Maternal separation modulates short-term behavioral and physiological indices of the stress response

Abstract Early-life stress produces an anxiogenic profile in adulthood, presumably by activating the otherwise quiescent hypothalamic–pituitary–adrenal (HPA) axis during the vulnerable ‘stress hyporesponsive period’. While the long-term effects of such early-life manipulations have been extensively characterized, little is known of the short-term effects. Here, we compared the short-term effects of two durations of maternal separation stress and one unseparated group (US) on behavioral and physiological indices of the stress response in rat pups. Separations included 3 h on each of 12 days, from postnatal day (PND) 2 to 13 (MS2–13) and 3 days of daily, 6-h separation from PND11–13 (MS11–13). On PND14 (Experiment 1), both MS2–13 and MS11–13 produced marked reductions in freezing toward an adult male conspecific along with reduced levels of glucocorticoid type 2 (GR) and CRF type-1 (CRF 1 ) receptor mRNA in the hippocampus. Group MS2–13 but not MS11–13 produced deficits in stressor-induced corticosterone secretion, accompanied by reductions in body weight. Our results suggest that GR and/or CRF 1 levels, not solely the magnitude of corticosterone secretion, may be involved in the modulation of freezing. In a second experiment, we aimed to extend these findings by testing male and female separated and unseparated pups' unconditioned defensive behaviors to cat odor on PND26, and subsequent cue + context conditioning and extinction throughout postnatal days 27–32. Our results show that maternal separation produced reductions in unconditioned freezing on PND26, with MS2–13 showing stronger deficits than MS11–13. However, separation did not affect any other defensive behaviors. Furthermore, separated rats failed to show conditioned freezing, although they did avoid the no-odor block conditioned cue. There were no sex differences other than weight. We suggest that maternal separation may have produced these changes by disrupting normal development of hippocampal regions involved in olfactory-mediated freezing, not in mechanisms of learning and memory per se . These findings may have direct relevance for understanding the mechanisms by which early-life adverse experiences produce short-term and lasting psychopathologies.