4.1 Article

Infant ultrasonic vocalizations predict adolescent social behavior in rats: Effects of early life adversity

Journal

DEVELOPMENTAL PSYCHOBIOLOGY
Volume 64, Issue 3, Pages -

Publisher

WILEY
DOI: 10.1002/dev.22260

Keywords

early life stress; limited bedding; play; prefrontal cortex; ultrasonic vocalization

Funding

  1. National Institute of Mental Health [R01MH107556]

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Early life adversity increases the risk of psychopathologies during adolescence, affecting brain development and social behavior. In a rat experiment, it was found that infant social communication predicts brain development and adolescent social behavior, providing clues for studying the relationship between early factors and vulnerability.
Early life adversity (ELA) increases risk for psychopathologies that often manifest during adolescence and involve disrupted social functioning. ELA affects development of the prefrontal cortex (PFC), which plays a role in social behavior. PFC oxytocin and vasopressin are important regulators of, first, mother-infant attachment, and, later, social behavior, and are implicated in psychiatric disorders. Here, we tested whether infant social communication is predictive of PFC development and adolescent social behavior. We used the limited bedding (LB) ELA model in rats during postnatal days (P)2-14, and measured isolation-induced ultrasonic vocalizations (USVs) at P10 to characterize differences in an early social response. Rats were tested for dyadic social interaction in adolescence (P34). Adolescent oxytocin receptor (Oxtr) and arginine-vasopressin receptor 1a mRNA were measured in the PFC. Relationships between infant USVs, adolescent behavior, and gene expression were assessed. LB-reared rats exhibited fewer USVs at P10. While social behaviors were not robustly affected by rearing, fewer total and complex-type infant USVs predicted fewer interactions in adolescence. LB increased Oxtr in both sexes but Oxtr was not directly predicted by USVs. Findings support the use of USVs as indicators of differential early life experience in rodents, toward further characterization of early factors associated with vulnerability.

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