Evidence map›Paper›PMID 36995973›Full record

ArticleBrain : a journal of neurology2023

Monitoring recovery after CNS demyelination, a novel tool to de-risk pro-remyelinating strategies.

Esther Henriet, Elodie M Martin, Pauline Jubin, Dominique Langui, Abdelkrim Mannioui, Bruno Stankoff, Catherine Lubetzki, Arseny Khakhalin, Bernard Zalc

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Assessing circuit function in the developingFrontiers in behavioral neuroscience · 2026
    Review
  3. Article
  4. 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

9 authors.

Esther HenrietSorbonne Université, Inserm, CNRS, ICM-GH Pitié-Salpêtrière, F-75013 Paris, France.
Elodie M MartinSorbonne Université, Inserm, CNRS, ICM-GH Pitié-Salpêtrière, F-75013 Paris, France.
Pauline JubinSorbonne Université, Inserm, CNRS, ICM-GH Pitié-Salpêtrière, F-75013 Paris, France.
Dominique LanguiSorbonne Université, Inserm, CNRS, ICM-GH Pitié-Salpêtrière, F-75013 Paris, France.
Abdelkrim ManniouiSorbonne Université, Inserm, CNRS, ICM-GH Pitié-Salpêtrière, F-75013 Paris, France.
Bruno StankoffSorbonne Université, Inserm, CNRS, ICM-GH Pitié-Salpêtrière, F-75013 Paris, France.ORCID 0000-0002-9631-4674
Catherine LubetzkiSorbonne Université, Inserm, CNRS, ICM-GH Pitié-Salpêtrière, F-75013 Paris, France.
Arseny KhakhalinBard College, 30 Campus Rd, Annandale-on-Hudson, NY 12504, USA.
Bernard ZalcSorbonne Université, Inserm, CNRS, ICM-GH Pitié-Salpêtrière, F-75013 Paris, France.ORCID 0000-0001-5484-2359

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In multiple sclerosis, while remarkable progress has been accomplished to control the inflammatory component of the disease, repair of demyelinated lesions is still an unmet need. Despite encouraging results generated in experimental models, several candidates favouring or promoting remyelination have not reached the expected outcomes in clinical trials. One possible reason for these failures is that, in most cases, during preclinical testing, efficacy was evaluated on histology only, while functional recovery had not been assessed. We have generated a Xenopus laevis transgenic model Tg(mbp:GFP-NTR) of conditional demyelination in which spontaneous remyelination can be accelerated using candidate molecules. Xenopus laevis is a classic model for in vivo studies of myelination because tadpoles are translucent. We reasoned that demyelination should translate into loss of sensorimotor functions followed by behavioural recovery upon remyelination. To this end, we measured the swimming speed and distance travelled before and after demyelination and during the ongoing spontaneous remyelination and have developed a functional assay based on the visual avoidance of a virtual collision. Here we show that alteration of these functional and clinical performances correlated well with the level of demyelination and that histological remyelination, assayed by counting in vivo the number of myelinating oligodendrocytes in the optic nerve, translated in clinical-functional recovery. This method was further validated in tadpoles treated with pro-remyelinating agents (clemastine, siponimod) showing that increased remyelination in the optic nerve was associated with functional improvement. Our data illustrate the potential interest of correlating histopathological parameters and functional-clinical parameters to screen molecules promoting remyelination in a simple in vivo model of conditional demyelination.

Indexed as

Multiple SclerosisRemyelinationAnimalsDisease Models, AnimalMyelin SheathOligodendrogliaOptic NerveXenopus laevismyelinoptic nerveregenerationvisual systemXenopus

Identifiers

PMID36995973
PMCPMC10232271

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.