Evidence map›Paper›PMID 28722023›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2018

Potential Involvement of Impaired BK

Maria Isabel Carreno-Munoz, Fabienne Martins, Maria Carmen Medrano, Elisabetta Aloisi, Susanna Pietropaolo, Corentin Dechaud, Enejda Subashi, Guillaume Bony, Melanie Ginger, Abdelmalik Moujahid and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Therapeutic efficacy of the BKCa channel opener chlorzoxazone in a mouse model of Fragile X syndrome.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Genes · 2021
    Review
  13. Channelopathies in fragile X syndrome.Nature reviews. Neuroscience · 2021
    Review
  14. A Highly Selective MNK Inhibitor Rescues Deficits Associated with Fragile X Syndrome in Mice.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Article
  15. Hyperexcitability and Homeostasis in Fragile X Syndrome.Frontiers in molecular neuroscience · 2021
    Article
  16. Article
  17. (ACS pharmacology & translational science · 2020
    Article
  18. Article
  19. Early Retinal Defects inFrontiers in cellular neuroscience · 2018
    Article
  20. Physiological Roles and Therapeutic Potential of CaFrontiers in molecular neuroscience · 2018
    Review
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

12 authors at 3 institutions in 2 countries.

Maria Isabel Carreno-MunozINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Fabienne MartinsINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Maria Carmen MedranoINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Elisabetta AloisiINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Susanna PietropaoloUniversity of Bordeaux, INCIA, Pessac, France.
Corentin DechaudINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Enejda SubashiINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Guillaume BonyINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Melanie GingerINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Abdelmalik MoujahidUniversity of the Basque Country (UPV/EHU), Donostia, Spain.
Andreas FrickINSERM, Neurocentre Magendie, U1215, Bordeaux, France.
Xavier LeinekugelINSERM, Neurocentre Magendie, U1215, Bordeaux, France.ORCID 0000-0003-2878-3791
Université de Bordeaux · FRCentre National de la Recherche Scientifique · FRUniversity of the Basque Country · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In fragile X syndrome (FXS), sensory hypersensitivity and impaired habituation is thought to result in attention overload and various behavioral abnormalities in reaction to the excessive and remanent salience of environment features that would normally be ignored. This phenomenon, termed sensory defensiveness, has been proposed as the potential cause of hyperactivity, hyperarousal, and negative reactions to changes in routine that are often deleterious for FXS patients. However, the lack of tools for manipulating sensory hypersensitivity has not allowed the experimental testing required to evaluate the relevance of this hypothesis. Recent work has shown that BMS-204352, a BK

Indexed as

AnimalsAnti-Anxiety AgentsDiazepamDisease Models, AnimalEnvironmentFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeGroomingIndolesLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitsMaleMice, KnockoutMotor ActivityNesting BehaviorNeurotransmitter AgentsPsychotropic DrugsAnti-Anxiety AgentsBKCa protein, mouseBMS204352DiazepamFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1IndolesLarge-Conductance Calcium-Activated Potassium Channel alpha SubunitsNeurotransmitter AgentsPsychotropic Drugs

Identifiers

PMID28722023
PMCPMC5770751
OpenAlexW2738288379

What OpenQuestion 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 OpenQuestion graph.