Maternal transfer of BDE-47 to offspring and neurobehavioral development in C57BL/6J mice
Abstract Polybrominated diphenyl ethers (PBDEs) are flame retardants used worldwide in a variety of commercial goods, and are now widely found in both environmental and biological samples. BDE-47 is one of the most pervasive of these PBDE congeners and therefore is of particular concern. In this stu...
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Veröffentlicht in: | Neurotoxicology and teratology 2012-11, Vol.34 (6), p.571-580 |
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description | Abstract Polybrominated diphenyl ethers (PBDEs) are flame retardants used worldwide in a variety of commercial goods, and are now widely found in both environmental and biological samples. BDE-47 is one of the most pervasive of these PBDE congeners and therefore is of particular concern. In this study C57BL/6J mice were exposed perinatally to 0.03, 0.1 or 1 mg/kg/day of BDE-47, a dose range chosen to encompass human exposure levels. Tissue levels of BDE-47 were measured in the blood, brain, fat and milk of dams and in whole fetal homogenate and blood and brain of pups on gestational day (GD) 15, and postnatal days (PNDs) 1, 10 and 21. From GD 15 to PND 1 levels of BDE-47 increased within dam tissues and then decreased from PNDs 1 to 21. Over the period of lactation levels in dam milk were comparatively high when compared to both brain and blood for all dose groups. Measurable levels of BDE-47 were found in the fetus on GD 15 confirming gestational exposure. From PNDs 1 to 21, levels of BDE-47 in pup tissue increased over the period of lactation due to the transfer of BDE-47 through milk. Behavioral tests of fine motor function and learning and memory were carried out between postnatal weeks 5–17 in order to evaluate the neurobehavioral toxicity of BDE-47. Behavioral deficits were only seen in the Barnes spatial maze where mice in the three exposure groups had longer latencies and traveled longer distances to find the escape hole when compared to vehicle control mice. These results support the conclusions that perinatal exposure to BDE-47 can have neurodevelopmental consequences, and that lactational exposure represents a significant exposure risk during development. |
doi_str_mv | 10.1016/j.ntt.2012.09.005 |
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BDE-47 is one of the most pervasive of these PBDE congeners and therefore is of particular concern. In this study C57BL/6J mice were exposed perinatally to 0.03, 0.1 or 1 mg/kg/day of BDE-47, a dose range chosen to encompass human exposure levels. Tissue levels of BDE-47 were measured in the blood, brain, fat and milk of dams and in whole fetal homogenate and blood and brain of pups on gestational day (GD) 15, and postnatal days (PNDs) 1, 10 and 21. From GD 15 to PND 1 levels of BDE-47 increased within dam tissues and then decreased from PNDs 1 to 21. Over the period of lactation levels in dam milk were comparatively high when compared to both brain and blood for all dose groups. Measurable levels of BDE-47 were found in the fetus on GD 15 confirming gestational exposure. From PNDs 1 to 21, levels of BDE-47 in pup tissue increased over the period of lactation due to the transfer of BDE-47 through milk. Behavioral tests of fine motor function and learning and memory were carried out between postnatal weeks 5–17 in order to evaluate the neurobehavioral toxicity of BDE-47. Behavioral deficits were only seen in the Barnes spatial maze where mice in the three exposure groups had longer latencies and traveled longer distances to find the escape hole when compared to vehicle control mice. These results support the conclusions that perinatal exposure to BDE-47 can have neurodevelopmental consequences, and that lactational exposure represents a significant exposure risk during development.</description><identifier>ISSN: 0892-0362</identifier><identifier>EISSN: 1872-9738</identifier><identifier>DOI: 10.1016/j.ntt.2012.09.005</identifier><identifier>PMID: 23022914</identifier><identifier>CODEN: NETEEC</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; BDE-47 ; Behavior ; Behavior, Animal - drug effects ; Bioaccumulation ; Biological and medical sciences ; Blood ; Brain ; Congeners ; Development ; Emergency ; Environmental Pollutants - pharmacokinetics ; Environmental Pollutants - toxicity ; Female ; Fetuses ; Fire retardant chemicals ; Flame retardant ; Halogenated Diphenyl Ethers ; Lactation ; Male ; Maternal transfer ; Maternal-Fetal Exchange ; Medical Education ; Medical sciences ; Memory ; Mice ; Mice, Inbred C57BL ; Milk ; Milk - metabolism ; Motor Activity - drug effects ; Motor skill learning ; Nervous System - drug effects ; Nervous System - embryology ; Nervous System - growth & development ; Neurodevelopment ; Perinatal exposure ; Polybrominated Biphenyls - pharmacokinetics ; Polybrominated Biphenyls - toxicity ; Polybrominated diphenyl ether ; polybrominated diphenyl ethers ; Pregnancy ; Prenatal Exposure Delayed Effects - chemically induced ; Prenatal Exposure Delayed Effects - metabolism ; Progeny ; Tissue Distribution ; Toxicity ; Toxicology</subject><ispartof>Neurotoxicology and teratology, 2012-11, Vol.34 (6), p.571-580</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><rights>2012 Elsevier Inc. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c635t-2c546f2efb496c1697773e53ef7117c49046e2ee4b2be1eaa1f7e01d7a5cafe13</citedby><cites>FETCH-LOGICAL-c635t-2c546f2efb496c1697773e53ef7117c49046e2ee4b2be1eaa1f7e01d7a5cafe13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S089203621200164X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26728101$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23022914$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koenig, Claire M</creatorcontrib><creatorcontrib>Lango, Jozsef</creatorcontrib><creatorcontrib>Pessah, Isaac N</creatorcontrib><creatorcontrib>Berman, Robert F</creatorcontrib><title>Maternal transfer of BDE-47 to offspring and neurobehavioral development in C57BL/6J mice</title><title>Neurotoxicology and teratology</title><addtitle>Neurotoxicol Teratol</addtitle><description>Abstract Polybrominated diphenyl ethers (PBDEs) are flame retardants used worldwide in a variety of commercial goods, and are now widely found in both environmental and biological samples. BDE-47 is one of the most pervasive of these PBDE congeners and therefore is of particular concern. In this study C57BL/6J mice were exposed perinatally to 0.03, 0.1 or 1 mg/kg/day of BDE-47, a dose range chosen to encompass human exposure levels. Tissue levels of BDE-47 were measured in the blood, brain, fat and milk of dams and in whole fetal homogenate and blood and brain of pups on gestational day (GD) 15, and postnatal days (PNDs) 1, 10 and 21. From GD 15 to PND 1 levels of BDE-47 increased within dam tissues and then decreased from PNDs 1 to 21. Over the period of lactation levels in dam milk were comparatively high when compared to both brain and blood for all dose groups. Measurable levels of BDE-47 were found in the fetus on GD 15 confirming gestational exposure. From PNDs 1 to 21, levels of BDE-47 in pup tissue increased over the period of lactation due to the transfer of BDE-47 through milk. Behavioral tests of fine motor function and learning and memory were carried out between postnatal weeks 5–17 in order to evaluate the neurobehavioral toxicity of BDE-47. Behavioral deficits were only seen in the Barnes spatial maze where mice in the three exposure groups had longer latencies and traveled longer distances to find the escape hole when compared to vehicle control mice. These results support the conclusions that perinatal exposure to BDE-47 can have neurodevelopmental consequences, and that lactational exposure represents a significant exposure risk during development.</description><subject>Animals</subject><subject>BDE-47</subject><subject>Behavior</subject><subject>Behavior, Animal - drug effects</subject><subject>Bioaccumulation</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Brain</subject><subject>Congeners</subject><subject>Development</subject><subject>Emergency</subject><subject>Environmental Pollutants - pharmacokinetics</subject><subject>Environmental Pollutants - toxicity</subject><subject>Female</subject><subject>Fetuses</subject><subject>Fire retardant chemicals</subject><subject>Flame retardant</subject><subject>Halogenated Diphenyl Ethers</subject><subject>Lactation</subject><subject>Male</subject><subject>Maternal transfer</subject><subject>Maternal-Fetal Exchange</subject><subject>Medical Education</subject><subject>Medical sciences</subject><subject>Memory</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Milk</subject><subject>Milk - metabolism</subject><subject>Motor Activity - drug effects</subject><subject>Motor skill learning</subject><subject>Nervous System - drug effects</subject><subject>Nervous System - embryology</subject><subject>Nervous System - growth & development</subject><subject>Neurodevelopment</subject><subject>Perinatal exposure</subject><subject>Polybrominated Biphenyls - pharmacokinetics</subject><subject>Polybrominated Biphenyls - toxicity</subject><subject>Polybrominated diphenyl ether</subject><subject>polybrominated diphenyl ethers</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects - chemically induced</subject><subject>Prenatal Exposure Delayed Effects - metabolism</subject><subject>Progeny</subject><subject>Tissue Distribution</subject><subject>Toxicity</subject><subject>Toxicology</subject><issn>0892-0362</issn><issn>1872-9738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kktv1DAUhSMEokPhB7BB2SCxSepX7FhIldqhvDSIBSDBynKc69ZDYg92MlL_PY5mKI8FK8vyd46PfW5RPMWoxgjzs23tp6kmCJMayRqh5l6xwq0glRS0vV-sUCtJhSgnJ8WjlLYIIcExelicEIoIkZitim8f9ATR66GcovbJQiyDLS9fXVVMlFPIG5t20fnrUvu-9DDH0MGN3rsQs6aHPQxhN4KfSufLdSMuN2f8fTk6A4-LB1YPCZ4c19Piy-urz-u31ebjm3fri01lOG2mipiGcUvAdkxyg7kUQlBoKFiBsTBMIsaBALCOdIBBa2wFINwL3RhtAdPT4vzgu5u7EXqTs-RoKocedbxVQTv194l3N-o67BVtEG5alg1eHA1i-DFDmtTokoFh0B7CnBSmpG2QlGxB8QE1MaQUwd5dg5FaKlFblStRSyUKSZUryZpnf-a7U_zqIAPPj4BORg8292Bc-s1xQdrsnbmXBw7yb-4dRJWMA2-gdxHMpPrg_hvj_B-1GZx3-cLvcAtpG-ZlCvJrVcoa9WmZnWV0MEHZkH2lPwHH7r5m</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Koenig, Claire M</creator><creator>Lango, Jozsef</creator><creator>Pessah, Isaac N</creator><creator>Berman, Robert F</creator><general>Elsevier Inc</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>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20121101</creationdate><title>Maternal transfer of BDE-47 to offspring and neurobehavioral development in C57BL/6J mice</title><author>Koenig, Claire M ; Lango, Jozsef ; Pessah, Isaac N ; Berman, Robert F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c635t-2c546f2efb496c1697773e53ef7117c49046e2ee4b2be1eaa1f7e01d7a5cafe13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>BDE-47</topic><topic>Behavior</topic><topic>Behavior, Animal - drug effects</topic><topic>Bioaccumulation</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Brain</topic><topic>Congeners</topic><topic>Development</topic><topic>Emergency</topic><topic>Environmental Pollutants - pharmacokinetics</topic><topic>Environmental Pollutants - toxicity</topic><topic>Female</topic><topic>Fetuses</topic><topic>Fire retardant chemicals</topic><topic>Flame retardant</topic><topic>Halogenated Diphenyl Ethers</topic><topic>Lactation</topic><topic>Male</topic><topic>Maternal transfer</topic><topic>Maternal-Fetal Exchange</topic><topic>Medical Education</topic><topic>Medical sciences</topic><topic>Memory</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Milk</topic><topic>Milk - metabolism</topic><topic>Motor Activity - drug effects</topic><topic>Motor skill learning</topic><topic>Nervous System - drug effects</topic><topic>Nervous System - embryology</topic><topic>Nervous System - growth & development</topic><topic>Neurodevelopment</topic><topic>Perinatal exposure</topic><topic>Polybrominated Biphenyls - pharmacokinetics</topic><topic>Polybrominated Biphenyls - toxicity</topic><topic>Polybrominated diphenyl ether</topic><topic>polybrominated diphenyl ethers</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects - chemically induced</topic><topic>Prenatal Exposure Delayed Effects - metabolism</topic><topic>Progeny</topic><topic>Tissue Distribution</topic><topic>Toxicity</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koenig, Claire M</creatorcontrib><creatorcontrib>Lango, Jozsef</creatorcontrib><creatorcontrib>Pessah, Isaac N</creatorcontrib><creatorcontrib>Berman, Robert F</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>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>Koenig, Claire M</au><au>Lango, Jozsef</au><au>Pessah, Isaac N</au><au>Berman, Robert F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maternal transfer of BDE-47 to offspring and neurobehavioral development in C57BL/6J mice</atitle><jtitle>Neurotoxicology and teratology</jtitle><addtitle>Neurotoxicol Teratol</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>34</volume><issue>6</issue><spage>571</spage><epage>580</epage><pages>571-580</pages><issn>0892-0362</issn><eissn>1872-9738</eissn><coden>NETEEC</coden><abstract>Abstract Polybrominated diphenyl ethers (PBDEs) are flame retardants used worldwide in a variety of commercial goods, and are now widely found in both environmental and biological samples. BDE-47 is one of the most pervasive of these PBDE congeners and therefore is of particular concern. In this study C57BL/6J mice were exposed perinatally to 0.03, 0.1 or 1 mg/kg/day of BDE-47, a dose range chosen to encompass human exposure levels. Tissue levels of BDE-47 were measured in the blood, brain, fat and milk of dams and in whole fetal homogenate and blood and brain of pups on gestational day (GD) 15, and postnatal days (PNDs) 1, 10 and 21. From GD 15 to PND 1 levels of BDE-47 increased within dam tissues and then decreased from PNDs 1 to 21. Over the period of lactation levels in dam milk were comparatively high when compared to both brain and blood for all dose groups. Measurable levels of BDE-47 were found in the fetus on GD 15 confirming gestational exposure. From PNDs 1 to 21, levels of BDE-47 in pup tissue increased over the period of lactation due to the transfer of BDE-47 through milk. Behavioral tests of fine motor function and learning and memory were carried out between postnatal weeks 5–17 in order to evaluate the neurobehavioral toxicity of BDE-47. Behavioral deficits were only seen in the Barnes spatial maze where mice in the three exposure groups had longer latencies and traveled longer distances to find the escape hole when compared to vehicle control mice. These results support the conclusions that perinatal exposure to BDE-47 can have neurodevelopmental consequences, and that lactational exposure represents a significant exposure risk during development.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>23022914</pmid><doi>10.1016/j.ntt.2012.09.005</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals BDE-47 Behavior Behavior, Animal - drug effects Bioaccumulation Biological and medical sciences Blood Brain Congeners Development Emergency Environmental Pollutants - pharmacokinetics Environmental Pollutants - toxicity Female Fetuses Fire retardant chemicals Flame retardant Halogenated Diphenyl Ethers Lactation Male Maternal transfer Maternal-Fetal Exchange Medical Education Medical sciences Memory Mice Mice, Inbred C57BL Milk Milk - metabolism Motor Activity - drug effects Motor skill learning Nervous System - drug effects Nervous System - embryology Nervous System - growth & development Neurodevelopment Perinatal exposure Polybrominated Biphenyls - pharmacokinetics Polybrominated Biphenyls - toxicity Polybrominated diphenyl ether polybrominated diphenyl ethers Pregnancy Prenatal Exposure Delayed Effects - chemically induced Prenatal Exposure Delayed Effects - metabolism Progeny Tissue Distribution Toxicity Toxicology |
title | Maternal transfer of BDE-47 to offspring and neurobehavioral development in C57BL/6J mice |
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