Evidence map›Paper›PMID 14977180›Full record

ArticleMolecular and cellular biochemistry

Functional coupling as a basic mechanism of feedback regulation of cardiac energy metabolism.

V A Saks, A V Kuznetsov, M Vendelin, K Guerrero, L Kay, E K Seppet

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-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

31 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
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  9. Age-related changes of myocardial ATP supply and demand mechanisms.Trends in endocrinology and metabolism: TEM · 2013
    Review
  10. Article
  11. Article
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  14. Review
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  16. Mitochondria in cardiomyocyte Ca2+ signaling.The international journal of biochemistry & cell biology · 2009
    Review
  17. Strong inference for systems biology.PLoS computational biology · 2009
    Article
  18. Article
  19. Mitochondria and energetic depression in cell pathophysiology.International journal of molecular sciences · 2009
    Review
  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

6 authors at 4 institutions in 3 countries.

V A SaksStructural and Quantitative Bioenergetics Research Group, Laboratory of Fundamental and Applied Bioenergetics, INSERM E0221, Joseph Fourier University, Grenoble, France. Valdur.Saks@ujf-grenoble.fr
A V Kuznetsov
M Vendelin
K Guerrero
L Kay
E K Seppet
Université Joseph Fourier · FRInserm · FRUniversity Hospital Innsbruck · ATUniversity of Tartu · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this review we analyze the concepts and the experimental data on the mechanisms of the regulation of energy metabolism in muscle cells. Muscular energetics is based on the force-length relationship, which in the whole heart is expressed as a Frank-Starling law, by which the alterations of left ventricle diastolic volume change linearly both the cardiac work and oxygen consumption. The second basic characteristics of the heart is the metabolic stability--almost constant levels of high energy phosphates, ATP and phosphocreatine, which are practically independent of the workload and the rate of oxygen consumption, in contrast to the fast-twitch skeletal muscle with no metabolic stability and rapid fatigue. Analysis of the literature shows that an increase in the rate of oxygen consumption by order of magnitude, due to Frank-Starling law, is observed without any significant changes in the intracellular calcium transients. Therefore, parallel activation of contraction and mitochondrial respiration by calcium ions may play only a minor role in regulation of respiration in the cells. The effective regulation of the respiration under the effect of Frank-Starling law and metabolic stability of the heart are explained by the mechanisms of functional coupling within supramolecular complexes in mitochondria, and at the subcellular level within the intracellular energetic units. Such a complex structural and functional organisation of heart energy metabolism can be described quantitatively by mathematical models.

Indexed as

Adenosine TriphosphateEnergy MetabolismFeedbackMyocardiumOxygen ConsumptionAdenosine Triphosphate

Identifiers

PMID14977180
OpenAlexW2145094126

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.