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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Authors | Pushparaj Gawai, Rohit Upadhyay, Sukanya G Gakare, Lopmudra Sarode, Shashank M Dravid, Rajesh R Ugale |
Journal | Behavioural pharmacology
(Behav Pharmacol)
Vol. 31
Issue 6
Pg. 524-534
(09 2020)
ISSN: 1473-5849 [Electronic] England |
PMID | 31860561
(Publication Type: Journal Article)
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Chemical References |
- Antipsychotic Agents
- NR2C NMDA receptor
- NR2D NMDA receptor
- Receptors, N-Methyl-D-Aspartate
- Dizocilpine Maleate
- Apomorphine
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Topics |
- Animals
- Antipsychotic Agents
(pharmacology)
- Apomorphine
(pharmacology)
- Disease Models, Animal
- Dizocilpine Maleate
(pharmacology)
- Male
- Maze Learning
- Mice
- Receptors, N-Methyl-D-Aspartate
(drug effects)
- Schizophrenia
(drug therapy)
- Social Interaction
(drug effects)
- Stereoisomerism
- Stereotyped Behavior
(drug effects)
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