1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      PACAP‐expressing neurons in the lateral habenula diminish negative emotional valence

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The lateral habenula (LHb) is a small, bilateral, epithalamic nucleus which processes aversive information. While primarily glutamatergic, LHb neurons express genes coding for many neuropeptides, such as Adcyap1 the gene encoding pituitary adenylate cyclase‐activating polypeptide (PACAP), which itself has been associated with anxiety and stress disorders. Using Cre‐dependent viral vectors, we targeted and characterized these neurons based on their anatomical projections and found that they projected to both the raphe and rostromedial tegmentum but only weakly to ventral tegmental area. Using RiboTag to capture ribosomal‐associated mRNA from these neurons and reanalysis of existing single cell RNA sequencing data, we did not identify a unique molecular phenotype that characterized these PACAP‐expressing neurons in LHb. In order to understand the function of these neurons, we conditionally expressed hM 3Dq DREADD selectively in LHb PACAP‐expressing neurons and chemogenetically excited these neurons during behavioral testing in the open field test, contextual fear conditioning, sucrose preference, novelty suppressed feeding, and conditioned place preference. We found that Gq activation of these neurons produce behaviors opposite to what is expected from the LHb as a whole—they decreased anxiety‐like and fear behavior and produced a conditioned place preference. In conclusion, PACAP‐expressing neurons in LHb represents a molecularly diverse population of cells that oppose the actions of the remainder of LHb neurons by being rewarding or diminishing the negative consequences of aversive events.

          Abstract

          While LHb PACAP‐expressing neurons do not define a distinct phenotypic class of LHb neurons, they are unique in behavioral control. Activation of these neurons reduces fear and anxiety and is directly rewarding.

          Related collections

          Most cited references66

          • Record: found
          • Abstract: found
          • Article: not found

          Genome-wide atlas of gene expression in the adult mouse brain.

          Molecular approaches to understanding the functional circuitry of the nervous system promise new insights into the relationship between genes, brain and behaviour. The cellular diversity of the brain necessitates a cellular resolution approach towards understanding the functional genomics of the nervous system. We describe here an anatomically comprehensive digital atlas containing the expression patterns of approximately 20,000 genes in the adult mouse brain. Data were generated using automated high-throughput procedures for in situ hybridization and data acquisition, and are publicly accessible online. Newly developed image-based informatics tools allow global genome-scale structural analysis and cross-correlation, as well as identification of regionally enriched genes. Unbiased fine-resolution analysis has identified highly specific cellular markers as well as extensive evidence of cellular heterogeneity not evident in classical neuroanatomical atlases. This highly standardized atlas provides an open, primary data resource for a wide variety of further studies concerning brain organization and function.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand.

            We evolved muscarinic receptors in yeast to generate a family of G protein-coupled receptors (GPCRs) that are activated solely by a pharmacologically inert drug-like and bioavailable compound (clozapine-N-oxide). Subsequent screening in human cell lines facilitated the creation of a family of muscarinic acetylcholine GPCRs suitable for in vitro and in situ studies. We subsequently created lines of telomerase-immortalized human pulmonary artery smooth muscle cells stably expressing all five family members and found that each one faithfully recapitulated the signaling phenotype of the parent receptor. We also expressed a G(i)-coupled designer receptor in hippocampal neurons (hM(4)D) and demonstrated its ability to induce membrane hyperpolarization and neuronal silencing. We have thus devised a facile approach for designing families of GPCRs with engineered ligand specificities. Such reverse-engineered GPCRs will prove to be powerful tools for selectively modulating signal-transduction pathways in vitro and in vivo.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Sucrose preference test for measurement of stress-induced anhedonia in mice

                Bookmark

                Author and article information

                Contributors
                neumaier@uw.edu
                Journal
                Genes Brain Behav
                Genes Brain Behav
                10.1111/(ISSN)1601-183X
                GBB
                Genes, Brain, and Behavior
                Blackwell Publishing Ltd (Oxford, UK )
                1601-1848
                1601-183X
                18 March 2022
                September 2022
                : 21
                : 7 ( doiID: 10.1111/gbb.v21.7 )
                : e12801
                Affiliations
                [ 1 ] Graduate Program in Neuroscience University of Washington Seattle Washington USA
                [ 2 ] Department of Psychiatry and Behavioral Sciences University of Washington Seattle Washington USA
                [ 3 ] Biobehavioral Imaging and Molecular Neuropsychopharmacology Unit, National Institute on Drug Abuse Intramural Research Program Baltimore Maryland USA
                [ 4 ] Department of Pharmacology University of Washington Seattle Washington USA
                [ 5 ] Department of Biology University of Washington Seattle Washington USA
                [ 6 ] Department of Anesthesiology and Pain Medicine University of Washington Seattle Washington USA
                [ 7 ] Center for Neurobiology of Addiction, Pain, and Emotion University of Washington Seattle Washington USA
                Author notes
                [*] [* ] Correspondence

                John F. Neumaier, Psychiatry and Behavioral Sciences, University of Washington, VA Puget Sound Health Care System 1660 S Columbian Way, Seattle, WA 98108, USA.

                Email: neumaier@ 123456uw.edu

                Author information
                https://orcid.org/0000-0003-4360-1503
                https://orcid.org/0000-0002-1763-7118
                Article
                GBB12801
                10.1111/gbb.12801
                9444940
                35304804
                7d9e08b3-4b79-44af-b21a-f759954c28b0
                © 2022 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ 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
                : 01 February 2022
                : 19 February 2022
                Page count
                Figures: 5, Tables: 0, Pages: 12, Words: 9275
                Funding
                Funded by: National Institute of Mental Health , doi 10.13039/100000025;
                Award ID: R01‐MH106532
                Funded by: National Institutes of Health , doi 10.13039/100000002;
                Award ID: T32‐NS099578
                Funded by: National Institute on Drug Abuse , doi 10.13039/100000026;
                Award ID: P30‐DA048736
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                September 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.1 mode:remove_FC converted:17.11.2022

                Neurosciences
                adcyap1,behavior,conditioned place preference,dreadd,fear learning,gene expression,lateral habenula,pacap,ribotag,rtqpcr

                Comments

                Comment on this article

                scite_

                Similar content373

                Cited by4

                Most referenced authors1,171