Age, β-endorphin, and sex dependent effects of maternal separation on locomotor activity, anxiety-like behavior, and alcohol reward

• Published in: Frontiers in behavioral neuroscience Vol. 17; p. 1155647
• Main Authors: Scopano, Madison R., Jones, Holly E., Stea, Sam G., Freeman, Maya Z., Grisel, Judith E.
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 05.04.2023; Frontiers Media S.A
• Subjects: adolescent; Adolescents; Alcohol; Animal models; Anxiety; Anxiety disorders; Behavior; Cameras; Children; conditioned place preference; Drug use; early life stress; Endorphins; EtOH reinforcement; Females; Gender differences; Genotypes; Locomotor activity; Maternal behavior; Mental disorders; Narcotics; Neuroscience; opioid; Place preference conditioning; Self-medication; Sex; sex differences; Stress; Stress response; Substance use; Teenagers; Weaning; development; conditioned place preference; opioid; adolescent; EtOH reinforcement; early life stress; sex differences; adverse childhood experiences
• ISSN: 1662-5153; 1662-5153
• DOI: 10.3389/fnbeh.2023.1155647

Childhood adversity is pervasive and linked to numerous disadvantages in adulthood, including physical health problems, mental illness, and substance use disorders. Initial sensitivity to the rewarding effects of alcohol predicts the risk of developing an alcohol use disorder, and may be linked to developmental stress. The opioid peptide β-endorphin (β-E) regulates the stress response and is also implicated in the risk for excessive alcohol consumption. We explored the influence of β-E in an animal model of early life adversity using controlled maternal separation by evaluating changes in locomotor activity, anxiety-like behavior, and the initial rewarding effects of alcohol in a single exposure conditioned place preference paradigm in control C57BL/6J and β-E deficient β-E +/+ 0.129S2-Pomc tm1Low/J; β-E -/- mice. Maternal separation (MS) occurred for 3 h each day from post-natal days (PND) 5-18 in approximately half the subjects. Maternal interactions increased following the separation protocol equally in both genotypes. MS and control subjects were tested as adolescents (PND 26-32) or adults (PND 58-72); the effects of MS were generally more pronounced in older subjects. Adults were more active than adolescents in the open field, and MS decreased activity in adolescent mice but increased it in adults. The increase in adult activity as a result of early life stress depended on both β-E and sex. β-E also influenced the effect of maternal separation on anxiety-like behavior in the Elevated Plus Maze. MS promoted rewarding effects of alcohol in male β-E deficient mice of either age, but had no effect in other groups. Taken together, these results suggest that the effects of MS develop over time and are β-E and sex dependent and may aid understanding of how individual differences influence the impact of adverse childhood experiences.