Chronic bupropion attenuated the anhedonic component of nicotine withdrawal in rats via inhibition of dopamine reuptake in the nucleus accumbens shell
Bupropion, a dopamine reuptake inhibitor, is an effective therapy for smoking cessation, but the behavioral and neurochemical mechanisms mediating its antismoking properties are relatively unknown. To explore the hypothesis that bupropion ameliorates nicotine withdrawal partly by a dopamine‐dependen...
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Veröffentlicht in: | The European journal of neuroscience 2007-05, Vol.25 (10), p.3099-3108 |
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description | Bupropion, a dopamine reuptake inhibitor, is an effective therapy for smoking cessation, but the behavioral and neurochemical mechanisms mediating its antismoking properties are relatively unknown. To explore the hypothesis that bupropion ameliorates nicotine withdrawal partly by a dopamine‐dependent mechanism, we investigated the effects of chronic bupropion on potassium‐stimulated dopamine overflow in the nucleus accumbens shell in nicotine‐withdrawing rats. We also assessed the effects of chronic bupropion on behavioral aspects of nicotine withdrawal measured by elevations in brain reward thresholds and somatic signs of withdrawal. Rats were treated with nicotine or saline for 7 days and then coadministration of bupropion or saline was initiated. After 14 days of coadministration of bupropion/saline and nicotine/saline, nicotine/saline administration was terminated, whereas bupropion/saline administration continued. These conditions mimic bupropion administration in human smokers. Cessation of nicotine administration in non‐bupropion‐treated rats elevated reward thresholds reflecting a reward deficit, increased somatic signs and diminished potassium‐evoked dopamine overflow in the nucleus accumbens shell. Chronic bupropion lowered reward thresholds and increased potassium‐evoked dopamine release regardless of previous nicotine exposure, possibly by inhibition of dopamine reuptake, and thus attenuated the anhedonic and neurochemical effects of nicotine withdrawal. Chronic bupropion blocked withdrawal‐associated increased somatic signs. Finally, acute experimenter‐administered nicotine enhanced brain reward function equally in all groups, indicating that bupropion does not alter the reward‐facilitating effects of experimenter‐administered nicotine. In conclusion, the bupropion‐induced increase in extracellular dopamine in the nucleus accumbens shell may ameliorate the anhedonia associated with nicotine withdrawal, which in turn may facilitate smoking cessation. |
doi_str_mv | 10.1111/j.1460-9568.2007.05546.x |
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To explore the hypothesis that bupropion ameliorates nicotine withdrawal partly by a dopamine‐dependent mechanism, we investigated the effects of chronic bupropion on potassium‐stimulated dopamine overflow in the nucleus accumbens shell in nicotine‐withdrawing rats. We also assessed the effects of chronic bupropion on behavioral aspects of nicotine withdrawal measured by elevations in brain reward thresholds and somatic signs of withdrawal. Rats were treated with nicotine or saline for 7 days and then coadministration of bupropion or saline was initiated. After 14 days of coadministration of bupropion/saline and nicotine/saline, nicotine/saline administration was terminated, whereas bupropion/saline administration continued. These conditions mimic bupropion administration in human smokers. Cessation of nicotine administration in non‐bupropion‐treated rats elevated reward thresholds reflecting a reward deficit, increased somatic signs and diminished potassium‐evoked dopamine overflow in the nucleus accumbens shell. Chronic bupropion lowered reward thresholds and increased potassium‐evoked dopamine release regardless of previous nicotine exposure, possibly by inhibition of dopamine reuptake, and thus attenuated the anhedonic and neurochemical effects of nicotine withdrawal. Chronic bupropion blocked withdrawal‐associated increased somatic signs. Finally, acute experimenter‐administered nicotine enhanced brain reward function equally in all groups, indicating that bupropion does not alter the reward‐facilitating effects of experimenter‐administered nicotine. In conclusion, the bupropion‐induced increase in extracellular dopamine in the nucleus accumbens shell may ameliorate the anhedonia associated with nicotine withdrawal, which in turn may facilitate smoking cessation.</description><identifier>ISSN: 0953-816X</identifier><identifier>EISSN: 1460-9568</identifier><identifier>DOI: 10.1111/j.1460-9568.2007.05546.x</identifier><identifier>PMID: 17561823</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; brain reward function ; Bupropion - pharmacology ; Bupropion - therapeutic use ; chronic bupropion ; Dopamine - metabolism ; Dopamine Uptake Inhibitors - pharmacology ; Dopamine Uptake Inhibitors - therapeutic use ; Drug Administration Schedule ; extracellular dopamine ; Male ; nicotine withdrawal ; Nucleus Accumbens - drug effects ; Nucleus Accumbens - metabolism ; nucleus accumbens shell ; Potassium - pharmacology ; rat ; Rats ; Rats, Wistar ; Reward ; Substance Withdrawal Syndrome - drug therapy ; Substance Withdrawal Syndrome - metabolism ; Substance Withdrawal Syndrome - physiopathology ; Synaptic Transmission - drug effects ; Synaptic Transmission - physiology ; Tobacco Use Disorder - drug therapy ; Tobacco Use Disorder - metabolism ; Tobacco Use Disorder - physiopathology ; Up-Regulation - drug effects ; Up-Regulation - physiology</subject><ispartof>The European journal of neuroscience, 2007-05, Vol.25 (10), p.3099-3108</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5026-d53b9a2b21a5f9b3b85816f57851384f57d5932b01d898b26f66a24b238693413</citedby><cites>FETCH-LOGICAL-c5026-d53b9a2b21a5f9b3b85816f57851384f57d5932b01d898b26f66a24b238693413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1460-9568.2007.05546.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1460-9568.2007.05546.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17561823$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Paterson, Neil E.</creatorcontrib><creatorcontrib>Balfour, David J.</creatorcontrib><creatorcontrib>Markou, Athina</creatorcontrib><title>Chronic bupropion attenuated the anhedonic component of nicotine withdrawal in rats via inhibition of dopamine reuptake in the nucleus accumbens shell</title><title>The European journal of neuroscience</title><addtitle>Eur J Neurosci</addtitle><description>Bupropion, a dopamine reuptake inhibitor, is an effective therapy for smoking cessation, but the behavioral and neurochemical mechanisms mediating its antismoking properties are relatively unknown. To explore the hypothesis that bupropion ameliorates nicotine withdrawal partly by a dopamine‐dependent mechanism, we investigated the effects of chronic bupropion on potassium‐stimulated dopamine overflow in the nucleus accumbens shell in nicotine‐withdrawing rats. We also assessed the effects of chronic bupropion on behavioral aspects of nicotine withdrawal measured by elevations in brain reward thresholds and somatic signs of withdrawal. Rats were treated with nicotine or saline for 7 days and then coadministration of bupropion or saline was initiated. After 14 days of coadministration of bupropion/saline and nicotine/saline, nicotine/saline administration was terminated, whereas bupropion/saline administration continued. These conditions mimic bupropion administration in human smokers. Cessation of nicotine administration in non‐bupropion‐treated rats elevated reward thresholds reflecting a reward deficit, increased somatic signs and diminished potassium‐evoked dopamine overflow in the nucleus accumbens shell. Chronic bupropion lowered reward thresholds and increased potassium‐evoked dopamine release regardless of previous nicotine exposure, possibly by inhibition of dopamine reuptake, and thus attenuated the anhedonic and neurochemical effects of nicotine withdrawal. Chronic bupropion blocked withdrawal‐associated increased somatic signs. Finally, acute experimenter‐administered nicotine enhanced brain reward function equally in all groups, indicating that bupropion does not alter the reward‐facilitating effects of experimenter‐administered nicotine. In conclusion, the bupropion‐induced increase in extracellular dopamine in the nucleus accumbens shell may ameliorate the anhedonia associated with nicotine withdrawal, which in turn may facilitate smoking cessation.</description><subject>Animals</subject><subject>brain reward function</subject><subject>Bupropion - pharmacology</subject><subject>Bupropion - therapeutic use</subject><subject>chronic bupropion</subject><subject>Dopamine - metabolism</subject><subject>Dopamine Uptake Inhibitors - pharmacology</subject><subject>Dopamine Uptake Inhibitors - therapeutic use</subject><subject>Drug Administration Schedule</subject><subject>extracellular dopamine</subject><subject>Male</subject><subject>nicotine withdrawal</subject><subject>Nucleus Accumbens - drug effects</subject><subject>Nucleus Accumbens - metabolism</subject><subject>nucleus accumbens shell</subject><subject>Potassium - pharmacology</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reward</subject><subject>Substance Withdrawal Syndrome - drug therapy</subject><subject>Substance Withdrawal Syndrome - metabolism</subject><subject>Substance Withdrawal Syndrome - physiopathology</subject><subject>Synaptic Transmission - drug effects</subject><subject>Synaptic Transmission - physiology</subject><subject>Tobacco Use Disorder - drug therapy</subject><subject>Tobacco Use Disorder - metabolism</subject><subject>Tobacco Use Disorder - physiopathology</subject><subject>Up-Regulation - drug effects</subject><subject>Up-Regulation - physiology</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU-P1CAYxonRuOPqVzCcvLXyp1B68GAm66hZVxM1eiPQ0pTZFipQZ_aL-HmlO5P1KhfewO954H0fACBGJc7r9b7EFUdFw7goCUJ1iRireHl8BDYPF4_BBjWMFgLznxfgWYx7hJDgFXsKLnDNOBaEbsCf7RC8sy3Uyxz8bL2DKiXjFpVMB9NgoHKD6e6R1k-zd8Yl6HuYD3yyzsCDTUMX1EGN0DoYVIrwt1W5Hqy2aTXMdOdnNa10MMuc1K1Z2dXdLe1olghV2y6TNi7COJhxfA6e9GqM5sV5vwTf3119274vrj_vPmzfXhctQ4QXHaO6UUQTrFjfaKoFy-32rBYMU1HlomMNJRrhTjRCE95zrkilCRW8oRWml-DVyTc3_2sxMcnJxjZ_QDnjlygJYoQTWmdQnMA2-BiD6eUc7KTCncRIrpnIvVxHL9fRyzUTeZ-JPGbpy_Mbi55M9094DiEDb07AwY7m7r-N5dXHm7XK-uKktzGZ44NehVvJa1oz-eNmJz_hese-ftnKHf0LISasaA</recordid><startdate>200705</startdate><enddate>200705</enddate><creator>Paterson, Neil E.</creator><creator>Balfour, David J.</creator><creator>Markou, Athina</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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>7TK</scope></search><sort><creationdate>200705</creationdate><title>Chronic bupropion attenuated the anhedonic component of nicotine withdrawal in rats via inhibition of dopamine reuptake in the nucleus accumbens shell</title><author>Paterson, Neil E. ; Balfour, David J. ; Markou, Athina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5026-d53b9a2b21a5f9b3b85816f57851384f57d5932b01d898b26f66a24b238693413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>brain reward function</topic><topic>Bupropion - pharmacology</topic><topic>Bupropion - therapeutic use</topic><topic>chronic bupropion</topic><topic>Dopamine - metabolism</topic><topic>Dopamine Uptake Inhibitors - pharmacology</topic><topic>Dopamine Uptake Inhibitors - therapeutic use</topic><topic>Drug Administration Schedule</topic><topic>extracellular dopamine</topic><topic>Male</topic><topic>nicotine withdrawal</topic><topic>Nucleus Accumbens - drug effects</topic><topic>Nucleus Accumbens - metabolism</topic><topic>nucleus accumbens shell</topic><topic>Potassium - pharmacology</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reward</topic><topic>Substance Withdrawal Syndrome - drug therapy</topic><topic>Substance Withdrawal Syndrome - metabolism</topic><topic>Substance Withdrawal Syndrome - physiopathology</topic><topic>Synaptic Transmission - drug effects</topic><topic>Synaptic Transmission - physiology</topic><topic>Tobacco Use Disorder - drug therapy</topic><topic>Tobacco Use Disorder - metabolism</topic><topic>Tobacco Use Disorder - physiopathology</topic><topic>Up-Regulation - drug effects</topic><topic>Up-Regulation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paterson, Neil E.</creatorcontrib><creatorcontrib>Balfour, David J.</creatorcontrib><creatorcontrib>Markou, Athina</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>The European journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paterson, Neil E.</au><au>Balfour, David J.</au><au>Markou, Athina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic bupropion attenuated the anhedonic component of nicotine withdrawal in rats via inhibition of dopamine reuptake in the nucleus accumbens shell</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>2007-05</date><risdate>2007</risdate><volume>25</volume><issue>10</issue><spage>3099</spage><epage>3108</epage><pages>3099-3108</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><abstract>Bupropion, a dopamine reuptake inhibitor, is an effective therapy for smoking cessation, but the behavioral and neurochemical mechanisms mediating its antismoking properties are relatively unknown. To explore the hypothesis that bupropion ameliorates nicotine withdrawal partly by a dopamine‐dependent mechanism, we investigated the effects of chronic bupropion on potassium‐stimulated dopamine overflow in the nucleus accumbens shell in nicotine‐withdrawing rats. We also assessed the effects of chronic bupropion on behavioral aspects of nicotine withdrawal measured by elevations in brain reward thresholds and somatic signs of withdrawal. Rats were treated with nicotine or saline for 7 days and then coadministration of bupropion or saline was initiated. After 14 days of coadministration of bupropion/saline and nicotine/saline, nicotine/saline administration was terminated, whereas bupropion/saline administration continued. These conditions mimic bupropion administration in human smokers. Cessation of nicotine administration in non‐bupropion‐treated rats elevated reward thresholds reflecting a reward deficit, increased somatic signs and diminished potassium‐evoked dopamine overflow in the nucleus accumbens shell. Chronic bupropion lowered reward thresholds and increased potassium‐evoked dopamine release regardless of previous nicotine exposure, possibly by inhibition of dopamine reuptake, and thus attenuated the anhedonic and neurochemical effects of nicotine withdrawal. Chronic bupropion blocked withdrawal‐associated increased somatic signs. Finally, acute experimenter‐administered nicotine enhanced brain reward function equally in all groups, indicating that bupropion does not alter the reward‐facilitating effects of experimenter‐administered nicotine. In conclusion, the bupropion‐induced increase in extracellular dopamine in the nucleus accumbens shell may ameliorate the anhedonia associated with nicotine withdrawal, which in turn may facilitate smoking cessation.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17561823</pmid><doi>10.1111/j.1460-9568.2007.05546.x</doi><tpages>10</tpages></addata></record> |
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subjects | Animals brain reward function Bupropion - pharmacology Bupropion - therapeutic use chronic bupropion Dopamine - metabolism Dopamine Uptake Inhibitors - pharmacology Dopamine Uptake Inhibitors - therapeutic use Drug Administration Schedule extracellular dopamine Male nicotine withdrawal Nucleus Accumbens - drug effects Nucleus Accumbens - metabolism nucleus accumbens shell Potassium - pharmacology rat Rats Rats, Wistar Reward Substance Withdrawal Syndrome - drug therapy Substance Withdrawal Syndrome - metabolism Substance Withdrawal Syndrome - physiopathology Synaptic Transmission - drug effects Synaptic Transmission - physiology Tobacco Use Disorder - drug therapy Tobacco Use Disorder - metabolism Tobacco Use Disorder - physiopathology Up-Regulation - drug effects Up-Regulation - physiology |
title | Chronic bupropion attenuated the anhedonic component of nicotine withdrawal in rats via inhibition of dopamine reuptake in the nucleus accumbens shell |
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