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Accumbal dopamine, noradrenaline and serotonin activity after naloxone-conditioned place aversion in morphine-dependent mice

► We evaluate the role of monoamines in naloxone-induced conditioned place aversion (CPA). ► We examined changes in the turnover of DA, NA and 5-HT in the nucleus accumbens (NAc). ► We examine the changes in TH mRNA in the ventral tegmental area (VTA). ► Morphine withdrawal Increases NA and DA turno...

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Published in:Neurochemistry international 2012-08, Vol.61 (3), p.433-440
Main Authors: Gómez-Milanés, Iván, Almela, Pilar, García-Carmona, Juan-Antonio, Salud García-Gutiérrez, M., Aracil-Fernández, Auxiliadora, Manzanares, Jorge, Victoria Milanés Maquilón, M., Luisa Laorden, M.
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container_title Neurochemistry international
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creator Gómez-Milanés, Iván
Almela, Pilar
García-Carmona, Juan-Antonio
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Aracil-Fernández, Auxiliadora
Manzanares, Jorge
Victoria Milanés Maquilón, M.
Luisa Laorden, M.
description ► We evaluate the role of monoamines in naloxone-induced conditioned place aversion (CPA). ► We examined changes in the turnover of DA, NA and 5-HT in the nucleus accumbens (NAc). ► We examine the changes in TH mRNA in the ventral tegmental area (VTA). ► Morphine withdrawal Increases NA and DA turnover in NAc and elevates TH expression in VTA. ► CPA is related to NA and DA activity and transcriptional regulation of TH. Dopamine (DA) neurons not only show a pattern signaling the magnitude, delay and probability of rewards but also code negative motivation and aversive events. Beside DA, other systems such as noradrenaline (NA) and serotonin (5-HT) may also be implicated in naloxone-induced conditioned place aversion (CPA; an index of the aversive consequences of withdrawal). The purpose of the present study was to evaluate: (i) the turnover of DA, NA and 5-HT in the nucleus accumbens (NAc), one of the most important substrates for aversive states, (ii) the changes in tyrosine hydroxylase (TH) gene expression in the ventral tegmental area, and (iii) total TH protein levels and TH phosphorylation in the NAc after naloxone-induced morphine withdrawal. DA, NA and 5-HT turnover was evaluated by high-performance liquid chromatography (HPLC). TH gene expression was determined by real time quantitative PCR (RT-PCR) and total TH and TH phosphorylated at Ser31 and Ser40 were analyzed by Western blot. Present results show that the aversion for environmental cues paired with opioid withdrawal was higher than that observed in the saline group treated with naloxone, which indicates that morphine pretreatment potentiated the ability of naloxone to produce place aversion. In addition, present data show that naloxone-induced CPA positively correlated with an increase of DA and NA turnover in the NAc, which paralleled an increase in TH gene expression in the VTA and TH phosphorylation and enhanced TH protein levels in the NAc. Thus, the present study indicates that naloxone-induced aversion in morphine-dependent mice enhances DA and NA activity in the NAc and suggests that transcriptional and post-transcriptional regulation of TH could be involved in the hyperactivity of mesolimbic dopaminergic system observed in morphine-withdrawn mice.
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Dopamine (DA) neurons not only show a pattern signaling the magnitude, delay and probability of rewards but also code negative motivation and aversive events. Beside DA, other systems such as noradrenaline (NA) and serotonin (5-HT) may also be implicated in naloxone-induced conditioned place aversion (CPA; an index of the aversive consequences of withdrawal). The purpose of the present study was to evaluate: (i) the turnover of DA, NA and 5-HT in the nucleus accumbens (NAc), one of the most important substrates for aversive states, (ii) the changes in tyrosine hydroxylase (TH) gene expression in the ventral tegmental area, and (iii) total TH protein levels and TH phosphorylation in the NAc after naloxone-induced morphine withdrawal. DA, NA and 5-HT turnover was evaluated by high-performance liquid chromatography (HPLC). TH gene expression was determined by real time quantitative PCR (RT-PCR) and total TH and TH phosphorylated at Ser31 and Ser40 were analyzed by Western blot. Present results show that the aversion for environmental cues paired with opioid withdrawal was higher than that observed in the saline group treated with naloxone, which indicates that morphine pretreatment potentiated the ability of naloxone to produce place aversion. In addition, present data show that naloxone-induced CPA positively correlated with an increase of DA and NA turnover in the NAc, which paralleled an increase in TH gene expression in the VTA and TH phosphorylation and enhanced TH protein levels in the NAc. 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Psychology ; Gene expression ; Gene regulation ; High-performance liquid chromatography ; Male ; Medical sciences ; Mice ; Morphine ; Morphine - administration &amp; dosage ; Motivation ; Naloxone ; Naloxone - pharmacology ; Neuropharmacology ; Noradrenaline ; Norepinephrine ; Norepinephrine - metabolism ; Nucleus accumbens ; Nucleus Accumbens - metabolism ; Opioids ; Pharmacology. Drug treatments ; Phosphorylation ; Polymerase chain reaction ; Post-transcription ; Real-Time Polymerase Chain Reaction ; Reinforcement ; Serotonin ; Serotonin - metabolism ; TH expression ; TH phosphorylation ; Tyrosine 3-monooxygenase ; Tyrosine 3-Monooxygenase - genetics ; Tyrosine 3-Monooxygenase - metabolism ; Vertebrates: nervous system and sense organs ; Western blotting</subject><ispartof>Neurochemistry international, 2012-08, Vol.61 (3), p.433-440</ispartof><rights>2012 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. 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Psychology</subject><subject>Gene expression</subject><subject>Gene regulation</subject><subject>High-performance liquid chromatography</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Morphine</subject><subject>Morphine - administration &amp; dosage</subject><subject>Motivation</subject><subject>Naloxone</subject><subject>Naloxone - pharmacology</subject><subject>Neuropharmacology</subject><subject>Noradrenaline</subject><subject>Norepinephrine</subject><subject>Norepinephrine - metabolism</subject><subject>Nucleus accumbens</subject><subject>Nucleus Accumbens - metabolism</subject><subject>Opioids</subject><subject>Pharmacology. 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Psychology</topic><topic>Gene expression</topic><topic>Gene regulation</topic><topic>High-performance liquid chromatography</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Morphine</topic><topic>Morphine - administration &amp; dosage</topic><topic>Motivation</topic><topic>Naloxone</topic><topic>Naloxone - pharmacology</topic><topic>Neuropharmacology</topic><topic>Noradrenaline</topic><topic>Norepinephrine</topic><topic>Norepinephrine - metabolism</topic><topic>Nucleus accumbens</topic><topic>Nucleus Accumbens - metabolism</topic><topic>Opioids</topic><topic>Pharmacology. Drug treatments</topic><topic>Phosphorylation</topic><topic>Polymerase chain reaction</topic><topic>Post-transcription</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Reinforcement</topic><topic>Serotonin</topic><topic>Serotonin - metabolism</topic><topic>TH expression</topic><topic>TH phosphorylation</topic><topic>Tyrosine 3-monooxygenase</topic><topic>Tyrosine 3-Monooxygenase - genetics</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gómez-Milanés, Iván</creatorcontrib><creatorcontrib>Almela, Pilar</creatorcontrib><creatorcontrib>García-Carmona, Juan-Antonio</creatorcontrib><creatorcontrib>Salud García-Gutiérrez, M.</creatorcontrib><creatorcontrib>Aracil-Fernández, Auxiliadora</creatorcontrib><creatorcontrib>Manzanares, Jorge</creatorcontrib><creatorcontrib>Victoria Milanés Maquilón, M.</creatorcontrib><creatorcontrib>Luisa Laorden, M.</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><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Neurochemistry international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gómez-Milanés, Iván</au><au>Almela, Pilar</au><au>García-Carmona, Juan-Antonio</au><au>Salud García-Gutiérrez, M.</au><au>Aracil-Fernández, Auxiliadora</au><au>Manzanares, Jorge</au><au>Victoria Milanés Maquilón, M.</au><au>Luisa Laorden, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Accumbal dopamine, noradrenaline and serotonin activity after naloxone-conditioned place aversion in morphine-dependent mice</atitle><jtitle>Neurochemistry international</jtitle><addtitle>Neurochem Int</addtitle><date>2012-08-01</date><risdate>2012</risdate><volume>61</volume><issue>3</issue><spage>433</spage><epage>440</epage><pages>433-440</pages><issn>0197-0186</issn><eissn>1872-9754</eissn><coden>NEUIDS</coden><abstract>► We evaluate the role of monoamines in naloxone-induced conditioned place aversion (CPA). ► We examined changes in the turnover of DA, NA and 5-HT in the nucleus accumbens (NAc). ► We examine the changes in TH mRNA in the ventral tegmental area (VTA). ► Morphine withdrawal Increases NA and DA turnover in NAc and elevates TH expression in VTA. ► CPA is related to NA and DA activity and transcriptional regulation of TH. Dopamine (DA) neurons not only show a pattern signaling the magnitude, delay and probability of rewards but also code negative motivation and aversive events. Beside DA, other systems such as noradrenaline (NA) and serotonin (5-HT) may also be implicated in naloxone-induced conditioned place aversion (CPA; an index of the aversive consequences of withdrawal). The purpose of the present study was to evaluate: (i) the turnover of DA, NA and 5-HT in the nucleus accumbens (NAc), one of the most important substrates for aversive states, (ii) the changes in tyrosine hydroxylase (TH) gene expression in the ventral tegmental area, and (iii) total TH protein levels and TH phosphorylation in the NAc after naloxone-induced morphine withdrawal. DA, NA and 5-HT turnover was evaluated by high-performance liquid chromatography (HPLC). TH gene expression was determined by real time quantitative PCR (RT-PCR) and total TH and TH phosphorylated at Ser31 and Ser40 were analyzed by Western blot. Present results show that the aversion for environmental cues paired with opioid withdrawal was higher than that observed in the saline group treated with naloxone, which indicates that morphine pretreatment potentiated the ability of naloxone to produce place aversion. In addition, present data show that naloxone-induced CPA positively correlated with an increase of DA and NA turnover in the NAc, which paralleled an increase in TH gene expression in the VTA and TH phosphorylation and enhanced TH protein levels in the NAc. Thus, the present study indicates that naloxone-induced aversion in morphine-dependent mice enhances DA and NA activity in the NAc and suggests that transcriptional and post-transcriptional regulation of TH could be involved in the hyperactivity of mesolimbic dopaminergic system observed in morphine-withdrawn mice.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>22713675</pmid><doi>10.1016/j.neuint.2012.06.011</doi><tpages>8</tpages></addata></record>
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subjects Analgesics
Animals
Aversion
Avoidance Learning
Biological and medical sciences
Blotting, Western
Chromatography, High Pressure Liquid
Conditioned place aversion
Conditioning, Operant
Dopamine
Dopamine - metabolism
Drug dependence
Fundamental and applied biological sciences. Psychology
Gene expression
Gene regulation
High-performance liquid chromatography
Male
Medical sciences
Mice
Morphine
Morphine - administration & dosage
Motivation
Naloxone
Naloxone - pharmacology
Neuropharmacology
Noradrenaline
Norepinephrine
Norepinephrine - metabolism
Nucleus accumbens
Nucleus Accumbens - metabolism
Opioids
Pharmacology. Drug treatments
Phosphorylation
Polymerase chain reaction
Post-transcription
Real-Time Polymerase Chain Reaction
Reinforcement
Serotonin
Serotonin - metabolism
TH expression
TH phosphorylation
Tyrosine 3-monooxygenase
Tyrosine 3-Monooxygenase - genetics
Tyrosine 3-Monooxygenase - metabolism
Vertebrates: nervous system and sense organs
Western blotting
title Accumbal dopamine, noradrenaline and serotonin activity after naloxone-conditioned place aversion in morphine-dependent mice
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