Changes in expression of c-Fos protein following cocaine-cue extinction learning
► Cocaine-cue extinction increased c-Fos expression in BLA and PL. ► Cocaine-cue and saline-cue extinction increased c-Fos expression in dSUB and IL. ► Number of lever responses correlated with c-Fos expression in NAc core and CPu. ► GluR2 expression was not altered after cocaine-cue extinction or c...
Gespeichert in:
Veröffentlicht in: | Behavioural brain research 2012-09, Vol.234 (1), p.100-106 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 106 |
---|---|
container_issue | 1 |
container_start_page | 100 |
container_title | Behavioural brain research |
container_volume | 234 |
creator | Nic Dhonnchadha, B.Á. Lovascio, B.F. Shrestha, N. Lin, A. Leite-Morris, K.A. Man, H.Y. Kaplan, G.B. Kantak, K.M. |
description | ► Cocaine-cue extinction increased c-Fos expression in BLA and PL. ► Cocaine-cue and saline-cue extinction increased c-Fos expression in dSUB and IL. ► Number of lever responses correlated with c-Fos expression in NAc core and CPu. ► GluR2 expression was not altered after cocaine-cue extinction or control training. ► Understanding extinction mechanisms may improve exposure therapy in cocaine addicts.
Extinguishing abnormally strengthened learned responses to cues associated with drugs of abuse remains a key tactic for alleviating addiction. To assist in developing pharmacotherapies to augment exposure therapy for relapse prevention, investigation into neurobiological underpinnings of drug-cue extinction learning is needed. We used regional analyses of c-Fos and GluR2 protein expression to delineate neural activity and plasticity that may be associated with cocaine-cue extinction learning. Rats were trained to self-administer cocaine paired with a light cue, and later underwent a single 2h extinction session for which cocaine was withheld but response-contingent cues were presented (cocaine-cue extinction). Control groups consisted of rats yoked to animals self-administering cocaine and receiving saline non-contingently followed by an extinction session, or rats trained to self-administer cocaine followed by a no-extinction session for which levers were retracted, and cocaine and cues were withheld. Among 11 brain sites examined, extinction training increased c-Fos expression in basolateral amygdala and prelimbic prefrontal cortex of cocaine-cue extinguished rats relative to both control conditions. In dorsal subiculum and infralimbic prefrontal cortex, extinction training increased c-Fos expression in both cocaine-cue and saline-cue extinguished rats relative to the no-extinction control condition. GluR2 protein expression was not altered in any site examined after extinction or control training. Findings suggest that basolateral amygdala and prelimbic prefrontal cortex neurons are activated during acquisition of cocaine-cue extinction learning, a process that is independent of changes in GluR2 abundance. Other sites are implicated in processing the significance of cues that are present early in extinction training. |
doi_str_mv | 10.1016/j.bbr.2012.06.010 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3412160</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0166432812004238</els_id><sourcerecordid>1030347951</sourcerecordid><originalsourceid>FETCH-LOGICAL-c451t-52e7873a98cd4f345b459e121cf668e7d8f95ba55714a06b6e4d845b10f6816f3</originalsourceid><addsrcrecordid>eNp9kU9P3DAQxa0KVBbaD9ALypFLUo_jP4kqVapWBSohwaE9W44zXrzK2oudhfbb49VS1F44zeH93pvRPEI-AW2Agvy8boYhNYwCa6hsKNB3ZAGdYrUSvD8ii8LImresOyGnOa8ppZwKeE9OGFMMpBILcre8N2GFufKhwt_bhDn7GKroKltfxlxtU5yxaC5OU3zyYVXZaI0PWNsdFsfsg533jglNCkX_QI6dmTJ-fJln5Nfl95_L6_rm9urH8ttNbbmAuRYMVada03d25K7lYuCiR2BgnZQdqrFzvRiMEAq4oXKQyMeuUECd7EC69ox8PeRud8MGR4thTmbS2-Q3Jv3R0Xj9vxL8vV7FR93yskXSEnDxEpDiww7zrDc-W5wmEzDusgba0parXkBB4YDaFHNO6F7XANX7JvRalyb0vglNpS5NFM_5v_e9Ov6-vgBfDgCWLz16TDpbj8Hi6BPaWY_RvxH_DMpMmjE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1030347951</pqid></control><display><type>article</type><title>Changes in expression of c-Fos protein following cocaine-cue extinction learning</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Nic Dhonnchadha, B.Á. ; Lovascio, B.F. ; Shrestha, N. ; Lin, A. ; Leite-Morris, K.A. ; Man, H.Y. ; Kaplan, G.B. ; Kantak, K.M.</creator><creatorcontrib>Nic Dhonnchadha, B.Á. ; Lovascio, B.F. ; Shrestha, N. ; Lin, A. ; Leite-Morris, K.A. ; Man, H.Y. ; Kaplan, G.B. ; Kantak, K.M.</creatorcontrib><description>► Cocaine-cue extinction increased c-Fos expression in BLA and PL. ► Cocaine-cue and saline-cue extinction increased c-Fos expression in dSUB and IL. ► Number of lever responses correlated with c-Fos expression in NAc core and CPu. ► GluR2 expression was not altered after cocaine-cue extinction or control training. ► Understanding extinction mechanisms may improve exposure therapy in cocaine addicts.
Extinguishing abnormally strengthened learned responses to cues associated with drugs of abuse remains a key tactic for alleviating addiction. To assist in developing pharmacotherapies to augment exposure therapy for relapse prevention, investigation into neurobiological underpinnings of drug-cue extinction learning is needed. We used regional analyses of c-Fos and GluR2 protein expression to delineate neural activity and plasticity that may be associated with cocaine-cue extinction learning. Rats were trained to self-administer cocaine paired with a light cue, and later underwent a single 2h extinction session for which cocaine was withheld but response-contingent cues were presented (cocaine-cue extinction). Control groups consisted of rats yoked to animals self-administering cocaine and receiving saline non-contingently followed by an extinction session, or rats trained to self-administer cocaine followed by a no-extinction session for which levers were retracted, and cocaine and cues were withheld. Among 11 brain sites examined, extinction training increased c-Fos expression in basolateral amygdala and prelimbic prefrontal cortex of cocaine-cue extinguished rats relative to both control conditions. In dorsal subiculum and infralimbic prefrontal cortex, extinction training increased c-Fos expression in both cocaine-cue and saline-cue extinguished rats relative to the no-extinction control condition. GluR2 protein expression was not altered in any site examined after extinction or control training. Findings suggest that basolateral amygdala and prelimbic prefrontal cortex neurons are activated during acquisition of cocaine-cue extinction learning, a process that is independent of changes in GluR2 abundance. Other sites are implicated in processing the significance of cues that are present early in extinction training.</description><identifier>ISSN: 0166-4328</identifier><identifier>EISSN: 1872-7549</identifier><identifier>DOI: 10.1016/j.bbr.2012.06.010</identifier><identifier>PMID: 22721675</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Basolateral amygdala ; Behavior, Addictive ; Behavior, Animal - drug effects ; Brain - drug effects ; Brain - metabolism ; c-Fos protein ; Cocaine ; Cocaine - pharmacology ; Extinction learning ; Extinction, Psychological - drug effects ; GluR2 protein ; Learning - drug effects ; Male ; Proto-Oncogene Proteins c-fos - metabolism ; Rats ; Rats, Wistar ; Receptors, AMPA - metabolism ; Self-administration</subject><ispartof>Behavioural brain research, 2012-09, Vol.234 (1), p.100-106</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><rights>2012 Elsevier B.V. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-52e7873a98cd4f345b459e121cf668e7d8f95ba55714a06b6e4d845b10f6816f3</citedby><cites>FETCH-LOGICAL-c451t-52e7873a98cd4f345b459e121cf668e7d8f95ba55714a06b6e4d845b10f6816f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0166432812004238$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22721675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nic Dhonnchadha, B.Á.</creatorcontrib><creatorcontrib>Lovascio, B.F.</creatorcontrib><creatorcontrib>Shrestha, N.</creatorcontrib><creatorcontrib>Lin, A.</creatorcontrib><creatorcontrib>Leite-Morris, K.A.</creatorcontrib><creatorcontrib>Man, H.Y.</creatorcontrib><creatorcontrib>Kaplan, G.B.</creatorcontrib><creatorcontrib>Kantak, K.M.</creatorcontrib><title>Changes in expression of c-Fos protein following cocaine-cue extinction learning</title><title>Behavioural brain research</title><addtitle>Behav Brain Res</addtitle><description>► Cocaine-cue extinction increased c-Fos expression in BLA and PL. ► Cocaine-cue and saline-cue extinction increased c-Fos expression in dSUB and IL. ► Number of lever responses correlated with c-Fos expression in NAc core and CPu. ► GluR2 expression was not altered after cocaine-cue extinction or control training. ► Understanding extinction mechanisms may improve exposure therapy in cocaine addicts.
Extinguishing abnormally strengthened learned responses to cues associated with drugs of abuse remains a key tactic for alleviating addiction. To assist in developing pharmacotherapies to augment exposure therapy for relapse prevention, investigation into neurobiological underpinnings of drug-cue extinction learning is needed. We used regional analyses of c-Fos and GluR2 protein expression to delineate neural activity and plasticity that may be associated with cocaine-cue extinction learning. Rats were trained to self-administer cocaine paired with a light cue, and later underwent a single 2h extinction session for which cocaine was withheld but response-contingent cues were presented (cocaine-cue extinction). Control groups consisted of rats yoked to animals self-administering cocaine and receiving saline non-contingently followed by an extinction session, or rats trained to self-administer cocaine followed by a no-extinction session for which levers were retracted, and cocaine and cues were withheld. Among 11 brain sites examined, extinction training increased c-Fos expression in basolateral amygdala and prelimbic prefrontal cortex of cocaine-cue extinguished rats relative to both control conditions. In dorsal subiculum and infralimbic prefrontal cortex, extinction training increased c-Fos expression in both cocaine-cue and saline-cue extinguished rats relative to the no-extinction control condition. GluR2 protein expression was not altered in any site examined after extinction or control training. Findings suggest that basolateral amygdala and prelimbic prefrontal cortex neurons are activated during acquisition of cocaine-cue extinction learning, a process that is independent of changes in GluR2 abundance. Other sites are implicated in processing the significance of cues that are present early in extinction training.</description><subject>Animals</subject><subject>Basolateral amygdala</subject><subject>Behavior, Addictive</subject><subject>Behavior, Animal - drug effects</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>c-Fos protein</subject><subject>Cocaine</subject><subject>Cocaine - pharmacology</subject><subject>Extinction learning</subject><subject>Extinction, Psychological - drug effects</subject><subject>GluR2 protein</subject><subject>Learning - drug effects</subject><subject>Male</subject><subject>Proto-Oncogene Proteins c-fos - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, AMPA - metabolism</subject><subject>Self-administration</subject><issn>0166-4328</issn><issn>1872-7549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9P3DAQxa0KVBbaD9ALypFLUo_jP4kqVapWBSohwaE9W44zXrzK2oudhfbb49VS1F44zeH93pvRPEI-AW2Agvy8boYhNYwCa6hsKNB3ZAGdYrUSvD8ii8LImresOyGnOa8ppZwKeE9OGFMMpBILcre8N2GFufKhwt_bhDn7GKroKltfxlxtU5yxaC5OU3zyYVXZaI0PWNsdFsfsg533jglNCkX_QI6dmTJ-fJln5Nfl95_L6_rm9urH8ttNbbmAuRYMVada03d25K7lYuCiR2BgnZQdqrFzvRiMEAq4oXKQyMeuUECd7EC69ox8PeRud8MGR4thTmbS2-Q3Jv3R0Xj9vxL8vV7FR93yskXSEnDxEpDiww7zrDc-W5wmEzDusgba0parXkBB4YDaFHNO6F7XANX7JvRalyb0vglNpS5NFM_5v_e9Ov6-vgBfDgCWLz16TDpbj8Hi6BPaWY_RvxH_DMpMmjE</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Nic Dhonnchadha, B.Á.</creator><creator>Lovascio, B.F.</creator><creator>Shrestha, N.</creator><creator>Lin, A.</creator><creator>Leite-Morris, K.A.</creator><creator>Man, H.Y.</creator><creator>Kaplan, G.B.</creator><creator>Kantak, K.M.</creator><general>Elsevier B.V</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120901</creationdate><title>Changes in expression of c-Fos protein following cocaine-cue extinction learning</title><author>Nic Dhonnchadha, B.Á. ; Lovascio, B.F. ; Shrestha, N. ; Lin, A. ; Leite-Morris, K.A. ; Man, H.Y. ; Kaplan, G.B. ; Kantak, K.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-52e7873a98cd4f345b459e121cf668e7d8f95ba55714a06b6e4d845b10f6816f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Basolateral amygdala</topic><topic>Behavior, Addictive</topic><topic>Behavior, Animal - drug effects</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>c-Fos protein</topic><topic>Cocaine</topic><topic>Cocaine - pharmacology</topic><topic>Extinction learning</topic><topic>Extinction, Psychological - drug effects</topic><topic>GluR2 protein</topic><topic>Learning - drug effects</topic><topic>Male</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, AMPA - metabolism</topic><topic>Self-administration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nic Dhonnchadha, B.Á.</creatorcontrib><creatorcontrib>Lovascio, B.F.</creatorcontrib><creatorcontrib>Shrestha, N.</creatorcontrib><creatorcontrib>Lin, A.</creatorcontrib><creatorcontrib>Leite-Morris, K.A.</creatorcontrib><creatorcontrib>Man, H.Y.</creatorcontrib><creatorcontrib>Kaplan, G.B.</creatorcontrib><creatorcontrib>Kantak, K.M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Behavioural brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nic Dhonnchadha, B.Á.</au><au>Lovascio, B.F.</au><au>Shrestha, N.</au><au>Lin, A.</au><au>Leite-Morris, K.A.</au><au>Man, H.Y.</au><au>Kaplan, G.B.</au><au>Kantak, K.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in expression of c-Fos protein following cocaine-cue extinction learning</atitle><jtitle>Behavioural brain research</jtitle><addtitle>Behav Brain Res</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>234</volume><issue>1</issue><spage>100</spage><epage>106</epage><pages>100-106</pages><issn>0166-4328</issn><eissn>1872-7549</eissn><abstract>► Cocaine-cue extinction increased c-Fos expression in BLA and PL. ► Cocaine-cue and saline-cue extinction increased c-Fos expression in dSUB and IL. ► Number of lever responses correlated with c-Fos expression in NAc core and CPu. ► GluR2 expression was not altered after cocaine-cue extinction or control training. ► Understanding extinction mechanisms may improve exposure therapy in cocaine addicts.
Extinguishing abnormally strengthened learned responses to cues associated with drugs of abuse remains a key tactic for alleviating addiction. To assist in developing pharmacotherapies to augment exposure therapy for relapse prevention, investigation into neurobiological underpinnings of drug-cue extinction learning is needed. We used regional analyses of c-Fos and GluR2 protein expression to delineate neural activity and plasticity that may be associated with cocaine-cue extinction learning. Rats were trained to self-administer cocaine paired with a light cue, and later underwent a single 2h extinction session for which cocaine was withheld but response-contingent cues were presented (cocaine-cue extinction). Control groups consisted of rats yoked to animals self-administering cocaine and receiving saline non-contingently followed by an extinction session, or rats trained to self-administer cocaine followed by a no-extinction session for which levers were retracted, and cocaine and cues were withheld. Among 11 brain sites examined, extinction training increased c-Fos expression in basolateral amygdala and prelimbic prefrontal cortex of cocaine-cue extinguished rats relative to both control conditions. In dorsal subiculum and infralimbic prefrontal cortex, extinction training increased c-Fos expression in both cocaine-cue and saline-cue extinguished rats relative to the no-extinction control condition. GluR2 protein expression was not altered in any site examined after extinction or control training. Findings suggest that basolateral amygdala and prelimbic prefrontal cortex neurons are activated during acquisition of cocaine-cue extinction learning, a process that is independent of changes in GluR2 abundance. Other sites are implicated in processing the significance of cues that are present early in extinction training.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>22721675</pmid><doi>10.1016/j.bbr.2012.06.010</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0166-4328 |
ispartof | Behavioural brain research, 2012-09, Vol.234 (1), p.100-106 |
issn | 0166-4328 1872-7549 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3412160 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Animals Basolateral amygdala Behavior, Addictive Behavior, Animal - drug effects Brain - drug effects Brain - metabolism c-Fos protein Cocaine Cocaine - pharmacology Extinction learning Extinction, Psychological - drug effects GluR2 protein Learning - drug effects Male Proto-Oncogene Proteins c-fos - metabolism Rats Rats, Wistar Receptors, AMPA - metabolism Self-administration |
title | Changes in expression of c-Fos protein following cocaine-cue extinction learning |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T22%3A59%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Changes%20in%20expression%20of%20c-Fos%20protein%20following%20cocaine-cue%20extinction%20learning&rft.jtitle=Behavioural%20brain%20research&rft.au=Nic%20Dhonnchadha,%20B.%C3%81.&rft.date=2012-09-01&rft.volume=234&rft.issue=1&rft.spage=100&rft.epage=106&rft.pages=100-106&rft.issn=0166-4328&rft.eissn=1872-7549&rft_id=info:doi/10.1016/j.bbr.2012.06.010&rft_dat=%3Cproquest_pubme%3E1030347951%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1030347951&rft_id=info:pmid/22721675&rft_els_id=S0166432812004238&rfr_iscdi=true |