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Behav Pharmacol ; 26(8 Spec No): 733-40, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26110222

ABSTRACT

The aims of this study were to investigate behaviour relevant to human autism spectrum disorder (ASD) and the fragile X syndrome in adolescent Fmr1 knockout (KO) mice and to evaluate the tissue levels of striatal monoamines. Fmr1 KO mice were evaluated in the open field, marble burying and three-chamber test for the presence of hyperactivity, anxiety, repetitive behaviour, sociability and observation of social novelty compared with wild-type (WT) mice. The Fmr1 KO mice expressed anxiety and hyperactivity in the open field compared with WT mice. This increased level of hyperactivity was confirmed in the three-chamber test. Fmr1 KO mice spent more time with stranger mice compared with the WT. However, after a correction for hyperactivity, their apparent increase in sociability became identical to that of the WT. Furthermore, the Fmr1 KO mice could not differentiate between a familiar or a novel mouse. Monoamines were measured by HPLC: Fmr1 KO mice showed an increase in the striatal dopamine level. We conclude that the fragile X syndrome model seems to be useful for understanding certain aspects of ASD and may have translational interest for studies of social behaviour when hyperactivity coexists in ASD patients.


Subject(s)
Anxiety/metabolism , Autism Spectrum Disorder/metabolism , Disease Models, Animal , Fragile X Mental Retardation Protein/metabolism , Hyperkinesis/metabolism , Social Behavior Disorders/metabolism , Animals , Anxiety/genetics , Autism Spectrum Disorder/genetics , Behavior, Animal/physiology , Biogenic Monoamines/metabolism , Female , Fragile X Mental Retardation Protein/genetics , Fragile X Syndrome/genetics , Hyperkinesis/genetics , Male , Mice , Mice, Knockout , Motor Activity , Social Behavior , Social Behavior Disorders/genetics
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