TY - JOUR T1 - Discriminative Stimulus Effects of the Mixed-Opioid Agonist/Antagonist Dezocine: Cross-Substitution by <em>Mu</em>and <em>Delta</em> Opioid Agonists JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 1009 LP - 1017 VL - 283 IS - 3 AU - Mitchell J. Picker Y1 - 1997/12/01 UR - http://jpet.aspetjournals.org/content/283/3/1009.abstract N2 - The purpose of this investigation was to evaluate the discriminative stimulus effects of the mixed-opioid agonist/antagonist dezocine. In pigeons trained to discriminate 1.7 mg/kg dezocine from saline, a series of opioids with activity at the mu opioid receptor substituted completely for the dezocine stimulus with a rank order of potency similar to that obtained in other assays sensitive to the effects of mu agonists (i.e., fentanyl &gt;[-]-cyclazocine &gt;buprenorphine = butorphanol &gt;l-methadone &gt;nalbuphine &gt;[-]-metazocine &gt;morphine). (-)-N-allylnormetazocine and (+)-propoxyphene substituted partially for the dezocine stimulus, an effect obtained even when tested up to doses that suppressed responding. Naloxone (0.1 - 10 mg/kg) antagonized the stimulus effects of dezocine, (+)-propoxyphene and fentanyl in a dose-related manner, whereas doses of naloxone that antagonized fentanyl’s rate-decreasing effects failed to antagonize the rate-decreasing effects of dezocine and (+)-propoxyphene. A 10-mg/kg dose of the mu-selective, noncompetitive antagonist β-funaltrexamine was more effective against the stimulus effects of dezocine and nalbuphine than against morphine and fentanyl. As was observed with naloxone, β-funaltrexamine failed to antagonize dezocine’s rate-decreasing effects. The delta agonists BW373U86 and SNC80 substituted partially for the dezocine stimulus, and these effects were reversed by doses of the delta-selective antagonist naltrindole (0.1 and 1.0 mg/kg) that had no effect on the dezocine stimulus. Naltrindole also antagonized the rate-decreasing effects produced by BW373U86 and SNC80, but not those of dezocine. Thekappa agonists bremazocine, spiradoline, U50,488 and U69,593 failed to substitute for the dezocine stimulus. Thekappa-selective antagonist norbinaltorphimine (1.0 mg/kg) failed to antagonize dezocine’s stimulus or rate-decreasing effects. The present findings indicate that dezocine shares similar stimulus effects with both mu and deltaagonists, its stimulus effects are reversed bymu-selective antagonists, and its rate-decreasing effects are not mediated by activity at mu,kappa or delta opioid receptors. The American Society for Pharmacology and Experimental Therapeutics ER -