Selective modulation of the glucocorticoid receptor with CORT108297 during chronic adolescent stress evokes sex specific effects in adulthood.
Adolescent animals are vulnerable to the effects of stress on brain development. We hypothesized that long-term effects of adolescent chronic stress are mediated by glucocorticoid receptor (GR) signaling. We used a specific GR modulator (CORT108297) to pharmacologically disrupt GR signaling in adolescent rats during exposure chronic variable stress (CVS). Male and female rats received 30mg/kg of drug concomitantly with a 2-week CVS protocol starting at PND46. Emotional reactivity (open field) and coping behaviors (forced swim test (FST)) were then tested in adulthood, 5 weeks after the end of the CVS protocol. Blood samples were collected two days before FST and serial samples after the onset of the swim test to determine baseline and stress response levels of HPA hormones respectively.\n\nOur results support differential behavioral, physiological and stress circuit reactivity to adolescent chronic stress exposure in males vs. females, with variable involvement of GR signaling. In response to adolescent stress, males had heightened reactivity to novelty and exhibited marked reduction in neuronal excitation following swim stress in adulthood, whereas females developed a passive coping strategy and enhanced HPA axis stress reactivity. Only the latter effect was attenuated by treatment with the GR modulator C108297. Our data suggest that adolescent stress differentially affects emotional behavior and circuit development in females, and that GR plays a role in driving some but not all sequelae of adolescent stress.