Central Oxytocin Administration Reduces Stress-Induced Corticosterone Release and Anxiety Behavior in Rats¹

TLDR

The study used central oxytocin infusions (10 or 100 ng/h for 5 days) in ovariectomized, estradiol‑treated female rats to assess corticosterone release during white‑noise stress and anxiety‑related behaviors on the elevated plus‑maze. Oxytocin dose‑dependently suppressed noise‑induced corticosterone and rearing, had no lasting effect after cessation, did not alter maze exploration in a familiar setting but increased open‑arm entries and time in an unfamiliar environment, indicating a central anxiolytic‑like effect on endocrine and behavioral responses to stress.

Abstract

Endocrine responses to noise stress and anxiety-related behaviors were measured in groups of ovariectomized, estradiol-treated female rats given central infusions of oxytocin. Control animals receiving isotonic saline showed a large increase in plasma corticosterone concentrations in response to 10 min of white noise. This response to noise stress was significantly and dose dependently decreased by oxytocin administered intracerebroventricularly at 10 or 100 ng/h for 5 days. Oxytocin also significantly decreased rearing behavior during this stress. When a second noise stress was given 3 days after cessation of oxytocin infusion, corticosterone responses did not differ between the control and previously oxytocin-infused animals. Administration of vasopressin had no significant effect on either the corticosterone or behavioral responses to noise stress. Anxiety-related behaviors were measured on the elevated plus-maze. No significant differences were seen in maze exploration between saline- and oxytocin-treated animals when housed and tested in the same environment. However, when animals were mildly stressed by testing in an unfamiliar environment, oxytocin-treated animals showed a higher proportion of open arm entries and spent significantly more time in the open arms of the maze. Thus, oxytocin exerts a central anxiolytic-like effect on both endocrine and behavioral systems and could play a role in moderating behavioral and physiological responses to stress.