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      Whole-Brain Wiring Diagram of Oxytocin System in Adult Mice

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          Abstract

          Oxytocin (Oxt) neurons regulate diverse physiological responses via direct connections with different neural circuits. However, the lack of comprehensive input-output wiring diagrams of Oxt neurons and their quantitative relationship with Oxt receptor (Oxtr) expression presents challenges to understanding circuit-specific Oxt functions. Here, we establish a whole-brain distribution and anatomic connectivity map of Oxt neurons, and their relationship with Oxtr expression using high-resolution 3D mapping methods in adult male and female mice. We use a flatmap to describe Oxt neuronal expression in four hypothalamic domains including under-characterized Oxt neurons in the tuberal nucleus (TU). Oxt neurons in the paraventricular hypothalamus (PVH) broadly project to nine functional circuits that control cognition, brain state, and somatic visceral response. In contrast, Oxt neurons in the supraoptic (SO) and accessory (AN) nuclei have limited central projection to a small subset of the nine circuits. Surprisingly, quantitative comparison between Oxt output and Oxtr expression showed no significant correlation across the whole brain, suggesting abundant indirect Oxt signaling in Oxtr-expressing areas. Unlike output, Oxt neurons in both the PVH and SO receive similar monosynaptic inputs from a subset of the nine circuits mainly in the thalamic, hypothalamic, and cerebral nuclei areas. Our results suggest that PVH-Oxt neurons serve as a central modulator to integrate external and internal information via largely reciprocal connection with the nine circuits while the SO-Oxt neurons act mainly as unidirectional Oxt hormonal output. In summary, our Oxt wiring diagram provides anatomic insights about distinct behavioral functions of Oxt signaling in the brain.

          SIGNIFICANCE STATEMENT Oxytocin (Oxt) neurons regulate diverse physiological functions from prosocial behavior to pain sensation via central projection in the brain. Thus, understanding detailed anatomic connectivity of Oxt neurons can provide insight on circuit-specific roles of Oxt signaling in regulating different physiological functions. Here, we use high-resolution mapping methods to describe the 3D distribution, monosynaptic input and long-range output of Oxt neurons, and their relationship with Oxt receptor (Oxtr) expression across the entire mouse brain. We found Oxt connections with nine functional circuits controlling cognition, brain state, and somatic visceral response. Furthermore, we identified a quantitatively unmatched Oxt-Oxtr relationship, suggesting broad indirect Oxt signaling. Together, our comprehensive Oxt wiring diagram advances our understanding of circuit-specific roles of Oxt neurons.

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          elastix: a toolbox for intensity-based medical image registration.

          Medical image registration is an important task in medical image processing. It refers to the process of aligning data sets, possibly from different modalities (e.g., magnetic resonance and computed tomography), different time points (e.g., follow-up scans), and/or different subjects (in case of population studies). A large number of methods for image registration are described in the literature. Unfortunately, there is not one method that works for all applications. We have therefore developed elastix, a publicly available computer program for intensity-based medical image registration. The software consists of a collection of algorithms that are commonly used to solve medical image registration problems. The modular design of elastix allows the user to quickly configure, test, and compare different registration methods for a specific application. The command-line interface enables automated processing of large numbers of data sets, by means of scripting. The usage of elastix for comparing different registration methods is illustrated with three example experiments, in which individual components of the registration method are varied.
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            The Allen Mouse Brain Common Coordinate Framework: A 3D Reference Atlas

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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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                Author and article information

                Journal
                J Neurosci
                J Neurosci
                jneuro
                J. Neurosci
                The Journal of Neuroscience
                Society for Neuroscience
                0270-6474
                1529-2401
                22 June 2022
                22 June 2022
                : 42
                : 25
                : 5021-5033
                Affiliations
                [1] 1Department of Neural and Behavioral Sciences, The Pennsylvania State University, Hershey, Pennsylvania 17033
                [2] 2Department of Pathology, The Pennsylvania State University, Hershey, Pennsylvania 17033
                [3] 3Program in Neuroscience, Harvard University, Boston, Massachusetts 02138
                Author notes
                Correspondence should be addressed to Yongsoo Kim at yuk17@ 123456psu.edu

                Author contributions: S.S. and Y.K. designed research; S.S., S.B.M., K.T.N., and M.C. performed research; Y.-t.W., D.J.V., T.E.A., and K.C.C. contributed unpublished reagents/analytic tools; S.S., S.B.M., K.T.N., Y.-t.W., M.C., and Y.K. analyzed data; S.S. and Y.K. wrote the first draft of the paper; S.S., S.B.M., K.T.N., T.E.A., K.C.C., and Y.K. edited the paper; S.S., S.B.M., and Y.K. wrote the paper.

                *S.S. and S.B.M. are co-first authors.

                Article
                JN-RM-0307-22
                10.1523/JNEUROSCI.0307-22.2022
                9233446
                35606144
                e1080a5c-5086-47e4-921c-9b52b4315072
                Copyright © 2022 Son et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 11 February 2022
                : 3 April 2022
                : 11 May 2022
                Funding
                Funded by: HHS | NIH | National Institute of Mental Health (NIMH), doi 10.13039/100000025;
                Award ID: R01MH116176
                Funded by: HHS | NIH | NIH Office of the Director (OD), doi 10.13039/100000052;
                Award ID: R24OD18559
                Categories
                Research Articles
                Systems/Circuits
                Custom metadata
                true

                anatomical connectivity,axonal output,brain mapping,oxytocin,synaptic input,wiring diagram

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