Antipsychotic-like profile of CIQ isomers in animal models of schizophrenia

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Abstract

Earlier, we have shown the efficacy of racemic (±) CIQ, a positive allosteric modulator of GluN2C/2D receptor against MK-801 induced impairment of prepulse inhibition as well as working memory. The present study investigated the antipsychotic-like profile of different CIQ (±, +,-) isomers against schizophrenia-like symptoms in series of behavioural animal models like apomorphine climbing, social isolation behaviour and NMDA receptor antagonist MK-801 induced cognitive deficits. Further, we also tested CIQ (±, +,-) isomers in neurodevelopmental model against MK-801induced deficits using open field test, Y-maze test and novel object recognition test. CIQ (±, +,-) isomers decreased climbing behaviour, increased social interaction and improved the MK-801 induced deficits in working memory in Y-maze. Further, CIQ (±, +) but not CIQ (-) improved the recognition memory in novel object recognition test as well as reduced hyperlocomotion and stereotyped behaviour. We conclude that CIQ (±, +) but not CIQ (-) exhibit the significant antipsychotic-like profile.

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Gawai, P., Upadhyay, R., Gakare, S. G., Sarode, L., Dravid, S. M., & Ugale, R. R. (2020). Antipsychotic-like profile of CIQ isomers in animal models of schizophrenia. Behavioural Pharmacology, 31(6), 524–534. https://doi.org/10.1097/FBP.0000000000000532

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