Evidence map›Paper›PMID 24012836›Full record

ArticleNeuroscience2013

Dominance of P/Q-type calcium channels in depolarization-induced presynaptic FM dye release in cultured hippocampal neurons.

B Nimmervoll, B E Flucher, G J Obermair

Open access · hybridAbstract read
In one paragraph

Article in Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Presynaptic αProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  4. Cav1.2 channelopathies causing autism: new hallmarks on Timothy syndrome.Pflugers Archiv : European journal of physiology · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. Review
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 1 institution in 1 country.

B NimmervollDivision of Physiology, Medical University Innsbruck, Fritz-Pregl-Str. 3, 6020 Innsbruck, Austria.
B E Flucher
G J Obermair
Innsbruck Medical University · AT

Funding

Austrian Science Fund FWF F 4406Austrian Science Fund FWF P 23479Austrian Science Fund FWF P 24079
6 · The paper itself

Abstract

Neurotransmitter release probability is related by high power to the local concentration of calcium in presynaptic terminals, which in turn is controlled by voltage-gated calcium channels. P/Q- and N-type channels trigger synaptic transmission in the majority of neurons of the central nervous system. However, whether and under which conditions both channel types act cooperatively or independently is still insufficiently understood. Previous studies suggested either a dominance of N- or P/Q-type channels, or a synergistic action of both channels, depending on the experimental paradigms. Thus, to provide insight into the properties of neurotransmitter release in cultured mouse hippocampal neurons, we used quantitative analysis of FM dye release from presynaptic boutons induced by high potassium membrane depolarization. Increasing extracellular potassium concentrations revealed a sigmoid dependence of FM dye release to the stimulation strength. Individual and combined application of the P/Q- and N-type channel-specific blockers ω-agatoxin-IVA and ω-conotoxin-GVIA, respectively, allowed us to specifically isolate the contribution of both channel types to release triggered with 40 mM KCl. Analysis of the release kinetics and the fractional release amplitude demonstrate that, whereas in only 15% of the synapses release depended exclusively on P/Q-type channels, the majority of synapses (85%) contained both N- and P/Q-type channels. Nevertheless, the kinetics of FM dye release in synapses containing both channel types was determined by the P/Q-type channels. Together, our data suggest a more direct coupling of P/Q-type channels to synaptic release compared to N-type channels, which may explain the high prevalence of neurological P/Q-type channelopathies.

Indexed as

AnimalsCadmium ChlorideCalciumCalcium Channel BlockersCalcium Channels, N-TypeCells, CulturedDose-Response Relationship, DrugEmbryo, MammalianFemaleFluorescent DyesHippocampusMiceMice, Inbred BALB CNeuronsomega-Agatoxin IVAomega-Conotoxin GVIACadmium ChlorideCalciumCalcium Channel BlockersCalcium Channels, N-TypeFluorescent DyesFM1 43omega-Agatoxin IVAomega-Conotoxin GVIAPotassium ChloridePyridinium CompoundsQuaternary Ammonium CompoundsAAgacalcium channel physiologyCa(V)CTxdays in vitroDIVextracellular potassium concentrationfractional release[K(+)]neurotransmitter releaseN-typeP/Q-typerelease amplituderelease time constantR(f)synapse functionvoltage-gated Ca(2+) channelvoltage-gated Ca(2+) channelsτω-agatoxin-IVAω-conotoxin GVIA

Identifiers

PMID24012836
PMCPMC3824072
OpenAlexW2085812990

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.