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Drug context differently regulates cocaine versus heroin self-administration and cocaine-versus heroin-induced Fos mRNA expression in the rat

Identifieur interne : 000289 ( PascalFrancis/Corpus ); précédent : 000288; suivant : 000290

Drug context differently regulates cocaine versus heroin self-administration and cocaine-versus heroin-induced Fos mRNA expression in the rat

Auteurs : Michele Celentano ; Daniele Caprioli ; Pasqua Di Pasquale ; Veronica Cardill ; Paolo Nencini ; Silvana Gaetani ; Aldo Badiani

Source :

RBID : Francis:09-0219985

Descripteurs français

English descriptors

Abstract

Rationale We have previously reported that cocaine self-administration is facilitated in male rats not residing in the test chambers (Non Resident rats) relative to rats living in the test chambers at all times (Resident rats). Surprisingly, the opposite was found for heroin. Materials and methods We predicted that, when given access to both cocaine and heroin on alternate days, Non Resident rats would take more cocaine relative to heroin than Resident rats. Heroin (25.0 μg/kg) and cocaine (400 μg/kg), were made alternately available for 14 self-administration sessions, on a fixed ratio (FR) schedule that was progressively increased from FR1 to FR5. Next, some rats underwent a progressive-ratio procedure for heroin and cocaine. The other rats continued to alternate heroin and cocaine self-administration for 12 additional sessions, during which the FR schedule was progressively increased from FR10 to FR100. The second aim of the study was to investigate Fos mRNA expression in Resident and Non Resident rats treated with non-contingent intravenous infusion of "self-administration doses" of heroin (25.0 μg/kg) and cocaine (400 μg/kg). Results We found that: (1) drug-taking context differentially modulates intravenous cocaine versus heroin self-administration; (2) very low doses of cocaine and heroin are sufficient to induce Fos mRNA expression in the posterior caudate; (3) drug-administration context differentially modulates cocaine- versus heroin-induced Fos mRNA expression. Conclusions Our study indicates that the context of drug taking can play a powerful role in modulating cocaine versus heroin intake in the laboratory rat.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A06       @2 2
A08 01  1  ENG  @1 Drug context differently regulates cocaine versus heroin self-administration and cocaine-versus heroin-induced Fos mRNA expression in the rat
A11 01  1    @1 CELENTANO (Michele)
A11 02  1    @1 CAPRIOLI (Daniele)
A11 03  1    @1 DI PASQUALE (Pasqua)
A11 04  1    @1 CARDILL (Veronica)
A11 05  1    @1 NENCINI (Paolo)
A11 06  1    @1 GAETANI (Silvana)
A11 07  1    @1 BADIANI (Aldo)
A14 01      @1 Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome @2 Rome @3 ITA @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut.
A14 02      @1 CRiN "Daniel Bovet", Sapienza University of Rome @2 Rome @3 ITA @Z 5 aut. @Z 7 aut.
A20       @1 349-360
A21       @1 2009
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A44       @0 0000 @1 © 2009 INIST-CNRS. All rights reserved.
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C01 01    ENG  @0 Rationale We have previously reported that cocaine self-administration is facilitated in male rats not residing in the test chambers (Non Resident rats) relative to rats living in the test chambers at all times (Resident rats). Surprisingly, the opposite was found for heroin. Materials and methods We predicted that, when given access to both cocaine and heroin on alternate days, Non Resident rats would take more cocaine relative to heroin than Resident rats. Heroin (25.0 μg/kg) and cocaine (400 μg/kg), were made alternately available for 14 self-administration sessions, on a fixed ratio (FR) schedule that was progressively increased from FR1 to FR5. Next, some rats underwent a progressive-ratio procedure for heroin and cocaine. The other rats continued to alternate heroin and cocaine self-administration for 12 additional sessions, during which the FR schedule was progressively increased from FR10 to FR100. The second aim of the study was to investigate Fos mRNA expression in Resident and Non Resident rats treated with non-contingent intravenous infusion of "self-administration doses" of heroin (25.0 μg/kg) and cocaine (400 μg/kg). Results We found that: (1) drug-taking context differentially modulates intravenous cocaine versus heroin self-administration; (2) very low doses of cocaine and heroin are sufficient to induce Fos mRNA expression in the posterior caudate; (3) drug-administration context differentially modulates cocaine- versus heroin-induced Fos mRNA expression. Conclusions Our study indicates that the context of drug taking can play a powerful role in modulating cocaine versus heroin intake in the laboratory rat.
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Format Inist (serveur)

NO : FRANCIS 09-0219985 INIST
ET : Drug context differently regulates cocaine versus heroin self-administration and cocaine-versus heroin-induced Fos mRNA expression in the rat
AU : CELENTANO (Michele); CAPRIOLI (Daniele); DI PASQUALE (Pasqua); CARDILL (Veronica); NENCINI (Paolo); GAETANI (Silvana); BADIANI (Aldo)
AF : Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome/Rome/Italie (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut.); CRiN "Daniel Bovet", Sapienza University of Rome/Rome/Italie (5 aut., 7 aut.)
DT : Publication en série; Niveau analytique
SO : Psychopharmacologia; ISSN 0033-3158; Coden PSYPAG; Allemagne; Da. 2009; Vol. 204; No. 2; Pp. 349-360; Bibl. 1 p.1/2
LA : Anglais
EA : Rationale We have previously reported that cocaine self-administration is facilitated in male rats not residing in the test chambers (Non Resident rats) relative to rats living in the test chambers at all times (Resident rats). Surprisingly, the opposite was found for heroin. Materials and methods We predicted that, when given access to both cocaine and heroin on alternate days, Non Resident rats would take more cocaine relative to heroin than Resident rats. Heroin (25.0 μg/kg) and cocaine (400 μg/kg), were made alternately available for 14 self-administration sessions, on a fixed ratio (FR) schedule that was progressively increased from FR1 to FR5. Next, some rats underwent a progressive-ratio procedure for heroin and cocaine. The other rats continued to alternate heroin and cocaine self-administration for 12 additional sessions, during which the FR schedule was progressively increased from FR10 to FR100. The second aim of the study was to investigate Fos mRNA expression in Resident and Non Resident rats treated with non-contingent intravenous infusion of "self-administration doses" of heroin (25.0 μg/kg) and cocaine (400 μg/kg). Results We found that: (1) drug-taking context differentially modulates intravenous cocaine versus heroin self-administration; (2) very low doses of cocaine and heroin are sufficient to induce Fos mRNA expression in the posterior caudate; (3) drug-administration context differentially modulates cocaine- versus heroin-induced Fos mRNA expression. Conclusions Our study indicates that the context of drug taking can play a powerful role in modulating cocaine versus heroin intake in the laboratory rat.
CC : 770E02; 770D03E01
FD : Médicament; Contexte; Cocaïne; Etude comparative; Héroïne; Substance toxicomanogène; Autoadministration; Expression génique; Gène fos; Rat; Animal; Opiacés; Peptide opioïde; Stimulant SNC; Récompense; Addiction; Toxicomanie; Abus de substance; Noyau caudé; Corps strié
FG : Rodentia; Mammalia; Vertebrata; Ester; Psychotrope; Encéphale; Noyau gris central; Système nerveux central
ED : Drug; Context; Cocaine; Comparative study; Heroin; Drug of abuse; Self administration; Gene expression; fos Gene; Rat; Animal; Opiates; Opioid peptide; CNS stimulant; Reward; Addiction; Drug addiction; Substance abuse; Caudate nucleus; Corpus striatum
EG : Rodentia; Mammalia; Vertebrata; Ester; Psychotropic; Encephalon; Basal ganglion; Central nervous system
SD : Medicamento; Contexto; Cocaína; Estudio comparativo; Heroína; Sustancia toxicomanógena; Autoadministración; Expresión genética; Gen fos; Rata; Animal; Opiados; Péptido opioide; Estimulante SNC; Recompensa; Adicción; Toxicomanía; Abuso de sustancias; Núcleo caudado; Cuerpo estriado
LO : INIST-1761.354000186087870140
ID : 09-0219985

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Francis:09-0219985

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</author>
<author>
<name sortKey="Badiani, Aldo" sort="Badiani, Aldo" uniqKey="Badiani A" first="Aldo" last="Badiani">Aldo Badiani</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome</s1>
<s2>Rome</s2>
<s3>ITA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
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<sZ>5 aut.</sZ>
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<affiliation>
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<s1>CRiN "Daniel Bovet", Sapienza University of Rome</s1>
<s2>Rome</s2>
<s3>ITA</s3>
<sZ>5 aut.</sZ>
<sZ>7 aut.</sZ>
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<series>
<title level="j" type="main">Psychopharmacologia</title>
<title level="j" type="abbreviated">Psychopharmacologia</title>
<idno type="ISSN">0033-3158</idno>
<imprint>
<date when="2009">2009</date>
</imprint>
</series>
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<title level="j" type="main">Psychopharmacologia</title>
<title level="j" type="abbreviated">Psychopharmacologia</title>
<idno type="ISSN">0033-3158</idno>
</seriesStmt>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Addiction</term>
<term>Animal</term>
<term>CNS stimulant</term>
<term>Caudate nucleus</term>
<term>Cocaine</term>
<term>Comparative study</term>
<term>Context</term>
<term>Corpus striatum</term>
<term>Drug</term>
<term>Drug addiction</term>
<term>Drug of abuse</term>
<term>Gene expression</term>
<term>Heroin</term>
<term>Opiates</term>
<term>Opioid peptide</term>
<term>Rat</term>
<term>Reward</term>
<term>Self administration</term>
<term>Substance abuse</term>
<term>fos Gene</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Médicament</term>
<term>Contexte</term>
<term>Cocaïne</term>
<term>Etude comparative</term>
<term>Héroïne</term>
<term>Substance toxicomanogène</term>
<term>Autoadministration</term>
<term>Expression génique</term>
<term>Gène fos</term>
<term>Rat</term>
<term>Animal</term>
<term>Opiacés</term>
<term>Peptide opioïde</term>
<term>Stimulant SNC</term>
<term>Récompense</term>
<term>Addiction</term>
<term>Toxicomanie</term>
<term>Abus de substance</term>
<term>Noyau caudé</term>
<term>Corps strié</term>
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<front>
<div type="abstract" xml:lang="en">Rationale We have previously reported that cocaine self-administration is facilitated in male rats not residing in the test chambers (Non Resident rats) relative to rats living in the test chambers at all times (Resident rats). Surprisingly, the opposite was found for heroin. Materials and methods We predicted that, when given access to both cocaine and heroin on alternate days, Non Resident rats would take more cocaine relative to heroin than Resident rats. Heroin (25.0 μg/kg) and cocaine (400 μg/kg), were made alternately available for 14 self-administration sessions, on a fixed ratio (FR) schedule that was progressively increased from FR1 to FR5. Next, some rats underwent a progressive-ratio procedure for heroin and cocaine. The other rats continued to alternate heroin and cocaine self-administration for 12 additional sessions, during which the FR schedule was progressively increased from FR10 to FR100. The second aim of the study was to investigate Fos mRNA expression in Resident and Non Resident rats treated with non-contingent intravenous infusion of "self-administration doses" of heroin (25.0 μg/kg) and cocaine (400 μg/kg). Results We found that: (1) drug-taking context differentially modulates intravenous cocaine versus heroin self-administration; (2) very low doses of cocaine and heroin are sufficient to induce Fos mRNA expression in the posterior caudate; (3) drug-administration context differentially modulates cocaine- versus heroin-induced Fos mRNA expression. Conclusions Our study indicates that the context of drug taking can play a powerful role in modulating cocaine versus heroin intake in the laboratory rat.</div>
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<s1>Drug context differently regulates cocaine versus heroin self-administration and cocaine-versus heroin-induced Fos mRNA expression in the rat</s1>
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<s1>CELENTANO (Michele)</s1>
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<s1>CAPRIOLI (Daniele)</s1>
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<s1>NENCINI (Paolo)</s1>
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<s1>GAETANI (Silvana)</s1>
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<s1>Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome</s1>
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<sZ>7 aut.</sZ>
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<s0>Rationale We have previously reported that cocaine self-administration is facilitated in male rats not residing in the test chambers (Non Resident rats) relative to rats living in the test chambers at all times (Resident rats). Surprisingly, the opposite was found for heroin. Materials and methods We predicted that, when given access to both cocaine and heroin on alternate days, Non Resident rats would take more cocaine relative to heroin than Resident rats. Heroin (25.0 μg/kg) and cocaine (400 μg/kg), were made alternately available for 14 self-administration sessions, on a fixed ratio (FR) schedule that was progressively increased from FR1 to FR5. Next, some rats underwent a progressive-ratio procedure for heroin and cocaine. The other rats continued to alternate heroin and cocaine self-administration for 12 additional sessions, during which the FR schedule was progressively increased from FR10 to FR100. The second aim of the study was to investigate Fos mRNA expression in Resident and Non Resident rats treated with non-contingent intravenous infusion of "self-administration doses" of heroin (25.0 μg/kg) and cocaine (400 μg/kg). Results We found that: (1) drug-taking context differentially modulates intravenous cocaine versus heroin self-administration; (2) very low doses of cocaine and heroin are sufficient to induce Fos mRNA expression in the posterior caudate; (3) drug-administration context differentially modulates cocaine- versus heroin-induced Fos mRNA expression. Conclusions Our study indicates that the context of drug taking can play a powerful role in modulating cocaine versus heroin intake in the laboratory rat.</s0>
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<s0>770E02</s0>
<s1>V</s1>
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<s1>IV</s1>
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<s0>Cocaine</s0>
<s2>NK</s2>
<s2>FR</s2>
<s2>FX</s2>
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<s0>Cocaína</s0>
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<s5>05</s5>
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<s5>06</s5>
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<s5>06</s5>
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<s5>08</s5>
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<s5>17</s5>
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<s0>Addiction</s0>
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<s5>18</s5>
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<s5>18</s5>
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<s5>20</s5>
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<s5>20</s5>
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<s5>20</s5>
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<s0>Corps strié</s0>
<s5>21</s5>
</fC03>
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<s0>Corpus striatum</s0>
<s5>21</s5>
</fC03>
<fC03 i1="20" i2="X" l="SPA">
<s0>Cuerpo estriado</s0>
<s5>21</s5>
</fC03>
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<s0>Rodentia</s0>
<s2>NS</s2>
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<s0>Rodentia</s0>
<s2>NS</s2>
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<s0>Rodentia</s0>
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<s0>Mammalia</s0>
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<s2>NS</s2>
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<s0>Vertebrata</s0>
<s2>NS</s2>
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<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
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<s0>Ester</s0>
<s5>37</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Ester</s0>
<s5>37</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Ester</s0>
<s5>37</s5>
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<s2>FX</s2>
<s5>38</s5>
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<s0>Psychotropic</s0>
<s2>FX</s2>
<s5>38</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Psicotropo</s0>
<s2>FX</s2>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Encéphale</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Encephalon</s0>
<s5>39</s5>
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<fC07 i1="06" i2="X" l="SPA">
<s0>Encéfalo</s0>
<s5>39</s5>
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<s0>Noyau gris central</s0>
<s5>40</s5>
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<s0>Basal ganglion</s0>
<s5>40</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Núcleo basal</s0>
<s5>40</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
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<s5>41</s5>
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<s0>Central nervous system</s0>
<s5>41</s5>
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<s0>Sistema nervioso central</s0>
<s5>41</s5>
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<s1>159</s1>
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</standard>
<server>
<NO>FRANCIS 09-0219985 INIST</NO>
<ET>Drug context differently regulates cocaine versus heroin self-administration and cocaine-versus heroin-induced Fos mRNA expression in the rat</ET>
<AU>CELENTANO (Michele); CAPRIOLI (Daniele); DI PASQUALE (Pasqua); CARDILL (Veronica); NENCINI (Paolo); GAETANI (Silvana); BADIANI (Aldo)</AU>
<AF>Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome/Rome/Italie (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut.); CRiN "Daniel Bovet", Sapienza University of Rome/Rome/Italie (5 aut., 7 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Psychopharmacologia; ISSN 0033-3158; Coden PSYPAG; Allemagne; Da. 2009; Vol. 204; No. 2; Pp. 349-360; Bibl. 1 p.1/2</SO>
<LA>Anglais</LA>
<EA>Rationale We have previously reported that cocaine self-administration is facilitated in male rats not residing in the test chambers (Non Resident rats) relative to rats living in the test chambers at all times (Resident rats). Surprisingly, the opposite was found for heroin. Materials and methods We predicted that, when given access to both cocaine and heroin on alternate days, Non Resident rats would take more cocaine relative to heroin than Resident rats. Heroin (25.0 μg/kg) and cocaine (400 μg/kg), were made alternately available for 14 self-administration sessions, on a fixed ratio (FR) schedule that was progressively increased from FR1 to FR5. Next, some rats underwent a progressive-ratio procedure for heroin and cocaine. The other rats continued to alternate heroin and cocaine self-administration for 12 additional sessions, during which the FR schedule was progressively increased from FR10 to FR100. The second aim of the study was to investigate Fos mRNA expression in Resident and Non Resident rats treated with non-contingent intravenous infusion of "self-administration doses" of heroin (25.0 μg/kg) and cocaine (400 μg/kg). Results We found that: (1) drug-taking context differentially modulates intravenous cocaine versus heroin self-administration; (2) very low doses of cocaine and heroin are sufficient to induce Fos mRNA expression in the posterior caudate; (3) drug-administration context differentially modulates cocaine- versus heroin-induced Fos mRNA expression. Conclusions Our study indicates that the context of drug taking can play a powerful role in modulating cocaine versus heroin intake in the laboratory rat.</EA>
<CC>770E02; 770D03E01</CC>
<FD>Médicament; Contexte; Cocaïne; Etude comparative; Héroïne; Substance toxicomanogène; Autoadministration; Expression génique; Gène fos; Rat; Animal; Opiacés; Peptide opioïde; Stimulant SNC; Récompense; Addiction; Toxicomanie; Abus de substance; Noyau caudé; Corps strié</FD>
<FG>Rodentia; Mammalia; Vertebrata; Ester; Psychotrope; Encéphale; Noyau gris central; Système nerveux central</FG>
<ED>Drug; Context; Cocaine; Comparative study; Heroin; Drug of abuse; Self administration; Gene expression; fos Gene; Rat; Animal; Opiates; Opioid peptide; CNS stimulant; Reward; Addiction; Drug addiction; Substance abuse; Caudate nucleus; Corpus striatum</ED>
<EG>Rodentia; Mammalia; Vertebrata; Ester; Psychotropic; Encephalon; Basal ganglion; Central nervous system</EG>
<SD>Medicamento; Contexto; Cocaína; Estudio comparativo; Heroína; Sustancia toxicomanógena; Autoadministración; Expresión genética; Gen fos; Rata; Animal; Opiados; Péptido opioide; Estimulante SNC; Recompensa; Adicción; Toxicomanía; Abuso de sustancias; Núcleo caudado; Cuerpo estriado</SD>
<LO>INIST-1761.354000186087870140</LO>
<ID>09-0219985</ID>
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