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      Lateral habenula glutamatergic neurons projecting to the dorsal raphe nucleus promote aggressive arousal in mice

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          Abstract

          The dorsal raphe nucleus (DRN) is known to control aggressive behavior in mice. Here, we found that glutamatergic projections from the lateral habenula (LHb) to the DRN were activated in male mice that experienced pre-exposure to a rival male mouse (“social instigation”) resulting in heightened intermale aggression. Both chemogenetic and optogenetic suppression of the LHb-DRN projection blocked heightened aggression after social instigation in male mice. In contrast, inhibition of this pathway did not affect basal levels of aggressive behavior, suggesting that the activity of the LHb-DRN projection is not necessary for the expression of species-typical aggressive behavior, but required for the increase of aggressive behavior resulting from social instigation. Anatomical analysis showed that LHb neurons synapse on non-serotonergic DRN neurons that project to the ventral tegmental area (VTA), and optogenetic activation of the DRN-VTA projection increased aggressive behaviors. Our results demonstrate that the LHb glutamatergic inputs to the DRN promote aggressive arousal induced by social instigation, which contributes to aggressive behavior by activating VTA-projecting non-serotonergic DRN neurons as one of its potential targets.

          Abstract

          The dorsal raphe nucleus (DRN) is known to modulate aggressive behaviour in rodents. Here the authors show that glutamatergic projections from the lateral habenula to DRN modulate aggression between male mice.

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          High-Performance Genetically Targetable Optical Neural Silencing via Light-Driven Proton Pumps

          The ability to silence the activity of genetically specified neurons in a temporally precise fashion would open up the ability to investigate the causal role of specific cell classes in neural computations, behaviors, and pathologies. Here we show that members of the class of light-driven outward proton pumps can mediate very powerful, safe, multiple-color silencing of neural activity. The gene archaerhodopsin-31 (Arch) from Halorubrum sodomense enables near-100% silencing of neurons in the awake brain when virally expressed in mouse cortex and illuminated with yellow light. Arch mediates currents of several hundred picoamps at low light powers, and supports neural silencing currents approaching 900 pA at light powers easily achievable in vivo. In addition, Arch spontaneously recovers from light-dependent inactivation, unlike light-driven chloride pumps that enter long-lasting inactive states in response to light. These properties of Arch are appropriate to mediate the optical silencing of significant brain volumes over behaviourally-relevant timescales. Arch function in neurons is well tolerated because pH excursions created by Arch illumination are minimized by self-limiting mechanisms to levels comparable to those mediated by channelrhodopsins2,3 or natural spike firing. To highlight how proton pump ecological and genomic diversity may support new innovation, we show that the blue-green light-drivable proton pump from the fungus Leptosphaeria maculans 4 (Mac) can, when expressed in neurons, enable neural silencing by blue light, thus enabling alongside other developed reagents the potential for independent silencing of two neural populations by blue vs. red light. Light-driven proton pumps thus represent a high-performance and extremely versatile class of “optogenetic” voltage and ion modulator, which will broadly empower new neuroscientific, biological, neurological, and psychiatric investigations.
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            AAV-Mediated Anterograde Transsynaptic Tagging: Mapping Corticocollicular Input-Defined Neural Pathways for Defense Behaviors.

            To decipher neural circuits underlying brain functions, viral tracers are widely applied to map input and output connectivity of neuronal populations. Despite the successful application of retrograde transsynaptic viruses for identifying presynaptic neurons of transduced neurons, analogous anterograde transsynaptic tools for tagging postsynaptically targeted neurons remain under development. Here, we discovered that adeno-associated viruses (AAV1 and AAV9) exhibit anterograde transsynaptic spread properties. AAV1-Cre from transduced presynaptic neurons effectively and specifically drives Cre-dependent transgene expression in selected postsynaptic neuronal targets, thus allowing axonal tracing and functional manipulations of the latter input-defined neuronal population. Its application in superior colliculus (SC) reveals that SC neuron subpopulations receiving corticocollicular projections from auditory and visual cortex specifically drive flight and freezing, two different types of defense behavior, respectively. Together with an intersectional approach, AAV-mediated anterograde transsynaptic tagging can categorize neurons by their inputs and molecular identity, and allow forward screening of distinct functional neural pathways embedded in complex brain circuits.
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              Deconstruction of a neural circuit for hunger

              Hunger is a complex behavioural state that elicits intense food seeking and consumption. These behaviours are rapidly recapitulated by activation of starvation-sensitive AGRP neurons, which present an entry point for reverse-engineering neural circuits for hunger. We mapped synaptic interactions of AGRP neurons with multiple cell populations and probed the contribution of these distinct circuits to feeding behaviour using optogenetic and pharmacogenetic techniques. An inhibitory circuit with paraventricular hypothalamus (PVH) neurons substantially accounted for acute AGRP neuron-evoked eating, whereas two other prominent circuits were insufficient. Within the PVH, we found that AGRP neurons target and inhibit oxytocin neurons, a small population that is selectively lost in Prader-Willi syndrome, a condition involving insatiable hunger. By developing strategies for evaluating molecularly-defined circuits, we show that AGRP neuron suppression of oxytocin neurons is critical for evoked feeding. These experiments reveal a new neural circuit that regulates hunger state and pathways associated with overeating disorders.
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                Author and article information

                Contributors
                aktakaha@human.tsukuba.ac.jp
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                21 July 2022
                21 July 2022
                2022
                : 13
                : 4039
                Affiliations
                [1 ]GRID grid.20515.33, ISNI 0000 0001 2369 4728, Laboratory of Behavioral Neurobiology, Faculty of Human Sciences, , University of Tsukuba, ; Tsukuba, Ibaraki 305-8577 Japan
                [2 ]GRID grid.20515.33, ISNI 0000 0001 2369 4728, Laboratory of Behavioral Neuroendocrinology, Faculty of Human Sciences, , University of Tsukuba, ; Tsukuba, Ibaraki 305-8577 Japan
                [3 ]GRID grid.59734.3c, ISNI 0000 0001 0670 2351, Nash Family Department of Neuroscience and Brain & Body Research Center, , Icahn School of Medicine at Mount Sinai, ; New York, NY 10029 USA
                [4 ]GRID grid.20515.33, ISNI 0000 0001 2369 4728, Department of Molecular Behavioral Physiology, Faculty of Medicine, , University of Tsukuba, ; Tsukuba, Ibaraki 305-8575 Japan
                [5 ]GRID grid.20515.33, ISNI 0000 0001 2369 4728, International Institute for Integrative Sleep Medicine (WPI-IIIS), , University of Tsukuba, ; Tsukuba, Ibaraki 305-8575 Japan
                [6 ]GRID grid.69566.3a, ISNI 0000 0001 2248 6943, Super-network Brain Physiology, Graduate School of Life Sciences, , Tohoku University, ; Sendai, Miyagi 980-8577 Japan
                [7 ]GRID grid.69566.3a, ISNI 0000 0001 2248 6943, Advanced Interdisciplinary Research Division, Frontier Research Institute for Interdisciplinary Sciences, , Tohoku University, ; Sendai, Miyagi 980-8578 Japan
                [8 ]GRID grid.419082.6, ISNI 0000 0004 1754 9200, Precursory Research for Embryonic Science and Technology, , Japan Science and Technology Agency, ; Kawaguchi, Saitama 332-0012 Japan
                [9 ]GRID grid.20515.33, ISNI 0000 0001 2369 4728, Department of Molecular Neurobiology, Faculty of Medicine, , University of Tsukuba, ; Tsukuba, Ibaraki 305-8575 Japan
                [10 ]GRID grid.20515.33, ISNI 0000 0001 2369 4728, Graduate School of Comprehensive Human Sciences, , University of Tsukuba, ; Tsukuba, Ibaraki 305-8575 Japan
                [11 ]GRID grid.59734.3c, ISNI 0000 0001 0670 2351, Department of Pharmacological Sciences and Department of Psychiatry, , Icahn School of Medicine at Mount Sinai, ; New York, NY 10029 USA
                [12 ]GRID grid.26091.3c, ISNI 0000 0004 1936 9959, Department of Neuropsychiatry, , Keio University School of Medicine, ; Shinjuku, Tokyo 160-8582 Japan
                [13 ]GRID grid.27476.30, ISNI 0000 0001 0943 978X, Department of Neuroscience II, Research Institute of Environmental Medicine, , Nagoya University, ; Nagoya, Aichi 464-8601 Japan
                [14 ]GRID grid.10698.36, ISNI 0000000122483208, Present Address: Bowles Center for Alcohol Studies, , University of North Carolina School of Medicine, ; Chapel Hill, 27599 NC USA
                Author information
                http://orcid.org/0000-0001-8325-9744
                http://orcid.org/0000-0003-0240-7608
                http://orcid.org/0000-0002-2711-4679
                http://orcid.org/0000-0002-0021-2586
                http://orcid.org/0000-0002-6139-8193
                http://orcid.org/0000-0002-1354-8468
                http://orcid.org/0000-0001-8829-1532
                http://orcid.org/0000-0003-4700-7894
                http://orcid.org/0000-0003-2511-0057
                http://orcid.org/0000-0001-6099-7306
                http://orcid.org/0000-0003-4474-6253
                http://orcid.org/0000-0002-6470-1805
                Article
                31728
                10.1038/s41467-022-31728-z
                9304121
                35864121
                eddf5657-35e8-48de-803a-8d42875a8b5d
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 14 May 2021
                : 29 June 2022
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100001691, MEXT | Japan Society for the Promotion of Science (JSPS);
                Award ID: JP19H05202
                Award ID: JP21H00183
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100009029, MEXT | JST | Adaptable and Seamless Technology Transfer Program through Target-Driven R and D (Adaptable and Seamless Technology Transfer Program through Target-Driven R&D);
                Award ID: JPMJTM20BW
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100002241, MEXT | Japan Science and Technology Agency (JST);
                Award ID: JPMJFR214A
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000025, U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH);
                Award ID: R01MH114882-01
                Award ID: R01MH104559
                Award ID: R01MH127820
                Award Recipient :
                Funded by: U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH)
                Funded by: U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH)
                Categories
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                © The Author(s) 2022

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                aggression,emotion
                Uncategorized
                aggression, emotion

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