Fabio Benfenati
TAAR1 Modulates Cortical Glutamate NMDA Receptor Function
Benfenati, Fabio; Espinoza, Stefano; Lignani, Gabriele; Caffino, Lucia; Maggi, Silvia; Sukhanov, Ilya; Leo, Damiana; Mus, Liudmila; Emanuele, Marco; Ronzitti, Giuseppe; Harmeier, Anja; Medrihan, Lucian; Sotnikova, Tatyana D; Chieregatti, Evelina; Hoener, Marius C; Tucci, Valter; Fumagalli, Fabio; Gainetdinov, Raul R
Authors
Stefano Espinoza
Gabriele Lignani
Lucia Caffino
Dr SILVIA MAGGI SILVIA.MAGGI@NOTTINGHAM.AC.UK
ASSISTANT PROFESSOR
Ilya Sukhanov
Damiana Leo
Liudmila Mus
Marco Emanuele
Giuseppe Ronzitti
Anja Harmeier
Lucian Medrihan
Tatyana D Sotnikova
Evelina Chieregatti
Marius C Hoener
Valter Tucci
Fabio Fumagalli
Raul R Gainetdinov
Abstract
Trace Amine-Associated Receptor 1 (TAAR1) is a G protein-coupled receptor expressed in the mammalian brain and known to influence subcortical monoaminergic transmission. Monoamines, such as dopamine, also play an important role within the prefrontal cortex (PFC) circuitry, which is critically involved in high-o5rder cognitive processes. TAAR1-selective ligands have shown potential antipsychotic, antidepressant, and pro-cognitive effects in experimental animal models; however, it remains unclear whether TAAR1 can affect PFC-related processes and functions. In this study, we document a distinct pattern of expression of TAAR1 in the PFC, as well as altered subunit composition and deficient functionality of the glutamate N-methyl-D-aspartate (NMDA) receptors in the pyramidal neurons of layer V of PFC in mice lacking TAAR1. The dysregulated cortical glutamate transmission in TAAR1-KO mice was associated with aberrant behaviors in several tests, indicating a perseverative and impulsive phenotype of mutants. Conversely, pharmacological activation of TAAR1 with selective agonists reduced premature impulsive responses observed in the fixed-interval conditioning schedule in normal mice. Our study indicates that TAAR1 plays an important role in the modulation of NMDA receptor-mediated glutamate transmission in the PFC and related functions. Furthermore, these data suggest that the development of TAAR1-based drugs could provide a novel therapeutic approach for the treatment of disorders related to aberrant cortical functions.
Citation
Benfenati, F., Espinoza, S., Lignani, G., Caffino, L., Maggi, S., Sukhanov, I., Leo, D., Mus, L., Emanuele, M., Ronzitti, G., Harmeier, A., Medrihan, L., Sotnikova, T. D., Chieregatti, E., Hoener, M. C., Tucci, V., Fumagalli, F., & Gainetdinov, R. R. (2015). TAAR1 Modulates Cortical Glutamate NMDA Receptor Function. Neuropsychopharmacology, 40(9), 2217-2227. https://doi.org/10.1038/npp.2015.65
Journal Article Type | Article |
---|---|
Acceptance Date | Feb 25, 2015 |
Online Publication Date | Mar 9, 2015 |
Publication Date | 2015-08 |
Deposit Date | Nov 4, 2019 |
Publicly Available Date | Nov 4, 2019 |
Journal | Neuropsychopharmacology |
Print ISSN | 0893-133X |
Electronic ISSN | 1740-634X |
Publisher | Nature Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 40 |
Issue | 9 |
Pages | 2217-2227 |
DOI | https://doi.org/10.1038/npp.2015.65 |
Keywords | Pharmacology; Psychiatry and Mental health |
Public URL | https://nottingham-repository.worktribe.com/output/3051783 |
Publisher URL | https://www.nature.com/articles/npp201565 |
Additional Information | Received: 21 October 2014; Revised: 21 February 2015; Accepted: 25 February 2015; First Online: 9 March 2015 |
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