Evidence map›Paper›PMID 22711953›Full record

ArticleThe Journal of physiology2012

Mitochondrial activation at the onset of contractions in isolated myofibres during successive contractile periods.

Paulo G Gandra, Leonardo Nogueira, Michael C Hogan

Abstract read
In one paragraph

Article in The Journal of physiology, 2012. 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
–field-weighted citation impact
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.

  1. Article
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  4. Review
  5. Article
  6. Article
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  14. Bang-bang model for regulation of local blood flow.Microcirculation (New York, N.Y. : 1994) · 2013
    Review
  15. Article
  16. Article
  17. Increasing temperature speeds intracellular PO2 kinetics during contractions in single Xenopus skeletal muscle fibers.American journal of physiology. Regulatory, integrative and comparative physiology · 2013
    Article
  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

3 authors.

Paulo G GandraDepartment of Medicine-0623, University of California, San Diego, 9500 Gilman Drive La Jolla, CA 92093-0623, USA.
Leonardo Nogueira
Michael C Hogan

Funding

Oxygen dependence of ROS generation in contracting single isolated myofibersR01AR040155 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HOGAN, MICHAEL C · 1996 to 2012
$3.4M
DETERMINANTS OF MUSCLE MAXIMAL O2 UPTAKE AND PERFORMANCER29AR040155 · NIAMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI HOGAN, MICHAEL C · 1991 to 1995
–
NIAMS NIH HHS AR-040155NIAMS NIH HHS R01 AR040155
6 · The paper itself

Abstract

At the onset of skeletal muscle repetitive contractions, there is a significant delay in the time to achieve oxidative phosphorylation steady state. The purpose of the present study was to examine the factors that limit oxidative phosphorylation at the onset of contractions. NAD(P)H was measured in real time during two contractile periods (2 min each) separated by 5 min of rest in intact single muscle fibres (n = 7) isolated from Xenopus laevis. The fibres were then loaded with the dye tetramethylrhodamine methyl ester perchlorate (TMRM) to evaluate the kinetics of the mitochondrial membrane potential (Δψ (m)) during two further successive contractile periods. At the onset of contractions in the first period, NAD(P)H exhibited a time delay (14.1 ± 1.3 s) before decreasing toward a steady state. In contrast, Δψ(m) decreased immediately after the first contraction and started to be reestablished after 10.7 ± 0.9 s, with restoration to the pre-stimulation values after approximately 32 s. In the second contractile period (5 min after the first), NAD(P)H decreased immediately (i.e. no time delay) after the first contraction and had a significantly shorter time constant compared to the first contractile bout (3.3 ± 0.3 vs. 5.0 ± 0.2 s, P < 0.05). During the second bout, Δψ(m) remained unchanged from pre-stimulation values. These results suggest: (1) that at the onset of contractions, oxidative phosphorylation is primarily limited by the activity of the electron transport chain complexes rather than by a limited level of substrates; and (2) when the muscle is 'primed' by previous contractile activity, the faster enhancement of the cellular respiratory rate is due to intrinsic factors within the myofibre.

Indexed as

AnimalsFemaleIn Vitro TechniquesMembrane Potential, MitochondrialMitochondriaMuscle ContractionMuscle Fibers, SkeletalNADPOxidative PhosphorylationOxygen ConsumptionXenopus laevisNADP

Identifiers

PMID22711953
PMCPMC3547273

What OpenQuestion holds

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Registered trials

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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.