Effects of nalfurafine on the reinforcing, thermal antinociceptive, and respiratory-depressant effects of oxycodone: modeling an abuse-deterrent opioid analgesic in rats

被引:41
作者
Townsend, E. Andrew [1 ,2 ]
Naylor, Jennifer E. [3 ]
Negus, S. Stevens [4 ]
Edwards, Shelley R. [5 ]
Qureshi, Hina N. [5 ]
McLendon, Hunter W. [6 ]
McCurdy, Christopher R. [7 ,8 ]
Kapanda, Coco N. [7 ]
do Carmo, Jussara M. [9 ]
da Silva, Fernanda S. [9 ]
Hall, John E. [9 ]
Sufka, Kenneth J. [10 ]
Freeman, Kevin B. [2 ]
机构
[1] Univ Mississippi, Med Ctr, Grad Program Neurosci, Jackson, MS 39216 USA
[2] Univ Mississippi, Med Ctr, Dept Psychiat & Human Behav, Jackson, MS 39216 USA
[3] US FDA, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[4] Virginia Commonwealth Univ, Dept Pharmacol & Toxicol, Richmond, VA USA
[5] Millsaps Coll, Jackson, MS 39210 USA
[6] Univ Mississippi, Med Ctr, Sch Med, Jackson, MS 39216 USA
[7] Univ Mississippi, Sch Pharm, Dept BioMol Sci, University, MS 38677 USA
[8] Univ Florida, Sch Pharm, Dept Med Chem, UF Translat Drug Dev Core, Gainesville, FL USA
[9] Univ Mississippi, Med Ctr, Deprtment Physiol & Biophys, Jackson, MS 39216 USA
[10] Univ Mississippi, Dept Psychol, University, MS 38677 USA
关键词
Abuse liability; Remitch; Plethysmography; RECEPTOR AGONIST; HEMODIALYSIS-PATIENTS; MORPHINE; COCAINE; MICE; HYDROCHLORIDE; ACTIVATION; LIABILITY; PRURITUS; EFFICACY;
D O I
10.1007/s00213-017-4652-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Strategies to reduce the misuse of mu opioid agonists are critically needed. Previous work has shown that kappa opioid agonists can diminish the abuse-related effects and augment the antinociceptive effects of mu agonists. However, use of traditional kappa agonists is limited by their dysphoric side effects. The current study examined the effects of nalfurafine, a clinically available atypical kappa agonist, on the reinforcing, thermal antinociceptive, and respiratory-depressant effects of oxycodone in male rats. To determine oxycodone/nalfurafine mixture proportions to be examined intravenously across procedures, a progressive ratio (PR) self-administration procedure compared the reinforcing effects of oxycodone (56 mu g/kg/inj) available alone or as a mixture with co-administered nalfurafine (0.32, 1, or 3.2 mu g/kg/inj), corresponding to oxycodone/nalfurafine proportions of 175:1, 56:1, and 18:1, respectively. Next, PR and thermal antinociception dose-effect functions were each determined for oxycodone, nalfurafine, and the same oxycodone/nalfurafine mixture proportions. Finally, the respiratory-depressant effects of equi-antinociceptive doses of oxycodone, nalfurafine, and the mixtures were compared. Nalfurafine decreased the reinforcing effects of oxycodone, and the 18:1 mixture did not function as a reinforcer. Oxycodone and nalfurafine each produced dose-dependent antinociception, and the mixtures produced additive antinociception. In addition, antinociceptive doses of the 56:1 and 18:1 mixtures did not produce respiratory depression. These results suggest that nalfurafine may augment the thermal antinociceptive effects while reducing the reinforcing and respiratory-depressant effects of oxycodone.
引用
收藏
页码:2597 / 2605
页数:9
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