Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.

<h4>Background</h4>Disruption of the circadian rhythm is a key feature of bipolar disorder. Variation in genes encoding components of the molecular circadian clock has been associated with increased risk of the disorder in clinical populations. Similarly in animal models, disruption of t...

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Main Authors: Robert Keers, Inti Pedroso, Gerome Breen, Kathy J Aitchison, Patrick M Nolan, Sven Cichon, Markus M Nöthen, Marcella Rietschel, Leonard C Schalkwyk, Cathy Fernandes
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0038263&type=printable
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author Robert Keers
Inti Pedroso
Gerome Breen
Kathy J Aitchison
Patrick M Nolan
Sven Cichon
Markus M Nöthen
Marcella Rietschel
Leonard C Schalkwyk
Cathy Fernandes
author_facet Robert Keers
Inti Pedroso
Gerome Breen
Kathy J Aitchison
Patrick M Nolan
Sven Cichon
Markus M Nöthen
Marcella Rietschel
Leonard C Schalkwyk
Cathy Fernandes
author_sort Robert Keers
collection DOAJ
description <h4>Background</h4>Disruption of the circadian rhythm is a key feature of bipolar disorder. Variation in genes encoding components of the molecular circadian clock has been associated with increased risk of the disorder in clinical populations. Similarly in animal models, disruption of the circadian clock can result in altered mood and anxiety which resemble features of human mania; including hyperactivity, reduced anxiety and reduced depression-like behaviour. One such mutant, after hours (Afh), an ENU-derived mutant with a mutation in a recently identified circadian clock gene Fbxl3, results in a disturbed (long) circadian rhythm of approximately 27 hours.<h4>Methodology</h4>Anxiety, exploratory and depression-like behaviours were evaluated in Afh mice using the open-field, elevated plus maze, light-dark box, holeboard and forced swim test. To further validate findings for human mania, polymorphisms in the human homologue of FBXL3, genotyped by three genome wide case control studies, were tested for association with bipolar disorder.<h4>Principal findings</h4>Afh mice showed reduced anxiety- and depression-like behaviour in all of the behavioural tests employed, and some evidence of increased locomotor activity in some tests. An analysis of three separate human data sets revealed a gene wide association between variation in FBXL3 and bipolar disorder (P = 0.009).<h4>Conclusions</h4>Our results are consistent with previous studies of mutants with extended circadian periods and suggest that disruption of FBXL3 is associated with mania-like behaviours in both mice and humans.
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spelling doaj-art-7016b763792444098cf9b53b590806d92025-08-20T03:25:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0176e3826310.1371/journal.pone.0038263Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.Robert KeersInti PedrosoGerome BreenKathy J AitchisonPatrick M NolanSven CichonMarkus M NöthenMarcella RietschelLeonard C SchalkwykCathy Fernandes<h4>Background</h4>Disruption of the circadian rhythm is a key feature of bipolar disorder. Variation in genes encoding components of the molecular circadian clock has been associated with increased risk of the disorder in clinical populations. Similarly in animal models, disruption of the circadian clock can result in altered mood and anxiety which resemble features of human mania; including hyperactivity, reduced anxiety and reduced depression-like behaviour. One such mutant, after hours (Afh), an ENU-derived mutant with a mutation in a recently identified circadian clock gene Fbxl3, results in a disturbed (long) circadian rhythm of approximately 27 hours.<h4>Methodology</h4>Anxiety, exploratory and depression-like behaviours were evaluated in Afh mice using the open-field, elevated plus maze, light-dark box, holeboard and forced swim test. To further validate findings for human mania, polymorphisms in the human homologue of FBXL3, genotyped by three genome wide case control studies, were tested for association with bipolar disorder.<h4>Principal findings</h4>Afh mice showed reduced anxiety- and depression-like behaviour in all of the behavioural tests employed, and some evidence of increased locomotor activity in some tests. An analysis of three separate human data sets revealed a gene wide association between variation in FBXL3 and bipolar disorder (P = 0.009).<h4>Conclusions</h4>Our results are consistent with previous studies of mutants with extended circadian periods and suggest that disruption of FBXL3 is associated with mania-like behaviours in both mice and humans.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0038263&type=printable
spellingShingle Robert Keers
Inti Pedroso
Gerome Breen
Kathy J Aitchison
Patrick M Nolan
Sven Cichon
Markus M Nöthen
Marcella Rietschel
Leonard C Schalkwyk
Cathy Fernandes
Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.
PLoS ONE
title Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.
title_full Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.
title_fullStr Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.
title_full_unstemmed Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.
title_short Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.
title_sort reduced anxiety and depression like behaviours in the circadian period mutant mouse afterhours
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0038263&type=printable
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