Please use this identifier to cite or link to this item: https://doi.org/10.3389/fnbeh.2013.00103
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dc.titleCo-segregation of hyperactivity, active coping styles, and cognitive dysfunction in mice selectively bred for low levels of anxiety
dc.contributor.authorYen, Y.-C
dc.contributor.authorAnderzhanova, E
dc.contributor.authorBunck, M
dc.contributor.authorSchuller, J
dc.contributor.authorLandgraf, R
dc.contributor.authorWotjak, C.T
dc.date.accessioned2020-10-27T11:17:53Z
dc.date.available2020-10-27T11:17:53Z
dc.date.issued2013
dc.identifier.citationYen, Y.-C, Anderzhanova, E, Bunck, M, Schuller, J, Landgraf, R, Wotjak, C.T (2013). Co-segregation of hyperactivity, active coping styles, and cognitive dysfunction in mice selectively bred for low levels of anxiety. Frontiers in Behavioral Neuroscience (AUG). ScholarBank@NUS Repository. https://doi.org/10.3389/fnbeh.2013.00103
dc.identifier.issn16625153
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181558
dc.description.abstractWe established mouse models of extremes in trait anxiety, which are based on selective breeding for low vs. normal vs. high open-arm exploration on the elevated plus-maze. Genetically selected low anxiety-related behavior (LAB) coincided with hyperactivity in the home cage. Given the fact that several psychiatric disorders such as schizophrenia, mania, and attention deficit hyperactivity disorder (ADHD) share hyperactivity symptom, we systematically examined LAB mice with respect to unique and overlapping endophenotypes of the three diseases. To this end Venn diagrams were used as an instrument for discrimination of possible models. We arranged the endophenotypes in Venn diagrams and translated them into different behavioral tests. LAB mice showed elevated levels of locomotion in the open field (OF) test with deficits in habituation, compared to mice bred for normal (NAB) and high anxiety-related behavior (HAB). Cross-breeding of hypoactive HAB and hyperactive LAB mice resulted in offspring showing a low level of locomotion comparable to HAB mice, indicating that the HAB alleles are dominant over LAB alleles in determining the level of locomotion. In a holeboard test, LAB mice spent less time in hole exploration, as shown in patients with schizophrenia and ADHD; however, LAB mice displayed no impairments in social interaction and prepulse inhibition (PPI), implying a unlikelihood of LAB as an animal model of schizophrenia. Although LAB mice displayed hyperarousal, active coping styles, and cognitive deficits, symptoms shared by mania and ADHD, they failed to reveal the classic manic endophenotypes, such as increased hedonia and object interaction. The neuroleptic haloperidol reduced locomotor activity in all mouse lines. The mood stabilizer lithium and the psychostimulant amphetamine, in contrast, selectively reduced hyperactivity in LAB mice. Based on the behavioral and pharmacological profiles, LAB mice are suggested as a novel rodent model of ADHD-like symptoms. © 2013 Yen, Anderzhanova, Bunck, Schuller, Landgraf and Wotjak.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectamphetamine
dc.subjecthaloperidol
dc.subjectlithium
dc.subjectallele
dc.subjectanimal behavior
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanxiety
dc.subjectarticle
dc.subjectattention deficit disorder
dc.subjectbehavioral test
dc.subjectbreeding
dc.subjectcognitive defect
dc.subjectcontrolled study
dc.subjectcoping behavior
dc.subjectcross breeding
dc.subjectdiscriminant analysis
dc.subjectelevated plus maze
dc.subjectendophenotype
dc.subjectexperimental test
dc.subjectexploratory behavior
dc.subjectfemale
dc.subjectgenetic selection
dc.subjecthabituation
dc.subjecthedonia
dc.subjectholeboard test
dc.subjecthyperactivity
dc.subjectmale
dc.subjectmania
dc.subjectmathematical analysis
dc.subjectmaze test
dc.subjectmouse
dc.subjectmouse strain
dc.subjectnonhuman
dc.subjectobject interaction
dc.subjectopen field test
dc.subjectprepulse inhibition
dc.subjectpsychologic test
dc.subjectschizophrenia
dc.subjectsocial interaction
dc.subjectstrain difference
dc.subjectvenn diagram
dc.typeArticle
dc.contributor.departmentPHYSIOLOGY
dc.description.doi10.3389/fnbeh.2013.00103
dc.description.sourcetitleFrontiers in Behavioral Neuroscience
dc.description.issueAUG
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