5-HT 1B receptor agonist attenuates cocaine self-administration after protracted abstinence and relapse in rats
The 5-HT receptor (5-HT R) agonist, CP94253, enhances cocaine intake during maintenance of self-administration (SA) but attenuates intake after 21 days of forced abstinence in male rats. We examined whether CP94253 attenuates cocaine intake in female rats after a period of abstinence, and if these a...
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Veröffentlicht in: | Journal of psychopharmacology (Oxford) 2021-10, Vol.35 (10), p.1216-1225 |
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container_title | Journal of psychopharmacology (Oxford) |
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creator | Scott, Samantha N Garcia, Raul Powell, Gregory L Doyle, Sophia M Ruscitti, Brielle Le, Tien Esquer, Aracely Blattner, Kevin M Blass, Benjamin E Neisewander, Janet L |
description | The 5-HT
receptor (5-HT
R) agonist, CP94253, enhances cocaine intake during maintenance of self-administration (SA) but attenuates intake after 21 days of forced abstinence in male rats.
We examined whether CP94253 attenuates cocaine intake in female rats after a period of abstinence, and if these attenuating effects persist or revert to enhancing cocaine intake during resumption (i.e. relapse) of daily cocaine SA.
Male and female rats trained to lever press on a fixed ratio 5 schedule of cocaine reinforcement underwent ⩾21 days of forced abstinence. They were then tested for the effects of CP94253 (5.6 mg/kg, SC) or vehicle on cocaine SA. During the test session, rats had 1-h access to the training dose of cocaine (0.75 mg/kg, IV) followed by 1-h access to a lower cocaine dose (0.075 mg/kg, IV). Rats then resumed cocaine SA for 15 days to mimic relapse and were retested as done previously. Subsequently, rats underwent abstinence again (21-60 days) and were tested for CP94253 effects on locomotion and cue reactivity (i.e. responding for light/tone cues previously paired with cocaine infusions).
Regardless of sex, CP94253 decreased cocaine intake after abstinence and during resumption of SA and decreased cue reactivity while having no effect on locomotion.
CP94253 decreases cocaine intake and cocaine seeking in both males and females even after resumption of cocaine SA. These findings suggest that the inhibitory effects of CP94253 observed after abstinence are long-lasting, and therefore, 5-HT
R agonists may have clinical efficacy as anti-relapse medications for cocaine use disorders. |
doi_str_mv | 10.1177/02698811211019279 |
format | Article |
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receptor (5-HT
R) agonist, CP94253, enhances cocaine intake during maintenance of self-administration (SA) but attenuates intake after 21 days of forced abstinence in male rats.
We examined whether CP94253 attenuates cocaine intake in female rats after a period of abstinence, and if these attenuating effects persist or revert to enhancing cocaine intake during resumption (i.e. relapse) of daily cocaine SA.
Male and female rats trained to lever press on a fixed ratio 5 schedule of cocaine reinforcement underwent ⩾21 days of forced abstinence. They were then tested for the effects of CP94253 (5.6 mg/kg, SC) or vehicle on cocaine SA. During the test session, rats had 1-h access to the training dose of cocaine (0.75 mg/kg, IV) followed by 1-h access to a lower cocaine dose (0.075 mg/kg, IV). Rats then resumed cocaine SA for 15 days to mimic relapse and were retested as done previously. Subsequently, rats underwent abstinence again (21-60 days) and were tested for CP94253 effects on locomotion and cue reactivity (i.e. responding for light/tone cues previously paired with cocaine infusions).
Regardless of sex, CP94253 decreased cocaine intake after abstinence and during resumption of SA and decreased cue reactivity while having no effect on locomotion.
CP94253 decreases cocaine intake and cocaine seeking in both males and females even after resumption of cocaine SA. These findings suggest that the inhibitory effects of CP94253 observed after abstinence are long-lasting, and therefore, 5-HT
R agonists may have clinical efficacy as anti-relapse medications for cocaine use disorders.</description><identifier>ISSN: 0269-8811</identifier><identifier>EISSN: 1461-7285</identifier><identifier>DOI: 10.1177/02698811211019279</identifier><identifier>PMID: 34049460</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Cocaine - administration & dosage ; Cocaine-Related Disorders - physiopathology ; Cues ; Female ; Locomotion - drug effects ; Male ; Pyridines - pharmacology ; Rats ; Rats, Sprague-Dawley ; Receptor, Serotonin, 5-HT1B - drug effects ; Receptor, Serotonin, 5-HT1B - metabolism ; Recurrence ; Reinforcement, Psychology ; Self Administration ; Serotonin 5-HT1 Receptor Agonists - pharmacology ; Time Factors</subject><ispartof>Journal of psychopharmacology (Oxford), 2021-10, Vol.35 (10), p.1216-1225</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1130-74da1548873c94d50023a00c926f267b7fbb7fcc71e14850a5fae4a1828afdf43</citedby><cites>FETCH-LOGICAL-c1130-74da1548873c94d50023a00c926f267b7fbb7fcc71e14850a5fae4a1828afdf43</cites><orcidid>0000-0003-0642-3875 ; 0000-0002-1096-1644</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34049460$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Scott, Samantha N</creatorcontrib><creatorcontrib>Garcia, Raul</creatorcontrib><creatorcontrib>Powell, Gregory L</creatorcontrib><creatorcontrib>Doyle, Sophia M</creatorcontrib><creatorcontrib>Ruscitti, Brielle</creatorcontrib><creatorcontrib>Le, Tien</creatorcontrib><creatorcontrib>Esquer, Aracely</creatorcontrib><creatorcontrib>Blattner, Kevin M</creatorcontrib><creatorcontrib>Blass, Benjamin E</creatorcontrib><creatorcontrib>Neisewander, Janet L</creatorcontrib><title>5-HT 1B receptor agonist attenuates cocaine self-administration after protracted abstinence and relapse in rats</title><title>Journal of psychopharmacology (Oxford)</title><addtitle>J Psychopharmacol</addtitle><description>The 5-HT
receptor (5-HT
R) agonist, CP94253, enhances cocaine intake during maintenance of self-administration (SA) but attenuates intake after 21 days of forced abstinence in male rats.
We examined whether CP94253 attenuates cocaine intake in female rats after a period of abstinence, and if these attenuating effects persist or revert to enhancing cocaine intake during resumption (i.e. relapse) of daily cocaine SA.
Male and female rats trained to lever press on a fixed ratio 5 schedule of cocaine reinforcement underwent ⩾21 days of forced abstinence. They were then tested for the effects of CP94253 (5.6 mg/kg, SC) or vehicle on cocaine SA. During the test session, rats had 1-h access to the training dose of cocaine (0.75 mg/kg, IV) followed by 1-h access to a lower cocaine dose (0.075 mg/kg, IV). Rats then resumed cocaine SA for 15 days to mimic relapse and were retested as done previously. Subsequently, rats underwent abstinence again (21-60 days) and were tested for CP94253 effects on locomotion and cue reactivity (i.e. responding for light/tone cues previously paired with cocaine infusions).
Regardless of sex, CP94253 decreased cocaine intake after abstinence and during resumption of SA and decreased cue reactivity while having no effect on locomotion.
CP94253 decreases cocaine intake and cocaine seeking in both males and females even after resumption of cocaine SA. These findings suggest that the inhibitory effects of CP94253 observed after abstinence are long-lasting, and therefore, 5-HT
R agonists may have clinical efficacy as anti-relapse medications for cocaine use disorders.</description><subject>Animals</subject><subject>Cocaine - administration & dosage</subject><subject>Cocaine-Related Disorders - physiopathology</subject><subject>Cues</subject><subject>Female</subject><subject>Locomotion - drug effects</subject><subject>Male</subject><subject>Pyridines - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor, Serotonin, 5-HT1B - drug effects</subject><subject>Receptor, Serotonin, 5-HT1B - metabolism</subject><subject>Recurrence</subject><subject>Reinforcement, Psychology</subject><subject>Self Administration</subject><subject>Serotonin 5-HT1 Receptor Agonists - pharmacology</subject><subject>Time Factors</subject><issn>0269-8811</issn><issn>1461-7285</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkMtOwzAQRS0EoqXwAWyQf8DgcZzYWUIFFKkSm7KOJvYYBbVJZLsL_p5EPDYsRiPN3HMXh7FrkLcAxtxJVdXWAigACbUy9Qlbgq5AGGXLU7ac_2IOLNhFSh9SQqWr8pwtCi11rSu5ZEMpNjsODzySozEPkeP70Hcpc8yZ-iNmStwNDrueeKJ9EOgP3RyImLuh5xgyRT7GYTq4TJ5jm_IU7h1x7P3Uu8cxEe96PhHpkp0F3Ce6-tkr9vb0uFtvxPb1-WV9vxUOoJDCaI9QamtN4WrtSylVgVK6WlVBVaY1oZ3GOQME2pYSy4CkEayyGHzQxYrBd6-LQ0qRQjPG7oDxswHZzPKaf_Im5uabGY_tgfwf8Wur-AIy5GrN</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Scott, Samantha N</creator><creator>Garcia, Raul</creator><creator>Powell, Gregory L</creator><creator>Doyle, Sophia M</creator><creator>Ruscitti, Brielle</creator><creator>Le, Tien</creator><creator>Esquer, Aracely</creator><creator>Blattner, Kevin M</creator><creator>Blass, Benjamin E</creator><creator>Neisewander, Janet L</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-0642-3875</orcidid><orcidid>https://orcid.org/0000-0002-1096-1644</orcidid></search><sort><creationdate>202110</creationdate><title>5-HT 1B receptor agonist attenuates cocaine self-administration after protracted abstinence and relapse in rats</title><author>Scott, Samantha N ; Garcia, Raul ; Powell, Gregory L ; Doyle, Sophia M ; Ruscitti, Brielle ; Le, Tien ; Esquer, Aracely ; Blattner, Kevin M ; Blass, Benjamin E ; Neisewander, Janet L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1130-74da1548873c94d50023a00c926f267b7fbb7fcc71e14850a5fae4a1828afdf43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Cocaine - administration & dosage</topic><topic>Cocaine-Related Disorders - physiopathology</topic><topic>Cues</topic><topic>Female</topic><topic>Locomotion - drug effects</topic><topic>Male</topic><topic>Pyridines - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor, Serotonin, 5-HT1B - drug effects</topic><topic>Receptor, Serotonin, 5-HT1B - metabolism</topic><topic>Recurrence</topic><topic>Reinforcement, Psychology</topic><topic>Self Administration</topic><topic>Serotonin 5-HT1 Receptor Agonists - pharmacology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scott, Samantha N</creatorcontrib><creatorcontrib>Garcia, Raul</creatorcontrib><creatorcontrib>Powell, Gregory L</creatorcontrib><creatorcontrib>Doyle, Sophia M</creatorcontrib><creatorcontrib>Ruscitti, Brielle</creatorcontrib><creatorcontrib>Le, Tien</creatorcontrib><creatorcontrib>Esquer, Aracely</creatorcontrib><creatorcontrib>Blattner, Kevin M</creatorcontrib><creatorcontrib>Blass, Benjamin E</creatorcontrib><creatorcontrib>Neisewander, Janet L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of psychopharmacology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scott, Samantha N</au><au>Garcia, Raul</au><au>Powell, Gregory L</au><au>Doyle, Sophia M</au><au>Ruscitti, Brielle</au><au>Le, Tien</au><au>Esquer, Aracely</au><au>Blattner, Kevin M</au><au>Blass, Benjamin E</au><au>Neisewander, Janet L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>5-HT 1B receptor agonist attenuates cocaine self-administration after protracted abstinence and relapse in rats</atitle><jtitle>Journal of psychopharmacology (Oxford)</jtitle><addtitle>J Psychopharmacol</addtitle><date>2021-10</date><risdate>2021</risdate><volume>35</volume><issue>10</issue><spage>1216</spage><epage>1225</epage><pages>1216-1225</pages><issn>0269-8811</issn><eissn>1461-7285</eissn><abstract>The 5-HT
receptor (5-HT
R) agonist, CP94253, enhances cocaine intake during maintenance of self-administration (SA) but attenuates intake after 21 days of forced abstinence in male rats.
We examined whether CP94253 attenuates cocaine intake in female rats after a period of abstinence, and if these attenuating effects persist or revert to enhancing cocaine intake during resumption (i.e. relapse) of daily cocaine SA.
Male and female rats trained to lever press on a fixed ratio 5 schedule of cocaine reinforcement underwent ⩾21 days of forced abstinence. They were then tested for the effects of CP94253 (5.6 mg/kg, SC) or vehicle on cocaine SA. During the test session, rats had 1-h access to the training dose of cocaine (0.75 mg/kg, IV) followed by 1-h access to a lower cocaine dose (0.075 mg/kg, IV). Rats then resumed cocaine SA for 15 days to mimic relapse and were retested as done previously. Subsequently, rats underwent abstinence again (21-60 days) and were tested for CP94253 effects on locomotion and cue reactivity (i.e. responding for light/tone cues previously paired with cocaine infusions).
Regardless of sex, CP94253 decreased cocaine intake after abstinence and during resumption of SA and decreased cue reactivity while having no effect on locomotion.
CP94253 decreases cocaine intake and cocaine seeking in both males and females even after resumption of cocaine SA. These findings suggest that the inhibitory effects of CP94253 observed after abstinence are long-lasting, and therefore, 5-HT
R agonists may have clinical efficacy as anti-relapse medications for cocaine use disorders.</abstract><cop>United States</cop><pmid>34049460</pmid><doi>10.1177/02698811211019279</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-0642-3875</orcidid><orcidid>https://orcid.org/0000-0002-1096-1644</orcidid></addata></record> |
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source | MEDLINE; SAGE Complete A-Z List |
subjects | Animals Cocaine - administration & dosage Cocaine-Related Disorders - physiopathology Cues Female Locomotion - drug effects Male Pyridines - pharmacology Rats Rats, Sprague-Dawley Receptor, Serotonin, 5-HT1B - drug effects Receptor, Serotonin, 5-HT1B - metabolism Recurrence Reinforcement, Psychology Self Administration Serotonin 5-HT1 Receptor Agonists - pharmacology Time Factors |
title | 5-HT 1B receptor agonist attenuates cocaine self-administration after protracted abstinence and relapse in rats |
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