Abstract
RationaleDysregulation of the serotonin (5-HT) system is a pathophysiological component in major depressive disorder (MDD), a condition closely associated with abnormal emotional responsivity to positive and negative feedback. However, the precise mechanism through which 5-HT tone biases feedback responsivity remains unclear. 5-HT2C receptors (5-HT2CRs) are closely linked with aspects of depressive symptomatology, including abnormalities in reinforcement processes and response to stress. Thus, we aimed to determine the impact of 5-HT2CR function on response to feedback in biased reinforcement learning.MethodsWe used two touchscreen assays designed to assess the impact of positive and negative feedback on probabilistic reinforcement in mice, including a novel valence-probe visual discrimination (VPVD) and a probabilistic reversal learning procedure (PRL). Systemic administration of a 5-HT2CR agonist and antagonist resulted in selective changes in the balance of feedback sensitivity bias on these tasks.ResultsSpecifically, on VPVD, SB 242084, the 5-HT2CR antagonist, impaired acquisition of a discrimination dependent on appropriate integration of positive and negative feedback. On PRL, SB 242084 at 1 mg/kg resulted in changes in behaviour consistent with reduced sensitivity to positive feedback. In contrast, WAY 163909, the 5-HT2CR agonist, resulted in changes associated with increased sensitivity to positive feedback and decreased sensitivity to negative feedback.ConclusionsThese results suggest that 5-HT2CRs tightly regulate feedback sensitivity bias in mice with consequent effects on learning and cognitive flexibility and specify a framework for the influence of 5-HT2CRs on sensitivity to reinforcement.
Highlights
Adaptive responding requires organisms to detect and integrate the consequences of their actions to guide future behaviour
Our findings indicate that 5-HT2CRs regulate responsivity to positive and negative feedback in these tasks
Following valence-probe visual discrimination (VPVD), we investigated the involvement of the 5HT2CR in reactivity to positive and negative feedback by testing animals on PRL (Fig. 2a) following acute administration of the antagonist SB 242084 and agonist WAY 163909
Summary
Adaptive responding requires organisms to detect and integrate the consequences of their actions to guide future behaviour. Abnormalities in feedback sensitivity appear to causally contribute to the development and maintenance of MDD (Clark et al 2009; Roiser et al 2012), with evidence that successful antidepressant treatment may reverse this response profile (Harmer et al 2006, 2009). This domain represents a promising candidate for the development of Psychopharmacology (2018) 235:2101–2111 targeted therapeutics directed at reversing cognitive profiles implicated in depressive states.
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