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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 |
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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. |
doi_str_mv | 10.1016/j.neuint.2012.06.011 |
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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. 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.</description><identifier>ISSN: 0197-0186</identifier><identifier>EISSN: 1872-9754</identifier><identifier>DOI: 10.1016/j.neuint.2012.06.011</identifier><identifier>PMID: 22713675</identifier><identifier>CODEN: NEUIDS</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>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</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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-e52bd5a10cd9c2968298caa68e0ff9de70e20e724486bb388b40d7915607e6943</citedby><cites>FETCH-LOGICAL-c425t-e52bd5a10cd9c2968298caa68e0ff9de70e20e724486bb388b40d7915607e6943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26363466$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22713675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Accumbal dopamine, noradrenaline and serotonin activity after naloxone-conditioned place aversion in morphine-dependent mice</title><title>Neurochemistry international</title><addtitle>Neurochem Int</addtitle><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.</description><subject>Analgesics</subject><subject>Animals</subject><subject>Aversion</subject><subject>Avoidance Learning</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Conditioned place aversion</subject><subject>Conditioning, Operant</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Drug dependence</subject><subject>Fundamental and applied biological sciences. 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 & 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. Drug treatments</subject><subject>Phosphorylation</subject><subject>Polymerase chain reaction</subject><subject>Post-transcription</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Reinforcement</subject><subject>Serotonin</subject><subject>Serotonin - metabolism</subject><subject>TH expression</subject><subject>TH phosphorylation</subject><subject>Tyrosine 3-monooxygenase</subject><subject>Tyrosine 3-Monooxygenase - genetics</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Western blotting</subject><issn>0197-0186</issn><issn>1872-9754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkU2r1DAUhoMo3vHqPxDJRnBhx5O0TZqNcLn4BRfc6DqkySlmaJOapIMX_PFmmFF34iofPO95Qx5CnjPYM2DizWEfcPOh7DkwvgexB8YekB0bJG-U7LuHZAdMyQbYIK7Ik5wPACAV9I_JFeeStUL2O_LzxtptGc1MXVzN4gO-piEm4xIGM9cjNcHRjCmWGHygxhZ_9OWemqlgopWJP2LAxsbgfPF16-g6G1tzR0y5XtCaWmJav9VhjcMVg8NQ6OItPiWPJjNnfHZZr8nX9---3H5s7j5_-HR7c9fYjvelwZ6PrjcMrFOWKzFwNVhjxIAwTcqhBOSAknfdIMaxHYaxAycV6wVIFKprr8mr89w1xe8b5qIXny3OswkYt6wZtIOATgn1P2gtapUUFe3OqE0x54STXpNfTLqvkD4p0gd9VqRPijQIXRXV2ItLwzYu6P6EfjupwMsLYLI185RMsD7_5UQr2k6c-t-eOaxfd_SYdLYeg0XnE9qiXfT_fskvKgSzFw</recordid><startdate>20120801</startdate><enddate>20120801</enddate><creator>Gómez-Milanés, Iván</creator><creator>Almela, Pilar</creator><creator>García-Carmona, Juan-Antonio</creator><creator>Salud García-Gutiérrez, M.</creator><creator>Aracil-Fernández, Auxiliadora</creator><creator>Manzanares, Jorge</creator><creator>Victoria Milanés Maquilón, M.</creator><creator>Luisa Laorden, M.</creator><general>Elsevier Ltd</general><general>Elsevier</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><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20120801</creationdate><title>Accumbal dopamine, noradrenaline and serotonin activity after naloxone-conditioned place aversion in morphine-dependent mice</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-e52bd5a10cd9c2968298caa68e0ff9de70e20e724486bb388b40d7915607e6943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Analgesics</topic><topic>Animals</topic><topic>Aversion</topic><topic>Avoidance Learning</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Conditioned place aversion</topic><topic>Conditioning, Operant</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>Drug dependence</topic><topic>Fundamental and applied biological sciences. 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 & 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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