Prior and delayed applications of dizocilpine or ethanol alter locomotor sensitization to morphine

Abstract

Three experiments compared the effects of prior versus delayed applications of dizocilpine (MK-801), a noncompetitive NMDA antagonist, to ethanol, a putative NMDA antagonist, on morphine locomotor activity. In Experiment 1, rats received MK-801 (0.1 mg/kg), ethanol (1 g/kg), or vehicle injections 30 min prior to morphine (0 or 10 mg/kg) injections for 14 days. The expression of morphine (0 or 3 mg/kg) locomotor sensitization was assessed 1 week later. Both MK-801 and ethanol attenuated morphine-induced locomotor activity. Chronic MK-801 with or without morphine eliminated morphine’s temporal pattern of activity calling into question the specificity of its effect on sensitization. In contrast, chronic ethanol administration attenuated morphine locomotor sensitization. In Experiment 2, the effects of the agents on the acute biphasic locomotor effects of morphine (hypoactivity followed by hyperactivity) were examined. Agents were administered 30 min prior to or 120 min after morphine (or vehicle). Neither agent at either administration time altered morphine’s acute locomotor effects. In Experiment 3, the effects of chronic delayed application of MK-801 or ethanol (120-min post-morphine administration for 14 days) on the expression of morphine locomotor sensitization were assessed. Results were similar to the prior application effects of Experiment 1. These data suggest that the delayed effects of morphine are important in changes seen with chronic administration and these may involve NMDA receptor activation. Further, in conjunction with our previous work, ethanol appears to alter plasticity effects of chronic morphine administration perhaps via its NMDA antagonist effects.