Evidence map›Paper›PMID 26308619›Full record

ArticlePloS one2015

Social Behavioral Deficits Coincide with the Onset of Seizure Susceptibility in Mice Lacking Serotonin Receptor 2c.

Julien Séjourné, Danielle Llaneza, Orsolya J Kuti, Damon T Page

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. iScience · 2022
    Article
  11. Article
  12. Article
  13. A 5-HTThe European journal of neuroscience · 2020
    Article
  14. Review
  15. (ACS pharmacology & translational science · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Autism-relevant behaviors are minimally impacted by conditional deletion of Pten in oxytocinergic neurons.Autism research : official journal of the International Society for Autism Research · 2016
    Article
  20. 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

4 authors at 2 institutions in 1 country.

Julien SéjournéDepartment of Neuroscience, The Scripps Research Institute, 130 Scripps Way, Jupiter, Florida, 33458, United States of America.
Danielle LlanezaDepartment of Neuroscience, The Scripps Research Institute, 130 Scripps Way, Jupiter, Florida, 33458, United States of America.
Orsolya J KutiDepartment of Brain and Cognitive Sciences and Picower Institute for Learning and Memory, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts, 02139, United States of America.
Damon T PageDepartment of Neuroscience, The Scripps Research Institute, 130 Scripps Way, Jupiter, Florida, 33458, United States of America.
Scripps Research Institute · USMassachusetts Institute of Technology · US

Funding

Impact of Pten mutations on brain growth and social behavioral development.R01MH105610 · NIMH · SCRIPPS FLORIDA · PI PAGE, DAMON THERON · 2015 to 2019
$2.4M
NIMH NIH HHS R01 MH105610NIMH NIH HHS R01MH105610
6 · The paper itself

Abstract

The development of social behavior is strongly influenced by the serotonin system. Serotonin 2c receptor (5-HT2cR) is particularly interesting in this context considering that pharmacological modulation of 5-HT2cR activity alters social interaction in adult rodents. However, the role of 5-HT2cR in the development of social behavior is unexplored. Here we address this using Htr2c knockout mice, which lack 5-HT2cR. We found that these animals exhibit social behavior deficits as adults but not as juveniles. Moreover, we found that the age of onset of these deficits displays similar timing as the onset of susceptibility to spontaneous death and audiogenic-seizures, consistent with the hypothesis that imbalanced excitation and inhibition (E/I) may contribute to social behavioral deficits. Given that autism spectrum disorder (ASD) features social behavioral deficits and is often co-morbid with epilepsy, and given that 5-HT2cR physically interacts with Pten, we tested whether a second site mutation in the ASD risk gene Pten can modify these phenotypes. The age of spontaneous death is accelerated in mice double mutant for Pten and Htr2c relative to single mutants. We hypothesized that pharmacological antagonism of 5-HT2cR activity in adult animals, which does not cause seizures, might modify social behavioral deficits in Pten haploinsufficient mice. SB 242084, a 5-HT2cR selective antagonist, can reverse the social behavior deficits observed in Pten haploinsufficient mice. Together, these results elucidate a role of 5-HT2cR in the modulation of social behavior and seizure susceptibility in the context of normal development and Pten haploinsufficiency.

Indexed as

Behavior, AnimalDisease SusceptibilitySocial BehaviorAnimalsBrainFemaleHaploinsufficiencyMaleMiceMice, Inbred C57BLMice, KnockoutPhenotypeReceptor, Serotonin, 5-HT2CSeizuresSerotoninReceptor, Serotonin, 5-HT2CSerotonin

Identifiers

PMID26308619
PMCPMC4550412
OpenAlexW1954851557

What OpenQuestion holds

Textmetadata
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.