Varying responses to the rat forced-swim test under diurnal and nocturnal conditions

Author(s): Connor, T. J., Harkin, A., Sanchez, C., Kelly, J. P., Leonard, B. E.

Journal/Book: Physiol Behav. 2000; 69: the Boulevard Langford Lane, Kidlington, Oxford Ox5 1GB, England. Pergamon-Elsevier Science Ltd. 531-539.

Abstract: The paradox that experiments in behavioural pharmacology employing nocturnal rodent species are carried out almost exclusively in the resting phase of the animals' circadian cycle has remained largely unexamined and unquestioned. This is despite the: fact that all major physiological systems in the body are intrinsically aligned with its natural circadian rhythm. The forced-swim test (FST) is a rodent model that is used extensively as a screening test for antidepressant activity. The objectives of the present study were to examine the behaviour of rats in the FST under diurnal and nocturnal conditions and, in addition, to profile the response of neurochemical. Neuroendocrine, and cellular indices of stress at time points up to 120 min following exposure to the FST. The time spent in escape-oriented activity was significantly Ices: when animals were tested in the dark phase. The profile of serum corticosterone and adrenal ascorbic acid concentrations indicates that the animals were less stressed by the test situation juring the active (i.e., dark) phase of their circadian cycle. Similarly, increases in blood enzymatic markers of stress-induced cellular damage were less marked following FST exposure in the nocturnal period. Characteristic stress-induced increases in 5-HT turnover in the frontal cortex and amygdala observed in the diurnal phase were reversed in the nocturnal period. In conclusion, circadian differences in behaviour in the FST may be related to parallel alterations in the ability of animals to adapt to exposure to stress.

Note: Article Connor TJ, Natl Univ Ireland Univ Coll Galway, Dept Pharmacol, Galway, IRELAND

Keyword(s): behaviour; circadian; diurnal; endocrine; forced-swim test; immobility; nocturnal; rat; serotonin; stress; PINEAL MELATONIN SYNTHESIS; IN-VIVO MICRODIALYSIS; PSYCHOLOGICAL STRESS; BEHAVIORAL DESPAIR; CIRCADIAN-RHYTHMS; IMMUNE CHANGES; BRAIN; RELEASE; CYCLE; HYPERGLYCEMIA

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