4.3 Article

Combined administration of buprenorphine and naltrexone produces antidepressant-like effects in mice

Journal

JOURNAL OF PSYCHOPHARMACOLOGY
Volume 29, Issue 7, Pages 812-821

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/0269881115586937

Keywords

Depression; anxiety; kappa opioid receptor; kappa antagonist; mu agonist

Funding

  1. Government of Saudi Arabia
  2. Royal Society
  3. NIDA [DA07315]

Ask authors/readers for more resources

Opiates have been used historically for the treatment of depression. Renewed interest in the use of opiates as antidepressants has focused on the development of kappa opioid receptor (-receptor) antagonists. Buprenorphine acts as a partial mu-opioid receptor agonist and a -receptor antagonist. By combining buprenorphine with the opioid antagonist naltrexone, the activation of mu-opioid receptors will be reduced and the -antagonist properties enhanced. We have established that a combination dose of buprenorphine (1 mg/kg) with naltrexone (1 mg/kg) functions as a short-acting -antagonist in the mouse tail withdrawal test. Furthermore, this dose combination is neither rewarding nor aversive in the conditioned place preference paradigm, and is without significant locomotor effects. We have shown for the first time that systemic co-administration of buprenorphine (1 mg/kg) with naltrexone (1 mg/kg) in CD-1 mice produced an antidepressant-like response in behaviours in both the forced swim test and novelty induced hypophagia task. Behaviours in the elevated plus maze and light dark box were not significantly altered by treatment with buprenorphine alone, or in combination with naltrexone. We propose that the combination of buprenorphine with naltrexone represents a novel, and potentially a readily translatable approach, to the treatment of depression.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available