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NMDA receptor antagonists ketamine and PCP have direct effects on the dopamine D2 and serotonin 5-HT2 receptors—implications for models of schizophrenia

Abstract

Ketamine and PCP are commonly used as selective NMDA receptor antagonists to model the putative hypoglutamate state of schizophrenia and to test new antipsychotics. Recent findings question the NMDA receptor selectivity of these agents. To examine this further, we measured the affinity of ketamine and PCP for the high-affinity states of the dopamine D2 and serotonin 5-HT2 receptor and found that ketamine shows very similar affinity at the NMDA receptor and D2 sites with a slightly lower affinity for 5-HT2 (0.5 μM, 0.5 μM and 15 μM respectively), while PCP shows similar affinity for the NMDA and 5-HT2 sites, with a slightly lower affinity for the D2 site (2 μM, 5 μM and 37 μM respectively). Further, ketamine and PCP in clinically relevant doses caused a significant increase in the incorporation of [35S]GTP-γ-S binding in CHO-cells expressing D2 receptors, which was prevented by raclopride, suggesting a partial agonist effect at the D2 receptor. Thus, ketamine and PCP may not produce a selective hypoglutamate state, but more likely produce a non-selective multi-system neurochemical perturbation via direct and indirect effects. These findings confound the inferences one can draw from the ketamine/PCP models of schizophrenia.

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Acknowledgements

We thank Dr H-C Guan for excellent assistance. We thank Professor HA Adams (Medizinische Hochschule Hannover, Germany) for donating a sample of S-ketamine. PS is a Janice Lieber Investigator of NARSAD and SK is supported by a Canada Research Chair in Schizophrenia and Therapeutic Neuroscience. This work was supported by NARSAD, the Ontario Mental Health Foundation, the Canadian Institutes for Health Research, the National Institute on Drug Abuse, the Stanley Foundation and by generous donations from Dr Karolina Jus and the Medland and O'Rorke families.

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Kapur, S., Seeman, P. NMDA receptor antagonists ketamine and PCP have direct effects on the dopamine D2 and serotonin 5-HT2 receptors—implications for models of schizophrenia. Mol Psychiatry 7, 837–844 (2002). https://doi.org/10.1038/sj.mp.4001093

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