Evidence map›Paper›PMID 9350620›Full record

ArticleThe Journal of physiology1997

Stimulation-induced changes in [Ca2+] in lizard motor nerve terminals.

G David, J N Barrett, E F Barrett

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  6. Target cell-specific involvement of presynaptic mitochondria in post-tetanic potentiation at hippocampal mossy fiber synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  7. Article
  8. Ca2+ dynamics along identified synaptic terminals in Drosophila larvae.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
    Article
  9. Functional compensation of P/Q by N-type channels blocks short-term plasticity at the calyx of Held presynaptic terminal.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Article
  10. Spatial Distribution of Calcium Entry Evoked by Single Action Potentials within the Presynaptic Active Zone.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Article
  11. Mitochondria and release at hippocampal synapses.Pflugers Archiv : European journal of physiology · 2003
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  12. Article
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  17. Measurement of action potential-induced presynaptic calcium domains at a cultured neuromuscular junction.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
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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.

G Davidgdavid@newssun.med.miami.edu
J N Barrett
E F Barrett

Funding

MYELINATED AXONS AND MOTOR TERMINALS--FUNCTIONAL STUDIESR01NS012404 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BARRETT, ELLEN F · 1985 to 2006
$1.7M
CONFOCAL LASER SCANNING MICROSCOPES10RR008368 · NCRR · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BARRETT, ELLEN F · 1994 to 1994
–
NCRR NIH HHS 1S10RR08368NINDS NIH HHS NS12404
6 · The paper itself

Abstract

1. Motor axons were injected ionophoretically with one of five Ca(2+)-sensitive dyes (fluo-3, Calcium Green-2, Calcium Green-5N, fluo-3FF and Oregon Green BAPTA-5N). Changes in fluorescence (delta F/Frest) within motor terminal boutons following a single action potential and brief stimulus trains were monitored with high temporal resolution using a confocal microscope. 2. Stimulation-induced increases in delta F/Frest were confined primarily to boutons, with roughly uniform increases in all the boutons of a terminal. The increase in delta F/Frest began prior to, and decayed more slowly than, the endplate potential (EPP) recorded in the underlying muscle fibre. delta F/Frest was graded with bath [Ca2+]. Both delta F/Frest and the EPP were reduced, but not eliminated, by omega-conotoxin GVIA (5-10 microM). 3. For dyes with lower affinity for Ca2+ (e.g. Oregon Green BAPTA-5N, Kd approximately 60 microM) stimulation-induced increases in delta F/Frest were measured in the presence of the K+ channel blocker 3,4-diaminopyridine (3,4-DAP, 100 microM). During brief stimulus trains (4 at 50 Hz) in 3,4-DAP, the EPP exhibited profound depression, but the fluorescence increase associated with each stimulus showed little decrement, suggesting that depression was not mediated by a reduction in Ca2+ entry. 4. For dyes with a higher affinity for Ca2+ (e.g. fluo-3, Kd approximately 0.5-1 microM) stimulation-induced increases in delta F/Frest could also be measured in normal physiological saline. Increases in delta F/Frest were much greater with 3,4-DAP present, but the amplitude decreased with successive stimuli due to partial dye saturation. 5. Calculations suggested that following a single action potential the average [Ca2+] within a bouton increased by up to 150 nM in normal saline and 940 nM in 3,4-DAP. With low affinity dyes the delta F/Frest measured near the membrane had a higher peak amplitude and a faster early decay than that measured in the centre of the bouton, suggesting that substantial spatial [Ca2+] gradients exist within boutons for at least 15 ms following stimulation.

Indexed as

Action PotentialsAnimalsAxonsCalciumCalcium Channel BlockersElectric StimulationElectrophysiologyFluorescent DyesImage Processing, Computer-AssistedIn Vitro TechniquesIontophoresisKineticsLizardsMembrane PotentialsMicroscopy, ConfocalMotor NeuronsCalciumCalcium Channel BlockersFluorescent Dyes

Identifiers

PMID9350620
PMCPMC1159938
OpenAlexW2038415660

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.