Increased rewarding properties of morphine in perinatally protein-malnourished rats
Abstract In the current research, we assessed the influence of a protein malnutrition schedule from the 14th day of gestation up to 40 days of age (D-rats) on the rewarding properties of morphine in adult rats by means of the conditioned place preference paradigm. Well-nourished animals (C-rats) adm...
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description | Abstract In the current research, we assessed the influence of a protein malnutrition schedule from the 14th day of gestation up to 40 days of age (D-rats) on the rewarding properties of morphine in adult rats by means of the conditioned place preference paradigm. Well-nourished animals (C-rats) administered with different doses of morphine (0.75, 1.5, 3, 6, 12 or 24 mg/kg i.p.) exhibited a conditioning place preference with doses of 3 and 6 mg/kg, whereas in D-rats such a conditioning effect was observed with doses of 1.5 and 3 mg/kg. No adverse effects were observed in either C- or D-rats for the higher doses of morphine. In addition, when animals of both groups were pretreated twice a day for 3 days with increasing doses of morphine (5, 10 and 20 mg/kg s.c.), only D-rats elicited sensitization to the conditioning effect with the lowest dose of morphine (0.75 mg/kg i.p.). Furthermore, sensitized D-rats showed a selective and significant increase in FosB expression in the nucleus accumbens (core and shell), basolateral amygdala and medial prefrontal cortex, brain areas that are functionally related to the rewarding neural circuit. These results demonstrate that a deficient nutritional status during the perinatal period results in adult subjects having neural alterations, leading to an increased responsiveness to morphine and/or enhanced reinforcement effects, which correlates with an overexpression of FosB in selective brain areas related to the rewarding network. |
doi_str_mv | 10.1016/j.neuroscience.2007.09.006 |
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Well-nourished animals (C-rats) administered with different doses of morphine (0.75, 1.5, 3, 6, 12 or 24 mg/kg i.p.) exhibited a conditioning place preference with doses of 3 and 6 mg/kg, whereas in D-rats such a conditioning effect was observed with doses of 1.5 and 3 mg/kg. No adverse effects were observed in either C- or D-rats for the higher doses of morphine. In addition, when animals of both groups were pretreated twice a day for 3 days with increasing doses of morphine (5, 10 and 20 mg/kg s.c.), only D-rats elicited sensitization to the conditioning effect with the lowest dose of morphine (0.75 mg/kg i.p.). Furthermore, sensitized D-rats showed a selective and significant increase in FosB expression in the nucleus accumbens (core and shell), basolateral amygdala and medial prefrontal cortex, brain areas that are functionally related to the rewarding neural circuit. These results demonstrate that a deficient nutritional status during the perinatal period results in adult subjects having neural alterations, leading to an increased responsiveness to morphine and/or enhanced reinforcement effects, which correlates with an overexpression of FosB in selective brain areas related to the rewarding network.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/j.neuroscience.2007.09.006</identifier><identifier>PMID: 17935891</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Amygdala - drug effects ; Amygdala - metabolism ; Amygdala - physiopathology ; Analgesics ; Animals ; Biological and medical sciences ; Brain - drug effects ; Brain - metabolism ; Brain - physiopathology ; conditioned place preference ; Conditioning (Psychology) - drug effects ; Conditioning (Psychology) - physiology ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Female ; Fetal Nutrition Disorders - physiopathology ; FosB expression ; Fundamental and applied biological sciences. Psychology ; Limbic System - drug effects ; Limbic System - metabolism ; Limbic System - physiopathology ; Medical sciences ; morphine ; Morphine - pharmacology ; Morphine Dependence - metabolism ; Morphine Dependence - physiopathology ; Narcotics - pharmacology ; Neurology ; Neuropharmacology ; Nucleus Accumbens - drug effects ; Nucleus Accumbens - metabolism ; Nucleus Accumbens - physiopathology ; perinatal undernutrition ; Pharmacology. Drug treatments ; Prefrontal Cortex - drug effects ; Prefrontal Cortex - metabolism ; Prefrontal Cortex - physiopathology ; Pregnancy ; Protein Deficiency - physiopathology ; Proto-Oncogene Proteins c-fos - drug effects ; Proto-Oncogene Proteins c-fos - metabolism ; Rats ; Rats, Wistar ; Reward ; sensitization ; Up-Regulation - drug effects ; Up-Regulation - physiology ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2007-12, Vol.150 (2), p.449-458</ispartof><rights>IBRO</rights><rights>2007 IBRO</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c519t-15c1e66c3bcc1c0bd1d7498e60518a0ae3ce475364855d7cbd76340896890cc53</citedby><cites>FETCH-LOGICAL-c519t-15c1e66c3bcc1c0bd1d7498e60518a0ae3ce475364855d7cbd76340896890cc53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuroscience.2007.09.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19940520$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17935891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Valdomero, A</creatorcontrib><creatorcontrib>Velazquez, E.E</creatorcontrib><creatorcontrib>de Olmos, S</creatorcontrib><creatorcontrib>De Olmos, J.S</creatorcontrib><creatorcontrib>Orsingher, O.A</creatorcontrib><creatorcontrib>Cuadra, G.R</creatorcontrib><title>Increased rewarding properties of morphine in perinatally protein-malnourished rats</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Abstract In the current research, we assessed the influence of a protein malnutrition schedule from the 14th day of gestation up to 40 days of age (D-rats) on the rewarding properties of morphine in adult rats by means of the conditioned place preference paradigm. Well-nourished animals (C-rats) administered with different doses of morphine (0.75, 1.5, 3, 6, 12 or 24 mg/kg i.p.) exhibited a conditioning place preference with doses of 3 and 6 mg/kg, whereas in D-rats such a conditioning effect was observed with doses of 1.5 and 3 mg/kg. No adverse effects were observed in either C- or D-rats for the higher doses of morphine. In addition, when animals of both groups were pretreated twice a day for 3 days with increasing doses of morphine (5, 10 and 20 mg/kg s.c.), only D-rats elicited sensitization to the conditioning effect with the lowest dose of morphine (0.75 mg/kg i.p.). Furthermore, sensitized D-rats showed a selective and significant increase in FosB expression in the nucleus accumbens (core and shell), basolateral amygdala and medial prefrontal cortex, brain areas that are functionally related to the rewarding neural circuit. These results demonstrate that a deficient nutritional status during the perinatal period results in adult subjects having neural alterations, leading to an increased responsiveness to morphine and/or enhanced reinforcement effects, which correlates with an overexpression of FosB in selective brain areas related to the rewarding network.</description><subject>Amygdala - drug effects</subject><subject>Amygdala - metabolism</subject><subject>Amygdala - physiopathology</subject><subject>Analgesics</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Brain - physiopathology</subject><subject>conditioned place preference</subject><subject>Conditioning (Psychology) - drug effects</subject><subject>Conditioning (Psychology) - physiology</subject><subject>Disease Models, Animal</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Fetal Nutrition Disorders - physiopathology</subject><subject>FosB expression</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Limbic System - drug effects</subject><subject>Limbic System - metabolism</subject><subject>Limbic System - physiopathology</subject><subject>Medical sciences</subject><subject>morphine</subject><subject>Morphine - pharmacology</subject><subject>Morphine Dependence - metabolism</subject><subject>Morphine Dependence - physiopathology</subject><subject>Narcotics - pharmacology</subject><subject>Neurology</subject><subject>Neuropharmacology</subject><subject>Nucleus Accumbens - drug effects</subject><subject>Nucleus Accumbens - metabolism</subject><subject>Nucleus Accumbens - physiopathology</subject><subject>perinatal undernutrition</subject><subject>Pharmacology. Drug treatments</subject><subject>Prefrontal Cortex - drug effects</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Prefrontal Cortex - physiopathology</subject><subject>Pregnancy</subject><subject>Protein Deficiency - physiopathology</subject><subject>Proto-Oncogene Proteins c-fos - drug effects</subject><subject>Proto-Oncogene Proteins c-fos - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reward</subject><subject>sensitization</subject><subject>Up-Regulation - drug effects</subject><subject>Up-Regulation - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQhi0EokvhL6AIid4SxvFHYg5IqOWjUqUeWs6WdzJLvSTOYieg_fc42khFnPDFkvXMzKvHw9gbDhUHrt_tq0BzHBN6CkhVDdBUYCoA_YRteNuIslFSPmUbEKBLqer6jL1IaQ_5KCmeszPeGKFawzfs7jpgJJeoKyL9drHz4XtxiOOB4uQpFeOuGMZ4ePCBCh-K_OyDm1zfHxdqIh_KwfVhnKNPD0sTN6WX7NnO9Ylerfc5-_b50_3l1_Lm9sv15cebEhU3U8kVctIaxRaRI2w73jXStKRB8daBI4EkGyW0bJXqGtx2jRYSWqNbA4hKnLOLU9-c5OdMabKDT0h97wKNc7I1KJXlmAy-P4GYraVIO3uIfnDxaDnYRand27-V2kWpBWOz0lz8ep0ybwfqHktXhxl4uwIuoet30QX06ZEzRkLOkbmrE0fZyS9P0a7jOh8JJ9uN_v_yfPinDfY--Dz5Bx0p7fNXhGzdcptqC_ZuWYJlB6ABzkGB-AMoKrGy</recordid><startdate>20071205</startdate><enddate>20071205</enddate><creator>Valdomero, A</creator><creator>Velazquez, E.E</creator><creator>de Olmos, S</creator><creator>De Olmos, J.S</creator><creator>Orsingher, O.A</creator><creator>Cuadra, G.R</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>7QG</scope><scope>7TK</scope></search><sort><creationdate>20071205</creationdate><title>Increased rewarding properties of morphine in perinatally protein-malnourished rats</title><author>Valdomero, A ; Velazquez, E.E ; de Olmos, S ; De Olmos, J.S ; Orsingher, O.A ; Cuadra, G.R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c519t-15c1e66c3bcc1c0bd1d7498e60518a0ae3ce475364855d7cbd76340896890cc53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Amygdala - drug effects</topic><topic>Amygdala - metabolism</topic><topic>Amygdala - physiopathology</topic><topic>Analgesics</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Brain - physiopathology</topic><topic>conditioned place preference</topic><topic>Conditioning (Psychology) - drug effects</topic><topic>Conditioning (Psychology) - physiology</topic><topic>Disease Models, Animal</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Fetal Nutrition Disorders - physiopathology</topic><topic>FosB expression</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Limbic System - drug effects</topic><topic>Limbic System - metabolism</topic><topic>Limbic System - physiopathology</topic><topic>Medical sciences</topic><topic>morphine</topic><topic>Morphine - pharmacology</topic><topic>Morphine Dependence - metabolism</topic><topic>Morphine Dependence - physiopathology</topic><topic>Narcotics - pharmacology</topic><topic>Neurology</topic><topic>Neuropharmacology</topic><topic>Nucleus Accumbens - drug effects</topic><topic>Nucleus Accumbens - metabolism</topic><topic>Nucleus Accumbens - physiopathology</topic><topic>perinatal undernutrition</topic><topic>Pharmacology. Drug treatments</topic><topic>Prefrontal Cortex - drug effects</topic><topic>Prefrontal Cortex - metabolism</topic><topic>Prefrontal Cortex - physiopathology</topic><topic>Pregnancy</topic><topic>Protein Deficiency - physiopathology</topic><topic>Proto-Oncogene Proteins c-fos - drug effects</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reward</topic><topic>sensitization</topic><topic>Up-Regulation - drug effects</topic><topic>Up-Regulation - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Valdomero, A</creatorcontrib><creatorcontrib>Velazquez, E.E</creatorcontrib><creatorcontrib>de Olmos, S</creatorcontrib><creatorcontrib>De Olmos, J.S</creatorcontrib><creatorcontrib>Orsingher, O.A</creatorcontrib><creatorcontrib>Cuadra, G.R</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>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Valdomero, A</au><au>Velazquez, E.E</au><au>de Olmos, S</au><au>De Olmos, J.S</au><au>Orsingher, O.A</au><au>Cuadra, G.R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased rewarding properties of morphine in perinatally protein-malnourished rats</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2007-12-05</date><risdate>2007</risdate><volume>150</volume><issue>2</issue><spage>449</spage><epage>458</epage><pages>449-458</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Abstract In the current research, we assessed the influence of a protein malnutrition schedule from the 14th day of gestation up to 40 days of age (D-rats) on the rewarding properties of morphine in adult rats by means of the conditioned place preference paradigm. Well-nourished animals (C-rats) administered with different doses of morphine (0.75, 1.5, 3, 6, 12 or 24 mg/kg i.p.) exhibited a conditioning place preference with doses of 3 and 6 mg/kg, whereas in D-rats such a conditioning effect was observed with doses of 1.5 and 3 mg/kg. No adverse effects were observed in either C- or D-rats for the higher doses of morphine. In addition, when animals of both groups were pretreated twice a day for 3 days with increasing doses of morphine (5, 10 and 20 mg/kg s.c.), only D-rats elicited sensitization to the conditioning effect with the lowest dose of morphine (0.75 mg/kg i.p.). Furthermore, sensitized D-rats showed a selective and significant increase in FosB expression in the nucleus accumbens (core and shell), basolateral amygdala and medial prefrontal cortex, brain areas that are functionally related to the rewarding neural circuit. These results demonstrate that a deficient nutritional status during the perinatal period results in adult subjects having neural alterations, leading to an increased responsiveness to morphine and/or enhanced reinforcement effects, which correlates with an overexpression of FosB in selective brain areas related to the rewarding network.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>17935891</pmid><doi>10.1016/j.neuroscience.2007.09.006</doi><tpages>10</tpages></addata></record> |
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subjects | Amygdala - drug effects Amygdala - metabolism Amygdala - physiopathology Analgesics Animals Biological and medical sciences Brain - drug effects Brain - metabolism Brain - physiopathology conditioned place preference Conditioning (Psychology) - drug effects Conditioning (Psychology) - physiology Disease Models, Animal Dose-Response Relationship, Drug Drug Administration Schedule Female Fetal Nutrition Disorders - physiopathology FosB expression Fundamental and applied biological sciences. Psychology Limbic System - drug effects Limbic System - metabolism Limbic System - physiopathology Medical sciences morphine Morphine - pharmacology Morphine Dependence - metabolism Morphine Dependence - physiopathology Narcotics - pharmacology Neurology Neuropharmacology Nucleus Accumbens - drug effects Nucleus Accumbens - metabolism Nucleus Accumbens - physiopathology perinatal undernutrition Pharmacology. Drug treatments Prefrontal Cortex - drug effects Prefrontal Cortex - metabolism Prefrontal Cortex - physiopathology Pregnancy Protein Deficiency - physiopathology Proto-Oncogene Proteins c-fos - drug effects Proto-Oncogene Proteins c-fos - metabolism Rats Rats, Wistar Reward sensitization Up-Regulation - drug effects Up-Regulation - physiology Vertebrates: nervous system and sense organs |
title | Increased rewarding properties of morphine in perinatally protein-malnourished rats |
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