Effects of systemic oxytocin receptor activation and blockade on risky decision making in female and male rats.

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Abstract
The neuropeptide oxytocin is traditionally known for its roles in parturition, lactation, and social behavior. Other data, however, show that oxytocin can modulate behaviors outside of these contexts, including drug self-administration and some aspects of cost-benefit decision making. Here we used a pharmacological approach to investigate the contributions of oxytocin signaling to decision making under risk of explicit punishment. Female and male Long-Evans rats were trained on a risky decision-making task in which they chose between a small, "safe" food reward and a large, "risky" food reward that was accompanied by varying probabilities of mild footshock. Once stable choice behavior emerged, rats were tested in the task following acute intraperitoneal injections of oxytocin or the oxytocin receptor antagonist L-368,899. Oxytocin dose-dependently reduced preference for the large, risky reward only in females, whereas L-368,899 dose-dependently reduced preference for the large, risky reward in both sexes. Control experiments showed that these effects could not be accounted for by drug-induced alterations in preference for the large reward or shock sensitivity. Together, these results reveal partially sex-dependent effects of oxytocin signaling on risky decision making in rats. (PsycInfo Database Record (c) 2025 APA, all rights reserved).
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Funding Information
  • National Institutes of Health (AG060778)
  • Evelyn F. McKnight Brain Research Foundation

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