Dopamine D2 Receptors in the Paraventricular Thalamus Attenuate Cocaine Locomotor Sensitization
Alterations in thalamic dopamine (DA) or DA D2 receptors (D2Rs) have been measured in drug addiction and schizophrenia, but the relevance of thalamic D2Rs for behavior is largely unknown. Using hybridization and mice expressing green fluorescent protein (GFP) under the promoter, we found that D2R ex...
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creator | Clark, Abigail M Leroy, Felix Martyniuk, Kelly M Feng, Wendy McManus, Erika Bailey, Matthew R Javitch, Jonathan A Balsam, Peter D Kellendonk, Christoph |
description | Alterations in thalamic dopamine (DA) or DA D2 receptors (D2Rs) have been measured in drug addiction and schizophrenia, but the relevance of thalamic D2Rs for behavior is largely unknown. Using
hybridization and mice expressing green fluorescent protein (GFP) under the
promoter, we found that D2R expression within the thalamus is enriched in the paraventricular nucleus (PVT) as well as in more ventral midline thalamic nuclei. Within the PVT, D2Rs are inhibitory as their activation inhibits neuronal action potentials in brain slices. Using Cre-dependent anterograde and retrograde viral tracers, we further determined that PVT neurons are reciprocally interconnected with multiple areas of the limbic system including the amygdala and the nucleus accumbens (NAc). Based on these anatomical findings, we analyzed the role of D2Rs in the PVT in behaviors that are supported by these areas and that also have relevance for schizophrenia and drug addiction. Male and female mice with selective overexpression of D2Rs in the PVT showed attenuated cocaine locomotor sensitization, whereas anxiety levels, fear conditioning, sensorimotor gating, and food-motivated behaviors were not affected. These findings suggest the importance of PVT inhibition by D2Rs in modulating the sensitivity to cocaine, a finding that may have novel implications for human drug use. |
doi_str_mv | 10.1523/ENEURO.0227-17.2017 |
format | Article |
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hybridization and mice expressing green fluorescent protein (GFP) under the
promoter, we found that D2R expression within the thalamus is enriched in the paraventricular nucleus (PVT) as well as in more ventral midline thalamic nuclei. Within the PVT, D2Rs are inhibitory as their activation inhibits neuronal action potentials in brain slices. Using Cre-dependent anterograde and retrograde viral tracers, we further determined that PVT neurons are reciprocally interconnected with multiple areas of the limbic system including the amygdala and the nucleus accumbens (NAc). Based on these anatomical findings, we analyzed the role of D2Rs in the PVT in behaviors that are supported by these areas and that also have relevance for schizophrenia and drug addiction. Male and female mice with selective overexpression of D2Rs in the PVT showed attenuated cocaine locomotor sensitization, whereas anxiety levels, fear conditioning, sensorimotor gating, and food-motivated behaviors were not affected. These findings suggest the importance of PVT inhibition by D2Rs in modulating the sensitivity to cocaine, a finding that may have novel implications for human drug use.</description><identifier>ISSN: 2373-2822</identifier><identifier>EISSN: 2373-2822</identifier><identifier>DOI: 10.1523/ENEURO.0227-17.2017</identifier><identifier>PMID: 29071300</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Animals ; Cocaine - pharmacology ; Dopamine Agonists - pharmacology ; Dopamine Antagonists - pharmacology ; Dopamine Uptake Inhibitors - pharmacology ; Dose-Response Relationship, Drug ; Fear - drug effects ; Female ; Locomotion - drug effects ; Locomotion - genetics ; Male ; Maze Learning - drug effects ; Membrane Potentials - drug effects ; Membrane Potentials - genetics ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Midline Thalamic Nuclei - drug effects ; New Research ; Quinpirole - pharmacology ; Receptors, Dopamine D2 - genetics ; Receptors, Dopamine D2 - metabolism ; Sulpiride - pharmacology ; Transduction, Genetic</subject><ispartof>eNeuro, 2017-09, Vol.4 (5), p.ENEURO.0227-17.2017</ispartof><rights>Copyright © 2017 Clark et al. 2017 Clark et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-18ab5b39073c1306bd1dcfff8261db892786c0dbfcaad97eb61816ead4e56a123</citedby><cites>FETCH-LOGICAL-c471t-18ab5b39073c1306bd1dcfff8261db892786c0dbfcaad97eb61816ead4e56a123</cites><orcidid>0000-0002-9734-8809 ; 0000-0003-1715-3233 ; 0000-0001-8908-9790 ; 0000-0001-7581-5499 ; 0000-0002-9570-7505 ; 0000-0001-7395-2967 ; 0000-0003-4190-4121 ; 0000-0003-3302-2188</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654238/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654238/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29071300$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Clark, Abigail M</creatorcontrib><creatorcontrib>Leroy, Felix</creatorcontrib><creatorcontrib>Martyniuk, Kelly M</creatorcontrib><creatorcontrib>Feng, Wendy</creatorcontrib><creatorcontrib>McManus, Erika</creatorcontrib><creatorcontrib>Bailey, Matthew R</creatorcontrib><creatorcontrib>Javitch, Jonathan A</creatorcontrib><creatorcontrib>Balsam, Peter D</creatorcontrib><creatorcontrib>Kellendonk, Christoph</creatorcontrib><title>Dopamine D2 Receptors in the Paraventricular Thalamus Attenuate Cocaine Locomotor Sensitization</title><title>eNeuro</title><addtitle>eNeuro</addtitle><description>Alterations in thalamic dopamine (DA) or DA D2 receptors (D2Rs) have been measured in drug addiction and schizophrenia, but the relevance of thalamic D2Rs for behavior is largely unknown. Using
hybridization and mice expressing green fluorescent protein (GFP) under the
promoter, we found that D2R expression within the thalamus is enriched in the paraventricular nucleus (PVT) as well as in more ventral midline thalamic nuclei. Within the PVT, D2Rs are inhibitory as their activation inhibits neuronal action potentials in brain slices. Using Cre-dependent anterograde and retrograde viral tracers, we further determined that PVT neurons are reciprocally interconnected with multiple areas of the limbic system including the amygdala and the nucleus accumbens (NAc). Based on these anatomical findings, we analyzed the role of D2Rs in the PVT in behaviors that are supported by these areas and that also have relevance for schizophrenia and drug addiction. Male and female mice with selective overexpression of D2Rs in the PVT showed attenuated cocaine locomotor sensitization, whereas anxiety levels, fear conditioning, sensorimotor gating, and food-motivated behaviors were not affected. These findings suggest the importance of PVT inhibition by D2Rs in modulating the sensitivity to cocaine, a finding that may have novel implications for human drug use.</description><subject>Animals</subject><subject>Cocaine - pharmacology</subject><subject>Dopamine Agonists - pharmacology</subject><subject>Dopamine Antagonists - pharmacology</subject><subject>Dopamine Uptake Inhibitors - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fear - drug effects</subject><subject>Female</subject><subject>Locomotion - drug effects</subject><subject>Locomotion - genetics</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Membrane Potentials - drug effects</subject><subject>Membrane Potentials - genetics</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Midline Thalamic Nuclei - drug effects</subject><subject>New Research</subject><subject>Quinpirole - pharmacology</subject><subject>Receptors, Dopamine D2 - genetics</subject><subject>Receptors, Dopamine D2 - metabolism</subject><subject>Sulpiride - pharmacology</subject><subject>Transduction, Genetic</subject><issn>2373-2822</issn><issn>2373-2822</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkF1rwjAUhsPYmOL8BYORP1CXD9vUm4Go-wCZw-l1OE3TmdE2JYnC9uvX4ibuKgfC8573PAjdUjKiMeP3i9fFdr0aEcZERMWIESouUJ9xwSOWMnZ5NvfQ0PtPQghNmKApvUY9NiGCckL6SM5tA5WpNZ4zvNZKN8E6j02Nw07jN3Bw0HVwRu1LcHizgxKqvcfTEHS9h6DxzCro8KVVtrItjN917U0w3xCMrW_QVQGl18Pfd4C2j4vN7Dlarp5eZtNlpMaChoimkMUZb2tx1RZLspzmqiiKlCU0z9IJE2miSJ4VCiCfCJ0l7SGJhnys4wQo4wP0cMxt9lmlc9WVhlI2zlTgvqQFI___1GYnP-xBxkk8ZjxtA_gxQDnrvdPFiaVEdsrlUbnslEsqZKe8pe7O156YP8H8B1vkgEg</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Clark, Abigail M</creator><creator>Leroy, Felix</creator><creator>Martyniuk, Kelly M</creator><creator>Feng, Wendy</creator><creator>McManus, Erika</creator><creator>Bailey, Matthew R</creator><creator>Javitch, Jonathan A</creator><creator>Balsam, Peter D</creator><creator>Kellendonk, Christoph</creator><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9734-8809</orcidid><orcidid>https://orcid.org/0000-0003-1715-3233</orcidid><orcidid>https://orcid.org/0000-0001-8908-9790</orcidid><orcidid>https://orcid.org/0000-0001-7581-5499</orcidid><orcidid>https://orcid.org/0000-0002-9570-7505</orcidid><orcidid>https://orcid.org/0000-0001-7395-2967</orcidid><orcidid>https://orcid.org/0000-0003-4190-4121</orcidid><orcidid>https://orcid.org/0000-0003-3302-2188</orcidid></search><sort><creationdate>20170901</creationdate><title>Dopamine D2 Receptors in the Paraventricular Thalamus Attenuate Cocaine Locomotor Sensitization</title><author>Clark, Abigail M ; Leroy, Felix ; Martyniuk, Kelly M ; Feng, Wendy ; McManus, Erika ; Bailey, Matthew R ; Javitch, Jonathan A ; Balsam, Peter D ; Kellendonk, Christoph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-18ab5b39073c1306bd1dcfff8261db892786c0dbfcaad97eb61816ead4e56a123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Cocaine - pharmacology</topic><topic>Dopamine Agonists - pharmacology</topic><topic>Dopamine Antagonists - pharmacology</topic><topic>Dopamine Uptake Inhibitors - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fear - drug effects</topic><topic>Female</topic><topic>Locomotion - drug effects</topic><topic>Locomotion - genetics</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Membrane Potentials - drug effects</topic><topic>Membrane Potentials - genetics</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Midline Thalamic Nuclei - drug effects</topic><topic>New Research</topic><topic>Quinpirole - pharmacology</topic><topic>Receptors, Dopamine D2 - genetics</topic><topic>Receptors, Dopamine D2 - metabolism</topic><topic>Sulpiride - pharmacology</topic><topic>Transduction, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Clark, Abigail M</creatorcontrib><creatorcontrib>Leroy, Felix</creatorcontrib><creatorcontrib>Martyniuk, Kelly M</creatorcontrib><creatorcontrib>Feng, Wendy</creatorcontrib><creatorcontrib>McManus, Erika</creatorcontrib><creatorcontrib>Bailey, Matthew R</creatorcontrib><creatorcontrib>Javitch, Jonathan A</creatorcontrib><creatorcontrib>Balsam, Peter D</creatorcontrib><creatorcontrib>Kellendonk, Christoph</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>eNeuro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clark, Abigail M</au><au>Leroy, Felix</au><au>Martyniuk, Kelly M</au><au>Feng, Wendy</au><au>McManus, Erika</au><au>Bailey, Matthew R</au><au>Javitch, Jonathan A</au><au>Balsam, Peter D</au><au>Kellendonk, Christoph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dopamine D2 Receptors in the Paraventricular Thalamus Attenuate Cocaine Locomotor Sensitization</atitle><jtitle>eNeuro</jtitle><addtitle>eNeuro</addtitle><date>2017-09-01</date><risdate>2017</risdate><volume>4</volume><issue>5</issue><spage>ENEURO.0227-17.2017</spage><pages>ENEURO.0227-17.2017-</pages><issn>2373-2822</issn><eissn>2373-2822</eissn><abstract>Alterations in thalamic dopamine (DA) or DA D2 receptors (D2Rs) have been measured in drug addiction and schizophrenia, but the relevance of thalamic D2Rs for behavior is largely unknown. Using
hybridization and mice expressing green fluorescent protein (GFP) under the
promoter, we found that D2R expression within the thalamus is enriched in the paraventricular nucleus (PVT) as well as in more ventral midline thalamic nuclei. Within the PVT, D2Rs are inhibitory as their activation inhibits neuronal action potentials in brain slices. Using Cre-dependent anterograde and retrograde viral tracers, we further determined that PVT neurons are reciprocally interconnected with multiple areas of the limbic system including the amygdala and the nucleus accumbens (NAc). Based on these anatomical findings, we analyzed the role of D2Rs in the PVT in behaviors that are supported by these areas and that also have relevance for schizophrenia and drug addiction. Male and female mice with selective overexpression of D2Rs in the PVT showed attenuated cocaine locomotor sensitization, whereas anxiety levels, fear conditioning, sensorimotor gating, and food-motivated behaviors were not affected. These findings suggest the importance of PVT inhibition by D2Rs in modulating the sensitivity to cocaine, a finding that may have novel implications for human drug use.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>29071300</pmid><doi>10.1523/ENEURO.0227-17.2017</doi><orcidid>https://orcid.org/0000-0002-9734-8809</orcidid><orcidid>https://orcid.org/0000-0003-1715-3233</orcidid><orcidid>https://orcid.org/0000-0001-8908-9790</orcidid><orcidid>https://orcid.org/0000-0001-7581-5499</orcidid><orcidid>https://orcid.org/0000-0002-9570-7505</orcidid><orcidid>https://orcid.org/0000-0001-7395-2967</orcidid><orcidid>https://orcid.org/0000-0003-4190-4121</orcidid><orcidid>https://orcid.org/0000-0003-3302-2188</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cocaine - pharmacology Dopamine Agonists - pharmacology Dopamine Antagonists - pharmacology Dopamine Uptake Inhibitors - pharmacology Dose-Response Relationship, Drug Fear - drug effects Female Locomotion - drug effects Locomotion - genetics Male Maze Learning - drug effects Membrane Potentials - drug effects Membrane Potentials - genetics Mice Mice, Inbred C57BL Mice, Transgenic Midline Thalamic Nuclei - drug effects New Research Quinpirole - pharmacology Receptors, Dopamine D2 - genetics Receptors, Dopamine D2 - metabolism Sulpiride - pharmacology Transduction, Genetic |
title | Dopamine D2 Receptors in the Paraventricular Thalamus Attenuate Cocaine Locomotor Sensitization |
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