Evidence map›Paper›PMID 21593394›Full record

ArticleJournal of neurophysiology2011

Effect of presynaptic membrane potential on electrical vs. chemical synaptic transmission.

Colin G Evans, Bjoern Ch Ludwar, Timothy Kang, Elizabeth C Cropper

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of neurophysiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Activity-dependent increases in [CaJournal of neurophysiology · 2017
    Article
  3. Effect of holding potential on the dynamics of homosynaptic facilitation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    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

4 authors at 1 institution in 1 country.

Colin G EvansFishberg Department of Neuroscience and Friedman Brain Institute, Mt. Sinai School of Medicine, New York, NY 10029, USA.
Bjoern Ch Ludwar
Timothy Kang
Elizabeth C Cropper
Allen Institute for Brain Science · US

Funding

NATIONAL RESOURCES FOR APLYSIAP40RR010294 · NCRR · UNIVERSITY OF MIAMI ROSENTEIL SCHOOL · PI SCHMALE, MICHAEL C · 1996 to 2011
$6.2M
NEURAL BASIS OF BEHAVIORAL PLASTICITY IN A SIMPLE SYSTEMR01MH051393 · NIMH · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI CROPPER, ELIZABETH C · 1993 to 2016
$6.1M
NCRR NIH HHS RR-10294NIMH NIH HHS MH-51393
6 · The paper itself

Abstract

The growing realization that electrical coupling is present in the mammalian brain has sparked renewed interest in determining its functional significance and contrasting it with chemical transmission. One question of interest is whether the two types of transmission can be selectively regulated, e.g., if a cell makes both types of connections can electrical transmission occur in the absence of chemical transmission? We explore this issue in an experimentally advantageous preparation. B21, the neuron we study, is an Aplysia sensory neuron involved in feeding that makes electrical and chemical connections with other identified cells. Previously we demonstrated that chemical synaptic transmission is membrane potential dependent. It occurs when B21 is centrally depolarized prior to and during peripheral activation, but does not occur if B21 is peripherally activated at its resting membrane potential. In this article we study effects of membrane potential on electrical transmission. We demonstrate that maximal potentiation occurs in different voltage ranges for the two types of transmission, with potentiation of electrical transmission occurring at more hyperpolarized potentials (i.e., requiring less central depolarization). Furthermore, we describe a physiologically relevant type of stimulus that induces both spiking and an envelope of depolarization in the somatic region of B21. This depolarization does not induce functional chemical synaptic transmission but is comparable to the depolarization needed to maximally potentiate electrical transmission. In this study we therefore characterize a situation in which electrical and chemical transmission can be selectively controlled by membrane potential.

Indexed as

AnimalsAplysiaElectrical SynapsesGanglia, InvertebrateMembrane PotentialsNeurotransmitter AgentsPresynaptic TerminalsSynaptic TransmissionNeurotransmitter Agents

Identifiers

PMID21593394
PMCPMC3154816
OpenAlexW2018563908

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.