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      Corticotropin-releasing hormone signaling from prefrontal cortex to lateral septum suppresses interaction with familiar mice

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          Abstract

          Social preference, the decision to interact with one member of the same species over another, is a key feature of optimizing social interactions. Thus, adult rodents favor interacting with novel conspecifics over familiar ones but whether this preference for social novelty stems from neural circuits facilitating interactions with novel conspecifics or suppressing interactions with familiar ones remains unknown. Here, we identify neurons in the infra-limbic area (ILA) of the mouse prefrontal cortex that express the neuropeptide corticotropin-releasing hormone (CRH) and project to the dorsal region of the rostral lateral septum (rLS). We show how release of CRH during familiar encounters disinhibits rLS neurons, thereby suppressing social interactions with familiar mice and contributing to social novelty preference. We further demonstrate how the maturation of CRH expression in ILA during the first two post-natal weeks enables the developmental shift from a preference for littermates in juveniles to a preference for novel mice in adults. Taken together, our findings suggest that the developmental maturation of CRH in ILA and its later release onto rLS is critical for controlling the preference for socially novel encounters exhibited by adult mice.

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          Social reward requires coordinated activity of accumbens oxytocin and 5HT

          Social behaviors in species as diverse as honey bees and humans promote group survival but often come at some cost to the individual. Although reinforcement of adaptive social interactions is ostensibly required for the evolutionary persistence of these behaviors, the neural mechanisms by which social reward is encoded by the brain are largely unknown. Here we demonstrate that in mice oxytocin (OT) acts as a social reinforcement signal within the nucleus accumbens (NAc) core, where it elicits a presynaptically expressed long-term depression of excitatory synaptic transmission in medium spiny neurons. Although the NAc receives OT receptor-containing inputs from several brain regions, genetic deletion of these receptors specifically from dorsal raphe nucleus, which provides serotonergic (5-HT) innervation to the NAc, abolishes the reinforcing properties of social interaction. Furthermore, OT-induced synaptic plasticity requires activation of NAc 5-HT1b receptors, the blockade of which prevents social reward. These results demonstrate that the rewarding properties of social interaction in mice require the coordinated activity of OT and 5-HT in the NAc, a mechanistic insight with implications for understanding the pathogenesis of social dysfunction in neuropsychiatric disorders such as autism.
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            Natural neural projection dynamics underlying social behavior.

            Social interaction is a complex behavior essential for many species and is impaired in major neuropsychiatric disorders. Pharmacological studies have implicated certain neurotransmitter systems in social behavior, but circuit-level understanding of endogenous neural activity during social interaction is lacking. We therefore developed and applied a new methodology, termed fiber photometry, to optically record natural neural activity in genetically and connectivity-defined projections to elucidate the real-time role of specified pathways in mammalian behavior. Fiber photometry revealed that activity dynamics of a ventral tegmental area (VTA)-to-nucleus accumbens (NAc) projection could encode and predict key features of social, but not novel object, interaction. Consistent with this observation, optogenetic control of cells specifically contributing to this projection was sufficient to modulate social behavior, which was mediated by type 1 dopamine receptor signaling downstream in the NAc. Direct observation of deep projection-specific activity in this way captures a fundamental and previously inaccessible dimension of mammalian circuit dynamics. Copyright © 2014 Elsevier Inc. All rights reserved.
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              Characterization of a 41-residue ovine hypothalamic peptide that stimulates secretion of corticotropin and beta-endorphin

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                Author and article information

                Journal
                0413066
                Cell
                Cell
                Cell
                0092-8674
                1097-4172
                29 August 2023
                29 August 2023
                07 September 2023
                18 September 2023
                : 186
                : 19
                : 4152-4171.e31
                Affiliations
                [1 ]Instituto de Neurociencias CSIC-UMH, San Juan de Alicante, Spain
                [2 ]Center for Theoretical Neuroscience, Columbia University, New York, USA
                [3 ]Department of Neuroscience, Columbia University, New York, USA
                [4 ]Zuckerman Mind Brain & Behavior Institute, New York, USA
                [5 ]School of Medicine, University of Washington, Seattle, USA
                Author notes
                Corresponding author: Félix Leroy ( felxfel@ 123456aol.com )
                Article
                EMS187521
                10.1016/j.cell.2023.08.010
                7615103
                37669667
                0454e41a-9986-4cec-946d-95639c4e4c8d

                This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/.

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                Categories
                Article

                Cell biology
                social novelty preference,lateral septum,pre-frontal cortex,corticotropinreleasing hormone,crf

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