Abstract

The purpose of our experiment was to examine the influence of co-administration of nicotine and mephedrone on anxiety-like behaviors, cognitive processes and the nicotine-induced behavioral sensitization as well as processes connected with induction of oxidative stress in the brain of male Swiss mice. The results revealed that co-administration of subthreshold doses of mephedrone and nicotine (0.05 mg/kg each) exerted marked anxiogenic profile in the elevated plus maze and displayed pro-cognitive action in the passive avoidance paradigm (nicotine 0.05 mg/kg and mephedrone 2.5 mg/kg). Furthermore, one of the main findings of the present study was that mephedrone, administered alone at the dose not affecting locomotor activity of mice (1 mg/kg), enhanced the expression of nicotine-induced locomotor sensitization. Moreover, mephedrone administered with nicotine decreased general antioxidant status and catalase activity as well as antioxidant enzymes activity in the hippocampus and prefrontal cortex and increased concentration of malondialdehyde, an indicator of lipid peroxidation processes. Considering the likelihood that mephedrone is taken as a part of polydrug combination with nicotine, the effects of this combination on mammalian organisms have been confirmed in our study. Understanding the consequences of co-administration of psychoactive substances on the central nervous system and oxidative processes in the brain provide the important toxicological significance, and may be useful in polydrug intoxication treatment. Electronic supplementary materialThe online version of this article (doi:10.1007/s11064-015-1566-5) contains supplementary material, which is available to authorized users.

Highlights

  • The purpose of our experiment was to examine the influence of co-administration of nicotine and mephedrone on anxiety-like behaviors, cognitive processes and the nicotine-induced behavioral sensitization as well as processes connected with induction of oxidative stress in the brain of male Swiss mice

  • The results revealed that coadministration of subthreshold doses of mephedrone and nicotine (0.05 mg/kg each) exerted marked anxiogenic profile in the elevated plus maze and displayed pro-cognitive action in the passive avoidance paradigm

  • Our results showed that animals treated with mephedrone and nicotine at the subthreshold doses demonstrated elevated level of anxiety in the elevated plus maze (EPM) test and displayed procognitive behaviors in the passive avoidance (PA) paradigm

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Summary

Introduction

The purpose of our experiment was to examine the influence of co-administration of nicotine and mephedrone on anxiety-like behaviors, cognitive processes and the nicotine-induced behavioral sensitization as well as processes connected with induction of oxidative stress in the brain of male Swiss mice. One of the main findings of the present study was that mephedrone, administered alone at the dose not affecting locomotor activity of mice (1 mg/kg), enhanced the expression of nicotine-induced locomotor sensitization. Legal highs or club drugs, various kinds of products containing psychoactive substances, were often taken as a part of the nightclub scene with alcohol, marijuana or amphetamines. This work was extended by the finding that mephedrone causes a rapid decrease in striatal DA and hippocampal 5-HT transporters function Mephedrone inhibits both synaptosomal DA and 5-HT uptake [5]. It is well established that psychostimulant drugs, including amphetamines or cocaine, have been found to exert potent neurotoxic effects due to their ability to increase the formation of reactive oxygen and nitrogen species (ROS and RNS) as well as intensification of lipids peroxidation processes [11]. The effects of nicotine have been extensively investigated in humans, and in animals and several cell systems [19,20,21,22,23,24]

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