Abstract

RationaleAbnormal oscillatory activity associated with N-methyl-D-aspartate (NMDA) receptor hypofunction is widely considered to contribute to the symptoms of schizophrenia.ObjectiveThis study aims to characterise the changes produced by NMDA receptor antagonists and antipsychotics on accumbal high-frequency oscillations (HFO; 130–180 Hz) in mice.MethodsLocal field potentials were recorded from the nucleus accumbens of freely moving mice.ResultsSystemic injection of ketamine and MK801 both dose-dependently increased the power of HFO and produced small increases in HFO frequency. The atypical antipsychotic drug, clozapine, produced a robust dose-dependent reduction in the frequency of MK801-enhanced HFO, whilst haloperidol, a typical antipsychotic drug, had little effect. Stimulation of NMDA receptors (directly or through the glycine site) as well as activation of 5-HT1A receptors, reduced the frequency of MK801-enhanced HFO, but other receptors known to be targets for clozapine, namely 5-HT2A, 5-HT7 and histamine H3 receptors had no effect.ConclusionsNMDA receptor antagonists and antipsychotics produce broadly similar fundamental effects on HFO, as reported previously for rats, but we did observe several notable differences. In mice, HFO at baseline were weak or not detectable unlike rats. Post-injection of NMDA receptor antagonists HFO was also weaker but significantly faster. Additionally, we found that atypical antipsychotic drugs may reduce the frequency of HFO by interacting with NMDA and/or 5-HT1A receptors.Electronic supplementary materialThe online version of this article (doi:10.1007/s00213-015-4073-0) contains supplementary material, which is available to authorized users.

Highlights

  • N-methyl-D-aspartate (NMDA) receptor hypofunction has been proposed to contribute to the symptoms of schizophrenia

  • We found that atypical antipsychotic drugs may reduce the frequency of high-frequency oscillations (HFO) by interacting with NMDA and/ or 5-HT1A receptors

  • Power spectra analysis of LFP recorded in the mouse nucleus accumbens (NAc) revealed the occurrence of weak spontaneous HFO (130– 180 Hz) in some, but not all mice

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Summary

Introduction

N-methyl-D-aspartate (NMDA) receptor hypofunction has been proposed to contribute to the symptoms of schizophrenia. Acute administration of NMDA receptor antagonists produces transient psychosis-like activity in healthy humans and exacerbates the pre-existing symptoms in stabilised schizophrenic individuals (Krystal et al 1994; Lahti et al 1995). This suggests that NMDA receptor antagonists can interact with neuronal networks that mediate psychosis. Acute application of NMDA receptor antagonists is known to influence oscillations recorded in LFP (Ma and Leung 2000; Psychopharmacology (2015) 232:4525–4535

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