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Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice
Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice
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Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice
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Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice
Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice

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Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice
Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice
Journal Article

Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice

2017
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Overview
Background Obsessive–compulsive disorder (OCD) is a severe neuropsychiatric condition affecting 1–3% of the worldwide population. OCD has a strong genetic component, and the SLC1A1 gene that encodes neuronal glutamate transporter EAAT3 is a strong candidate for this disorder. To evaluate the impact of reduced EAAT3 expression in vivo, we studied male EAAT3 heterozygous and wild-type littermate mice using a battery of behavioral paradigms relevant to anxiety (open field test, elevated plus maze) and compulsivity (marble burying), as well as locomotor activity induced by amphetamine. Using high-performance liquid chromatography, we also determined tissue neurotransmitter levels in cortex, striatum and thalamus—brain areas that are relevant to OCD. Results Compared to wild-type littermates, EAAT3 heterozygous male mice have unaltered baseline anxiety-like, compulsive-like behavior and locomotor activity. Administration of acute amphetamine (5 mg/kg intraperitoneally) increased locomotion with no differences across genotypes. Tissue levels of glutamate, GABA, dopamine and serotonin did not vary between EAAT3 heterozygous and wild-type mice. Conclusions Our results indicate that reduced EAAT3 expression does not impact neurotransmitter content in the corticostriatal circuit nor alter anxiety or compulsive-like behaviors.