Evidence map›Paper›PMID 39201269›Full record

ReviewInternational journal of molecular sciences2024

Glutamate, Gangliosides, and the Synapse: Electrostatics at Work in the Brain.

Henri Chahinian, Nouara Yahi, Jacques Fantini

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Gangliosides in molecular interactions and cell regulation.The Journal of biological chemistry · 2026
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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.

Henri ChahinianFaculty of Sciences, Department of Biology, University of Aix-Marseille, INSERM UA16, 13015 Marseille, France.ORCID 0000-0002-9516-4168
Nouara YahiFaculty of Sciences, Department of Biology, University of Aix-Marseille, INSERM UA16, 13015 Marseille, France.
Jacques FantiniFaculty of Sciences, Department of Biology, University of Aix-Marseille, INSERM UA16, 13015 Marseille, France.ORCID 0000-0001-8653-5521

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synapse is a piece of information transfer machinery replacing the electrical conduction of nerve impulses at the end of the neuron. Like many biological mechanisms, its functioning is heavily affected by time constraints. The solution selected by evolution is based on chemical communication that, in theory, cannot compete with the speed of nerve conduction. Nevertheless, biochemical and biophysical compensation mechanisms mitigate this intrinsic weakness: (i) through the high concentrations of neurotransmitters inside the synaptic vesicles; (ii) through the concentration of neurotransmitter receptors in lipid rafts, which are signaling platforms; indeed, the presence of raft lipids, such as gangliosides and cholesterol, allows a fine tuning of synaptic receptors by these lipids; (iii) through the negative electrical charges of the gangliosides, which generate an attractive (for cationic neurotransmitters, such as serotonin) or repulsive (for anionic neurotransmitters, such as glutamate) electric field. This electric field controls the flow of glutamate in the tripartite synapse involving pre- and post-synaptic neurons and the astrocyte. Changes in the expression of brain gangliosides can disrupt the functioning of the glutamatergic synapse, causing fatal diseases, such as Rett syndrome. In this review, we propose an in-depth analysis of the role of gangliosides in the glutamatergic synapse, highlighting the primordial and generally overlooked role played by the electric field of synaptic gangliosides.

Indexed as

BrainGangliosidesGlutamic AcidStatic ElectricitySynapsesAnimalsHumansNeuronsNeurotransmitter AgentsSynaptic TransmissionGangliosidesGlutamic AcidNeurotransmitter Agentsastrocytebrainelectrostatic surface potentialgangliosideglutamatelipid raftneuronreceptorsphingolipidsynapse

Identifiers

PMID39201269
PMCPMC11354842

What Socratic 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 Socratic graph.