Methylphenidate, but not citalopram, decreases impulsive choice in rats performing a temporal discounting task

• Published in: Frontiers in psychiatry Vol. 15; p. 1385502
• Main Authors: Koloski, Miranda F., Terry, Alyssa, Lee, Noelle, Ramanathan, Dhakshin S.
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 08.05.2024
• Subjects: citalopram; impulsivity; methylphenidate; nucleus accumbens; Psychiatry; temporal discounting; impulsivity; temporal discounting; methylphenidate; nucleus accumbens; citalopram
• ISSN: 1664-0640; 1664-0640
• DOI: 10.3389/fpsyt.2024.1385502

Drugs targeting monoamine systems remain the most common treatment for disorders with impulse control impairments. There is a body of literature suggesting that drugs affecting serotonin reuptake and dopamine reuptake can modulate distinct aspects of impulsivity - though such tests are often performed using distinct behavioral tasks prohibiting easy comparisons. Here, we directly compare pharmacologic agents that affect dopamine (methylphenidate) vs serotonin (citalopram) manipulations on choice impulsivity in a temporal discounting task where rats could choose between a small, immediate reward or a large reward delayed at either 2 or 10s. In control conditions, rats preferred the large reward at a small (2s) delay and discounted the large reward at a long (10s) delay. Methylphenidate, a dopamine transport inhibitor that blocks reuptake of dopamine, dose-dependently increased large reward preference in the long delay (10s) block. Citalopram, a selective serotonin reuptake inhibitor, had no effect on temporal discounting behavior. Impulsive behavior on the temporal discounting task was at least partially mediated by the nucleus accumbens shell. Bilateral lesions to the nucleus accumbens shell reduced choice impulsivity during the long delay (10s) block. Following lesions, methylphenidate did not impact impulsivity. Our results suggest that striatal dopaminergic systems modulate choice impulsivity via actions within the nucleus accumbens shell, whereas serotonin systems may regulate different aspects of behavioral inhibition/impulsivity.