Enhanced cognitive flexibility and phasic striatal dopamine dynamics in a mouse model of low striatal tonic dopamine

• Published in: Neuropsychopharmacology (New York, N.Y.) N.Y.), 2024-09, Vol.49 (10), p.1600-1608
• Main Authors: Delaney, Jena, Nathani, Sanya, Tan, Victor, Chavez, Carson, Orr, Alexander, Paek, Joon, Faraji, Mojdeh, Setlow, Barry, Urs, Nikhil M
• Format: Article
• Language: English
• Subjects: Animals; Breakpoints; Catecholamines; Cognition - physiology; Corpus Striatum - metabolism; Dopamine; Dopamine - metabolism; Dopamine Plasma Membrane Transport Proteins - deficiency; Dopamine Plasma Membrane Transport Proteins - metabolism; Dopamine transporter; Flexibility; Hyperactivity; Male; Mental disorders; Mice; Mice, Inbred C57BL; Mice, Knockout; Neostriatum; Neuromodulation; Norepinephrine; Norepinephrine - metabolism; Norepinephrine Plasma Membrane Transport Proteins - metabolism; Norepinephrine transporter; Phenotypes; Prefrontal cortex; Prefrontal Cortex - metabolism; Reversal learning; Reversal Learning - physiology; Reward
• ISSN: 0893-133X; 1740-634X; 1740-634X
• DOI: 10.1038/s41386-024-01868-5

The catecholamine neuromodulators dopamine and norepinephrine are implicated in motor function, motivation, and cognition. Although roles for striatal dopamine in these aspects of behavior are well established, the specific roles for cortical catecholamines in regulating striatal dopamine dynamics and behavior are less clear. We recently showed that elevating cortical dopamine but not norepinephrine suppresses hyperactivity in dopamine transporter knockout (DAT-KO) mice, which have elevated striatal dopamine levels. In contrast, norepinephrine transporter knockout (NET-KO) mice have a phenotype distinct from DAT-KO mice, as they show elevated extracellular cortical catecholamines but reduced baseline striatal dopamine levels. Here we evaluated the consequences of altered catecholamine levels in NET-KO mice on cognitive flexibility and striatal dopamine dynamics. In a probabilistic reversal learning task, NET-KO mice showed enhanced reversal learning, which was consistent with larger phasic dopamine transients (dLight) in the dorsomedial striatum (DMS) during reward delivery and reward omission, compared to WT controls. Selective depletion of dorsal medial prefrontal cortex (mPFC) norepinephrine in WT mice did not alter performance on the reversal learning task but reduced nestlet shredding. Surprisingly, NET-KO mice did not show altered breakpoints in a progressive ratio task, suggesting intact food motivation. Collectively, these studies show novel roles of cortical catecholamines in the regulation of tonic and phasic striatal dopamine dynamics and cognitive flexibility, updating our current views on dopamine regulation and informing future therapeutic strategies to counter multiple psychiatric disorders.