Article ID Journal Published Year Pages File Type
2035487 Cell 2014 11 Pages PDF
Abstract

•Oxtr Cre BAC transgenic mice target a subset of Sst-positive cortical interneurons•OxtrINs respond to Oxytocin by increasing their firing rate•OxtrINs in mPFC are required for female social interest in male mice during estrus•Oxytocin action in mPFC is required for female sociosexual behavior

SummaryHuman imaging studies have revealed that intranasal administration of the “prosocial” hormone oxytocin (OT) activates the frontal cortex, and this action of OT correlates with enhanced brain function in autism. Here, we report the discovery of a population of somatostatin (Sst)-positive, regular spiking interneurons that express the oxytocin receptor (OxtrINs). Silencing of OxtrINs in the medial prefrontal cortex (mPFC) of female mice resulted in loss of social interest in male mice specifically during the sexually receptive phase of the estrous cycle. This sociosexual deficit was also present in mice in which the Oxtr gene was conditionally deleted from the mPFC and in control mice infused with an Oxtr antagonist. Our data demonstrate a gender-, cell type-, and state-specific role for OT/Oxtr signaling in the mPFC and identify a latent cortical circuit element that may modulate other complex social behaviors in response to OT.PaperFlick To view the video inline, enable JavaScript on your browser. However, you can download and view the video by clicking on the icon belowHelp with MP4 filesOptionsDownload video (124260 K)

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