Abstract

Metabotropic glutamate subtype 5 (mGlu5) receptors are implicated in various forms of synaptic plasticity, including drugs of abuse. In drug-addicted individuals, associative memories can drive relapse to drug use. The present study investigated the potential of the mGlu5 receptor positive allosteric modulator (PAM), VU-29 (30 mg/kg, i.p.), to inhibit the maintenance of a learned association between ethanol and environmental context by using conditioned place preference (CPP) in rats. The ethanol-CPP was established by the administration of ethanol (1.0 g/kg, i.p. ×10 days) using an unbiased procedure. Following ethanol conditioning, VU-29 was administered at various post-conditioning times (ethanol free state at the home cage) to ascertain if there was a temporal window during which VU-29 would be effective. Our experiments indicated that VU-29 did not affect the expression of ethanol-induced CPP when it was given over two post-conditioning days. However, the expression of ethanol-CPP was inhibited by 10-day home cage administration of VU-29, but not by first 2-day or last 2-day injection of VU-29 during the 10-day period. These findings reveal that VU-29 can inhibit the maintenance of ethanol-induced CPP, and that treatment duration contributes to this effect of VU-29. Furthermore, VU-29 effect was reversed by pretreatment with either MTEP (the mGlu5 receptor antagonist), or MK-801 (the N-methyl-D-aspartate-NMDA receptor antagonist). Thus, the inhibitory effect of VU-29 is dependent on the functional interaction between mGlu5 and NMDA receptors. Because a reduction in ethanol-associated cues can reduce relapse, mGlu5 receptor PAM would be useful for therapy of alcoholism. Future research is required to confirm the current findings.

Highlights

  • Addiction to ethanol and other drugs of abuse results in part from exceptionally strong, maladaptive associations formed between contextual cues and the rewarding properties of the drug [1,2,3]

  • Our study revealed that the Metabotropic glutamate subtype 5 (mGlu5) receptor positive allosteric modulator (PAM), VU-29 administered to rats in the neutral environment of the home cage, was sufficient to diminish the previously expressed preference for the ethanol-paired chamber

  • A important observation is that mGlu5 PAM modulation with VU-29 attenuated maladaptive memories involved in ethanol relapse following withdrawal, and that this VU-29 effect is dependent on the time of its administration

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Summary

Introduction

Addiction to ethanol and other drugs of abuse results in part from exceptionally strong, maladaptive associations formed between contextual cues and the rewarding properties of the drug [1,2,3] These drug-associated contextual memories are long lasting, highly resistant to extinction, and contribute to the high rate of relapse in ethanol-dependent individuals, as well as the reinstatement of ethanol-seeking behavior [4,5,6,7,8]. Extinction is usually performed either by administering injections of a vehicle in both the original drug-paired and the original vehicle-paired chambers or by repeating CPP tests until preference is no longer observed. Such a procedure should facilitate the extinction of cue–drug memories to reduce relapse [15]

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