Evidence map›Paper›PMID 30044951›Full record

ArticleMolecular and cellular neurosciences2018

Physiological signature of a novel potentiator of AMPA receptor signalling.

Blanka R Szulc, Stephen T Hilton, Arnaud J Ruiz

Open access · hybridAbstract read
In one paragraph

Article in Molecular and cellular neurosciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 92% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 1 institution in 1 country.

Blanka R SzulcDepartment of Pharmacology, School of Pharmacy, University College London, London, UK.
Stephen T HiltonDepartment of Pharmacology, School of Pharmacy, University College London, London, UK. Electronic address: s.hilton@ucl.ac.uk.
Arnaud J RuizDepartment of Pharmacology, School of Pharmacy, University College London, London, UK. Electronic address: a.ruiz@ucl.ac.uk.
University College London · GB

Funding

Medical Research Council G0801316Medical Research Council G1000629
6 · The paper itself

Abstract

We have synthesized a novel small molecule based on the pyrrolidinone-containing core structure of clausenamide, which is a candidate anti-dementia drug. The synthetic route yielded multi-gram quantities of an isomeric racemate mixture in a short number of steps. When tested in hippocampal slices from young adult rats the compound enhanced AMPA receptor-mediated signalling at mossy fibre synapses, and potentiated inward currents evoked by local application of l-glutamate onto CA3 pyramidal neurons. It facilitated the induction of mossy fibre LTP, but the magnitude of potentiation was smaller than that observed in untreated slices. The racemic mixture was separated and it was shown that only the (-) enantiomer was active. Toxicity analysis indicated that cell lines tolerated the compound at concentrations well above those enhancing synaptic transmission. Our results unveil a small molecule whose physiological signature resembles that of a potent nootropic drug.

Indexed as

AnimalsCA3 Region, HippocampalGlutamic AcidLong-Term PotentiationMaleMossy Fibers, HippocampalNootropic AgentsPyrrolidinonesRatsRats, Sprague-DawleyReceptors, AMPASynaptic TransmissionGlutamic AcidNootropic AgentsPyrrolidinonesReceptors, AMPA

Identifiers

PMID30044951
PMCPMC6525152
OpenAlexW2884516137

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.