Dopamine-mediated striatal activity and function is enhanced in GlyRα2 knockout animals

Autor(en): Devoght, Jens
Comhair, Joris
Morelli, Giovanni
Rigo, Jean-Michel
D'Hooge, Rudi
Touma, Chadi 
Palme, Rupert
Dewachter, Ilse
Vandeven, Martin
Harvey, Robert J.
Schiffmann, Serge N.
Piccart, Elisabeth
Brone, Bert
Stichwörter: ADENYLATE-CYCLASE ACTIVITY; AMPHETAMINE; C-FOS; DELTA-FOSB; DORSAL STRIATUM; DRUG SEEKING; Multidisciplinary Sciences; NEURONS; NUCLEUS; Science & Technology - Other Topics; TEGMENTAL AREA; VENTRAL STRIATUM
Erscheinungsdatum: 2023
Herausgeber: CELL PRESS
Journal: ISCIENCE
Volumen: 26
Ausgabe: 8
Zusammenfassung: 
The glycine receptor alpha 2 (GlyR alpha 2) is a ligand-gated ion channel which upon activation induces a chloride conductance. Here, we investigated the role of GlyRa2 in dopamine-stimulated striatal cell activity and behavior. We show that depletion of GlyR alpha 2 enhances dopamine-induced increases in the activity of putative dopamine D1 receptor-expressing striatal projection neurons, but does not alter midbrain dopamine neuron activity. We next show that the locomotor response to d-amphetamine is enhanced in GlyRa2 knockout animals, and that this increase correlates with c-fos expression in the dorsal striatum. 3-Dmodeling revealed an increase in the neuronal ensemble size in the striatum in response to D-amphetamine in GlyR alpha 2 KO mice. Finally, we show enhanced appetitive conditioning in GlyR alpha 2 KO animals that is likely due to increased motivation, but not changes in associative learning or hedonic response. Taken together, we show that GlyR alpha 2 is an important regulator of dopamine-stimulated striatal activity and function.
DOI: 10.1016/j.isci.2023.107400

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