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X-WR-CALNAME:Bordeaux Neurocampus
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X-WR-CALDESC:Évènements pour Bordeaux Neurocampus
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DTSTART:20250330T010000
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DTSTART;TZID=Europe/Paris:20250207T113000
DTEND;TZID=Europe/Paris:20250207T113000
DTSTAMP:20260403T205024
CREATED:20240710T170228Z
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UID:173129-1738927800-1738927800@www.bordeaux-neurocampus.fr
SUMMARY:PhD seminar - Bita Moghaddam
DESCRIPTION:Venue: Centre Broca \n\nIn the frame of the Girls and Women of Science Day \nBita Moghaddam\nRuth Matarazzo Professor of Behavioral Neuroscience\nProfessor of Psychiatry\nOregon Health and Science University\, USA\nLab website https://www.moghaddamlab.org/\nhttps://en.wikipedia.org/wiki/Bita_Moghaddam \nTitle\nEvolution of the Glutamate Models of Psychosis \nAbstract\nPsychosis is a hallmark of schizophrenia. It typically emerges in late adolescence and is associated with striatal dopamine abnormalities. Most genes implicated in the risk for schizophrenia involve ubiquitous targets that do not explain the latent expression of psychosis or dopaminergic disruptions. Here\, we describe an etiologically relevant mechanism for adolescent onset of dopamine abnormalities and psychosis. We focused on GRIN2A\, which encodes the GluN2A subunit of the NMDA receptor. Both common variants in this gene as well as rare missense and protein-truncating variants were recently identified as genetic risk factors for schizophrenia. We find that GluN2A levels decline throughout adolescence in midbrain regions that contain dopamine neurons. This led us to reason that variants that reduce GRIN2A function could augment this natural adolescent developmental process and contribute to the emergence of psychosis at this age. Consistent with this mechanism\, virally mediated Grin2a knockout in rat adolescent dopamine neurons resulted in a phenotype mirroring psychosis. These included disruptions in salience attribution and dopamine release during prediction error signaling. Overall\, these data provide mechanistic insight into how variants of GRIN2A may lead to the latent presentation of psychosis and abnormalities in dopamine dynamics in schizophrenia. Our approach provides a model with construct and face validity to aid future discovery of course altering treatments for schizophrenia. \nSuggested papers:\nhttps://www.cell.com/fulltext/S0896-6273(03)00757-8 \nhttps://www.pnas.org/doi/abs/10.1073/pnas.0308455101 \nhttps://www.nature.com/articles/npp2011181 \nhttps://www.biorxiv.org/content/10.1101/2024.10.28.620713v1.abstract \nShare some pizza with the speaker!\nPhD students and post docs\, you can meet the speaker after the talk. On registration. \n
URL:https://www.bordeaux-neurocampus.fr/event/phd-seminar-bita-moghaddam/
CATEGORIES:A la une,Conférences mensuelles,Pour les scientifiques
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