Evidence map›Paper›PMID 39223257›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2024

Therapeutic efficacy of the BKCa channel opener chlorzoxazone in a mouse model of Fragile X syndrome.

Celeste Ferraguto, Marion Piquemal-Lagoueillat, Valerie Lemaire, Maïté M Moreau, Stefania Trazzi, Beatrice Uguagliati, Elisabetta Ciani, Sandrine S Bertrand, Eric Louette, Bruno Bontempi and 1 more

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Article
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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

11 authors.

Celeste Ferraguto *Univ. Bordeaux, CNRS, EPHE, INCIA, UMR 5287, Bordeaux, France.
Marion Piquemal-Lagoueillat *Univ. Bordeaux, CNRS, EPHE, INCIA, UMR 5287, Bordeaux, France.
Valerie LemaireUniv. Bordeaux, CNRS, EPHE, INCIA, UMR 5287, Bordeaux, France.
Maïté M MoreauUniv. Bordeaux, INSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Stefania TrazziDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0003-2623-2769
Beatrice UguagliatiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Elisabetta CianiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Sandrine S BertrandUniv. Bordeaux, CNRS, EPHE, INCIA, UMR 5287, Bordeaux, France.
Eric LouetteAssetsup, Le Boulinier, Rueil-Malmaison, France.
Bruno BontempiUniv. Bordeaux, CNRS, EPHE, INCIA, UMR 5287, Bordeaux, France.
Susanna PietropaoloUniv. Bordeaux, CNRS, EPHE, INCIA, UMR 5287, Bordeaux, France. susanna.pietropaolo@u-bordeaux.fr.

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-23-CE37-0013-02Université de Bordeaux (University of Bordeaux) GPR BRAIN_2030
6 · The paper itself

Abstract

Fragile X syndrome (FXS) is an X-linked neurodevelopmental disorder characterized by several behavioral abnormalities, including hyperactivity, anxiety, sensory hyper-responsiveness, and autistic-like symptoms such as social deficits. Despite considerable efforts, effective pharmacological treatments are still lacking, prompting the need for exploring the therapeutic value of existing drugs beyond their original approved use. One such repurposed drug is chlorzoxazone which is classified as a large-conductance calcium-dependent potassium (BKCa) channel opener. Reduced BKCa channel functionality has been reported in FXS patients, suggesting that molecules activating these channels could serve as promising treatments for this syndrome. Here, we sought to characterize the therapeutic potential of chlorzoxazone using the Fmr1-KO mouse model of FXS which recapitulates the main phenotypes of FXS, including BKCa channel alterations. Chlorzoxazone, administered either acutely or chronically, rescued hyperactivity and acoustic hyper-responsiveness as well as impaired social interactions exhibited by Fmr1-KO mice. Chlorzoxazone was more efficacious in alleviating these phenotypes than gaboxadol and metformin, two repurposed treatments for FXS that do not target BKCa channels. Systemic administration of chlorzoxazone modulated the neuronal activity-dependent gene c-fos in selected brain areas of Fmr1-KO mice, corrected aberrant hippocampal dendritic spines, and was able to rescue impaired BKCa currents recorded from hippocampal and cortical neurons of these mutants. Collectively, these findings provide further preclinical support for BKCa channels as a valuable therapeutic target for treating FXS and encourage the repurposing of chlorzoxazone for clinical applications in FXS and other related neurodevelopmental diseases.

Indexed as

ChlorzoxazoneDisease Models, AnimalFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitsMice, KnockoutAnimalsHippocampusMaleMiceMice, Inbred C57BLBKCa protein, mouseChlorzoxazoneFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Large-Conductance Calcium-Activated Potassium Channel alpha Subunits

Identifiers

PMID39223257
PMCPMC11480417

What Socratic holds

Textmetadata
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.