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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurotoxicology and teratology 2012-11, Vol.34 (6), p.571-580
Hauptverfasser: Koenig, Claire M, Lango, Jozsef, Pessah, Isaac N, Berman, Robert F
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 580
container_issue 6
container_start_page 571
container_title Neurotoxicology and teratology
container_volume 34
creator Koenig, Claire M
Lango, Jozsef
Pessah, Isaac N
Berman, Robert F
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
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3501584</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S089203621200164X</els_id><sourcerecordid>1328509944</sourcerecordid><originalsourceid>FETCH-LOGICAL-c635t-2c546f2efb496c1697773e53ef7117c49046e2ee4b2be1eaa1f7e01d7a5cafe13</originalsourceid><addsrcrecordid>eNp9kktv1DAUhSMEokPhB7BB2SCxSepX7FhIldqhvDSIBSDBynKc69ZDYg92MlL_PY5mKI8FK8vyd46PfW5RPMWoxgjzs23tp6kmCJMayRqh5l6xwq0glRS0vV-sUCtJhSgnJ8WjlLYIIcExelicEIoIkZitim8f9ATR66GcovbJQiyDLS9fXVVMlFPIG5t20fnrUvu-9DDH0MGN3rsQs6aHPQxhN4KfSufLdSMuN2f8fTk6A4-LB1YPCZ4c19Piy-urz-u31ebjm3fri01lOG2mipiGcUvAdkxyg7kUQlBoKFiBsTBMIsaBALCOdIBBa2wFINwL3RhtAdPT4vzgu5u7EXqTs-RoKocedbxVQTv194l3N-o67BVtEG5alg1eHA1i-DFDmtTokoFh0B7CnBSmpG2QlGxB8QE1MaQUwd5dg5FaKlFblStRSyUKSZUryZpnf-a7U_zqIAPPj4BORg8292Bc-s1xQdrsnbmXBw7yb-4dRJWMA2-gdxHMpPrg_hvj_B-1GZx3-cLvcAtpG-ZlCvJrVcoa9WmZnWV0MEHZkH2lPwHH7r5m</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1328509944</pqid></control><display><type>article</type><title>Maternal transfer of BDE-47 to offspring and neurobehavioral development in C57BL/6J mice</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Koenig, Claire M ; Lango, Jozsef ; Pessah, Isaac N ; Berman, Robert F</creator><creatorcontrib>Koenig, Claire M ; Lango, Jozsef ; Pessah, Isaac N ; Berman, Robert F</creatorcontrib><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><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 &amp; 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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26728101$$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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0892-0362
ispartof Neurotoxicology and teratology, 2012-11, Vol.34 (6), p.571-580
issn 0892-0362
1872-9738
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3501584
source MEDLINE; Elsevier ScienceDirect Journals Complete
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-18T22%3A01%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Maternal%20transfer%20of%20BDE-47%20to%20offspring%20and%20neurobehavioral%20development%20in%20C57BL/6J%20mice&rft.jtitle=Neurotoxicology%20and%20teratology&rft.au=Koenig,%20Claire%20M&rft.date=2012-11-01&rft.volume=34&rft.issue=6&rft.spage=571&rft.epage=580&rft.pages=571-580&rft.issn=0892-0362&rft.eissn=1872-9738&rft.coden=NETEEC&rft_id=info:doi/10.1016/j.ntt.2012.09.005&rft_dat=%3Cproquest_pubme%3E1328509944%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1328509944&rft_id=info:pmid/23022914&rft_els_id=1_s2_0_S089203621200164X&rfr_iscdi=true