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Dr. Ávila-Macaya, Ariel
Nombre de publicación
Dr. Ávila-Macaya, Ariel
Nombre completo
Ávila Macaya, Ariel Salvatore
Facultad
Email
aavila@ucsc.cl
ORCID
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- PublicationMice lacking neuronal calcium sensor-1 show social and cognitive deficits(Elsevier, 2020)
;Ng, Enoch ;Georgiou, John; ;Trought, Kathleen ;Mun, Ho-Suk ;Hodgson, Meggie ;Servinis, Panayiotis ;Roder, John C. ;Collingridge, Graham L.Wong, Albert H.CNeuronal calcium sensor-1 or Frequenin is a calcium sensor widely expressed in the nervous system, with roles in neurotransmission, neurite outgrowth, synaptic plasticity, learning, and motivated behaviours. Neuronal calcium sensor-1 has been implicated in neuropsychiatric disorders including autism spectrum disorder, schizophrenia, and bipolar disorder. However, the role of neuronal calcium sensor-1 in behavioural phenotypes and brain changes relevant to autism spectrum disorder have not been evaluated. We show that neuronal calcium sensor-1 deletion in the mouse leads to a mild deficit in social approach and impaired displaced object recognition without affecting social interactions, behavioural flexibility, spatial reference memory, anxiety-like behaviour, or sensorimotor gating. Morphologically, neuronal calcium sensor-1 deletion leads to increased dendritic arbour complexity in the frontal cortex. At the level of hippocampal synaptic plasticity, neuronal calcium sensor-1 deletion leads to a reduction in long-term potentiation in the dentate gyrus, but not area Cornu Ammonis 1. Metabotropic glutamate receptor-induced long-term depression was unaffected in both dentate and Cornu Ammonis 1. These studies identify roles for neuronal calcium sensor-1 in specific subregions of the brain including a phenotype relevant to neuropsychiatric disorders.