Developmental exposure to polychlorinated biphenyls reduces amphetamine behavioral sensitization in Long–Evans rats
Abstract PCBs have long been known to affect dopamine (DA) function in the brain. The current study used an amphetamine behavioral sensitization paradigm in rats developmentally exposed to PCBs. Long–Evans rats were given perinatal exposure to 0, 3, or 6 mg/kg/day PCBs and behavioral sensitization t...
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creator | Poon, Emily Monaikul, Supida Kostyniak, Paul J Chi, Lai Har Schantz, Susan L Sable, Helen J.K |
description | Abstract PCBs have long been known to affect dopamine (DA) function in the brain. The current study used an amphetamine behavioral sensitization paradigm in rats developmentally exposed to PCBs. Long–Evans rats were given perinatal exposure to 0, 3, or 6 mg/kg/day PCBs and behavioral sensitization to d -amphetamine (AMPH) was assessed in one adult male and female/litter. Non-exposed (control) males showed increasing locomotor activity to repeated injections of 0.5 mg/kg AMPH, typical of behavioral sensitization. PCB-exposed males showed greater activation to the initial acute AMPH injection, but sensitization occurred later and was blunted relative to controls. Sensitization in control females took longer to develop than in the males, but no exposure-related differences were observed. Analysis of whole brain and serum AMPH content following a final IP injection of 0.5 mg/kg revealed no differences among the exposure groups. Overall, these results indicated developmental PCB exposure can alter the motor-stimulating effects of repeated AMPH injections. Males developmentally exposed to PCBs appeared to be pre-sensitized to AMPH, but quickly showed behavioral tolerance to the same drug dose. Results also revealed the behavioral effect was not due to exposure-induced alterations in AMPH metabolism following PCB exposure. |
doi_str_mv | 10.1016/j.ntt.2013.04.005 |
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The current study used an amphetamine behavioral sensitization paradigm in rats developmentally exposed to PCBs. Long–Evans rats were given perinatal exposure to 0, 3, or 6 mg/kg/day PCBs and behavioral sensitization to d -amphetamine (AMPH) was assessed in one adult male and female/litter. Non-exposed (control) males showed increasing locomotor activity to repeated injections of 0.5 mg/kg AMPH, typical of behavioral sensitization. PCB-exposed males showed greater activation to the initial acute AMPH injection, but sensitization occurred later and was blunted relative to controls. Sensitization in control females took longer to develop than in the males, but no exposure-related differences were observed. Analysis of whole brain and serum AMPH content following a final IP injection of 0.5 mg/kg revealed no differences among the exposure groups. Overall, these results indicated developmental PCB exposure can alter the motor-stimulating effects of repeated AMPH injections. Males developmentally exposed to PCBs appeared to be pre-sensitized to AMPH, but quickly showed behavioral tolerance to the same drug dose. Results also revealed the behavioral effect was not due to exposure-induced alterations in AMPH metabolism following PCB exposure.</description><identifier>ISSN: 0892-0362</identifier><identifier>EISSN: 1872-9738</identifier><identifier>DOI: 10.1016/j.ntt.2013.04.005</identifier><identifier>PMID: 23623962</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Administration, Oral ; Amphetamine ; Animals ; Behavioral pharmacology ; Behavioral sensitization ; Central Nervous System Sensitization - drug effects ; Dextroamphetamine - pharmacokinetics ; Dextroamphetamine - pharmacology ; Dose-Response Relationship, Drug ; Emergency ; Female ; Male ; Medical Education ; Motor Activity - drug effects ; Neurotoxicology ; Polychlorinated biphenyls ; Polychlorinated Biphenyls - administration & dosage ; Polychlorinated Biphenyls - toxicity ; Pregnancy ; Rats ; Rats, Long-Evans ; Time Factors</subject><ispartof>Neurotoxicology and teratology, 2013-07, Vol.38, p.6-12</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><rights>2013 Elsevier Inc. All rights reserved. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-c020bbea5166cd67142afe7a6a13bbe8e15a3f08346e1237ff77c0359b9d26963</citedby><cites>FETCH-LOGICAL-c539t-c020bbea5166cd67142afe7a6a13bbe8e15a3f08346e1237ff77c0359b9d26963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ntt.2013.04.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,315,781,785,886,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23623962$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Poon, Emily</creatorcontrib><creatorcontrib>Monaikul, Supida</creatorcontrib><creatorcontrib>Kostyniak, Paul J</creatorcontrib><creatorcontrib>Chi, Lai Har</creatorcontrib><creatorcontrib>Schantz, Susan L</creatorcontrib><creatorcontrib>Sable, Helen J.K</creatorcontrib><title>Developmental exposure to polychlorinated biphenyls reduces amphetamine behavioral sensitization in Long–Evans rats</title><title>Neurotoxicology and teratology</title><addtitle>Neurotoxicol Teratol</addtitle><description>Abstract PCBs have long been known to affect dopamine (DA) function in the brain. The current study used an amphetamine behavioral sensitization paradigm in rats developmentally exposed to PCBs. Long–Evans rats were given perinatal exposure to 0, 3, or 6 mg/kg/day PCBs and behavioral sensitization to d -amphetamine (AMPH) was assessed in one adult male and female/litter. Non-exposed (control) males showed increasing locomotor activity to repeated injections of 0.5 mg/kg AMPH, typical of behavioral sensitization. PCB-exposed males showed greater activation to the initial acute AMPH injection, but sensitization occurred later and was blunted relative to controls. Sensitization in control females took longer to develop than in the males, but no exposure-related differences were observed. Analysis of whole brain and serum AMPH content following a final IP injection of 0.5 mg/kg revealed no differences among the exposure groups. Overall, these results indicated developmental PCB exposure can alter the motor-stimulating effects of repeated AMPH injections. Males developmentally exposed to PCBs appeared to be pre-sensitized to AMPH, but quickly showed behavioral tolerance to the same drug dose. Results also revealed the behavioral effect was not due to exposure-induced alterations in AMPH metabolism following PCB exposure.</description><subject>Administration, Oral</subject><subject>Amphetamine</subject><subject>Animals</subject><subject>Behavioral pharmacology</subject><subject>Behavioral sensitization</subject><subject>Central Nervous System Sensitization - drug effects</subject><subject>Dextroamphetamine - pharmacokinetics</subject><subject>Dextroamphetamine - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Emergency</subject><subject>Female</subject><subject>Male</subject><subject>Medical Education</subject><subject>Motor Activity - drug effects</subject><subject>Neurotoxicology</subject><subject>Polychlorinated biphenyls</subject><subject>Polychlorinated Biphenyls - administration & dosage</subject><subject>Polychlorinated Biphenyls - toxicity</subject><subject>Pregnancy</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Time Factors</subject><issn>0892-0362</issn><issn>1872-9738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UsGO0zAQtRCI7RY-gAvKkUvL2G7sREgroWUXkCpxAM6W40y2LokdbCfacuIf-EO-BFddVsCB00hv3nsezxtCnlFYU6Di5X7tUlozoHwNmzVA-YAsaCXZqpa8ekgWUNVsBVywM3Ie4x4ApKDwmJyxjPFasAWZ3uCMvR8HdEn3Bd6OPk4Bi-SL0fcHs-t9sE4nbIvGjjt0hz4WAdvJYCz0kJGkB-uwaHCnZ-tDNonook32m07Wu8K6Yuvdzc_vP65m7bJYp_iEPOp0H_HpXV2Sz9dXny7frbYf3r6_fL1dmZLXaWWAQdOgLqkQphWSbpjuUGqhKc94hbTUvIOKbwRSxmXXSWmAl3VTt0zUgi_Jxcl3nJoBW5M_mQdUY7CDDgfltVV_d5zdqRs_Ky4pp9l4SV7cGQT_dcKY1GCjwb7XDv0UFRVM1qISQmYqPVFN8DEG7O6foaCOcam9ynGpY1wKNirHlTXP_5zvXvE7n0x4dSJg3tJsMahoLDqDrQ1okmq9_a_9xT9q01tnje6_4AHj3k_B5fUrqiJToD4e7-V4LpQDUEZr_gs0YsAt</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>Poon, Emily</creator><creator>Monaikul, Supida</creator><creator>Kostyniak, Paul J</creator><creator>Chi, Lai Har</creator><creator>Schantz, Susan L</creator><creator>Sable, Helen J.K</creator><general>Elsevier Inc</general><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>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20130701</creationdate><title>Developmental exposure to polychlorinated biphenyls reduces amphetamine behavioral sensitization in Long–Evans rats</title><author>Poon, Emily ; Monaikul, Supida ; Kostyniak, Paul J ; Chi, Lai Har ; Schantz, Susan L ; Sable, Helen J.K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-c020bbea5166cd67142afe7a6a13bbe8e15a3f08346e1237ff77c0359b9d26963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Administration, Oral</topic><topic>Amphetamine</topic><topic>Animals</topic><topic>Behavioral pharmacology</topic><topic>Behavioral sensitization</topic><topic>Central Nervous System Sensitization - drug effects</topic><topic>Dextroamphetamine - pharmacokinetics</topic><topic>Dextroamphetamine - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Emergency</topic><topic>Female</topic><topic>Male</topic><topic>Medical Education</topic><topic>Motor Activity - drug effects</topic><topic>Neurotoxicology</topic><topic>Polychlorinated biphenyls</topic><topic>Polychlorinated Biphenyls - administration & dosage</topic><topic>Polychlorinated Biphenyls - toxicity</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Rats, Long-Evans</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poon, Emily</creatorcontrib><creatorcontrib>Monaikul, Supida</creatorcontrib><creatorcontrib>Kostyniak, Paul J</creatorcontrib><creatorcontrib>Chi, Lai Har</creatorcontrib><creatorcontrib>Schantz, Susan L</creatorcontrib><creatorcontrib>Sable, Helen J.K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neurotoxicology and teratology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poon, Emily</au><au>Monaikul, Supida</au><au>Kostyniak, Paul J</au><au>Chi, Lai Har</au><au>Schantz, Susan L</au><au>Sable, Helen J.K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental exposure to polychlorinated biphenyls reduces amphetamine behavioral sensitization in Long–Evans rats</atitle><jtitle>Neurotoxicology and teratology</jtitle><addtitle>Neurotoxicol Teratol</addtitle><date>2013-07-01</date><risdate>2013</risdate><volume>38</volume><spage>6</spage><epage>12</epage><pages>6-12</pages><issn>0892-0362</issn><eissn>1872-9738</eissn><abstract>Abstract PCBs have long been known to affect dopamine (DA) function in the brain. The current study used an amphetamine behavioral sensitization paradigm in rats developmentally exposed to PCBs. Long–Evans rats were given perinatal exposure to 0, 3, or 6 mg/kg/day PCBs and behavioral sensitization to d -amphetamine (AMPH) was assessed in one adult male and female/litter. Non-exposed (control) males showed increasing locomotor activity to repeated injections of 0.5 mg/kg AMPH, typical of behavioral sensitization. PCB-exposed males showed greater activation to the initial acute AMPH injection, but sensitization occurred later and was blunted relative to controls. Sensitization in control females took longer to develop than in the males, but no exposure-related differences were observed. Analysis of whole brain and serum AMPH content following a final IP injection of 0.5 mg/kg revealed no differences among the exposure groups. Overall, these results indicated developmental PCB exposure can alter the motor-stimulating effects of repeated AMPH injections. Males developmentally exposed to PCBs appeared to be pre-sensitized to AMPH, but quickly showed behavioral tolerance to the same drug dose. Results also revealed the behavioral effect was not due to exposure-induced alterations in AMPH metabolism following PCB exposure.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23623962</pmid><doi>10.1016/j.ntt.2013.04.005</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Amphetamine Animals Behavioral pharmacology Behavioral sensitization Central Nervous System Sensitization - drug effects Dextroamphetamine - pharmacokinetics Dextroamphetamine - pharmacology Dose-Response Relationship, Drug Emergency Female Male Medical Education Motor Activity - drug effects Neurotoxicology Polychlorinated biphenyls Polychlorinated Biphenyls - administration & dosage Polychlorinated Biphenyls - toxicity Pregnancy Rats Rats, Long-Evans Time Factors |
title | Developmental exposure to polychlorinated biphenyls reduces amphetamine behavioral sensitization in Long–Evans rats |
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