Evidence map›Paper›PMID 15538948›Full record

ArticleBMC neuroscience2004

Bi-directional modulation of AMPA receptor unitary conductance by synaptic activity.

Andreas Lüthi, Martin A Wikström, Mary J Palmer, Paul Matthews, Tim A Benke, John T R Isaac, Graham L Collingridge

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

34 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
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  3. Activity-dependent diffusion trapping of AMPA receptors as a key step for expression of early LTP.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
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  12. Persistent CaMKII activation mediates learning-induced long-lasting enhancement of synaptic inhibition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
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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

7 authors at 3 institutions in 3 countries.

Andreas LüthiMRC Centre for Synaptic Plasticity, Department of Anatomy, University of Bristol, Bristol, BS8 1TD, UK. Andreas.Luthi@fmi.ch <Andreas.Luthi@fmi.ch>
Martin A Wikström
Mary J Palmer
Paul Matthews
Tim A Benke
John T R Isaac
Graham L Collingridge
University of Bristol · GBNational Institutes of Health · USUniversity of Colorado Health · US

Funding

Mechanisms of Synaptic Plasticity and Development of Circuit FunctionZIANS003011 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI ISAAC, JOHN · 2009 to 2010
$3.7M
Synaptic Plasticity in Developing Cortical NetworksZ01NS003011 · NINDS · NEUROLOGICAL DISORDERS AND STROKE · PI ISAAC, JOHN · 2005 to 2008
$2.4M
Medical Research Council G9532377
6 · The paper itself

Abstract

backgroundKnowledge of how synapses alter their efficiency of communication is central to the understanding of learning and memory. The most extensively studied forms of synaptic plasticity are long-term potentiation (LTP) and its counterpart long-term depression (LTD) of AMPA receptor-mediated synaptic transmission. In the CA1 region of the hippocampus, it has been shown that LTP often involves a rapid increase in the unitary conductance of AMPA receptor channels. However, LTP can also occur in the absence of any alteration in AMPA receptor unitary conductance. In the present study we have used whole-cell dendritic recording, failures analysis and non-stationary fluctuation analysis to investigate the mechanism of depotentiation of LTP.

resultsWe find that when LTP involves an increase in unitary conductance, subsequent depotentiation invariably involves the return of unitary conductance to pre-LTP values. In contrast, when LTP does not involve a change in unitary conductance then depotentiation also occurs in the absence of any change in unitary conductance, indicating a reduction in the number of activated receptors as the most likely mechanism.

conclusionsThese data show that unitary conductance can be bi-directionally modified by synaptic activity. Furthermore, there are at least two distinct mechanisms to restore synaptic strength from a potentiated state, which depend upon the mechanism of the previous potentiation.

Indexed as

Long-Term PotentiationLong-Term Synaptic DepressionAnimalsCells, CulturedElectric ConductivityHippocampusModels, NeurologicalPatch-Clamp TechniquesRatsReceptors, AMPAReceptors, N-Methyl-D-AspartateReceptors, AMPAReceptors, N-Methyl-D-Aspartate

Identifiers

PMID15538948
PMCPMC535344
OpenAlexW1604295762

What OpenQuestion holds

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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.