Journal
PSYCHOLOGICAL MEDICINE
Volume 53, Issue 14, Pages 6434-6445Publisher
CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291722002963
Keywords
5-HT2A; cognitive flexibility; computational modeling; LSD; probabilistic reversal learning; psychedelics; reinforcement learning; serotonin
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The study aimed to investigate how LSD affects probabilistic reversal learning in healthy individuals. The results showed that LSD increased the reward and punishment learning rates, decreased stimulus stickiness, and induced a state of heightened plasticity.
Background. The non-selective serotonin 2A (5-HT2A) receptor agonist lysergic acid diethylamide (LSD) holds promise as a treatment for some psychiatric disorders. Psychedelic drugs such as LSD have been suggested to have therapeutic actions through their effects on learning. The behavioural effects of LSD in humans, however, remain incompletely understood. Here we examined how LSD affects probabilistic reversal learning (PRL) in healthy humans. Methods. Healthy volunteers received intravenous LSD (75 mu g in 10mL saline) or placebo (10 mL saline) in a within-subjects design and completed a PRL task. Participants had to learn through trial and error which of three stimuli was rewarded most of the time, and these contingencies switched in a reversal phase. Computational models of reinforcement learning (RL) were fitted to the behavioural data to assess how LSD affected the updating ('learning rates') and deployment of value representations ('reinforcement sensitivity') during choice, as well as 'stimulus stickiness' (choice repetition irrespective of reinforcement history). Results. Raw data measures assessing sensitivity to immediate feedback ('win-stay' and 'lose-shift' probabilities) were unaffected, whereas LSD increased the impact of the strength of initial learning on perseveration. Computational modelling revealed that the most pronounced effect of LSD was the enhancement of the reward learning rate. The punishment learning rate was also elevated. Stimulus stickiness was decreased by LSD, reflecting heightened exploration. Reinforcement sensitivity differed by phase. Conclusions. Increased RL rates suggest LSD induced a state of heightened plasticity. These results indicate a potential mechanism through which revision of maladaptive associations could occur in the clinical application of LSD.
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