Evidence map›Paper›PMID 12598609›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2003

Modulation of spike-mediated synaptic transmission by presynaptic background Ca2+ in leech heart interneurons.

Andrei I Ivanov, Ronald L Calabrese

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Activity-dependent increases in [CaJournal of neurophysiology · 2017
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Peptide neuromodulation of synaptic dynamics in an oscillatory network.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. T-type channels-secretion coupling: evidence for a fast low-threshold exocytosis.Pflugers Archiv : European journal of physiology · 2006
    Review
  13. 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.

Andrei I IvanovBiology Department, Emory University, Atlanta, Georgia 30322, USA. aivanov@biology.emory.edu
Ronald L Calabrese
Emory University · US

Funding

NEUROMODULATORY INFLUENCES ON MOTOR SYSTEMSR01NS024072 · NINDS · EMORY UNIVERSITY · PI CALABRESE, RONALD L · 1985 to 2011
$3.6M
Neuromodulatory Influences on Motor SystemsR56NS024072 · NINDS · EMORY UNIVERSITY · PI CALABRESE, RONALD L · 2013 to 2013
$386k
NINDS NIH HHS NS24072NINDS NIH HHS R01 NS024072NINDS NIH HHS R56 NS024072
6 · The paper itself

Abstract

At the core of the rhythmically active leech heartbeat central pattern generator are pairs of mutually inhibitory interneurons. Synaptic transmission between these interneurons consists of spike-mediated and graded components, both of which wax and wane on a cycle-by-cycle basis. Low-threshold Ca2+ currents gate the graded component. Ca imaging experiments indicate that these low-threshold currents are widespread in the neurons and that they contribute to neuron-wide changes in internal background Ca2+ concentration (Ivanov and Calabrese, 2000). During normal rhythmic activity, background Ca2+ concentration oscillates, and thus graded synaptic transmission waxes and wanes as the neurons move from the depolarized to the inhibited phases of their activity. Here we show that in addition to gating graded transmitter release, the background Ca2+ concentration changes evoked by low-threshold Ca2+ currents modulate spike-mediated synaptic transmission. We develop stimulation paradigms to simulate the changes in baseline membrane potential that accompany rhythmic bursting. Using Ca imaging and electrophysiological measurements, we show that the strength of spike-mediated synaptic transmission follows the changes in background Ca2+ concentration that these baseline potential changes evoke and that it does not depend on previous spike activity. Moreover, we show using internal EGTA and photo-release of caged Ca2+ and caged Ca2+ chelator that changes in internal Ca2+ concentration modulate spike-mediated synaptic transmission. Thus activity-dependent changes in background Ca2+, which have been implicated in homeostatic regulation of intrinsic membrane currents and synaptic strength, may also regulate synaptic transmission in an immediate way to modulate synaptic strength cycle by cycle in rhythmically active networks.

Indexed as

Action PotentialsSynaptic TransmissionAnimalsCalciumCells, CulturedChelating AgentsDiazonium CompoundsEgtazic AcidElectric ConductivityHeartInterneuronsKineticsLeechesMembrane PotentialsMicroscopy, FluorescenceNeuronal PlasticityCalciumChelating Agentsdiazo-2Diazonium CompoundsEgtazic AcidPhenoxyacetates

Identifiers

PMID12598609
PMCPMC6742253
OpenAlexW2108716566

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.