CRISPR-mediated knockdown of oxytocin receptor in extended amygdala reduces stress-induced social avoidance and vigilance

Oxytocin receptors (OTR) within the extended amygdala and nucleus accumbens have been implicated in modulating social behaviors, particularly following stress. The effects of OTR could be mediated by modulating the activity of pre-synaptic axon terminals or via post-synaptic neurons or glia. Using a viral-mediated CRISPR/Cas9 gene editing system in California mice ( Peromyscus californicus ), we selectively knocked down OTR in the anteromedial bed nucleus of the stria terminalis (BNST) or the nucleus accumbens (NAc) to examine their roles modulating social approach and vigilance behaviors. Knockdown of OTR in the BNST attenuated stress-induced decreases of social approach and increases of social vigilance behaviors in adult female California mice, similar to prior pharmacological studies. These effects were more prominent in the large arena social interaction where mice could control proximity to a social target with a barrier (wire cage). In a small arena interaction test where focal mice freely interacted with target mice, effects of BNST OTR knockdown were muted. This suggests that within the BNST OTR are more important for modulating behavioral responses to more distal stimuli versus more proximal social contexts. In mice with OTR knockdown in the NAc, few behavioral changes were observed which is consistent with previous findings of the importance of presynaptic OTR, which were unaffected by our gene editing strategy, driving social approach behaviors in the NAc. Interestingly, BNST OTR knockdown increased exploratory behavior toward a non-social stimulus after stress, pointing to a potentially broader role for BNST OTR function. Our findings highlight the region- and context-specific functions of OTR in social behavior and the advantages of using a selective gene-editing tool to dissect the neural circuits that influence social and stress-related responses.