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Acta Physiologica 2011; Volume 203, Supplement 686
Joint Congress of FEPS and Turkish Society of Physiological Sciences
9/3/2011-9/7/2011
Istanbul, Turkey
THE EFFECT OF CITALOPRAM, A SELECTIVE SEROTONIN REUPTAKE INHIBITOR, ON MEMORY ALTERATIONS INDUCED BY SELECTIVE RAPID EYE MOVEMENT SLEEP DEPRIVATION IN RATS
Abstract number: PC090
Aricanli1 Nurcan, Hakan Karadag1 Çetin, Oztrk2 Levent
1Department of Pharmacology Trakya University Faculty of Medicine, Edirne, TURKEY
2Department of Physiology Trakya University Faculty of Medicine, Edirne, TURKEY
Objective:
We aimed to investigate the effects of citalopram, a selective serotonin reuptake inhibitor, on memory alterations induced by selective rapid eye movement (REM) sleep deprivation.
Methods:
Sixty male Wistar albino rats (average weight, 200 300g) were equally divided into five groups: Group 1 (n=12) normal sleep + placebo (%0.9 NaCl); Group 2 (n=12) REM sleep deprivation by modified platform technique + placebo; Group 3, 4, and 5 (for each n= 12) REM sleep deprivation and 5, 10, and 20 mg/kg single dose citalopram, respectively. All the study groups, except Group 1, underwent REM sleep deprivation between the 1st -13th days of the study. Drug interventions were applied between the 8th 13th days of the study. The rats were trained 4 times daily between Day 8 and Day 12 of the study (acquisition phase). At the 13th day, the platform was removed, and the probe test was performed for 30 seconds (retrieval).
Results:
REM sleep deprivation led to statistically significant impairments in various learning parameters (p<0.05), and increased thigmotaxis (p<0.001); these impairments were not seen in citalopram groups. However, a dose-response relationship was not found in the effects of citalopram. In probe trials, REM sleep deprivation did not cause any significant impairment.
Conclusions:
REM sleep deprivation retards learning by increasing thigmotaxis and the negative effects of REM sleep deprivation on learning may be prevented by citalopram.
To cite this abstract, please use the following information:
Acta Physiologica 2011; Volume 203, Supplement 686 :PC090