Evidence map›Paper›PMID 21473759›Full record

ArticleBMC pharmacology2011

Altered 5-HT2C receptor agonist-induced responses and 5-HT2C receptor RNA editing in the amygdala of serotonin transporter knockout mice.

Pablo R Moya, Meredith A Fox, Catherine L Jensen, Justin L Laporte, Helen T French, Jens R Wendland, Dennis L Murphy

Open access · hybridAbstract read
In one paragraph

Article in BMC pharmacology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  10. 5-HTThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
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  16. Review
  17. Dissociation of frontotemporal dementia-related deficits and neuroinflammation in progranulin haploinsufficient mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    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

7 authors at 3 institutions in 2 countries.

Pablo R MoyaLaboratory of Clinical Science, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA. moyap@mail.nih.gov
Meredith A Fox
Catherine L Jensen
Justin L Laporte
Helen T French
Jens R Wendland
Dennis L Murphy
National Institutes of Health · USNational Institute of Mental Health · USNational Institute of Mental Health · CZ

Funding

Genetic Mouse Models for the Study of Serotonin Function and BehaviorZIAMH000332 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MURPHY, DENNIS L · 2009 to 2014
$4.9M
Intramural NIH HHS
6 · The paper itself

Abstract

backgroundThe serotonin 5-HT2C receptor (5-HT2CR) is expressed in amygdala, a region involved in anxiety and fear responses and implicated in the pathogenesis of several psychiatric disorders such as acute anxiety and post traumatic stress disorder. In humans and in rodent models, there is evidence of both anxiogenic and anxiolytic actions of 5-HT2C ligands. In this study, we determined the responsiveness of 5-HT2CR in serotonin transporter (SERT) knockout (-/-) mice, a model characterized by increased anxiety-like and stress-responsive behaviors.

resultsIn the three-chamber social interaction test, the 5-HT2B/2C agonist mCPP decreased sociability and sniffing in SERT wildtype (+/+) mice, both indicative of the well-documented anxiogenic effect of mCPP. This 5-HT2C-mediated response was absent in SERT-/- mice. Likewise, in the open field test, the selective 5-HT2C agonist RO 60-0175 induced an anxiogenic response in SERT+/+ mice, but not in SERT-/- mice. Since 5-HT2CR pre-mRNA is adenosine-to-inosine (A-to-I) edited, we also evaluated the 5-HT2CR RNA editing profiles of SERT+/+ and SERT-/- mice in amygdala. Compared to SERT+/+ mice, SERT-/- mice showed a decrease in less edited, highly functional 5-HT2C isoforms, and an increase in more edited isoforms with reduced signaling efficiency.

conclusionsThese results indicate that the 5-HT2CR in the amygdala of SERT-/- mice has increased RNA editing, which could explain, at least in part, the decreased behavioral responses to 5-HT2C agonists in SERT-/- mice. These alterations in 5-HT2CR in amygdala may be relevant to humans with SERT polymorphisms that alter SERT expression, function, and emotional behaviors.

Indexed as

RNA EditingAmygdalaAnimalsAnxietyBehavior, AnimalEthylaminesIndolesInterpersonal RelationsMaleMiceMice, Inbred C57BLMice, KnockoutPiperazinesReceptor, Serotonin, 5-HT2CRNA PrecursorsSerotonin 5-HT2 Receptor Agonists1-(3-chlorophenyl)piperazineEthylaminesIndolesPiperazinesReceptor, Serotonin, 5-HT2CRNA PrecursorsRo 60-0175Serotonin 5-HT2 Receptor AgonistsSerotonin Plasma Membrane Transport Proteins

Identifiers

PMID21473759
PMCPMC3080299
OpenAlexW1995545760

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Registered trials

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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.