metabolic labeling and high resolution mass spectrometry. We reported the half-lives and synthesis rates of several proteins in the two cardiac mitochondrial subpopulations, subsarcolemmal and interfibrillar (SSM and IFM), in Sprague Dawley rats. In the present study, we tested the hypothesis that the mitochondrial protein synthesis rate is reduced in heart failure, with possible differential changes in SSM versus IFM. Six to seven week old male Sprague Dawley rats underwent transverse aortic constriction (TAC) and developed moderate heart failure after 22weeks. Heart failure and sham rats of the same age received heavy water (5% in drinking water) for up to 80days. Cardiac SSM and IFM were isolated from both groups and the proteins were separated by 1D gel electrophoresis. Heart failure reduced protein content and increased the turnover rate of several proteins involved in fatty acid oxidation, electron transport chain and ATP synthesis, while it decreased the turnover of other proteins, including pyruvate dehydrogenase subunit in IFM, but not in SSM. Because of these bidirectional changes, the average overall half-life of proteins was not altered by heart failure in both SSM and IFM. The kinetic measurements of individual mitochondrial proteins presented in this study may contribute to a better understanding of the mechanisms responsible for mitochondrial alterations in the failing heart.

Indexed as

Protein BiosynthesisAnimalsBody WeightCell RespirationCitrate (si)-SynthaseDeuterium OxideHalf-LifeHeart FailureHeart VentriclesMaleMitochondria, HeartMitochondrial ProteinsOrgan SizeOxidation-ReductionPressureProtein StabilityCitrate (si)-SynthaseDeuterium OxideMitochondrial ProteinsProteomeCardiac failureDeuteriumMitochondriaProteome dynamics

Identifiers

PMID24995939
PMCPMC5363075
OpenAlexW2016951642

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.