| Literature DB >> 33020267 |
Natalia Duque-Wilckens1,2,3, Lisette Y Torres1, Sae Yokoyama1, Vanessa A Minie1, Amy M Tran1, Stela P Petkova4, Rebecca Hao1, Stephanie Ramos-Maciel1, Roberto A Rios1, Kenneth Jackson5, Francisco J Flores-Ramirez6, Israel Garcia-Carachure6, Patricia A Pesavento5, Sergio D Iñiguez6, Valery Grinevich7, Brian C Trainor8.
Abstract
Oxytocin increases the salience of both positive and negative social contexts and it is thought that these diverse actions on behavior are mediated in part through circuit-specific action. This hypothesis is based primarily on manipulations of oxytocin receptor function, leaving open the question of whether different populations of oxytocin neurons mediate different effects on behavior. Here we inhibited oxytocin synthesis in a stress-sensitive population of oxytocin neurons specifically within the medioventral bed nucleus of the stria terminalis (BNSTmv). Oxytocin knockdown prevented social stress-induced increases in social vigilance and decreases in social approach. Viral tracing of BNSTmv oxytocin neurons revealed fibers in regions controlling defensive behaviors, including lateral hypothalamus, anterior hypothalamus, and anteromedial BNST (BNSTam). Oxytocin infusion into BNSTam in stress naïve mice increased social vigilance and reduced social approach. These results show that a population of extrahypothalamic oxytocin neurons plays a key role in controlling stress-induced social anxiety behaviors.Entities:
Keywords: California mouse; anxiety; bed nucleus of the stria terminalis; extended amygdala; morpholino
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Year: 2020 PMID: 33020267 PMCID: PMC7585015 DOI: 10.1073/pnas.2011890117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205