Evidence map›Paper›PMID 26480028›Full record

ArticlePloS one2015

Synaptic Efficacy as a Function of Ionotropic Receptor Distribution: A Computational Study.

Sushmita L Allam, Jean-Marie C Bouteiller, Eric Y Hu, Nicolas Ambert, Renaud Greget, Serge Bischoff, Michel Baudry, Theodore W Berger

Abstract read
In one paragraph

Article in PloS one, 2015. 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
–field-weighted citation impact
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.

  1. Glutamate and GABA in Microglia-Neuron Cross-Talk in Alzheimer's Disease.International journal of molecular sciences · 2021
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Inflammation, Glutamate, and Glia: A Trio of Trouble in Mood Disorders.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Review
  8. 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

8 authors.

Sushmita L AllamCenter for Neural Engineering, Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America.
Jean-Marie C BouteillerCenter for Neural Engineering, Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America; Rhenovia Pharma, Mulhouse, France.
Eric Y HuCenter for Neural Engineering, Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America.
Nicolas AmbertRhenovia Pharma, Mulhouse, France.
Renaud GregetRhenovia Pharma, Mulhouse, France.
Serge BischoffRhenovia Pharma, Mulhouse, France.
Michel BaudryRhenovia Pharma, Mulhouse, France; Graduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA, United States of America.
Theodore W BergerCenter for Neural Engineering, Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, United States of America.

Funding

TrainingP41EB001978 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KHOO, MICHAEL C K · 2003 to 2017
$18.1M
Predictive modeling of bioelectric activity on mammalian multilayered neuronal stU01GM104604 · NIGMS · UNIVERSITY OF UTAH · PI BERGER, THEODORE W., LAZZI, GIANLUCA · 2012 to 2016
$2.8M
Simulation of learning: models and biological validationR01NS057128 · NINDS · WESTERN UNIVERSITY OF HEALTH SCIENCES · PI BAUDRY, MICHEL · 2009 to 2012
$2.2M
NIBIB NIH HHS P41 EB001978NIBIB NIH HHS P41 EB001978-24NIGMS NIH HHS U01 GM104604NINDS NIH HHS 1R01NS057128-01A2NINDS NIH HHS R01 NS057128
6 · The paper itself

Abstract

Glutamatergic synapses are the most prevalent functional elements of information processing in the brain. Changes in pre-synaptic activity and in the function of various post-synaptic elements contribute to generate a large variety of synaptic responses. Previous studies have explored postsynaptic factors responsible for regulating synaptic strength variations, but have given far less importance to synaptic geometry, and more specifically to the subcellular distribution of ionotropic receptors. We analyzed the functional effects resulting from changing the subsynaptic localization of ionotropic receptors by using a hippocampal synaptic computational framework. The present study was performed using the EONS (Elementary Objects of the Nervous System) synaptic modeling platform, which was specifically developed to explore the roles of subsynaptic elements as well as their interactions, and that of synaptic geometry. More specifically, we determined the effects of changing the localization of ionotropic receptors relative to the presynaptic glutamate release site, on synaptic efficacy and its variations following single pulse and paired-pulse stimulation protocols. The results indicate that changes in synaptic geometry do have consequences on synaptic efficacy and its dynamics.

Indexed as

Computer SimulationModels, NeurologicalAnimalsGlutamic AcidHippocampusHumansReceptors, AMPAReceptors, N-Methyl-D-AspartateSynapsesGlutamic AcidReceptors, AMPAReceptors, N-Methyl-D-Aspartate

Identifiers

PMID26480028
PMCPMC4610697

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.