The neuropeptide oxytocin facilitates pro-social behavior and prevents social avoidance in rodents
Résumé
Social avoidance and social phobia are core symptoms of various psychopathologies but their underlying aetiology remains poorly understood. Therefore, this study aims to reveal pro-social effects of the neuropeptide oxytocin, under both basal and stress-induced social avoidance conditions in rodents using a social-preference paradigm. We initially show that intracerebroventricular (icv) application of an oxytocin receptor antagonist (OTR-A) in naïve male rats (0.75µg/5µl) or mice (20µg/2µl) reduced social exploration of a novel con-specific indicative of attenuated social preference. Prior exposure of male rats to a single social defeat resulted in loss of their social preference and social avoidance, which could be restored by icv infusion of synthetic oxytocin (0.1µg/5µl) 10 min prior to the social preference test. The amygdala has been implicated in both social and oxytocin-mediated actions, but bilateral OTR-A (0.1 µg/1µl) or oxytocin (OT; 0.01 µg/1µl) administration into various subnuclei of the amygdala did not affect basal or stress-induced social preference behavior, respectively. Finally, we demonstrate the social specificity of these OT-mediated effects by showing that neither an arginine vasopressin V1a receptor antagonist (0.75µg/5µl, icv) nor the anxiogenic drug pentylenetetrazol (15mg/kg, i.p.) altered social preference while OTR-A did not affect state anxiety. Overall, the data indicate that the basal activity of the endogenous brain oxytocin system is sufficient to promote pro-social behavior in rodents while synthetic oxytocin shows potential to reverse stress-induced social avoidance and might support treatment of social phobia and social dysfunction in humans.
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