Dose-related effects of the acetylcholinesterase inhibitor tacrine on cocaine and food self-administration in rats
Rationale Acetylcholine (ACh) is involved in brain reward and learning functions and contributes to opiate- and psychostimulant-motivated behaviors. Tacrine is a centrally acting, reversible cholinesterase inhibitor that also inhibits monoamine oxidase (MAO) and blocks reuptake of dopamine (DA) and...
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creator | Grasing, Kenneth He, Shuangteng Yang, Yungao |
description | Rationale
Acetylcholine (ACh) is involved in brain reward and learning functions and contributes to opiate- and psychostimulant-motivated behaviors. Tacrine is a centrally acting, reversible cholinesterase inhibitor that also inhibits monoamine oxidase (MAO) and blocks reuptake of dopamine (DA) and serotonin.
Objectives
To determine the effects of pretreatment with tacrine on self-administration of cocaine and nondrug reinforcers.
Materials and methods
Male Wistar rats were trained to self-administer cocaine under a fixed-ratio-5 (FR-5) schedule during 2-h multiple-component sessions in which 0.1, 0.2, and 0.4 mg/kg per injection of cocaine were each available for 40 min. Other animals self-administered 45 mg food pellets under FR-30 or 20% Ensure (liquid food) under FR-5 in amounts of 30, 60, or 120 μl. Vehicle or tacrine was administered as single intravenous doses 20 min before self-administration of cocaine, food pellets, or liquid food.
Results
Although pretreatment with 0.032 mg/kg of tacrine increased self-administration of food pellets, pretreatment with higher doses of tacrine attenuated self-administration of cocaine, food pellets, or liquid food. Tacrine’s ED
50
value for attenuating self-administration of 0.1 mg/kg per injection of cocaine was more than sixfold lower than values for attenuating liquid food- or food pellet-reinforced behavior. However, ED
50
values for attenuating self-administration of higher doses of cocaine were similar to those observed for 30 or 60 μl of liquid food.
Conclusions
Tacrine can selectively attenuate self-administration of low-dose cocaine, but its effects on higher doses of cocaine are similar to its ability to decrease self-administration of nondrug reinforcers. |
doi_str_mv | 10.1007/s00213-007-0944-3 |
format | Article |
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Acetylcholine (ACh) is involved in brain reward and learning functions and contributes to opiate- and psychostimulant-motivated behaviors. Tacrine is a centrally acting, reversible cholinesterase inhibitor that also inhibits monoamine oxidase (MAO) and blocks reuptake of dopamine (DA) and serotonin.
Objectives
To determine the effects of pretreatment with tacrine on self-administration of cocaine and nondrug reinforcers.
Materials and methods
Male Wistar rats were trained to self-administer cocaine under a fixed-ratio-5 (FR-5) schedule during 2-h multiple-component sessions in which 0.1, 0.2, and 0.4 mg/kg per injection of cocaine were each available for 40 min. Other animals self-administered 45 mg food pellets under FR-30 or 20% Ensure (liquid food) under FR-5 in amounts of 30, 60, or 120 μl. Vehicle or tacrine was administered as single intravenous doses 20 min before self-administration of cocaine, food pellets, or liquid food.
Results
Although pretreatment with 0.032 mg/kg of tacrine increased self-administration of food pellets, pretreatment with higher doses of tacrine attenuated self-administration of cocaine, food pellets, or liquid food. Tacrine’s ED
50
value for attenuating self-administration of 0.1 mg/kg per injection of cocaine was more than sixfold lower than values for attenuating liquid food- or food pellet-reinforced behavior. However, ED
50
values for attenuating self-administration of higher doses of cocaine were similar to those observed for 30 or 60 μl of liquid food.
Conclusions
Tacrine can selectively attenuate self-administration of low-dose cocaine, but its effects on higher doses of cocaine are similar to its ability to decrease self-administration of nondrug reinforcers.</description><identifier>ISSN: 0033-3158</identifier><identifier>EISSN: 1432-2072</identifier><identifier>DOI: 10.1007/s00213-007-0944-3</identifier><identifier>PMID: 17917719</identifier><identifier>CODEN: PSYPAG</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Animals ; Appetitive Behavior - drug effects ; Association Learning - drug effects ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Cholinesterase Inhibitors - pharmacology ; Cocaine ; Cocaine - administration & dosage ; Cocaine-Related Disorders - psychology ; Comparative studies ; Cues ; Dose-Response Relationship, Drug ; Food Preferences - drug effects ; Injections, Intravenous ; Male ; Medical sciences ; Motivation ; Neuropharmacology ; Neurosciences ; Neurotransmitters ; Original Investigation ; Pharmacology ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Premedication ; Psychiatry ; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer ; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) ; Psychology ; Psychology. Psychoanalysis. Psychiatry ; Psychopharmacology ; Rats ; Rats, Wistar ; Reinforcement Schedule ; Rodents ; Self Administration ; Tacrine - pharmacology</subject><ispartof>Psychopharmacologia, 2008, Vol.196 (1), p.133-142</ispartof><rights>Springer-Verlag 2007</rights><rights>2008 INIST-CNRS</rights><rights>Springer-Verlag 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-9fb23e330576c514f29aedeb83d9eead2c5be5f08766a07c3421a9332ad3e6f53</citedby><cites>FETCH-LOGICAL-c430t-9fb23e330576c514f29aedeb83d9eead2c5be5f08766a07c3421a9332ad3e6f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00213-007-0944-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00213-007-0944-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,4009,27902,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19998855$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17917719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grasing, Kenneth</creatorcontrib><creatorcontrib>He, Shuangteng</creatorcontrib><creatorcontrib>Yang, Yungao</creatorcontrib><title>Dose-related effects of the acetylcholinesterase inhibitor tacrine on cocaine and food self-administration in rats</title><title>Psychopharmacologia</title><addtitle>Psychopharmacology</addtitle><addtitle>Psychopharmacology (Berl)</addtitle><description>Rationale
Acetylcholine (ACh) is involved in brain reward and learning functions and contributes to opiate- and psychostimulant-motivated behaviors. Tacrine is a centrally acting, reversible cholinesterase inhibitor that also inhibits monoamine oxidase (MAO) and blocks reuptake of dopamine (DA) and serotonin.
Objectives
To determine the effects of pretreatment with tacrine on self-administration of cocaine and nondrug reinforcers.
Materials and methods
Male Wistar rats were trained to self-administer cocaine under a fixed-ratio-5 (FR-5) schedule during 2-h multiple-component sessions in which 0.1, 0.2, and 0.4 mg/kg per injection of cocaine were each available for 40 min. Other animals self-administered 45 mg food pellets under FR-30 or 20% Ensure (liquid food) under FR-5 in amounts of 30, 60, or 120 μl. Vehicle or tacrine was administered as single intravenous doses 20 min before self-administration of cocaine, food pellets, or liquid food.
Results
Although pretreatment with 0.032 mg/kg of tacrine increased self-administration of food pellets, pretreatment with higher doses of tacrine attenuated self-administration of cocaine, food pellets, or liquid food. Tacrine’s ED
50
value for attenuating self-administration of 0.1 mg/kg per injection of cocaine was more than sixfold lower than values for attenuating liquid food- or food pellet-reinforced behavior. However, ED
50
values for attenuating self-administration of higher doses of cocaine were similar to those observed for 30 or 60 μl of liquid food.
Conclusions
Tacrine can selectively attenuate self-administration of low-dose cocaine, but its effects on higher doses of cocaine are similar to its ability to decrease self-administration of nondrug reinforcers.</description><subject>Animals</subject><subject>Appetitive Behavior - drug effects</subject><subject>Association Learning - drug effects</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cholinesterase Inhibitors - pharmacology</subject><subject>Cocaine</subject><subject>Cocaine - administration & dosage</subject><subject>Cocaine-Related Disorders - psychology</subject><subject>Comparative studies</subject><subject>Cues</subject><subject>Dose-Response Relationship, Drug</subject><subject>Food Preferences - drug effects</subject><subject>Injections, Intravenous</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Motivation</subject><subject>Neuropharmacology</subject><subject>Neurosciences</subject><subject>Neurotransmitters</subject><subject>Original Investigation</subject><subject>Pharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Premedication</subject><subject>Psychiatry</subject><subject>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer</subject><subject>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</subject><subject>Psychology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reinforcement Schedule</subject><subject>Rodents</subject><subject>Self Administration</subject><subject>Tacrine - pharmacology</subject><issn>0033-3158</issn><issn>1432-2072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kctqHDEQRUVIsMcTf0A2QQTinWK9-qFlcJ5gyMZZN9VSKSPTIzmSZuG_t5oZGAhEG12oU6WruoS8E_yT4Hy4LZxLoViTjButmXpFNkIrySQf5Guy4VwppkQ3XpKrUh55O3rUF-RSDEYMgzAbkr-kgizjAhUdRe_R1kKTp3WHFCzW58Xu0hIilooZCtIQd2EONWVaweZWoClSmyysEqKjPiVHCy6egduHGErNUEODQqRNlbfkjYel4PXp3pLf374-3P1g97--_7z7fM-sVrwy42epUCneDb3thPbSADqcR-UMIjhpuxk7z8eh74EPVmkpwCglwSnsfae25OY49ymnv4fmf9qHYnFZIGI6lEnyzrTliAZ--Ad8TIccm7dJitGMum_glogjZHMqJaOfnnLYQ36eBJ_WNKZjGtMq1zQm1XrenwYf5j26c8dp_Q34eAKgWFh8hmhDOXPGmHHs1q_II1daKf7BfHb4_9dfAFqwozI</recordid><startdate>2008</startdate><enddate>2008</enddate><creator>Grasing, Kenneth</creator><creator>He, Shuangteng</creator><creator>Yang, Yungao</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7QG</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>2008</creationdate><title>Dose-related effects of the acetylcholinesterase inhibitor tacrine on cocaine and food self-administration in rats</title><author>Grasing, Kenneth ; He, Shuangteng ; Yang, Yungao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-9fb23e330576c514f29aedeb83d9eead2c5be5f08766a07c3421a9332ad3e6f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Appetitive Behavior - drug effects</topic><topic>Association Learning - drug effects</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cholinesterase Inhibitors - pharmacology</topic><topic>Cocaine</topic><topic>Cocaine - administration & dosage</topic><topic>Cocaine-Related Disorders - psychology</topic><topic>Comparative studies</topic><topic>Cues</topic><topic>Dose-Response Relationship, Drug</topic><topic>Food Preferences - drug effects</topic><topic>Injections, Intravenous</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Motivation</topic><topic>Neuropharmacology</topic><topic>Neurosciences</topic><topic>Neurotransmitters</topic><topic>Original Investigation</topic><topic>Pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Premedication</topic><topic>Psychiatry</topic><topic>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer</topic><topic>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</topic><topic>Psychology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reinforcement Schedule</topic><topic>Rodents</topic><topic>Self Administration</topic><topic>Tacrine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grasing, Kenneth</creatorcontrib><creatorcontrib>He, Shuangteng</creatorcontrib><creatorcontrib>Yang, Yungao</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>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Psychopharmacologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grasing, Kenneth</au><au>He, Shuangteng</au><au>Yang, Yungao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dose-related effects of the acetylcholinesterase inhibitor tacrine on cocaine and food self-administration in rats</atitle><jtitle>Psychopharmacologia</jtitle><stitle>Psychopharmacology</stitle><addtitle>Psychopharmacology (Berl)</addtitle><date>2008</date><risdate>2008</risdate><volume>196</volume><issue>1</issue><spage>133</spage><epage>142</epage><pages>133-142</pages><issn>0033-3158</issn><eissn>1432-2072</eissn><coden>PSYPAG</coden><abstract>Rationale
Acetylcholine (ACh) is involved in brain reward and learning functions and contributes to opiate- and psychostimulant-motivated behaviors. Tacrine is a centrally acting, reversible cholinesterase inhibitor that also inhibits monoamine oxidase (MAO) and blocks reuptake of dopamine (DA) and serotonin.
Objectives
To determine the effects of pretreatment with tacrine on self-administration of cocaine and nondrug reinforcers.
Materials and methods
Male Wistar rats were trained to self-administer cocaine under a fixed-ratio-5 (FR-5) schedule during 2-h multiple-component sessions in which 0.1, 0.2, and 0.4 mg/kg per injection of cocaine were each available for 40 min. Other animals self-administered 45 mg food pellets under FR-30 or 20% Ensure (liquid food) under FR-5 in amounts of 30, 60, or 120 μl. Vehicle or tacrine was administered as single intravenous doses 20 min before self-administration of cocaine, food pellets, or liquid food.
Results
Although pretreatment with 0.032 mg/kg of tacrine increased self-administration of food pellets, pretreatment with higher doses of tacrine attenuated self-administration of cocaine, food pellets, or liquid food. Tacrine’s ED
50
value for attenuating self-administration of 0.1 mg/kg per injection of cocaine was more than sixfold lower than values for attenuating liquid food- or food pellet-reinforced behavior. However, ED
50
values for attenuating self-administration of higher doses of cocaine were similar to those observed for 30 or 60 μl of liquid food.
Conclusions
Tacrine can selectively attenuate self-administration of low-dose cocaine, but its effects on higher doses of cocaine are similar to its ability to decrease self-administration of nondrug reinforcers.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>17917719</pmid><doi>10.1007/s00213-007-0944-3</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Appetitive Behavior - drug effects Association Learning - drug effects Biological and medical sciences Biomedical and Life Sciences Biomedicine Cholinesterase Inhibitors - pharmacology Cocaine Cocaine - administration & dosage Cocaine-Related Disorders - psychology Comparative studies Cues Dose-Response Relationship, Drug Food Preferences - drug effects Injections, Intravenous Male Medical sciences Motivation Neuropharmacology Neurosciences Neurotransmitters Original Investigation Pharmacology Pharmacology. Drug treatments Pharmacology/Toxicology Premedication Psychiatry Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) Psychology Psychology. Psychoanalysis. Psychiatry Psychopharmacology Rats Rats, Wistar Reinforcement Schedule Rodents Self Administration Tacrine - pharmacology |
title | Dose-related effects of the acetylcholinesterase inhibitor tacrine on cocaine and food self-administration in rats |
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