Abstract

The serotonin (5-HT) system, particularly the 5-HT2C receptor, has consistently been implicated in behavioural control. However, while some studies have focused on the role 5-HT2C receptors play in regulating motivation to work for reward, others have highlighted its importance in response restraint. To date, it is unclear how 5-HT transmission at this receptor regulates the balance of response invigoration and restraint in anticipation of future reward. In addition, it remains to be established how 5-HT2C receptors gate the influence of internal versus cue-driven processes over reward-guided actions. To elucidate these issues, we investigated the effects of administering the 5-HT2C receptor antagonist SB242084, both systemically and directly into the nucleus accumbens core (NAcC), in rats performing a Go/No-Go task for small or large rewards. The results were compared to the administration of d-amphetamine into the NAcC, which has previously been shown to promote behavioural activation. Systemic perturbation of 5-HT2C receptors—but crucially not intra-NAcC infusions—consistently boosted rats’ performance and instrumental vigour on Go trials when they were required to act. Concomitantly, systemic administration also reduced their ability to withhold responding for rewards on No-Go trials, particularly late in the holding period. Notably, these effects were often apparent only when the reward on offer was small. By contrast, inducing a hyperdopaminergic state in the NAcC with d-amphetamine strongly impaired response restraint on No-Go trials both early and late in the holding period, as well as speeding action initiation. Together, these findings suggest that 5-HT2C receptor transmission, outside the NAcC, shapes the vigour of ongoing goal-directed action as well as the likelihood of responding as a function of expected reward.

Highlights

  • The central neurotransmitter serotonin (5-HT) has been implicated in the motivational control of behaviour (McElroy et al 1982; Soubrié 1986; Kulichenko and Pavlenko 2004; Cools et al 2011)

  • These No-Go errors were often followed by lever pressing within the No-Go holding interval (F1, 12 = 12.40, p = 0.004). This deficit in withholding actions generalised to the pre-cue period, where intra-nucleus accumbens core (NAcC) d-amphetamine substantially increased the numbers of aborted trials. These findings demonstrate that intra-NAcC d-amphetamine significantly biased behavioural strategies towards action over inaction, speeding action initiation and impairing action restraint

  • We studied the role of 5-HT2C receptors – an important modulator of instrumental vigour (Simpson et al 2011; Bailey et al 2016, 2018; Browne et al 2017) – in controlling action and restraint

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Summary

Introduction

The central neurotransmitter serotonin (5-HT) has been implicated in the motivational control of behaviour (McElroy et al 1982; Soubrié 1986; Kulichenko and Pavlenko 2004; Cools et al 2011). A second issue is that the study of action vigour often uses internally guided instrumental paradigms, whilst those investigating the role of serotonin in action restraint have predominantly used stimulus-driven tasks. Such differences are likely to be important as 5-HT has been implicated in gating sensory processing (Petzold et al 2009), and it has recently been shown that administration of a 5-HT2C receptor antagonist can reduce the influence of cues over decision-making policies (Adams et al 2017). An important open question concerns whether the influence of 5-HT2C in behavioural control depends on the level of reward expectation and if this varies as a function of temporal proximity to rewardpredicting cues

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