Evidence map›Paper›PMID 25936642›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2015

Mice Lacking the Serotonin Htr2B Receptor Gene Present an Antipsychotic-Sensitive Schizophrenic-Like Phenotype.

Pothitos M Pitychoutis, Arnauld Belmer, Imane Moutkine, Joëlle Adrien, Luc Maroteaux

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Pooled it
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  5. Development of a Peripherally Restricted 5-HTJACC. Basic to translational science · 2023
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  7. A conserved role forSleep advances : a journal of the Sleep Research Society · 2023
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  16. Identification ofeLife · 2020
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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

5 authors at 2 institutions in 2 countries.

Pothitos M PitychoutisINSERM UMR S-839, Université Pierre et Marie Curie-Paris6, Institut du Fer à Moulin, Paris, France.
Arnauld BelmerINSERM UMR S-839, Université Pierre et Marie Curie-Paris6, Institut du Fer à Moulin, Paris, France.
Imane MoutkineINSERM UMR S-839, Université Pierre et Marie Curie-Paris6, Institut du Fer à Moulin, Paris, France.
Joëlle AdrienINSERM UMR S-975, Universite Pierre et Marie Curie-Paris6, Paris, France.
Luc MaroteauxINSERM UMR S-839, Université Pierre et Marie Curie-Paris6, Institut du Fer à Moulin, Paris, France.ORCID http://orcid.org/0000-0002-9499-8603
Inserm · FRUniversity of Dayton · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Impulsivity and hyperactivity share common ground with numerous mental disorders, including schizophrenia. Recently, a population-specific serotonin 2B (5-HT2B) receptor stop codon (ie, HTR2B Q20*) was reported to segregate with severely impulsive individuals, whereas 5-HT2B mutant (Htr2B(-/-)) mice also showed high impulsivity. Interestingly, in the same cohort, early-onset schizophrenia was more prevalent in HTR2B Q*20 carriers. However, the putative role of 5-HT2B receptor in the neurobiology of schizophrenia has never been investigated. We assessed the effects of the genetic and the pharmacological ablation of 5-HT2B receptors in mice subjected to a comprehensive series of behavioral test screenings for schizophrenic-like symptoms and investigated relevant dopaminergic and glutamatergic neurochemical alterations in the cortex and the striatum. Domains related to the positive, negative, and cognitive symptom clusters of schizophrenia were affected in Htr2B(-/-) mice, as shown by deficits in sensorimotor gating, in selective attention, in social interactions, and in learning and memory processes. In addition, Htr2B(-/-) mice presented with enhanced locomotor response to the psychostimulants dizocilpine and amphetamine, and with robust alterations in sleep architecture. Moreover, ablation of 5-HT2B receptors induced a region-selective decrease of dopamine and glutamate concentrations in the dorsal striatum. Importantly, selected schizophrenic-like phenotypes and endophenotypes were rescued by chronic haloperidol treatment. We report herein that 5-HT2B receptor deficiency confers a wide spectrum of antipsychotic-sensitive schizophrenic-like behavioral and psychopharmacological phenotypes in mice and provide first evidence for a role of 5-HT2B receptors in the neurobiology of psychotic disorders.

Indexed as

AmphetamineAnimalsAntipsychotic AgentsCohort StudiesConditioning, PsychologicalCuesDisease Models, AnimalDizocilpine MaleateFearInhibition, PsychologicalMaleMiceMice, TransgenicMotor ActivityReceptor, Serotonin, 5-HT2BRecognition, PsychologyAmphetamineAntipsychotic AgentsDizocilpine MaleateReceptor, Serotonin, 5-HT2B

Identifiers

PMID25936642
PMCPMC4864652
OpenAlexW1561479775

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.