Abstract
It is known that chronic high levels of corticosterone (CORT) enhance aversive responses such as avoidance and contextual freezing. In contrast, chronic CORT does not alter defensive behavior induced by the exposure to a predator odor. Since different defense-related responses have been associated with specific anxiety disorders found in clinical settings, the observation that chronic CORT alters some defensive behaviors but not others might be relevant to the understanding of the neurobiology of anxiety. In the present study, we investigated the effects of chronic CORT administration (through surgical implantation of a 21-day release 200 mg pellet) on avoidance acquisition and escape expression by male Wistar rats (200 g in weight at the beginning of the experiments, N = 6-10/group) tested in the elevated T-maze (ETM). These defensive behaviors have been associated with generalized anxiety and panic disorder, respectively. Since the tricyclic antidepressant imipramine is successfully used to treat both conditions, the effects of combined treatment with chronic imipramine (15 mg, ip) and CORT were also investigated. Results showed that chronic CORT facilitated avoidance performance, an anxiogenic-like effect (P < 0.05), without changing escape responses. Imipramine significantly reversed the anxiogenic effect of CORT (P < 0.05), although the drug did not exhibit anxiolytic effects by itself. Confirming previous observations, imipramine inhibited escape responses, a panicolytic-like effect. Unlike chronic CORT, imipramine also decreased locomotor activity in an open field. These data suggest that chronic CORT specifically altered ETM avoidance, a fact that should be relevant to a better understanding of the physiopathology of generalized anxiety and panic disorder.
Highlights
It has been shown that short-term glucocorticoid secretion is essential for the maintenance of several behavioral events, and crucial for the expression of fear/anxiety responses [1,2,3]
In order to better understand how CORT administration alters defensive responses related to anxiety disorders found in clinical settings, in the present study we investigated the effects of chronic CORT (200 mg pellets, 21-day release) on avoidance acquisition and escape expression by male Wistar rats tested in the elevated T-maze (ETM) [8]
Three-factor ANOVA showed a significant effect of trials [F(2,58) = 27.15; P < 0.001], CORT [F(1,29) = 5.10; P < 0.05], imipramine [F(1,29) = 11.53; P < 0.001], and CORT by imipramine interaction [F(1,29) = 9.78; P < 0.001]
Summary
It has been shown that short-term glucocorticoid secretion is essential for the maintenance of several behavioral events, and crucial for the expression of fear/anxiety responses [1,2,3]. Clinical observations suggest that chronic high levels of glucocorticoids, which are most often a result of prolonged stress, lead to maladaptive anxiety and/or depressive disorders [3]. A number of experimental studies have demonstrated the anxiogenic effects of the exogenous administration of glucocorticoids. It has been observed, for instance, that post-training injections of corticosterone (CORT) enhance the animals’ performance in several aversive tasks, facilitating responses such as inhibitory avoidance and contextual freezing [2]. Chronic CORT does not alter defensive behavior induced by an innate fear stimulus, i.e., exposure to a predator odor [4]
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