Evidence map›Paper›PMID 24523520›Full record

ArticleJournal of neurophysiology2014

Distinct roles for Cav2.1-2.3 in activity-dependent synaptic dynamics.

Ulises M Ricoy, Matthew E Frerking

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Functional Postnatal Maturation of the Medial Olivocochlear Efferent-Outer Hair Cell Synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  5. Article
  6. Review
  7. Article
  8. In vitro and in vivo phosphorylation of the CaChannels (Austin, Tex.) · 2018
    Review
  9. Article
  10. C-terminal splice variants of P/Q-type CaThe Journal of biological chemistry · 2017
    Article
  11. Article
  12. Review
  13. Review: CaThe open neurology journal · 2016
    Article
  14. 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

2 authors at 1 institution in 1 country.

Ulises M RicoyDepartment of Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon.
Matthew E FrerkingDepartment of Behavioral Neuroscience, Oregon Health and Science University, Portland, Oregon frerking@ohsu.edu.
Oregon Health & Science University · US

Funding

Hippocampal synaptic dynamics during realistic patterns of afferent activityR01MH077120 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI FRERKING, MATTHEW E · 2008 to 2012
$1.3M
Excitatory synaptic transmission onto hippocampal interneuronsR01NS064317 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI FRERKING, MATTHEW E · 2010 to 2013
$1.2M
NIMH NIH HHS MH-077120NINDS NIH HHS NS-064317
6 · The paper itself

Abstract

Synaptic transmission throughout most of the CNS is steeply dependent on presynaptic calcium influx through the voltage-gated calcium channels Cav2.1-Cav2.3. In addition to triggering exocytosis, this calcium influx also recruits short-term synaptic plasticity. During the complex patterns of presynaptic activity that occur in vivo, several forms of plasticity combine to generate a synaptic output that is dynamic, in which the size of a given excitatory postsynaptic potential (EPSP) in response to a given spike depends on the short-term history of presynaptic activity. It remains unclear whether the different Cav2 channels play distinct roles in defining these synaptic dynamics and, if so, under what conditions different Cav2 family members most effectively determine synaptic output. We examined these questions by measuring the effects of calcium channel-selective toxins on synaptic transmission at the Schaffer collateral synapse in hippocampal slices from adult mice in response to both low-frequency stimulation and complex stimulus trains derived from in vivo recordings. Blockade of Cav2.1 had a greater inhibitory effect on synaptic transmission during low-frequency components of the stimulus train than on synaptic transmission during high-frequency components of the train, indicating that Cav2.1 had a greater fractional contribution to synaptic transmission at low frequencies than at high frequencies. Relative to Cav2.1, Cav2.2 had a disproportionately reduced contribution to synaptic transmission at frequencies >20 Hz, while Cav2.3 had a disproportionately increased contribution to synaptic transmission at frequencies >1 Hz. These activity-dependent effects of different Cav2 family members shape the filtering characteristics of GABAB receptor-mediated presynaptic inhibition. Thus different Cav2 channels vary in their coupling to synaptic transmission over different frequency ranges, with consequences for the frequency tuning of both synaptic dynamics and presynaptic neuromodulation.

Indexed as

AnimalsCalcium Channel BlockersCalcium Channels, N-TypeCalcium Channels, R-TypeCation Transport ProteinsElectric StimulationExcitatory Postsynaptic PotentialsGABA-B Receptor AgonistsHippocampusMice, Inbred C57BLReceptors, GABA-BSynapsesSynaptic TransmissionTissue Culture TechniquesCacna1b protein, mouseCacna1e protein, mouseCalcium Channel BlockersCalcium Channels, N-TypeCalcium Channels, R-TypeCation Transport ProteinsGABA-B Receptor AgonistsReceptors, GABA-Bcalcium channelsglutamatehippocampusplasticitysynaptic dynamics

Identifiers

PMID24523520
PMCPMC4044429
OpenAlexW2035439766

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.