Abstract

While the contribution of Mu Opioid Receptors (MORs) to hedonic aspects of reward processing is well-established, the notion that these receptors may also regulate motivation to gain a reward, and possibly other related cognitive dimensions, has been less investigated. The prefrontal cortex (PFC) is a critical site for these processes. Our previous functional magnetic resonance imaging study found alterations of functional connectivity (FC) in reward/aversion networks in MOR knockout mice. Here we pursued voxelwise seed-based FC analyses using the same dataset with a focus on the PFC. We observed significant reduction of PFC FC in mutant mice, predominantly with the nucleus accumbens, supporting the notion of altered reward-driven top-down controls. We tested motivation for palatable food in a classical operant self-administration paradigm, and found delayed performance for mutant mice. We then evaluated motivational and cognitive abilities of MOR knockout mice in TouchScreen-based behavioral tests. Learning was delayed and stimulus/reward association was impaired, suggesting lower hedonic reward value and reduced motivation. Perseverative responses were decreased, while discriminatory behavior and attention were unchanged, indicative of increased inhibitory controls with otherwise intact cognitive performance. Together, our data suggest that MORs contribute to enhance reward-seeking and facilitate perseverative behaviors. The possibility that MOR blockade could reduce maladaptive compulsivity deserves further investigation in addiction and self-control disorder research.

Highlights

  • While the contribution of Mu Opioid Receptors (MORs) to hedonic aspects of reward processing is well-established, the notion that these receptors may regulate motivation to gain a reward, and possibly other related cognitive dimensions, has been less investigated

  • The two quantification methods concurred to indicate that the prefrontal cortex (PFC) displays highest reduction of correlated activity with the nucleus accumbens (NAc) (23% of NAc voxels corresponding to 449 NAc voxels overall)

  • We combined PFC seed-based functional connectivity (FC) analysis by MRI, operant self-administration procedure and Touchscreen-based autoshaping/5-CSRT tasks to investigate whether MORs regulate reward-driven motivated behavior, and related cognitive controls

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Summary

Introduction

While the contribution of Mu Opioid Receptors (MORs) to hedonic aspects of reward processing is well-established, the notion that these receptors may regulate motivation to gain a reward, and possibly other related cognitive dimensions, has been less investigated. MOR mutant mice showed normal transfer but reduced sensitivity to outcome devaluation, whereas the opposite was observed for DOR knockout mice, and local pharmacology using specific antagonists identified the nucleus accumbens (NAc) shell and core as main sites mediating these aspects of opioid-regulated incentive motivation[9]. These experiments provide evidence that opioid receptors, and MORs in particular, do more than just attributing hedonic values to rewards, and contribute to reward-guided decision making[10]. This observation supports the notion that MORs contribute to reward-driven motivation and action, as well as perhaps other aspects of executive controls involving the PFC12,13

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