Dexmedetomidine induces conditioned place preference in rats: Involvement of opioid receptors

Uskur T., Barlas M. A., Akkan A. G., Shahzadi A., Uzbay T.

BEHAVIOURAL BRAIN RESEARCH, vol.296, pp.163-168, 2016 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 296
  • Publication Date: 2016
  • Doi Number: 10.1016/j.bbr.2015.09.017
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.163-168
  • Istanbul University Affiliated: Yes


Dexmedetomidine (DEX) is an alpha-2 adrenergic agonist drug recently introduced to anesthesia practice. Certain agents used in anesthesia practice have been associated with abuse and addiction problems; however, few studies have investigated the role of DEX on addictive processes. Here, the effects and possible mechanisms of action of DEX on conditioned place preference (CPP), a model used for measuring the rewarding effects of drug abuse in rats, was investigated. The CPP apparatus was considered "biased" as the animals preferred the grid side to the mesh side. Male Wistar albino rats weighing 250-300 g were divided into several groups, including control (saline), morphine (10 mg/kg), DEX (2.5-20 mu g/kg), naloxone alone (0.5 mg/kg) and a combination (0.5 mg/kg naloxone plus 20 mu g/kg DEX) (n=7-8 for each group). The CPP effects of morphine, DEX, saline and the combination were evaluated. All the drug and saline administrations except naloxone were performed by intraperitoneal (ip) injections. Naloxone was injected subcutaneously (Sc) when given alone or in combination with DEX. Morphine (10 mg/kg) and DEX (5-20 mu g/kg) produced CPP that were statistically significant relative to saline-injected rats. DEX-induced CPP was significantly reversed by pretreatment with naloxone, an opioid antagonist. Naloxone alone treatment did not cause any significant effect on CPP. Our results suggest that DEX produces CPP effects similar to morphine in rats and that opioidergic mechanism may be responsible for DEX-induced CPP. Thus, DEX might have the potential to be addictive, and this possibility should be considered during clinical application of this drug. (C) 2015 Elsevier B.V. All rights reserved.