Evidence map›Paper›PMID 9450940›Full record

ArticleThe Journal of general physiology1998

Modulation of the frequency of spontaneous sarcoplasmic reticulum Ca2+ release events (Ca2+ sparks) by myoplasmic [Mg2+] in frog skeletal muscle.

A Lacampagne, M G Klein, M F Schneider

Abstract read
In one paragraph

Article in The Journal of general physiology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Calcium sparks in intact skeletal muscle fibers of the frog.The Journal of general physiology · 2001
    Article
  14. Article
  15. Calcium release in skeletal muscle: from K+ contractures to Ca2+ sparks.Journal of muscle research and cell motility · 2001
    Review
  16. Article
  17. Article
  18. Two mechanisms for termination of individual Ca2+ sparks in skeletal muscle.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  19. Article
  20. Involvement of multiple intracellular release channels in calcium sparks of skeletal muscle.Proceedings of the National Academy of Sciences of the United States of America · 2000
    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.

A LacampagneDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
M G Klein
M F Schneider

Funding

EXCITATION-CONTRACTION COUPLING IN CUT MUSCLE FIBERSR01NS023346 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI SCHNEIDER, MARTIN F · 1985 to 2006
$2.2M
LOCAL CALCIUM RELEASE EVENTS IN SKELETAL MUSCLER01AR044197 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI KLEIN, MICHAEL G · 1996 to 2005
$1.3M
NIAMS NIH HHS R01 AR044197NIAMS NIH HHS R01-AR44197NINDS NIH HHS R01 NS023346NINDS NIH HHS R01-NS23346
6 · The paper itself

Abstract

The modulation by internal free [Mg2+] of spontaneous calcium release events (Ca2+ "sparks") from the sarcoplasmic reticulum (SR) was studied in depolarized notched frog skeletal muscle fibers using a laser scanning confocal microscope in line-scan mode (x vs. t). Over the range of [Mg2+] from 0.13 to 1.86 mM, decreasing the [Mg2+] induced an increase in the frequency of calcium release events in proportion to [Mg2+]-1.6. The change of event frequency was not due to changes in [Mg-ATP] or [ATP]. Analysis of individual SR calcium release event properties showed that the variation in event frequency induced by the change of [Mg2+] was not accompanied by any changes in the spatiotemporal spread (i.e., spatial half width or temporal half duration) of Ca2+ sparks. The increase in event frequency also had no effect on the distribution of event amplitudes. Finally, the rise time of calcium sparks was independent of the [Mg2+], indicating that the open time of the SR channel or channels underlying spontaneous calcium release events was not altered by [Mg2+] over the range tested. These results suggest that in resting skeletal fibers, [Mg2+] modulates the SR calcium release channel opening frequency by modifying the average closed time of the channel without altering the open time. A kinetic reaction scheme consistent with our results and those of bilayer and SR vesicle experiments indicates that physiological levels of resting Mg2+ may inhibit channel opening by occupying the site for calcium activation of the SR calcium release channel.

Indexed as

Adenine NucleotidesAnimalsCalciumElectrophysiologyImage CytometryImage Processing, Computer-AssistedKineticsMagnesiumMicroscopy, ConfocalMuscle Fibers, SkeletalMuscle, SkeletalRana pipiensRyanodine Receptor Calcium Release ChannelSarcoplasmic ReticulumSpectrometry, FluorescenceAdenine NucleotidesCalciumMagnesiumRyanodine Receptor Calcium Release Channel

Identifiers

PMID9450940
PMCPMC2222774

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.