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      The Dorsal Raphe Regulates the Duration of Attack through the Medial Orbitofrontal Cortex and Medial Amygdala

      research-article
      1 , 2 , 1 ,
      eNeuro
      Society for Neuroscience
      aggression, dorsal raphe, medial amygdala, neurocircuit, optogenetics, orbitofrontal cortex

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          Abstract

          The dorsal raphe (DR) is an evolutionarily conserved brain structure that is involved in aggressive behavior. It projects onto numerous cortical and limbic areas underlying attack behavior. The specific neurocircuit through which the DR regulates aggression, however, is largely unclear. In this study we show that DR neurons expressing CaMKIIα are activated by attack behavior in mice. These neurons project to the medial aspect of the orbitofrontal cortex (OFC; MeOC) and the medial amygdala (MeA), two key regions within the neural circuit known to control aggressive behavior. Using an in vivo optogenetic approach, we show that attack bouts are shortened by inhibiting CaMKIIα + neurons in the DR and their axons at the MeOC and prolonged by stimulating the DR-MeOC axons during an attack. By contrast, stimulating the axons of CaMKIIα + DR neurons at the MeA shortens attack. Notably, neither the DR-MeOC or DR-MeA pathway initiates attack when stimulated. These results indicate that the DR-MeOC and DR-MeA pathways regulate the duration of attack behavior in opposite directions, revealing a circuit mechanism for the control of attack by the DR.

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          Most cited references68

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          The Logic of Animal Conflict

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            Neural mechanisms of aggression.

            Unchecked aggression and violence exact a significant toll on human societies. Aggression is an umbrella term for behaviours that are intended to inflict harm. These behaviours evolved as adaptations to deal with competition, but when expressed out of context, they can have destructive consequences. Uncontrolled aggression has several components, such as impaired recognition of social cues and enhanced impulsivity. Molecular approaches to the study of aggression have revealed biological signals that mediate the components of aggressive behaviour. These signals may provide targets for therapeutic intervention for individuals with extreme aggressive outbursts. This Review summarizes the complex interactions between genes, biological signals, neural circuits and the environment that influence the development and expression of aggressive behaviour.
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              Ultrafast optogenetic control.

              Channelrhodopsins such as channelrhodopsin-2 (ChR2) can drive spiking with millisecond precision in a wide variety of cells, tissues and animal species. However, several properties of this protein have limited the precision of optogenetic control. First, when ChR2 is expressed at high levels, extra spikes (for example, doublets) can occur in response to a single light pulse, with potential implications as doublets may be important for neural coding. Second, many cells cannot follow ChR2-driven spiking above the gamma (approximately 40 Hz) range in sustained trains, preventing temporally stationary optogenetic access to a broad and important neural signaling band. Finally, rapid optically driven spike trains can result in plateau potentials of 10 mV or more, causing incidental upstates with information-processing implications. We designed and validated an engineered opsin gene (ChETA) that addresses all of these limitations (profoundly reducing extra spikes, eliminating plateau potentials and allowing temporally stationary, sustained spike trains up to at least 200 Hz).
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                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                14 October 2020
                22 October 2020
                Sep-Oct 2020
                : 7
                : 5
                : ENEURO.0331-20.2020
                Affiliations
                [1 ]Section on Synapse Development Plasticity, National Institute of Mental Health, National Institutes of Health , Bethesda, MD 20892
                [2 ]National Institute of General Medical Sciences, National Institutes of Health , Bethesda, MD 20892
                Author notes

                The authors declare no competing financial interests.

                Author contributions: J.N. and Z.L. designed research; J.N. performed research; J.N. analyzed data; J.N. and Z.L. wrote the paper.

                This work was supported by the Intramural Research Program of the National Institute of Mental Health Grant 1Z1AMH002881 (to Z.L.) and the National Institute of General Medical Sciences Postdoctoral Research Associate Training (PRAT) Program 1FI2GM119962-01 (to J.N.).

                Correspondence should be addressed to Zheng Li at lizheng2@ 123456mail.nih.gov .
                Author information
                https://orcid.org/0000-0003-2513-7831
                https://orcid.org/0000-0002-2978-2531
                Article
                eN-NWR-0331-20
                10.1523/ENEURO.0331-20.2020
                7665904
                33055195
                743b771a-5d85-49d2-8621-aeda26789631
                Copyright © 2020 Nordman and Li

                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
                : 27 July 2020
                : 21 September 2020
                : 25 September 2020
                Page count
                Figures: 7, Tables: 2, Equations: 0, References: 68, Pages: 15, Words: 00
                Funding
                Funded by: Intramural Research Program of the National Institute of Mental Health
                Award ID: 1Z1AMH002881
                Funded by: HHS | NIH | National Institute of General Medical Sciences Postdoctoral Research Associate Training Program
                Award ID: 1FI2GM119962-01
                Categories
                1
                Research Article: New Research
                Cognition and Behavior
                Custom metadata
                September/October 2020

                aggression,dorsal raphe,medial amygdala,neurocircuit,optogenetics,orbitofrontal cortex

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