The circadian glucocorticoid rhythm provides important information on the functioning of the hypothalamicpituitary-adrenal axis in individuals. Frequent repeated blood sampling can limit the kinds of studies conducted on this rhythm, particularly in small laboratory rodents that have limited blood volumes and are easily stressed by handling. We developed an extraction and assay protocol to measure fecal corticosterone metabolites in repeated samples collected from undisturbed male and female adult Sprague-Dawley rats. This fecal measure provides a noninvasive method to assess changes in corticosterone within a single animal over time, with sufficient temporal acuity to quantify several characteristics of the circadian rhythm: e.g. the nadir, acrophase, and asymmetry (saw-tooth) of the rhythm. Males excreted more immunoreactive fecal corticoids than did females. Across the estrous cycle, females produced more fecal corticoids on proestrus (the day of the preovulatory luteinizing hormone surge) than during estrus or metestrus. These results establish a baseline from which to study environmental, psychological, and physiological disturbances of the circadian corticosterone rhythm within individual rats.

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In the túngara frog, Physalaemus pustulosus, males alter calling behavior with changes in their social environment, adding ‘chucks’ to their advertisement calls in response to the calls of conspecific males. Other studies demonstrate that adding chucks increases the attractiveness of calls to females but also increases the risk of bat predation. In the current study, subcutaneous injections of the neuropeptide hormone arginine vasotocin (AVT) significantly increased chuck production in male túngara frogs. The effects of AVT on chuck production did not depend on the presence of playback stimuli, suggesting that AVT increased either the males’ general motivation to produce chucks or their responsiveness to the calls of distant males. Injections of AVT also increased the probability that males would call and decreased the latency to call after injection, supporting the hypothesis that AVT influences motivation to call. Finally, AVT inhibited a drop in call rate after the termination of a playback stimulus and increased call rate at a lower dose of AVT. The effects of AVT on chucks and call rate appear to be independent of each other, as there was no correlation between change in chuck production and change in call rate in individual males. We conclude that AVT may play an important role in socially-mediated call changes that result from competition for mates. The behavioral changes induced by AVT might increase a male’s attractiveness to females, and also may be consistent with an aggressive response to another túngara frog male.

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