Evidence map›Paper›PMID 15548652›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

Functional compensation of P/Q by N-type channels blocks short-term plasticity at the calyx of Held presynaptic terminal.

Carlota González Inchauspe, Francisco J Martini, Ian D Forsythe, Osvaldo D Uchitel

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

77 citing papers in PubMed, 138 citations in OpenAlex.

  1. Presynaptic CaCell reports · 2026
    Article
  2. Presynaptic CabioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. CaThe Journal of physiology · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Neurotransmitter Release Site Replenishment and Presynaptic Plasticity.International journal of molecular sciences · 2020
    Review
  12. Review
  13. Review
  14. Review
  15. Presynaptic Calcium Channels.International journal of molecular sciences · 2019
    Review
  16. The Role of CaCell reports · 2019
    Article
  17. CaNeuron · 2019
    Article
  18. Control of Excitation/Inhibition Balance in a Hippocampal Circuit by Calcium Sensor Protein Regulation of Presynaptic Calcium Channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  19. Molecular moieties masking CaThe Journal of general physiology · 2018
    Article
  20. New Insights Into the Role of CaFrontiers in molecular neuroscience · 2018
    Article

17 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

4 authors at 3 institutions in 3 countries.

Carlota González InchauspeInstituto de Fisiología, Biología Molecular y Neurociencias, Consejo Nacional de Investigaciones Científicas y Técnicas, Departamento de Fisiología, Biología Molecular y Celular, Universidad de Buenos Aires, Argentina.
Francisco J Martini
Ian D Forsythe
Osvaldo D Uchitel
Fundación Ciencias Exactas y Naturales · ARUniversity of Buenos Aires · ARUniversity of Leicester · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Calcium channels of the P/Q subtype mediate transmitter release at the neuromuscular junction and at many central synapses, such as the calyx of Held. Transgenic mice in which alpha1A channels are ablated provide a powerful tool with which to test compensatory mechanisms at the synapse and to explore mechanisms of presynaptic regulation associated with expression of P/Q channels. Using the calyx of Held preparation from the knock-out (KO) mice, we show here that N-type channels functionally compensate for the absence of P/Q subunits at the calyx and evoke giant synaptic currents [approximately two-thirds of the magnitude of wild-type (WT) responses]. However, although evoked paired-pulse facilitation is prominent in WT, this facilitation is greatly diminished in the KO. In addition, direct recording of presynaptic calcium currents revealed that the major functional difference was the absence of calcium-dependent facilitation at the calyx in the P/Q KO animals. We conclude that one physiological function of P/Q channels is to provide additional facilitatory drive, so contributing to maintenance of transmission as vesicles are depleted during high throughput synaptic transmission.

Indexed as

AnimalsBrain StemCalciumCalcium Channels, N-TypeCalcium Channels, P-TypeCalcium Channels, Q-TypeEvoked PotentialsIn Vitro TechniquesMiceMice, KnockoutNeuronal PlasticityPresynaptic TerminalsProtein SubunitsSynapsesSynaptic TransmissionCalciumCalcium Channels, N-TypeCalcium Channels, P-TypeCalcium Channels, Q-TypeProtein Subunits

Identifiers

PMID15548652
PMCPMC6730293
OpenAlexW2007589527

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.