Evidence map›Paper›PMID 19622784›Full record

Trial reportAmerican journal of physiology. Endocrinology and metabolism2009

Magnitude and control of mitochondrial sensitivity to ADP.

Jeroen A L Jeneson, Joep P J Schmitz, Nicole M A van den Broek, Natal A W van Riel, Peter A J Hilbers, Klaas Nicolay, Jeanine J Prompers

Abstract readClinical Trial
In one paragraph

Trial report in American journal of physiology. Endocrinology and metabolism, 2009. 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
2.4field-weighted citation impact, top 11% 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, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Oxidative phosphorylation KBiochimica et biophysica acta. Bioenergetics · 2021
    Article
  6. Article
  7. Neuronal control of astrocytic respiration through a variant of the Crabtree effect.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  8. In-vivoAnalytical biochemistry · 2017
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. On the kinetics of anaerobic power.Theoretical biology & medical modelling · 2012
    Article
  18. Article
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Jeroen A L JenesonBiomedical NMR, Dept. of Biomedical Engineering, Eindhoven University of Technology, 5600 MB Eindhoven, The Netherlands. j.a.l.jeneson@tue.nl
Joep P J Schmitz
Nicole M A van den Broek
Natal A W van Riel
Peter A J Hilbers
Klaas Nicolay
Jeanine J Prompers
Eindhoven University of Technology · NL

Funding

Integrated Modeling of Cardiac Metabolism and TransportR01HL072011 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BEARD, DANIEL A · 2004 to 2016
$4.0M
NHLBI NIH HHS HL-072011NHLBI NIH HHS R01 HL072011
6 · The paper itself

Abstract

The transduction function for ADP stimulation of mitochondrial ATP synthesis in skeletal muscle was reconstructed in vivo and in silico to investigate the magnitude and origin of mitochondrial sensitivity to cytoplasmic ADP concentration changes. Dynamic in vivo measurements of human leg muscle phosphocreatine (PCr) content during metabolic recovery from contractions were performed by (31)P-NMR spectroscopy. The cytoplasmic ADP concentration ([ADP]) and rate of oxidative ATP synthesis (Jp) at each time point were calculated from creatine kinase equilibrium and the derivative of a monoexponential fit to the PCr recovery data, respectively. Reconstructed [ADP]-Jp relations for individual muscles containing more than 100 data points were kinetically characterized by nonlinear curve fitting yielding an apparent kinetic order and ADP affinity of 1.9 +/- 0.2 and 0.022 +/- 0.003 mM, respectively (means +/- SD; n = 6). Next, in silico [ADP]-Jp relations for skeletal muscle were generated using a computational model of muscle oxidative ATP metabolism whereby model parameters corresponding to mitochondrial enzymes were randomly changed by 50-150% to determine control of mitochondrial ADP sensitivity. The multiparametric sensitivity analysis showed that mitochondrial ADP ultrasensitivity is an emergent property of the integrated mitochondrial enzyme network controlled primarily by kinetic properties of the adenine nucleotide translocator.

Indexed as

Adenosine DiphosphateAdenosine TriphosphateAdultComputer SimulationDrug ResistanceExerciseFemaleHumansKineticsMaleMitochondria, MuscleModels, BiologicalMuscle, SkeletalSignal TransductionYoung AdultAdenosine DiphosphateAdenosine Triphosphate

Identifiers

PMID19622784
PMCPMC3833997
OpenAlexW2169202177

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.