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      Monosynaptic retrograde tracing of neurons expressing the G‐protein coupled receptor Gpr151 in the mouse brain

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          Abstract

          GPR151 is a G‐protein coupled receptor for which the endogenous ligand remains unknown. In the nervous system of vertebrates, its expression is enriched in specific diencephalic structures, where the highest levels are observed in the habenular area. The habenula has been implicated in a range of different functions including behavioral flexibility, decision making, inhibitory control, and pain processing, which makes it a promising target for treating psychiatric and neurological disease. This study aimed to further characterize neurons expressing the Gpr151 gene, by tracing the afferent connectivity of this diencephalic cell population. Using pseudotyped rabies virus in a transgenic Gpr151‐Cre mouse line, monosynaptic afferents of habenular and thalamic Gpr151‐expressing neuronal populations could be visualized. The habenular and thalamic Gpr151 systems displayed both shared and distinct connectivity patterns. The habenular neurons primarily received input from basal forebrain structures, the bed nucleus of stria terminalis, the lateral preoptic area, the entopeduncular nucleus, and the lateral hypothalamic area. The Gpr151‐expressing neurons in the paraventricular nucleus of the thalamus was primarily contacted by medial hypothalamic areas as well as the zona incerta and projected to specific forebrain areas such as the prelimbic cortex and the accumbens nucleus. Gpr151 mRNA was also detected at low levels in the lateral posterior thalamic nucleus which received input from areas associated with visual processing, including the superior colliculus, zona incerta, and the visual and retrosplenial cortices. Knowledge about the connectivity of Gpr151‐expressing neurons will facilitate the interpretation of future functional studies of this receptor.

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          Most cited references48

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          A FLEX switch targets Channelrhodopsin-2 to multiple cell types for imaging and long-range circuit mapping.

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            A prefrontal cortex-brainstem neuronal projection that controls response to behavioural challenge.

            The prefrontal cortex (PFC) is thought to participate in high-level control of the generation of behaviours (including the decision to execute actions); indeed, imaging and lesion studies in human beings have revealed that PFC dysfunction can lead to either impulsive states with increased tendency to initiate action, or to amotivational states characterized by symptoms such as reduced activity, hopelessness and depressed mood. Considering the opposite valence of these two phenotypes as well as the broad complexity of other tasks attributed to PFC, we sought to elucidate the PFC circuitry that favours effortful behavioural responses to challenging situations. Here we develop and use a quantitative method for the continuous assessment and control of active response to a behavioural challenge, synchronized with single-unit electrophysiology and optogenetics in freely moving rats. In recording from the medial PFC (mPFC), we observed that many neurons were not simply movement-related in their spike-firing patterns but instead were selectively modulated from moment to moment, according to the animal's decision to act in a challenging situation. Surprisingly, we next found that direct activation of principal neurons in the mPFC had no detectable causal effect on this behaviour. We tested whether this behaviour could be causally mediated by only a subclass of mPFC cells defined by specific downstream wiring. Indeed, by leveraging optogenetic projection-targeting to control cells with specific efferent wiring patterns, we found that selective activation of those mPFC cells projecting to the brainstem dorsal raphe nucleus (DRN), a serotonergic nucleus implicated in major depressive disorder, induced a profound, rapid and reversible effect on selection of the active behavioural state. These results may be of importance in understanding the neural circuitry underlying normal and pathological patterns of action selection and motivation in behaviour.
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              Habenular α5* nicotinic receptor signaling controls nicotine intake

              Genetic variation in CHRNA5, the gene encoding the α5 nicotinic acetylcholine receptor (nAChR) subunit, increases vulnerability to tobacco addiction and lung cancer, but underlying mechanisms are unknown. Here, we report dramatically increased nicotine consumption in mice with null mutation in Chrna5. This effect was `rescued' in knockout mice by re-expressing α5 subunits in medial habenula (MHb), and recapitulated in rats through α5 subunit knockdown in MHb. Remarkably, α5 subunit knockdown in MHb did not alter the rewarding effects of nicotine but abolished the inhibitory effects of higher nicotine doses on brain reward systems. The MHb extends projections almost exclusively to the interpeduncular nucleus (IPN). We found diminished IPN activation in response to nicotine in α5 knockout mice and disruption of IPN signaling increased nicotine intake in rats. Our findings suggest that nicotine activates the habenulo-interpeduncular pathway through α5-containing nAChRs, triggering an inhibitory motivational signal that acts to limit nicotine intake.
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                Author and article information

                Contributors
                anders.tingstrom@med.lu.se
                Journal
                J Comp Neurol
                J. Comp. Neurol
                10.1002/(ISSN)1096-9861
                CNE
                The Journal of Comparative Neurology
                John Wiley and Sons Inc. (Hoboken )
                0021-9967
                1096-9861
                24 July 2017
                15 October 2017
                : 525
                : 15 ( doiID: 10.1002/cne.v525.15 )
                : 3227-3250
                Affiliations
                [ 1 ] Psychiatric Neuromodulation Unit Department of Clinical Sciences, Faculty of Medicine, Lund University Lund Sweden
                [ 2 ] Biomedical Services Division Faculty of Medicine, Lund University Lund Sweden
                [ 3 ] Department of Neuroscience Karolinska Institute Stockholm Sweden
                Author notes
                [*] [* ] Correspondence Anders Tingström, Psychiatric Neuromodulation Unit, Biomedical Center, D11, Klinikgatan 30, Lund 221 84, Sweden. Email: anders.tingstrom@ 123456med.lu.se
                Author information
                http://orcid.org/0000-0003-2416-1768
                Article
                CNE24273
                10.1002/cne.24273
                5601234
                28657115
                ae332259-14bf-40c2-baf4-e06c5ea4aa67
                © 2017 The Authors The Journal of Comparative Neurology Published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 07 November 2016
                : 16 June 2017
                : 19 June 2017
                Page count
                Figures: 11, Tables: 3, Pages: 25, Words: 11304
                Funding
                Funded by: Swedish Research Council
                Funded by: Royal Physiographic Society of Lund
                Funded by: Vetenskapsrådet
                Funded by: Stiftelsen Professor Bror Gadelius minnesfond
                Funded by: Kungliga Fysiografiska Sällskapet i Lund
                Funded by: Gyllenstiernska Krapperupsstiftelsen
                Funded by: Stiftelsen Ellen och Henrik Sjöbrings minnesfond
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                cne24273
                October 15, 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.1.9 mode:remove_FC converted:18.09.2017

                Neurology
                habenula,rabies,thalamus,rrid: imsr_jax:000664,rrid: imsr_jax:024109,rrid: ab_10743815,rrid: ab_2571870,rrid: scr_003070

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