Evidence map›Paper›PMID 16267232›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2005

Neuronal L-type calcium channels open quickly and are inhibited slowly.

Thomas D Helton, Weifeng Xu, Diane Lipscombe

Abstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing 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

117 citing papers in PubMed.

  1. Evaluation of Aldosterone Suppression by Cinnarizine, a Putative Cav1.3 Inhibitor.The Journal of clinical endocrinology and metabolism · 2025
    Trial
  2. Skin capillary endothelial cells form a network of spatiotemporally conserved CaProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Impact of CaInternational journal of molecular sciences · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. The Impact of Overexpression of the Mouse Ortholog ofBiological psychiatry global open science · 2025
    Article
  8. Article
  9. Inactivation of CaV1 and CaV2 channels.The Journal of general physiology · 2025
    Review
  10. Review
  11. Evaluation of fourChannels (Austin, Tex.) · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. A biochemical description of postsynaptic plasticity-with timescales ranging from milliseconds to seconds.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Review
  17. Article
  18. Electrically regulated cell-based intervention for viral infections.Bioengineering & translational medicine · 2023
    Article
  19. Review
  20. Review

57 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.

Thomas D HeltonDepartment of Neuroscience, Brown University, Providence, Rhode Island 02912, USA.
Weifeng Xu
Diane Lipscombe

Funding

NEURONAL CALCIUM CHANNELS--REGULATION AND FUNCTIONR01NS029967 · NINDS · BROWN UNIVERSITY · PI LIPSCOMBE, DIANE · 1997 to 2009
$3.0M
Training Programs in Systems and Behavioral NeuroscienceT32MH019118 · NIMH · BROWN UNIVERSITY · PI CONNORS, BARRY W · 1989 to 2013
$1.9M
NEURONAL CALIUM CHANNELS--REGULATION AND FUNCTIONR29NS029967 · NINDS · BROWN UNIVERSITY · PI LIPSCOMBE, DIANE · 1992 to 1996
–
NIMH NIH HHS MH19118NIMH NIH HHS T32 MH019118NINDS NIH HHS NS29967NINDS NIH HHS R01 NS029967
6 · The paper itself

Abstract

Neuronal L-type calcium channels are essential for regulating activity-dependent gene expression, but they are thought to open too slowly to contribute to action potential-dependent calcium entry. A complication of studying native L-type channels is that they represent a minor fraction of the whole-cell calcium current in most neurons. Dihydropyridine antagonists are therefore widely used to establish the contribution of L-type channels to various neuronal processes and to study their underlying biophysical properties. The effectiveness of these antagonists on L-type channels, however, varies with stimulus and channel subtype. Here, we study recombinant neuronal L-type calcium channels, CaV1.2 and CaV1.3. We show that these channels open with fast kinetics and carry substantial calcium entry in response to individual action potential waveforms, contrary to most studies of native L-type currents. Neuronal CaV1.3 L-type channels were as efficient as CaV2.2 N-type channels at supporting calcium entry during action potential-like stimuli. We conclude that the apparent slow activation of native L-type currents and their lack of contribution to single action potentials reflect the state-dependent nature of the dihydropyridine antagonists used to study them, not the underlying properties of L-type channels.

Indexed as

Action PotentialsAnimalsCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeIon Channel GatingKineticsMiceNeuronsRatsCacna1d protein, mouseCacna1d protein, ratCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeL-type calcium channel alpha(1C)

Identifiers

PMID16267232
PMCPMC6725800

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.