Abstract

Cocaine dependence is a psychiatric condition for which effective medications are still lacking. Published data indicate that an increase in nociceptin/orphanin FQ (N/OFQ) transmission by NOP receptor activation attenuates cocaine-induced place conditioning and the locomotor sensitization effects of cocaine. This suggests that the activation of the N/OFQ receptor (NOP) may attenuate the motivation for psychostimulants. To further explore this possibility, we investigated the effect of the potent and selective NOP receptor agonist Ro 64-6198 on cocaine intake under 1 h short access (ShA) and 6 h long access (LgA) operant self-administration conditions in rats. We used Marchigian Sardinian alcohol-preferring (msP) rats and Wistar control rats. msP rats were used because we recently found that this rat line, originally selected for excessive alcohol drinking and preference, exhibits a greater propensity to escalate cocaine self-administration following LgA training. msP rats are also characterized by innate overexpression of the N/OFQ-NOP system compared with Wistar rats. Wistar and msP rats both exhibited an increase in cocaine self-administration under LgA conditions, with a higher trend toward escalation in msP rats. In Wistar rats, the intraperitoneal administration of Ro 64-6198 (0. 1 and 3 mg/kg) significantly decreased ShA cocaine self-administration. In Wistar rats that underwent LgA cocaine self-administration training, Ro 64-6198 induced no significant effect either during the first hour of self-administration or after the entire 6 h session. In msP rats, Ro 64-6198 significantly reduced cocaine self-administration both under ShA conditions and in the first hour of the LgA session. At the end of the 6 h session, the effect of Ro 64-6198 was no longer observed in msP rats. The highest dose of Ro 64-6198 (3 mg/kg) did not affect saccharin self-administration in msP rats but reduced saccharin self-administration in Wistar rats. Altogether, these data suggest that NOP receptor activation attenuates cocaine self-administration, and this effect tends to be more pronounced in a rat line with innately higher NOP receptor expression and that more robustly escalates cocaine intake.

Highlights

  • Cocaine is the most commonly abusedillicit psychostimulant, and its use is linked to serious physical, psychiatric, socioeconomic, and legal problems [1]

  • We recently found that Marchigian Sardinian alcohol-preferring (msP) rats exhibited alterations of functional magnetic resonance imaging activity and an increase in nucleus accumbens dopamine release in response to an amphetamine challenge compared with Wistar rats. msP rats exhibited a higher propensity to escalate cocaine intake under extended access (6 h/day) self-administration conditions [5]

  • The present study found that cocaine intake was similar in Wistar and msP rats under short access (ShA) self-administration conditions, but Wistar rats received a slightly higher number of infusions

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Summary

Introduction

Cocaine is the most commonly abusedillicit psychostimulant, and its use is linked to serious physical, psychiatric, socioeconomic, and legal problems [1]. We recently found that Marchigian Sardinian alcohol-preferring (msP) rats, which are genetically selected for excessive alcohol drinking and preference, exhibit neurophysiological and pharmacological traits that confer a predisposition to psychostimulant abuse [5]. MsP rats are characterized by inherited neurophysiological adaptations of several neurotransmitter systems that may contribute to their vulnerable phenotype [6,7,8]. One such system consists of nociceptin/orphanin-FQ (N/OFQ) peptide and its NOP receptor, known for being structurally similar to dynorphin A and kappa opioid, respectively [9, 10]. The activation of NOP receptors has been shown to attenuate the motivation for various drugs of abuse [11,12,13,14,15,16,17,18]

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