Evidence map›Paper›PMID 14990680›Full record

ArticleThe Journal of physiology2004

The elementary events of Ca2+ release elicited by membrane depolarization in mammalian muscle.

L Csernoch, J Zhou, M D Stern, G Brum, E Ríos

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2004. 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
2.2field-weighted citation impact, top 13% 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, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Improper Remodeling of Organelles Deputed to CaInternational journal of molecular sciences · 2021
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Sparks and embers of skeletal muscle: the exciting events of contractile activation.Pflugers Archiv : European journal of physiology · 2007
    Review
  18. Ca(2+) sparks operated by membrane depolarization require isoform 3 ryanodine receptor channels in skeletal muscle.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  19. 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

5 authors at 3 institutions in 3 countries.

L CsernochDepartment of Physiology, University of Debrecen, Hungary.
J Zhou
M D Stern
G Brum
E Ríos
University of Debrecen · HUNational Institutes of Health · USUniversidad de la República · UY

Funding

Skeletal Muscle. Ca Release Control Inside the Sarcoplasmic Reticulum.R01AR049184 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI RIOS, EDUARDO · 2003 to 2013
$3.1M
CALCIUM MOVEMENTS IN EXCITATION-CONTRACTION COUPLINGR01AR032808 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI RIOS, EDUARDO · 1986 to 2011
$1.6M
STOCHASTIC SIMULATION OF EXCITATION-CONTRACTION COUPLINGZ01AG000844 · NIA · NATIONAL INSTITUTE ON AGING · PI STERN, MICHAEL D · 1997 to 2008
$1.1M
NIAMS NIH HHS R01 AR032808NIAMS NIH HHS R01 AR049184
6 · The paper itself

Abstract

Cytosolic [Ca(2+)] transients elicited by voltage clamp depolarization were examined by confocal line scanning of rat skeletal muscle fibres. Ca(2+) sparks were observed in the fibres' membrane-permeabilized ends, but not in responses to voltage in the membrane-intact area. Elementary events of the depolarization-evoked response could be separated either at low voltages (near -50 mV) or at -20 mV in partially inactivated cells. These were of lower amplitude, narrower and of much longer duration than sparks, similar to 'lone embers' observed in the permeabilized segments. Their average amplitude was 0.19 and spatial half-width 1.3 microm. Other parameters depended on voltage. At -50 mV average duration was 111 ms and latency 185 ms. At -20 mV duration was 203 ms and latency 24 ms. Ca(2+) release current, calculated on an average of events, was nearly steady at 0.5-0.6 pA. Accordingly, simulations of the fluorescence event elicited by a subresolution source of 0.5 pA open for 100 ms had morphology similar to the experimental average. Because 0.5 pA is approximately the current measured for single RyR channels in physiological conditions, the elementary fluorescence events in rat muscle probably reflect opening of a single RyR channel. A reconstruction of cell-averaged release flux at -20 mV based on the observed distribution of latencies and calculated elementary release had qualitatively correct but slower kinetics than the release flux in prior whole-cell measurements. The qualitative agreement indicates that global Ca(2+) release flux results from summation of these discrete events. The quantitative discrepancies suggest that the partial inactivation strategy may lead to events of greater duration than those occurring physiologically in fully polarized cells.

Indexed as

AnimalsCalciumCalcium SignalingCell MembraneComputer SimulationElectrophysiologyFluorescent DyesImage Processing, Computer-AssistedIn Vitro TechniquesMaleMembrane PotentialsMicroscopy, ConfocalMuscle Fibers, SkeletalMuscle, SkeletalPatch-Clamp TechniquesRatsCalciumFluorescent Dyes

Identifiers

PMID14990680
PMCPMC1665048
OpenAlexW2101170098

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.