Abstract
To investigate the contribution of individual serotonin (5-hydroxytryptamine; 5-HT) receptors to mood control, we have used homologous recombination to generate mice lacking specific serotonergic receptor subtypes. In the present report, we demonstrate that mice without 5-HT1A receptors display decreased exploratory activity and increased fear of aversive environments (open or elevated spaces). 5-HT1A knockout mice also exhibited a decreased immobility in the forced swim test, an effect commonly associated with antidepressant treatment. Although 5-HT1A receptors are involved in controlling the activity of serotonergic neurons, 5-HT1A knockout mice had normal levels of 5-HT and 5-hydroxyindoleacetic acid, possibly because of an up-regulation of 5-HT1B autoreceptors. Heterozygote 5-HT1A mutants expressed approximately one-half of wild-type receptor density and displayed intermediate phenotypes in most behavioral tests. These results demonstrate that 5-HT1A receptors are involved in the modulation of exploratory and fear-related behaviors and suggest that reductions in 5-HT1A receptor density due to genetic defects or environmental stressors might result in heightened anxiety.
MeSH Terms
Animals
Anxiety Disorders/genetics,metabolism
Autoradiography
Brain/metabolism
Disease Models, Animal
Female
Humans
Male
Mice
Mice, Inbred C57BL
Mice, Inbred Strains
Mice, Knockout
Motor Activity
Neurons/metabolism
Receptors, Serotonin/deficiency,genetics,physiology
Receptors, Serotonin, 5-HT1
Recombination, Genetic
Serotonin/metabolism
Tritium
Chemicals
Receptors, Serotonin
Receptors, Serotonin, 5-HT1
Tritium
Serotonin
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Ramboz S
Center for Neurobiology and Behavior, Columbia University, 722 West 168th Street, New York, NY 10032, USA.
Oosting R
Amara D A
Kung H F
Blier P
Mendelsohn M
Mann J J
Brunner D
Hen R
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