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Postnatal maternal separation increases hypothalamic corticotropin-releasing factor (CRF) gene expression and hypothalamic-pituitary-adrenal (HPA) and behavioral responses to stress. We report here that environmental enrichment during the peripubertal period completely reverses the effects of maternal separation on both HPA and behavioral responses to stress, with no effect on CRF mRNA expression. We conclude that environmental enrichment leads to a functional reversal of the effects of maternal separation through compensation for, rather than reversal of, the neural effects of early life adversity
Behavior. --- Behavioral-responses. --- Compensation. --- Corticotropin-releasing factor. --- Corticotropin-releasing-factor. --- Crf. --- Depression. --- Early experience,environmental enrichment,maternal separation,stress,corticotropin-releasing factor,glucocorticoid receptors. --- Early experience. --- Enrichment. --- Environmental enrichment. --- Expression. --- Gene-expression. --- Gene. --- Generations. --- Hippocampus. --- Hypothalamic-pituitary-adrenal. --- Increase. --- Increases. --- Life. --- Maternal separation. --- Maternal. --- Pituitary-adrenal responses. --- Prenatal stress. --- Rat. --- Reactivity. --- Receptor messenger-rna. --- Response. --- Responses. --- Separation. --- Stress reactivity. --- Stress. --- Transmission.
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Behavioural responses to psychostimulant drugs can be profoundly affected by early environmental influences. The aim of this study was to describe the effects of repeated brief separations of rat pups from their dams during the early neonatal period on cocaine self-administration behaviour as adults. Lister hooded rats exposed to a repeated maternal separation procedure (REMS) showed altered acquisition and maintenance of cocaine self-administration as adults, the effects being dose and gender-dependent. Overall, the patterns of acquisition of self-administration across three doses of cocaine (0.05, 0.08 and 0.5 mg/injection) suggested a rightward shift in the acquisition dose-effect functions for the REMS animals relative to control animals. At 0.05 mg/injection, there was a retarded acquisition of cocaine self-administration in male and female neonatally separated rats. At 0.08 mg/injection there was a facilitated acquisition in female neonatally separated subjects. After establishment of stable self-administration of the training dose, in the same cohort of subjects, rightward and downward shifts in the cocaine self-administration dose-effect functions were determined for female and male REMS subjects, respectively, relative to their controls. The dose-effect function for both female groups was shifted to the left of that of the respective male groups, although the lighter body weights of the females meant that they administered a higher unit dose per unit body weight than the males. Whereas male REMS subjects tended to self-administer less cocaine than the controls at the dose eliciting maximal responding (0.03 mg/injection) and to make fewer lever responses overall at each dose tested, female REMS subjects self-administered significantly more cocaine than their respective controls at a dose of 0.03 mg/injection. There was no differential sensitivity to the rate-altering effects of the selective dopamine D-2 receptor antagonist, eticlopride, or to the selecti
Acquisition. --- Adult rats. --- Adult-rat. --- Adult-rats. --- Adult. --- Alters. --- Animal. --- Animals. --- Behaviour. --- Body weight. --- Body-weight. --- Cocaine. --- Control. --- Corticotropin-releasing factor. --- D-amphetamine. --- D2 receptor. --- Different schedules. --- Dopamine-receptors. --- Dopamine. --- Drug. --- Drugs. --- Early environment. --- Environment. --- Eticlopride. --- Female. --- Females. --- Function. --- Group. --- Individual vulnerability. --- Intravenous self-administration. --- Isolation rearing. --- Isolation. --- Locomotor response. --- Maintenance. --- Male. --- Males. --- Maternal separation. --- Maternal. --- Mesolimbic dopamine. --- Messenger-rna. --- Neonatal. --- Nucleus-accumbens. --- Pattern. --- Patterns. --- Pituitary-adrenal responses. --- Post weaning. --- Pups. --- Rat. --- Rats. --- Rearing. --- Receptor antagonist. --- Receptor. --- Response. --- Responses. --- Reward. --- Sch 23390. --- Sensitivity. --- Separation. --- Stress. --- Time. --- Training. --- Weight.
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