Monoamine oxidase A rather than monoamine oxidase B inhibition increases nicotine reinforcement in rats
Although nicotine is considered to be responsible for the addictive properties of tobacco, growing evidence underlines the importance of non‐nicotine components in smoking reinforcement. It has been shown that tobacco smoke contains monoamine oxidase (MAO) A and B inhibitors and decreases MAO‐A and...
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creator | Guillem, Karine Vouillac, Caroline Azar, Marc R. Parsons, Loren H. Koob, George F. Cador, Martine Stinus, Luis |
description | Although nicotine is considered to be responsible for the addictive properties of tobacco, growing evidence underlines the importance of non‐nicotine components in smoking reinforcement. It has been shown that tobacco smoke contains monoamine oxidase (MAO) A and B inhibitors and decreases MAO‐A and MAO‐B activity in smokers. Here, we investigated the effects of clorgyline hydrochloride (irreversible MAO‐A inhibitor; 2 mg/kg/day), selegiline (irreversible MAO‐B inhibitor; 4 mg/kg) and the beta‐carboline norharmane hydrochloride (reversible MAO‐B inhibitor; 5 mg/kg/day) treatments on nicotine self‐administration (30 µg/kg/infusion, free base) in rats. Independent of the responsiveness to novelty and locomotor activity stimulation, only clorgyline hydrochloride treatment increased the intake of nicotine in a fixed‐ratio schedule (FR5) of reinforcement. When a progressive‐ratio schedule was implemented, both clorgyline hydrochloride and norharmane hydrochloride treatments potentiated the reinforcing effects of nicotine, whereas selegiline had no effect. Taken together, these results indicate that MAO‐A inhibition interacts with nicotine to enhance its rewarding effects in rats and suggest that other compounds present in tobacco, such as beta‐carboline, may also play an important role in sustaining smoking behavior in humans. |
doi_str_mv | 10.1111/j.1460-9568.2006.05217.x |
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It has been shown that tobacco smoke contains monoamine oxidase (MAO) A and B inhibitors and decreases MAO‐A and MAO‐B activity in smokers. Here, we investigated the effects of clorgyline hydrochloride (irreversible MAO‐A inhibitor; 2 mg/kg/day), selegiline (irreversible MAO‐B inhibitor; 4 mg/kg) and the beta‐carboline norharmane hydrochloride (reversible MAO‐B inhibitor; 5 mg/kg/day) treatments on nicotine self‐administration (30 µg/kg/infusion, free base) in rats. Independent of the responsiveness to novelty and locomotor activity stimulation, only clorgyline hydrochloride treatment increased the intake of nicotine in a fixed‐ratio schedule (FR5) of reinforcement. When a progressive‐ratio schedule was implemented, both clorgyline hydrochloride and norharmane hydrochloride treatments potentiated the reinforcing effects of nicotine, whereas selegiline had no effect. Taken together, these results indicate that MAO‐A inhibition interacts with nicotine to enhance its rewarding effects in rats and suggest that other compounds present in tobacco, such as beta‐carboline, may also play an important role in sustaining smoking behavior in humans.</description><identifier>ISSN: 0953-816X</identifier><identifier>EISSN: 1460-9568</identifier><identifier>DOI: 10.1111/j.1460-9568.2006.05217.x</identifier><identifier>PMID: 17229101</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Analysis of Variance ; Animals ; Behavior, Animal - drug effects ; Cotinine - blood ; Drug Interactions ; fixed ratio ; Male ; Monoamine Oxidase - physiology ; Monoamine Oxidase Inhibitors - blood ; Monoamine Oxidase Inhibitors - pharmacology ; Motor Activity - drug effects ; Nicotine - administration & dosage ; Nicotine - blood ; Nicotinic Agonists - administration & dosage ; Nicotinic Agonists - blood ; novelty ; progressive ratio ; Rats ; Rats, Wistar ; Reinforcement (Psychology) ; Reinforcement Schedule ; selective MAOI ; Self Administration - methods ; Time Factors</subject><ispartof>The European journal of neuroscience, 2006-12, Vol.24 (12), p.3532-3540</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4367-d1fab3aa183bb0a0774a70325866ef843d0a17abcf9fcb0d6ff266edc92ced0a3</citedby><cites>FETCH-LOGICAL-c4367-d1fab3aa183bb0a0774a70325866ef843d0a17abcf9fcb0d6ff266edc92ced0a3</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.1460-9568.2006.05217.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1460-9568.2006.05217.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17229101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guillem, Karine</creatorcontrib><creatorcontrib>Vouillac, Caroline</creatorcontrib><creatorcontrib>Azar, Marc R.</creatorcontrib><creatorcontrib>Parsons, Loren H.</creatorcontrib><creatorcontrib>Koob, George F.</creatorcontrib><creatorcontrib>Cador, Martine</creatorcontrib><creatorcontrib>Stinus, Luis</creatorcontrib><title>Monoamine oxidase A rather than monoamine oxidase B inhibition increases nicotine reinforcement in rats</title><title>The European journal of neuroscience</title><addtitle>Eur J Neurosci</addtitle><description>Although nicotine is considered to be responsible for the addictive properties of tobacco, growing evidence underlines the importance of non‐nicotine components in smoking reinforcement. It has been shown that tobacco smoke contains monoamine oxidase (MAO) A and B inhibitors and decreases MAO‐A and MAO‐B activity in smokers. Here, we investigated the effects of clorgyline hydrochloride (irreversible MAO‐A inhibitor; 2 mg/kg/day), selegiline (irreversible MAO‐B inhibitor; 4 mg/kg) and the beta‐carboline norharmane hydrochloride (reversible MAO‐B inhibitor; 5 mg/kg/day) treatments on nicotine self‐administration (30 µg/kg/infusion, free base) in rats. Independent of the responsiveness to novelty and locomotor activity stimulation, only clorgyline hydrochloride treatment increased the intake of nicotine in a fixed‐ratio schedule (FR5) of reinforcement. When a progressive‐ratio schedule was implemented, both clorgyline hydrochloride and norharmane hydrochloride treatments potentiated the reinforcing effects of nicotine, whereas selegiline had no effect. Taken together, these results indicate that MAO‐A inhibition interacts with nicotine to enhance its rewarding effects in rats and suggest that other compounds present in tobacco, such as beta‐carboline, may also play an important role in sustaining smoking behavior in humans.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Cotinine - blood</subject><subject>Drug Interactions</subject><subject>fixed ratio</subject><subject>Male</subject><subject>Monoamine Oxidase - physiology</subject><subject>Monoamine Oxidase Inhibitors - blood</subject><subject>Monoamine Oxidase Inhibitors - pharmacology</subject><subject>Motor Activity - drug effects</subject><subject>Nicotine - administration & dosage</subject><subject>Nicotine - blood</subject><subject>Nicotinic Agonists - administration & dosage</subject><subject>Nicotinic Agonists - blood</subject><subject>novelty</subject><subject>progressive ratio</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reinforcement (Psychology)</subject><subject>Reinforcement Schedule</subject><subject>selective MAOI</subject><subject>Self Administration - methods</subject><subject>Time Factors</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtP4zAURq0RaCiPvzDKanbJ2HFiJwsWgGgB8RDiqdlYjnNNXRqbsVNR_j0OrZgFG7zxlb_zXUsHoYTgjMTzZ5aRguG0LlmV5RizDJc54dnyBxp9BhtohOuSphVhj1toO4QZxrhiRfkTbRGe5zXBZISeLpx1sjMWErc0rQyQHCRe9lPwST-VNum-5IeJsVPTmN44G0flIb6GxBrl-oHzYKx2XkEHto_AsC7sok0t5wH21vcOuhsf3x6dpOdXk9Ojg_NUFZTxtCVaNlRKUtGmwRJzXkiOaV5WjIGuCtpiSbhslK61anDLtM5j0qo6VxAzuoN-r_a-ePdvAaEXnQkK5nNpwS2CIFENLWsawWoFKu9C8KDFized9G-CYDFIFjMxuBSDSzFIFh-SxTJWf63_WDQdtP-La6sR2F8Br2YOb99eLI7PLocp9tNV34Qelp996Z8F45SX4uFyIm6u_z6OT-7HYkLfAdMynQI</recordid><startdate>200612</startdate><enddate>200612</enddate><creator>Guillem, Karine</creator><creator>Vouillac, Caroline</creator><creator>Azar, Marc R.</creator><creator>Parsons, Loren H.</creator><creator>Koob, George F.</creator><creator>Cador, Martine</creator><creator>Stinus, Luis</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>200612</creationdate><title>Monoamine oxidase A rather than monoamine oxidase B inhibition increases nicotine reinforcement in rats</title><author>Guillem, Karine ; Vouillac, Caroline ; Azar, Marc R. ; Parsons, Loren H. ; Koob, George F. ; Cador, Martine ; Stinus, Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4367-d1fab3aa183bb0a0774a70325866ef843d0a17abcf9fcb0d6ff266edc92ced0a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Cotinine - blood</topic><topic>Drug Interactions</topic><topic>fixed ratio</topic><topic>Male</topic><topic>Monoamine Oxidase - physiology</topic><topic>Monoamine Oxidase Inhibitors - blood</topic><topic>Monoamine Oxidase Inhibitors - pharmacology</topic><topic>Motor Activity - drug effects</topic><topic>Nicotine - administration & dosage</topic><topic>Nicotine - blood</topic><topic>Nicotinic Agonists - administration & dosage</topic><topic>Nicotinic Agonists - blood</topic><topic>novelty</topic><topic>progressive ratio</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reinforcement (Psychology)</topic><topic>Reinforcement Schedule</topic><topic>selective MAOI</topic><topic>Self Administration - methods</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guillem, Karine</creatorcontrib><creatorcontrib>Vouillac, Caroline</creatorcontrib><creatorcontrib>Azar, Marc R.</creatorcontrib><creatorcontrib>Parsons, Loren H.</creatorcontrib><creatorcontrib>Koob, George F.</creatorcontrib><creatorcontrib>Cador, Martine</creatorcontrib><creatorcontrib>Stinus, Luis</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>Guillem, Karine</au><au>Vouillac, Caroline</au><au>Azar, Marc R.</au><au>Parsons, Loren H.</au><au>Koob, George F.</au><au>Cador, Martine</au><au>Stinus, Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monoamine oxidase A rather than monoamine oxidase B inhibition increases nicotine reinforcement in rats</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>2006-12</date><risdate>2006</risdate><volume>24</volume><issue>12</issue><spage>3532</spage><epage>3540</epage><pages>3532-3540</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><abstract>Although nicotine is considered to be responsible for the addictive properties of tobacco, growing evidence underlines the importance of non‐nicotine components in smoking reinforcement. It has been shown that tobacco smoke contains monoamine oxidase (MAO) A and B inhibitors and decreases MAO‐A and MAO‐B activity in smokers. Here, we investigated the effects of clorgyline hydrochloride (irreversible MAO‐A inhibitor; 2 mg/kg/day), selegiline (irreversible MAO‐B inhibitor; 4 mg/kg) and the beta‐carboline norharmane hydrochloride (reversible MAO‐B inhibitor; 5 mg/kg/day) treatments on nicotine self‐administration (30 µg/kg/infusion, free base) in rats. Independent of the responsiveness to novelty and locomotor activity stimulation, only clorgyline hydrochloride treatment increased the intake of nicotine in a fixed‐ratio schedule (FR5) of reinforcement. When a progressive‐ratio schedule was implemented, both clorgyline hydrochloride and norharmane hydrochloride treatments potentiated the reinforcing effects of nicotine, whereas selegiline had no effect. 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subjects | Analysis of Variance Animals Behavior, Animal - drug effects Cotinine - blood Drug Interactions fixed ratio Male Monoamine Oxidase - physiology Monoamine Oxidase Inhibitors - blood Monoamine Oxidase Inhibitors - pharmacology Motor Activity - drug effects Nicotine - administration & dosage Nicotine - blood Nicotinic Agonists - administration & dosage Nicotinic Agonists - blood novelty progressive ratio Rats Rats, Wistar Reinforcement (Psychology) Reinforcement Schedule selective MAOI Self Administration - methods Time Factors |
title | Monoamine oxidase A rather than monoamine oxidase B inhibition increases nicotine reinforcement in rats |
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