Evidence map›Paper›PMID 30001411›Full record

ArticlePloS one2018

Using MRI to predict the fate of excitotoxic lesions in rats.

Thibault Cholvin, Lisa Giorgi, Nathalie Baril, Jean-Michel Brezun, Bruno Poucet, Franck A Chaillan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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
0.2field-weighted citation impact, top 52% 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, 3 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

6 authors at 1 institution in 1 country.

Thibault CholvinAix Marseille Univ, CNRS, LNC, Laboratoire de Neurosciences Cognitives, Marseille, France.ORCID 0000-0002-9964-7693
Lisa GiorgiAix Marseille Univ, CNRS, LNC, Laboratoire de Neurosciences Cognitives, Marseille, France.
Nathalie BarilAix Marseille Univ, CNRS, Fédération 3C, Marseille, France.
Jean-Michel BrezunAix Marseille Univ, CNRS, Institut des Sciences du Mouvement (UMR 7287), Equipe "Plasticité des Systèmes Nerveux et Musculaire" (PSNM), Faculté des Sciences du Sport, Marseille, France.ORCID 0000-0002-6567-8264
Bruno PoucetAix Marseille Univ, CNRS, LNC, Laboratoire de Neurosciences Cognitives, Marseille, France.
Franck A ChaillanAix Marseille Univ, CNRS, LNC, Laboratoire de Neurosciences Cognitives, Marseille, France.ORCID 0000-0002-5518-9627
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Excitotoxic lesions are frequently used to assess the role of cerebral structures in cognitive processes in rodents. However, the precise site and extent of these lesions remain unknown without histological verifications. Using a 7-Teslas MRI system and a T2-weighted turbo-RARE sequence, MR images were acquired at several time points following NMDA lesions (1h, 6h, 24h, 48h, 1 week and 2 weeks). NMDA infusions into the parenchyma induced a clear and delineable hyperintense signal from 1h up to 1-week post-surgery. Hyperintensity volumes were compared with NeuN and Cresyl violet histological quantifications of the lesion magnitude. NMDA-induced hypersignal is observed as soon as 1h post-injection and is a reliable estimate of the presence (or absence) of a lesion. Compared to NeuN, Cresyl violet staining underestimates the extent of the lesion in significant proportions. The MRI hyperintensity generated by NMDA instillation into the parenchyma can be used as a powerful tool to confirm the diffusion of the drug into the cerebral tissue, to ascertain the locus of injection and predict with a high success rate the fate of NMDA lesions as soon as 1h post-surgery. This approach could be very useful in a large variety of lesion studies in rodents.

Indexed as

Magnetic Resonance ImagingAnimalsCerebellumCognitionMaleNeurotoxicity SyndromesN-MethylaspartateRatsRats, Long-EvansN-Methylaspartate

Identifiers

PMID30001411
PMCPMC6042754
OpenAlexW2834636902

What OpenQuestion holds

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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.