Evidence map›Paper›PMID 19114636›Full record

ArticleThe Journal of general physiology2009

The skeletal L-type Ca(2+) current is a major contributor to excitation-coupled Ca(2+) entry.

Roger A Bannister, Isaac N Pessah, Kurt G Beam

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

76 citing papers in PubMed, 111 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. ERG1A KScientific reports · 2025
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  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. MgInternational journal of molecular sciences · 2020
    Article
  14. Article
  15. Article
  16. Sarcopenia: Aging-Related Loss of Muscle Mass and Function.Physiological reviews · 2019 · on this map
    Review
  17. Article
  18. A skeletal muscle L-type CaThe Journal of biological chemistry · 2018
    Article
  19. Review
  20. Store-operated CaCommunications biology · 2018
    Article

16 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Roger A BannisterDepartment of Physiology and Biophysics, School of Medicine, University of Colorado Denver, Aurora, CO 80045, USA.
Isaac N Pessah
Kurt G Beam
University of Colorado Denver · USUniversity of California, Davis · US

Funding

SIGNALING BETWEEN CALCIUM CHANNELSP01AR044750 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI ALLEN, PAUL D · 1997 to 2006
$9.3M
Structure Function Studies of RyR1 in a Myogenic KnockoutR01AR043140 · NIAMS · CHILDREN'S HOSPITAL BOSTON · PI ALLEN, PAUL D · 1996 to 2010
$4.8M
NIAMS NIH HHS AR43140NIAMS NIH HHS AR44750NIAMS NIH HHS P01 AR044750NIAMS NIH HHS R01 AR043140
6 · The paper itself

Abstract

The term excitation-coupled Ca(2+) entry (ECCE) designates the entry of extracellular Ca(2+) into skeletal muscle cells, which occurs in response to prolonged depolarization or pulse trains and depends on the presence of both the 1,4-dihydropyridine receptor (DHPR) in the plasma membrane and the type 1 ryanodine receptor in the sarcoplasmic reticulum (SR) membrane. The ECCE pathway is blocked by pharmacological agents that also block store-operated Ca(2+) entry, is inhibited by dantrolene, is relatively insensitive to the DHP antagonist nifedipine (1 microM), and is permeable to Mn(2+). Here, we have examined the effects of these agents on the L-type Ca(2+) current conducted via the DHPR. We found that the nonspecific cation channel antagonists (2-APB, SKF 96356, La(3+), and Gd(3+)) and dantrolene all inhibited the L-type Ca(2+) current. In addition, complete (>97%) block of the L-type current required concentrations of nifedipine >10 microM. Like ECCE, the L-type Ca(2+) channel displays permeability to Mn(2+) in the absence of external Ca(2+) and produces a Ca(2+) current that persists during prolonged ( approximately 10-second) depolarization. This current appears to contribute to the Ca(2+) transient observed during prolonged KCl depolarization of intact myotubes because (1) the transients in normal myotubes decayed more rapidly in the absence of external Ca(2+); (2) the transients in dysgenic myotubes expressing SkEIIIK (a DHPR alpha(1S) pore mutant thought to conduct only monovalent cations) had a time course like that of normal myotubes in Ca(2+)-free solution and were unaffected by Ca(2+) removal; and (3) after block of SR Ca(2+) release by 200 microM ryanodine, normal myotubes still displayed a large Ca(2+) transient, whereas no transient was detectable in SkEIIIK-expressing dysgenic myotubes. Collectively, these results indicate that the skeletal muscle L-type channel is a major contributor to the Ca(2+) entry attributed to ECCE.

Indexed as

AnimalsCalciumCalcium Channel BlockersCalcium Channels, L-TypeCalcium SignalingDantroleneManganeseMiceMice, TransgenicMuscle Fibers, SkeletalMuscle, SkeletalNifedipinePatch-Clamp TechniquesCalciumCalcium Channel BlockersCalcium Channels, L-TypeDantroleneManganeseNifedipine

Identifiers

PMID19114636
PMCPMC2606935
OpenAlexW2147705281

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.