4.2 Article

Differential Effects of Olanzapine and Haloperidol on MK-801-induced Memory Impairment in Mice

Journal

CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE
Volume 14, Issue 3, Pages 279-285

Publisher

KOREAN COLL NEUROPSYCHOPHARMACOLOGY
DOI: 10.9758/cpn.2016.14.3.279

Keywords

Olanzapine; Haloperidol; Memory; NMDA antagonist; Neurogenesis

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2015R1D1A3A01016360]
  2. National Research Foundation of Korea [2015R1D1A3A01016360] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Objective: We investigated the differential effects of the antipsychotic drugs olanzapine and haloperidol on MK-801-induced memory impairment and neurogenesis in mice. Methods: MK-801 (0,1 mg/kg) was administered 20 minutes prior to behavioral testing over 9 days. Beginning on the sixth day of MK-801 treatment, either olanzapine (0,05 mg/kg) or haloperidol (0,05 mg/kg) was administered 40 minutes prior to MK-801 for the final 4 days. Spatial memory performance was measured using a Morris water maze (MWM) test for 9 days (four trials/day). Immunohistochemistry with bromodeoxyuridine (BrdU) was used to identify newborn cells labeled in tissue sections from the dentate gyrus of the hippocampus. Results: MK-801 administration over 9 days significantly impaired memory performance in the MWM test compared to untreated controls (p<0.05) and these deficits were blocked by treatment with olanzapine (p<0.05) but not haloperidol. The administration of MK -801 also resulted in a decrease in the number of BrdU labeled cells in the dentate gyrus (28.6%; p<0.01), which was prevented by treatment with olanzapine (p<0.05) but not haloperidol. Conclusion: These results suggest that olanzapine has a protective effect against cognitive impairments induced by MK-801 in mice via the stimulating effects of neurogenesis.

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