DOI: 10.1007/s12640-017-9718-9 Pages: 121-133
Article Type: ORIGINAL ARTICLE

Suppression of Methamphetamine Self-Administration by Ketamine Pre-treatment Is Absent in the Methylazoxymethanol (MAM) Rat Model of Schizophrenia

1. Masaryk University, Department of Pharmacology, Faculty of Medicine

2. Masaryk University, CEITEC - Central European Institute of Technology

3. University of Catania, Department of Biomedical and Biotechnological Sciences, Section of Pharmacology, School of Medicine

Correspondence to:
Jana Ruda-Kucerova
Tel: +420 549 494 238
Email: jkucer@med.muni.cz

Close

Abstract

Ketamine may prove to be a potential candidate in treating the widespread drug addiction/substance abuse epidemic among patients with schizophrenia. Clinical studies have shown ketamine to reduce cocaine and heroin cravings. However, the use of ketamine remains controversial as it may exacerbate the symptoms of schizophrenia. Therefore, the aim of this study is to characterize the effects of ketamine on drug addiction in schizophrenia using the methylazoxymethanol (MAM) acetate rat model on operant IV methamphetamine (METH) self-administration. MAM was administered intraperitoneally (22 mg/kg) on gestational day 17. Locomotor activity test and later IV self-administration (IVSA) were then performed in the male offspring followed by a period of forced abstinence and relapse of METH taking. After reaching stable intakes in the relapse phase, ketamine (5 mg/kg) was administered intraperitoneally 30 min prior to the self-administration session. As documented previously, the MAM rats showed a lack of habituation in the locomotor activity test but developed stable maintenance of METH self-administration with no difference in operant behaviour to control animals. Results show that ketamine treatment significantly reduced the METH intake in the control animals but not in MAM animals. Ketamine effect on METH self-administration may be explained by increased glutamatergic signalling in the prefrontal cortex caused by the N-methyl-D-aspartate antagonism and disinhibition of GABA interneurons which was shown to be impaired in the MAM rats. This mechanism may at least partly explain the clinically proven anti-craving potential of ketamine and allow development of more specific anti-craving medications with fewer risks.

To access the full text, please Sign in

If you have institutional access, please click here

  • Accepted: Mar 1, 2017
  • Online: Apr 18, 2017
  • Revised: Feb 22, 2017

Article Tools