Nicotine Indirectly Inhibits [3H]Dopamine Uptake at Concentrations That Do Not Directly Promote [3H]Dopamine Release in Rat Striatum

: The effects of both (–)‐ and (+)‐nicotine isomers were examined on in vitro uptake and release of [3H]dopamine in rat striatum. Both isomers inhibited uptake of [3H]dopamine in chopped tissue at concentrations well below those necessary for promoting release of preloaded [3H]dopamine. (–)‐Nicotine...

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Veröffentlicht in:Journal of neurochemistry 1991-02, Vol.56 (2), p.603-610
Hauptverfasser: Izenwasser, Sari, Jacocks, Henry M., Rosenberger, John G., Cox, Brian M.
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container_issue 2
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creator Izenwasser, Sari
Jacocks, Henry M.
Rosenberger, John G.
Cox, Brian M.
description : The effects of both (–)‐ and (+)‐nicotine isomers were examined on in vitro uptake and release of [3H]dopamine in rat striatum. Both isomers inhibited uptake of [3H]dopamine in chopped tissue at concentrations well below those necessary for promoting release of preloaded [3H]dopamine. (–)‐Nicotine was more potent than (+)‐nicotine both at inhibiting uptake and at promoting release. Unlike other dopamine uptake inhibitors, however, nicotine inhibited only 50% of the total uptake. In the presence of 1 nM nicotine, the residual [3H]dopamine uptake was less sensitive to inhibition by cocaine than uptake in the absence of nicotine. Nicotine did not compete against the binding of [3H]GBR 12935, a selective dopamine uptake inhibitor. The nicotinic receptor agonists carbachol and 1,1‐dimethyl‐4‐phenylpiperazinium iodide also inhibited uptake, whereas the nicotinic antagonists chlorisondamine and mecamylamine blocked nicotine's effect. Thus, the effect of nicotine on dopamine uptake appears to be mediated by a receptor similar to the nicotinic acetylcholine receptor. These receptors do not seem to be on the terminals that are accumulating dopamine, however, since tetrodotoxin prevented the effect of nicotine on [3H]dopamine uptake and nicotine had no effect on uptake in a synaptosomal preparation.
doi_str_mv 10.1111/j.1471-4159.1991.tb08192.x
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Both isomers inhibited uptake of [3H]dopamine in chopped tissue at concentrations well below those necessary for promoting release of preloaded [3H]dopamine. (–)‐Nicotine was more potent than (+)‐nicotine both at inhibiting uptake and at promoting release. Unlike other dopamine uptake inhibitors, however, nicotine inhibited only 50% of the total uptake. In the presence of 1 nM nicotine, the residual [3H]dopamine uptake was less sensitive to inhibition by cocaine than uptake in the absence of nicotine. Nicotine did not compete against the binding of [3H]GBR 12935, a selective dopamine uptake inhibitor. The nicotinic receptor agonists carbachol and 1,1‐dimethyl‐4‐phenylpiperazinium iodide also inhibited uptake, whereas the nicotinic antagonists chlorisondamine and mecamylamine blocked nicotine's effect. Thus, the effect of nicotine on dopamine uptake appears to be mediated by a receptor similar to the nicotinic acetylcholine receptor. 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Psychology ; Male ; Mecamylamine - pharmacology ; Microbiology ; Mycology ; Nicotine ; Nicotine - administration &amp; dosage ; Nicotine - metabolism ; Nicotine - pharmacology ; Piperazines - metabolism ; Rats ; Rats, Inbred Strains ; Receptors, Nicotinic - drug effects ; Receptors, Nicotinic - physiology ; Synaptosomes - drug effects ; Synaptosomes - metabolism ; Systematics</subject><ispartof>Journal of neurochemistry, 1991-02, Vol.56 (2), p.603-610</ispartof><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3993-b46fb1c6e7265642c24ae7fa63a76b8d5c5236370312f6c19be47421e46587c33</citedby><cites>FETCH-LOGICAL-c3993-b46fb1c6e7265642c24ae7fa63a76b8d5c5236370312f6c19be47421e46587c33</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.1471-4159.1991.tb08192.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-4159.1991.tb08192.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=19661668$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1988558$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Izenwasser, Sari</creatorcontrib><creatorcontrib>Jacocks, Henry M.</creatorcontrib><creatorcontrib>Rosenberger, John G.</creatorcontrib><creatorcontrib>Cox, Brian M.</creatorcontrib><title>Nicotine Indirectly Inhibits [3H]Dopamine Uptake at Concentrations That Do Not Directly Promote [3H]Dopamine Release in Rat Striatum</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>: The effects of both (–)‐ and (+)‐nicotine isomers were examined on in vitro uptake and release of [3H]dopamine in rat striatum. Both isomers inhibited uptake of [3H]dopamine in chopped tissue at concentrations well below those necessary for promoting release of preloaded [3H]dopamine. (–)‐Nicotine was more potent than (+)‐nicotine both at inhibiting uptake and at promoting release. Unlike other dopamine uptake inhibitors, however, nicotine inhibited only 50% of the total uptake. In the presence of 1 nM nicotine, the residual [3H]dopamine uptake was less sensitive to inhibition by cocaine than uptake in the absence of nicotine. Nicotine did not compete against the binding of [3H]GBR 12935, a selective dopamine uptake inhibitor. The nicotinic receptor agonists carbachol and 1,1‐dimethyl‐4‐phenylpiperazinium iodide also inhibited uptake, whereas the nicotinic antagonists chlorisondamine and mecamylamine blocked nicotine's effect. Thus, the effect of nicotine on dopamine uptake appears to be mediated by a receptor similar to the nicotinic acetylcholine receptor. These receptors do not seem to be on the terminals that are accumulating dopamine, however, since tetrodotoxin prevented the effect of nicotine on [3H]dopamine uptake and nicotine had no effect on uptake in a synaptosomal preparation.</description><subject>Animals</subject><subject>Binding, Competitive</subject><subject>Biological and medical sciences</subject><subject>Carbachol - pharmacology</subject><subject>Chlorisondamine - pharmacology</subject><subject>Cocaine</subject><subject>Cocaine - pharmacology</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - metabolism</subject><subject>Dimethylphenylpiperazinium Iodide - pharmacology</subject><subject>Dopamine - metabolism</subject><subject>Dopamine release</subject><subject>Dopamine uptake</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Mecamylamine - pharmacology</subject><subject>Microbiology</subject><subject>Mycology</subject><subject>Nicotine</subject><subject>Nicotine - administration &amp; dosage</subject><subject>Nicotine - metabolism</subject><subject>Nicotine - pharmacology</subject><subject>Piperazines - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Receptors, Nicotinic - drug effects</subject><subject>Receptors, Nicotinic - physiology</subject><subject>Synaptosomes - drug effects</subject><subject>Synaptosomes - metabolism</subject><subject>Systematics</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUU1v1DAQtRCoLC0_ASlCgluCx3YchwNStaW0qNqi0p4QshzvRPWSxIvtVbt3fjiJdmnhiC9j-X2M9R4hr4EWMJ53qwJEBbmAsi6grqFIDVVQs-L-CZk9QE_JjFLGck4Fe05exLiiFKSQcEAOoFaqLNWM_Fo465MbMDsfli6gTd12vN66xqWYfeNn30_82vQT4WadzA_MTMrmfrA4pGCS80PMrm_HtxOfLfw4_nh8Cb73Cf-1uMIOTcTMDdnVqPmagjNp0x-RZ63pIr7cz0Nyc_rxen6WX1x-Op8fX-SW1zXPGyHbBqzEislSCmaZMFi1RnJTyUYtS1syLnlFObBWWqgbFJVggEKWqrKcH5K3O9918D83GJPuXbTYdWZAv4lajUkp4Gokvt8RbfAxBmz1OrjehK0GqqcK9EpPOespZz1VoPcV6PtR_Gq_ZdP0uHyU7jIf8Td73ERrujaYwbr4F01KkHLifdjx7lyH2__4gf68mEvK-W_k9qOb</recordid><startdate>199102</startdate><enddate>199102</enddate><creator>Izenwasser, Sari</creator><creator>Jacocks, Henry M.</creator><creator>Rosenberger, John G.</creator><creator>Cox, Brian M.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>199102</creationdate><title>Nicotine Indirectly Inhibits [3H]Dopamine Uptake at Concentrations That Do Not Directly Promote [3H]Dopamine Release in Rat Striatum</title><author>Izenwasser, Sari ; Jacocks, Henry M. ; Rosenberger, John G. ; Cox, Brian M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3993-b46fb1c6e7265642c24ae7fa63a76b8d5c5236370312f6c19be47421e46587c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Binding, Competitive</topic><topic>Biological and medical sciences</topic><topic>Carbachol - pharmacology</topic><topic>Chlorisondamine - pharmacology</topic><topic>Cocaine</topic><topic>Cocaine - pharmacology</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - metabolism</topic><topic>Dimethylphenylpiperazinium Iodide - pharmacology</topic><topic>Dopamine - metabolism</topic><topic>Dopamine release</topic><topic>Dopamine uptake</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Mecamylamine - pharmacology</topic><topic>Microbiology</topic><topic>Mycology</topic><topic>Nicotine</topic><topic>Nicotine - administration &amp; dosage</topic><topic>Nicotine - metabolism</topic><topic>Nicotine - pharmacology</topic><topic>Piperazines - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Receptors, Nicotinic - drug effects</topic><topic>Receptors, Nicotinic - physiology</topic><topic>Synaptosomes - drug effects</topic><topic>Synaptosomes - metabolism</topic><topic>Systematics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Izenwasser, Sari</creatorcontrib><creatorcontrib>Jacocks, Henry M.</creatorcontrib><creatorcontrib>Rosenberger, John G.</creatorcontrib><creatorcontrib>Cox, Brian M.</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Izenwasser, Sari</au><au>Jacocks, Henry M.</au><au>Rosenberger, John G.</au><au>Cox, Brian M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nicotine Indirectly Inhibits [3H]Dopamine Uptake at Concentrations That Do Not Directly Promote [3H]Dopamine Release in Rat Striatum</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1991-02</date><risdate>1991</risdate><volume>56</volume><issue>2</issue><spage>603</spage><epage>610</epage><pages>603-610</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: The effects of both (–)‐ and (+)‐nicotine isomers were examined on in vitro uptake and release of [3H]dopamine in rat striatum. Both isomers inhibited uptake of [3H]dopamine in chopped tissue at concentrations well below those necessary for promoting release of preloaded [3H]dopamine. (–)‐Nicotine was more potent than (+)‐nicotine both at inhibiting uptake and at promoting release. Unlike other dopamine uptake inhibitors, however, nicotine inhibited only 50% of the total uptake. In the presence of 1 nM nicotine, the residual [3H]dopamine uptake was less sensitive to inhibition by cocaine than uptake in the absence of nicotine. Nicotine did not compete against the binding of [3H]GBR 12935, a selective dopamine uptake inhibitor. The nicotinic receptor agonists carbachol and 1,1‐dimethyl‐4‐phenylpiperazinium iodide also inhibited uptake, whereas the nicotinic antagonists chlorisondamine and mecamylamine blocked nicotine's effect. Thus, the effect of nicotine on dopamine uptake appears to be mediated by a receptor similar to the nicotinic acetylcholine receptor. These receptors do not seem to be on the terminals that are accumulating dopamine, however, since tetrodotoxin prevented the effect of nicotine on [3H]dopamine uptake and nicotine had no effect on uptake in a synaptosomal preparation.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1988558</pmid><doi>10.1111/j.1471-4159.1991.tb08192.x</doi><tpages>8</tpages></addata></record>
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subjects Animals
Binding, Competitive
Biological and medical sciences
Carbachol - pharmacology
Chlorisondamine - pharmacology
Cocaine
Cocaine - pharmacology
Corpus Striatum - drug effects
Corpus Striatum - metabolism
Dimethylphenylpiperazinium Iodide - pharmacology
Dopamine - metabolism
Dopamine release
Dopamine uptake
Dose-Response Relationship, Drug
Fundamental and applied biological sciences. Psychology
Male
Mecamylamine - pharmacology
Microbiology
Mycology
Nicotine
Nicotine - administration & dosage
Nicotine - metabolism
Nicotine - pharmacology
Piperazines - metabolism
Rats
Rats, Inbred Strains
Receptors, Nicotinic - drug effects
Receptors, Nicotinic - physiology
Synaptosomes - drug effects
Synaptosomes - metabolism
Systematics
title Nicotine Indirectly Inhibits [3H]Dopamine Uptake at Concentrations That Do Not Directly Promote [3H]Dopamine Release in Rat Striatum
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