Early developmental exposure to methylphenidate reduces cocaine-induced potentiation of brain stimulation reward in rats

Methylphenidate (MPH) is prescribed for the treatment of attention and hyperactivity disorders. We showed previously that early developmental exposure to MPH in rats causes behavioral alterations during adulthood, including reduced cocaine reward in place conditioning studies. Here we examined if ea...

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Veröffentlicht in:Biological psychiatry (1969) 2005-01, Vol.57 (2), p.120-125
Hauptverfasser: Mague, Stephen D., Andersen, Susan L., Carlezon, William A.
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container_title Biological psychiatry (1969)
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creator Mague, Stephen D.
Andersen, Susan L.
Carlezon, William A.
description Methylphenidate (MPH) is prescribed for the treatment of attention and hyperactivity disorders. We showed previously that early developmental exposure to MPH in rats causes behavioral alterations during adulthood, including reduced cocaine reward in place conditioning studies. Here we examined if early MPH exposure alters the ability of cocaine to potentiate the rewarding effects of electrical stimulation of the medial forebrain bundle (MFB) using intracranial self-stimulation (ICSS). Rats received MPH or saline during pre-adolescence (P20–35) and were implanted with MFB stimulating electrodes at adulthood (P60). Rats then were tested with cocaine in the ICSS paradigm. Cocaine dose-dependently decreased ICSS thresholds in all rats, but the threshold-lowering effects of cocaine were smaller in rats exposed to MPH during pre-adolescence. There were no differences between groups in sensitivity to the rewarding effects of MFB stimulation itself. Early developmental exposure to MPH reduces the reward-related effects of cocaine in the ICSS paradigm. These results are consistent with previous studies in which early exposure to MPH reduced the ability of cocaine to establish conditioned place preferences, as well as the rewarding effects of sucrose and sexual behavior. Reduced sensitivity to these various types of reward may reflect general dysfunctions of brain reward systems.
doi_str_mv 10.1016/j.biopsych.2004.10.037
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We showed previously that early developmental exposure to MPH in rats causes behavioral alterations during adulthood, including reduced cocaine reward in place conditioning studies. Here we examined if early MPH exposure alters the ability of cocaine to potentiate the rewarding effects of electrical stimulation of the medial forebrain bundle (MFB) using intracranial self-stimulation (ICSS). Rats received MPH or saline during pre-adolescence (P20–35) and were implanted with MFB stimulating electrodes at adulthood (P60). Rats then were tested with cocaine in the ICSS paradigm. Cocaine dose-dependently decreased ICSS thresholds in all rats, but the threshold-lowering effects of cocaine were smaller in rats exposed to MPH during pre-adolescence. There were no differences between groups in sensitivity to the rewarding effects of MFB stimulation itself. Early developmental exposure to MPH reduces the reward-related effects of cocaine in the ICSS paradigm. These results are consistent with previous studies in which early exposure to MPH reduced the ability of cocaine to establish conditioned place preferences, as well as the rewarding effects of sucrose and sexual behavior. Reduced sensitivity to these various types of reward may reflect general dysfunctions of brain reward systems.</description><subject>addiction</subject><subject>ADHD</subject><subject>Age Factors</subject><subject>Anatomical correlates of behavior</subject><subject>anhedonia</subject><subject>Animals</subject><subject>Association Learning - drug effects</subject><subject>Behavioral psychophysiology</subject><subject>Biological and medical sciences</subject><subject>Central Nervous System Stimulants - pharmacology</subject><subject>Cocaine - pharmacology</subject><subject>depression</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electric Stimulation</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Long-Term Potentiation - drug effects</subject><subject>Male</subject><subject>Medial Forebrain Bundle - physiology</subject><subject>Methylphenidate - pharmacology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychology. Psychophysiology</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reinforcement (Psychology)</subject><subject>Self Stimulation - drug effects</subject><subject>Stimulants</subject><issn>0006-3223</issn><issn>1873-2402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9vFCEYh4nR2G31KzRc9DYrMDMwe9M01Zo08aJn8g68ZNkwwwhM7X572eyaHj2R98fz489DyC1nW864_HTYjj4u-Wj2W8FYV8Mta9UrsuGDahvRMfGabBhjsmmFaK_Idc6HOioh-FtyxXvZi0HuNuT5HlI4UotPGOIy4VwgUHxeYl4T0hLphGV_DMseZ2-hIE1oV4OZmmjAz9j4-TRbusRSyx6KjzONjo6pbtNc_LSGc5jwDyRLa5qg5HfkjYOQ8f1lvSG_vt7_vHtoHn98-3735bEx7U6WRnEhrBtQ4TB2g-BorGFM4MgY9M6B3aGUjoHqYTAtEx3fIRg5gOGdcky1N-Tj-dwlxd8r5qInnw2GADPGNWupWjl0ilVQnkGTYs4JnV6SnyAdNWf65Fwf9D_n-uT8lFfntXh7uWEdJ7QvtYvkCny4AJANBJdgNj6_cLLrVf1T5T6fOaw-njwmnY3Hudr1CU3RNvr_veUv1y-nEg</recordid><startdate>20050115</startdate><enddate>20050115</enddate><creator>Mague, Stephen D.</creator><creator>Andersen, Susan L.</creator><creator>Carlezon, William A.</creator><general>Elsevier Inc</general><general>Elsevier Science</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>20050115</creationdate><title>Early developmental exposure to methylphenidate reduces cocaine-induced potentiation of brain stimulation reward in rats</title><author>Mague, Stephen D. ; Andersen, Susan L. ; Carlezon, William A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-7122df8e7e8b4821ecdc002eb00a5ffad9e66f0a75a8c302419eac68ac147f073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>addiction</topic><topic>ADHD</topic><topic>Age Factors</topic><topic>Anatomical correlates of behavior</topic><topic>anhedonia</topic><topic>Animals</topic><topic>Association Learning - drug effects</topic><topic>Behavioral psychophysiology</topic><topic>Biological and medical sciences</topic><topic>Central Nervous System Stimulants - pharmacology</topic><topic>Cocaine - pharmacology</topic><topic>depression</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electric Stimulation</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Long-Term Potentiation - drug effects</topic><topic>Male</topic><topic>Medial Forebrain Bundle - physiology</topic><topic>Methylphenidate - pharmacology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychology. Psychophysiology</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reinforcement (Psychology)</topic><topic>Self Stimulation - drug effects</topic><topic>Stimulants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mague, Stephen D.</creatorcontrib><creatorcontrib>Andersen, Susan L.</creatorcontrib><creatorcontrib>Carlezon, William A.</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>Biological psychiatry (1969)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mague, Stephen D.</au><au>Andersen, Susan L.</au><au>Carlezon, William A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early developmental exposure to methylphenidate reduces cocaine-induced potentiation of brain stimulation reward in rats</atitle><jtitle>Biological psychiatry (1969)</jtitle><addtitle>Biol Psychiatry</addtitle><date>2005-01-15</date><risdate>2005</risdate><volume>57</volume><issue>2</issue><spage>120</spage><epage>125</epage><pages>120-125</pages><issn>0006-3223</issn><eissn>1873-2402</eissn><coden>BIPCBF</coden><abstract>Methylphenidate (MPH) is prescribed for the treatment of attention and hyperactivity disorders. 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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects addiction
ADHD
Age Factors
Anatomical correlates of behavior
anhedonia
Animals
Association Learning - drug effects
Behavioral psychophysiology
Biological and medical sciences
Central Nervous System Stimulants - pharmacology
Cocaine - pharmacology
depression
Dose-Response Relationship, Drug
Electric Stimulation
Female
Fundamental and applied biological sciences. Psychology
Long-Term Potentiation - drug effects
Male
Medial Forebrain Bundle - physiology
Methylphenidate - pharmacology
Psychology. Psychoanalysis. Psychiatry
Psychology. Psychophysiology
rat
Rats
Rats, Sprague-Dawley
Reinforcement (Psychology)
Self Stimulation - drug effects
Stimulants
title Early developmental exposure to methylphenidate reduces cocaine-induced potentiation of brain stimulation reward in rats
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