Mephedrone (4-methylmethcathinone) supports intravenous self-administration in Sprague-Dawley and Wistar rats
Recreational use of the drug 4‐methylmethcathinone (mephedrone; 4‐MMC) became increasingly popular in the United Kingdom in recent years, spurred in part by the fact that it was not criminalized until April 2010. Although several fatalities have been associated with consumption of 4‐MMC and cautions...
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Veröffentlicht in: | Addiction biology 2013-09, Vol.18 (5), p.786-799 |
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creator | Aarde, Shawn M. Angrish, Deepshikha Barlow, Deborah J. Wright Jr, M. Jerry Vandewater, Sophia A. Creehan, Kevin M. Houseknecht, Karen L. Dickerson, Tobin J. Taffe, Michael A. |
description | Recreational use of the drug 4‐methylmethcathinone (mephedrone; 4‐MMC) became increasingly popular in the United Kingdom in recent years, spurred in part by the fact that it was not criminalized until April 2010. Although several fatalities have been associated with consumption of 4‐MMC and cautions for recreational users about its addictive potential have appeared on Internet forums, very little information about abuse liability for this drug is available. This study was conducted to determine if 4‐MMC serves as a reinforcer in a traditional intravenous self‐administration model. Groups of male Wistar and Sprague‐Dawley rats were prepared with intravenous catheters and trained to self‐administer 4‐MMC in 1‐hour sessions. Per‐infusion doses of 0.5 and 1.0 mg/kg were consistently self‐administered, resulting in greater than 80% discrimination for the drug‐paired lever and mean intakes of about 2–3 mg/kg/hour. Dose‐substitution studies after acquisition demonstrated that the number of responses and/or the total amount of drug self‐administered varied as a function of dose. In addition, radiotelemetry devices were used to show that self‐administered 4‐MMC was capable of increasing locomotor activity (Wistar) and decreasing body temperature (Sprague‐Dawley). Pharmacokinetic studies found that the T1/2 of 4‐MMC was about 1 hour in vivo in rat plasma and 90 minutes using in vitro liver microsomal assays. This study provides evidence of stimulant‐typical abuse liability for 4‐MMC in the traditional pre‐clinical self‐administration model. |
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Jerry ; Vandewater, Sophia A. ; Creehan, Kevin M. ; Houseknecht, Karen L. ; Dickerson, Tobin J. ; Taffe, Michael A.</creator><creatorcontrib>Aarde, Shawn M. ; Angrish, Deepshikha ; Barlow, Deborah J. ; Wright Jr, M. Jerry ; Vandewater, Sophia A. ; Creehan, Kevin M. ; Houseknecht, Karen L. ; Dickerson, Tobin J. ; Taffe, Michael A.</creatorcontrib><description>Recreational use of the drug 4‐methylmethcathinone (mephedrone; 4‐MMC) became increasingly popular in the United Kingdom in recent years, spurred in part by the fact that it was not criminalized until April 2010. Although several fatalities have been associated with consumption of 4‐MMC and cautions for recreational users about its addictive potential have appeared on Internet forums, very little information about abuse liability for this drug is available. This study was conducted to determine if 4‐MMC serves as a reinforcer in a traditional intravenous self‐administration model. Groups of male Wistar and Sprague‐Dawley rats were prepared with intravenous catheters and trained to self‐administer 4‐MMC in 1‐hour sessions. Per‐infusion doses of 0.5 and 1.0 mg/kg were consistently self‐administered, resulting in greater than 80% discrimination for the drug‐paired lever and mean intakes of about 2–3 mg/kg/hour. Dose‐substitution studies after acquisition demonstrated that the number of responses and/or the total amount of drug self‐administered varied as a function of dose. In addition, radiotelemetry devices were used to show that self‐administered 4‐MMC was capable of increasing locomotor activity (Wistar) and decreasing body temperature (Sprague‐Dawley). Pharmacokinetic studies found that the T1/2 of 4‐MMC was about 1 hour in vivo in rat plasma and 90 minutes using in vitro liver microsomal assays. This study provides evidence of stimulant‐typical abuse liability for 4‐MMC in the traditional pre‐clinical self‐administration model.</description><identifier>ISSN: 1355-6215</identifier><identifier>EISSN: 1369-1600</identifier><identifier>DOI: 10.1111/adb.12038</identifier><identifier>PMID: 23363010</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Abuse ; Analysis of Variance ; Animals ; Body Temperature Regulation - drug effects ; Cathinone ; Central Nervous System Stimulants - administration & dosage ; Central Nervous System Stimulants - pharmacokinetics ; Central Nervous System Stimulants - pharmacology ; Dose-Response Relationship, Drug ; Drug Substitution ; Humans ; Infusions, Intravenous ; Male ; Methamphetamine - administration & dosage ; Methamphetamine - analogs & derivatives ; Methamphetamine - pharmacokinetics ; Methamphetamine - pharmacology ; Motor Activity - drug effects ; Rats ; Rats, Sprague-Dawley ; Rats, Wistar ; reinforcement ; Reinforcement Schedule ; Reward ; Self Administration ; Species Specificity ; stimulant ; Substance-Related Disorders ; thermoregulation</subject><ispartof>Addiction biology, 2013-09, Vol.18 (5), p.786-799</ispartof><rights>2013 The Authors, Addiction Biology © 2013 Society for the Study of Addiction</rights><rights>2013 The Authors, Addiction Biology © 2013 Society for the Study of Addiction.</rights><rights>2013 Society for the Study of Addiction</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4808-fe8bb9119bf4d4ec26a07ad767fbff004ef209c6c30af5711222c662f55a23ae3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fadb.12038$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fadb.12038$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23363010$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aarde, Shawn M.</creatorcontrib><creatorcontrib>Angrish, Deepshikha</creatorcontrib><creatorcontrib>Barlow, Deborah J.</creatorcontrib><creatorcontrib>Wright Jr, M. Jerry</creatorcontrib><creatorcontrib>Vandewater, Sophia A.</creatorcontrib><creatorcontrib>Creehan, Kevin M.</creatorcontrib><creatorcontrib>Houseknecht, Karen L.</creatorcontrib><creatorcontrib>Dickerson, Tobin J.</creatorcontrib><creatorcontrib>Taffe, Michael A.</creatorcontrib><title>Mephedrone (4-methylmethcathinone) supports intravenous self-administration in Sprague-Dawley and Wistar rats</title><title>Addiction biology</title><addtitle>Addiction Biology</addtitle><description>Recreational use of the drug 4‐methylmethcathinone (mephedrone; 4‐MMC) became increasingly popular in the United Kingdom in recent years, spurred in part by the fact that it was not criminalized until April 2010. Although several fatalities have been associated with consumption of 4‐MMC and cautions for recreational users about its addictive potential have appeared on Internet forums, very little information about abuse liability for this drug is available. This study was conducted to determine if 4‐MMC serves as a reinforcer in a traditional intravenous self‐administration model. Groups of male Wistar and Sprague‐Dawley rats were prepared with intravenous catheters and trained to self‐administer 4‐MMC in 1‐hour sessions. Per‐infusion doses of 0.5 and 1.0 mg/kg were consistently self‐administered, resulting in greater than 80% discrimination for the drug‐paired lever and mean intakes of about 2–3 mg/kg/hour. Dose‐substitution studies after acquisition demonstrated that the number of responses and/or the total amount of drug self‐administered varied as a function of dose. In addition, radiotelemetry devices were used to show that self‐administered 4‐MMC was capable of increasing locomotor activity (Wistar) and decreasing body temperature (Sprague‐Dawley). Pharmacokinetic studies found that the T1/2 of 4‐MMC was about 1 hour in vivo in rat plasma and 90 minutes using in vitro liver microsomal assays. This study provides evidence of stimulant‐typical abuse liability for 4‐MMC in the traditional pre‐clinical self‐administration model.</description><subject>Abuse</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Body Temperature Regulation - drug effects</subject><subject>Cathinone</subject><subject>Central Nervous System Stimulants - administration & dosage</subject><subject>Central Nervous System Stimulants - pharmacokinetics</subject><subject>Central Nervous System Stimulants - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Substitution</subject><subject>Humans</subject><subject>Infusions, Intravenous</subject><subject>Male</subject><subject>Methamphetamine - administration & dosage</subject><subject>Methamphetamine - analogs & derivatives</subject><subject>Methamphetamine - pharmacokinetics</subject><subject>Methamphetamine - pharmacology</subject><subject>Motor Activity - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rats, Wistar</subject><subject>reinforcement</subject><subject>Reinforcement Schedule</subject><subject>Reward</subject><subject>Self Administration</subject><subject>Species Specificity</subject><subject>stimulant</subject><subject>Substance-Related Disorders</subject><subject>thermoregulation</subject><issn>1355-6215</issn><issn>1369-1600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1v1DAQhi0EoqVw4A-gSFzKwa0_YntzQSottEgtIPFRiYvlJOOuS-IEO2nZf89st6wAH-yR55lXM_MS8pyzA47n0LX1ARdMLh6QXS51Rblm7OE6VopqwdUOeZLzNWNcGCUfkx0hpZaMs13SX8C4hDYNEYr9kvYwLVfd-m7ctAwRv18VeR7HIU25CHFK7gbiMOciQ-epa_sQQ8bfKQwR88XnMbmrGeiJu-1gVbjYFpcIuFQgk5-SR951GZ7dv3vk67u3X47P6PnH0_fHR-e0KRdsQT0s6rrivKp92ZbQCO2Yca3RxtfeM1aCF6xqdCOZ88pwLoRotBZeKSekA7lHXm90x7nuoW1g3XhnxxR6l1Z2cMH-m4lhaa-GGyt1ybmqUGD_XiANP2fIk-1DbqDrXASc3vKyElrI0ghEX_6HXg9zijgeUrhlI6XgSL34u6NtK3-cQOBwA9wGXNw2z5ldW2zRYntnsT06eXMXYAXdVOB-4de2wqUfVhtplL38cGq_G_3t7OITqsjfnuGp1g</recordid><startdate>201309</startdate><enddate>201309</enddate><creator>Aarde, Shawn M.</creator><creator>Angrish, Deepshikha</creator><creator>Barlow, Deborah J.</creator><creator>Wright Jr, M. 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Jerry</creatorcontrib><creatorcontrib>Vandewater, Sophia A.</creatorcontrib><creatorcontrib>Creehan, Kevin M.</creatorcontrib><creatorcontrib>Houseknecht, Karen L.</creatorcontrib><creatorcontrib>Dickerson, Tobin J.</creatorcontrib><creatorcontrib>Taffe, Michael A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Animal Behavior Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Addiction biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aarde, Shawn M.</au><au>Angrish, Deepshikha</au><au>Barlow, Deborah J.</au><au>Wright Jr, M. Jerry</au><au>Vandewater, Sophia A.</au><au>Creehan, Kevin M.</au><au>Houseknecht, Karen L.</au><au>Dickerson, Tobin J.</au><au>Taffe, Michael A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mephedrone (4-methylmethcathinone) supports intravenous self-administration in Sprague-Dawley and Wistar rats</atitle><jtitle>Addiction biology</jtitle><addtitle>Addiction Biology</addtitle><date>2013-09</date><risdate>2013</risdate><volume>18</volume><issue>5</issue><spage>786</spage><epage>799</epage><pages>786-799</pages><issn>1355-6215</issn><eissn>1369-1600</eissn><abstract>Recreational use of the drug 4‐methylmethcathinone (mephedrone; 4‐MMC) became increasingly popular in the United Kingdom in recent years, spurred in part by the fact that it was not criminalized until April 2010. Although several fatalities have been associated with consumption of 4‐MMC and cautions for recreational users about its addictive potential have appeared on Internet forums, very little information about abuse liability for this drug is available. This study was conducted to determine if 4‐MMC serves as a reinforcer in a traditional intravenous self‐administration model. Groups of male Wistar and Sprague‐Dawley rats were prepared with intravenous catheters and trained to self‐administer 4‐MMC in 1‐hour sessions. Per‐infusion doses of 0.5 and 1.0 mg/kg were consistently self‐administered, resulting in greater than 80% discrimination for the drug‐paired lever and mean intakes of about 2–3 mg/kg/hour. Dose‐substitution studies after acquisition demonstrated that the number of responses and/or the total amount of drug self‐administered varied as a function of dose. In addition, radiotelemetry devices were used to show that self‐administered 4‐MMC was capable of increasing locomotor activity (Wistar) and decreasing body temperature (Sprague‐Dawley). Pharmacokinetic studies found that the T1/2 of 4‐MMC was about 1 hour in vivo in rat plasma and 90 minutes using in vitro liver microsomal assays. This study provides evidence of stimulant‐typical abuse liability for 4‐MMC in the traditional pre‐clinical self‐administration model.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>23363010</pmid><doi>10.1111/adb.12038</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abuse Analysis of Variance Animals Body Temperature Regulation - drug effects Cathinone Central Nervous System Stimulants - administration & dosage Central Nervous System Stimulants - pharmacokinetics Central Nervous System Stimulants - pharmacology Dose-Response Relationship, Drug Drug Substitution Humans Infusions, Intravenous Male Methamphetamine - administration & dosage Methamphetamine - analogs & derivatives Methamphetamine - pharmacokinetics Methamphetamine - pharmacology Motor Activity - drug effects Rats Rats, Sprague-Dawley Rats, Wistar reinforcement Reinforcement Schedule Reward Self Administration Species Specificity stimulant Substance-Related Disorders thermoregulation |
title | Mephedrone (4-methylmethcathinone) supports intravenous self-administration in Sprague-Dawley and Wistar rats |
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