Developmental toxicity in rats of a hemoglobin-based oxygen carrier results from impeded function of the inverted visceral yolk sac
•Infusion HBOC into pregnant rats causes developmental toxicity.•Sensitive from GD 7 to 11 when inverted yolk sac placenta (invYSP) supplies nutrition.•Controls for protein content, oncotic properties and Hb show effects are due to Hb.•Whole embryo culture verified HBOC interference with invYSP func...
Gespeichert in:
Veröffentlicht in: | Reproductive toxicology (Elmsford, N.Y.) N.Y.), 2015-04, Vol.52, p.108-117 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 117 |
---|---|
container_issue | |
container_start_page | 108 |
container_title | Reproductive toxicology (Elmsford, N.Y.) |
container_volume | 52 |
creator | Stump, D.G. Holson, J.F. Harris, C. Pearce, L.B. Watson, R.E. DeSesso, J.M. |
description | •Infusion HBOC into pregnant rats causes developmental toxicity.•Sensitive from GD 7 to 11 when inverted yolk sac placenta (invYSP) supplies nutrition.•Controls for protein content, oncotic properties and Hb show effects are due to Hb.•Whole embryo culture verified HBOC interference with invYSP function.•Humans lack invYSP and are unlikely to be affected by HBOC.
HBOC-201 is a bovine-derived, cross-linked, and stabilized hemoglobin (250kDa) in physiological saline. Daily intravenous infusions of HBOC (1.95, 3.90, or 5.85g/kg/day) during gestational days (GDs) 6–18 in Sprague-Dawley rats caused fetal mortality, reduced birth weight, and malformations. Subsequent single-day infusions (5.85g/kg/day) showed that developmental toxicity was limited to GDs 7–9 when histiotrophic nutrition via the inverted visceral yolk sac (invVYS) is essential. Histiotrophic nutrition is receptor-mediated endocytosis of bulk maternal proteins and subsequent lysosomal degradation providing amino acids and other nutrients for embryonic growth. Controls for protein content, oncotic properties, and hemoglobin content indicated that toxicity was due to hemoglobin. Rat whole embryo cultures verified HBOC interference with invVYS transport capacity and resultant deficient embryonic nutrition. These mechanisms of action are not expected to impact human development based on differences in VYS morphology and function, although a complete understanding of early human embryonic nutrition is lacking. |
doi_str_mv | 10.1016/j.reprotox.2015.01.005 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7127137</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0890623815000064</els_id><sourcerecordid>1732809860</sourcerecordid><originalsourceid>FETCH-LOGICAL-c640t-78e85e78abff41b6c7b0fba0c035c978c0f96a78f2bbcf752c518502d888b7413</originalsourceid><addsrcrecordid>eNqFkUFv1DAQhS0EokvhL1Q-ckk6Tjaxc0GgAgWpEhc4W7Yz3vWSxMF2ou6ZP45X21Zw4jSH-ebNzHuEXDEoGbD2-lAGnINP_r6sgDUlsBKgeUY2TPC6YBzEc7IB0UHRVrW4IK9iPADAlnf8JbmompZxAd2G_P6IKw5-HnFKaqBZzxmXjtRNNKgUqbdU0T2Ofjd47aZCq4g99ffHHU7UqBAcBhowLkOGbfAjdeOMfWbsMpnk_HSSSHvMiiuGlBuriwZDXnb0w08alXlNXlg1RHzzUC_Jj8-fvt98Ke6-3X69-XBXmHYLqeACRYNcKG3tlunWcA1WKzBQN6bjwoDtWsWFrbQ2ljeVaZhooOqFEJpvWX1J3p1150WP2Jv8cj5DzsGNKhylV07-25ncXu78KjmrOKt5Fnj7IBD8rwVjkuPpl2FQE_olSsbrKrsqWshoe0ZN8DEGtE9rGMhTgvIgHxOUpwQlMJkTzINXfx_5NPYYWQbenwHMVq3ZfhmNw8lg7wKaJHvv_rfjD7tstYY</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1732809860</pqid></control><display><type>article</type><title>Developmental toxicity in rats of a hemoglobin-based oxygen carrier results from impeded function of the inverted visceral yolk sac</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Stump, D.G. ; Holson, J.F. ; Harris, C. ; Pearce, L.B. ; Watson, R.E. ; DeSesso, J.M.</creator><creatorcontrib>Stump, D.G. ; Holson, J.F. ; Harris, C. ; Pearce, L.B. ; Watson, R.E. ; DeSesso, J.M.</creatorcontrib><description>•Infusion HBOC into pregnant rats causes developmental toxicity.•Sensitive from GD 7 to 11 when inverted yolk sac placenta (invYSP) supplies nutrition.•Controls for protein content, oncotic properties and Hb show effects are due to Hb.•Whole embryo culture verified HBOC interference with invYSP function.•Humans lack invYSP and are unlikely to be affected by HBOC.
HBOC-201 is a bovine-derived, cross-linked, and stabilized hemoglobin (250kDa) in physiological saline. Daily intravenous infusions of HBOC (1.95, 3.90, or 5.85g/kg/day) during gestational days (GDs) 6–18 in Sprague-Dawley rats caused fetal mortality, reduced birth weight, and malformations. Subsequent single-day infusions (5.85g/kg/day) showed that developmental toxicity was limited to GDs 7–9 when histiotrophic nutrition via the inverted visceral yolk sac (invVYS) is essential. Histiotrophic nutrition is receptor-mediated endocytosis of bulk maternal proteins and subsequent lysosomal degradation providing amino acids and other nutrients for embryonic growth. Controls for protein content, oncotic properties, and hemoglobin content indicated that toxicity was due to hemoglobin. Rat whole embryo cultures verified HBOC interference with invVYS transport capacity and resultant deficient embryonic nutrition. These mechanisms of action are not expected to impact human development based on differences in VYS morphology and function, although a complete understanding of early human embryonic nutrition is lacking.</description><identifier>ISSN: 0890-6238</identifier><identifier>EISSN: 1873-1708</identifier><identifier>DOI: 10.1016/j.reprotox.2015.01.005</identifier><identifier>PMID: 25617809</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Abnormalities, Drug-Induced ; Animals ; Blood Substitutes ; Embryo Culture Techniques ; Embryonic Development - drug effects ; Female ; Fetal Death - etiology ; Gestational Age ; Hemoglobin-based oxygen carrier ; Hemoglobins - administration & dosage ; Hemoglobins - toxicity ; Histiotrophic ; Infant, Low Birth Weight ; Models, Animal ; Placenta ; Pregnancy ; Rats ; Rats, Sprague-Dawley ; Species Specificity ; Visceral yolk sac ; Whole embryo culture ; Yolk Sac - drug effects ; Yolk Sac - physiology</subject><ispartof>Reproductive toxicology (Elmsford, N.Y.), 2015-04, Vol.52, p.108-117</ispartof><rights>2015</rights><rights>Copyright © 2015. Published by Elsevier Inc.</rights><rights>Copyright © 2015 Published by Elsevier Inc. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c640t-78e85e78abff41b6c7b0fba0c035c978c0f96a78f2bbcf752c518502d888b7413</citedby><cites>FETCH-LOGICAL-c640t-78e85e78abff41b6c7b0fba0c035c978c0f96a78f2bbcf752c518502d888b7413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.reprotox.2015.01.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25617809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stump, D.G.</creatorcontrib><creatorcontrib>Holson, J.F.</creatorcontrib><creatorcontrib>Harris, C.</creatorcontrib><creatorcontrib>Pearce, L.B.</creatorcontrib><creatorcontrib>Watson, R.E.</creatorcontrib><creatorcontrib>DeSesso, J.M.</creatorcontrib><title>Developmental toxicity in rats of a hemoglobin-based oxygen carrier results from impeded function of the inverted visceral yolk sac</title><title>Reproductive toxicology (Elmsford, N.Y.)</title><addtitle>Reprod Toxicol</addtitle><description>•Infusion HBOC into pregnant rats causes developmental toxicity.•Sensitive from GD 7 to 11 when inverted yolk sac placenta (invYSP) supplies nutrition.•Controls for protein content, oncotic properties and Hb show effects are due to Hb.•Whole embryo culture verified HBOC interference with invYSP function.•Humans lack invYSP and are unlikely to be affected by HBOC.
HBOC-201 is a bovine-derived, cross-linked, and stabilized hemoglobin (250kDa) in physiological saline. Daily intravenous infusions of HBOC (1.95, 3.90, or 5.85g/kg/day) during gestational days (GDs) 6–18 in Sprague-Dawley rats caused fetal mortality, reduced birth weight, and malformations. Subsequent single-day infusions (5.85g/kg/day) showed that developmental toxicity was limited to GDs 7–9 when histiotrophic nutrition via the inverted visceral yolk sac (invVYS) is essential. Histiotrophic nutrition is receptor-mediated endocytosis of bulk maternal proteins and subsequent lysosomal degradation providing amino acids and other nutrients for embryonic growth. Controls for protein content, oncotic properties, and hemoglobin content indicated that toxicity was due to hemoglobin. Rat whole embryo cultures verified HBOC interference with invVYS transport capacity and resultant deficient embryonic nutrition. These mechanisms of action are not expected to impact human development based on differences in VYS morphology and function, although a complete understanding of early human embryonic nutrition is lacking.</description><subject>Abnormalities, Drug-Induced</subject><subject>Animals</subject><subject>Blood Substitutes</subject><subject>Embryo Culture Techniques</subject><subject>Embryonic Development - drug effects</subject><subject>Female</subject><subject>Fetal Death - etiology</subject><subject>Gestational Age</subject><subject>Hemoglobin-based oxygen carrier</subject><subject>Hemoglobins - administration & dosage</subject><subject>Hemoglobins - toxicity</subject><subject>Histiotrophic</subject><subject>Infant, Low Birth Weight</subject><subject>Models, Animal</subject><subject>Placenta</subject><subject>Pregnancy</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Species Specificity</subject><subject>Visceral yolk sac</subject><subject>Whole embryo culture</subject><subject>Yolk Sac - drug effects</subject><subject>Yolk Sac - physiology</subject><issn>0890-6238</issn><issn>1873-1708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EokvhL1Q-ckk6Tjaxc0GgAgWpEhc4W7Yz3vWSxMF2ou6ZP45X21Zw4jSH-ebNzHuEXDEoGbD2-lAGnINP_r6sgDUlsBKgeUY2TPC6YBzEc7IB0UHRVrW4IK9iPADAlnf8JbmompZxAd2G_P6IKw5-HnFKaqBZzxmXjtRNNKgUqbdU0T2Ofjd47aZCq4g99ffHHU7UqBAcBhowLkOGbfAjdeOMfWbsMpnk_HSSSHvMiiuGlBuriwZDXnb0w08alXlNXlg1RHzzUC_Jj8-fvt98Ke6-3X69-XBXmHYLqeACRYNcKG3tlunWcA1WKzBQN6bjwoDtWsWFrbQ2ljeVaZhooOqFEJpvWX1J3p1150WP2Jv8cj5DzsGNKhylV07-25ncXu78KjmrOKt5Fnj7IBD8rwVjkuPpl2FQE_olSsbrKrsqWshoe0ZN8DEGtE9rGMhTgvIgHxOUpwQlMJkTzINXfx_5NPYYWQbenwHMVq3ZfhmNw8lg7wKaJHvv_rfjD7tstYY</recordid><startdate>20150401</startdate><enddate>20150401</enddate><creator>Stump, D.G.</creator><creator>Holson, J.F.</creator><creator>Harris, C.</creator><creator>Pearce, L.B.</creator><creator>Watson, R.E.</creator><creator>DeSesso, J.M.</creator><general>Elsevier Inc</general><general>Published by 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>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20150401</creationdate><title>Developmental toxicity in rats of a hemoglobin-based oxygen carrier results from impeded function of the inverted visceral yolk sac</title><author>Stump, D.G. ; Holson, J.F. ; Harris, C. ; Pearce, L.B. ; Watson, R.E. ; DeSesso, J.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c640t-78e85e78abff41b6c7b0fba0c035c978c0f96a78f2bbcf752c518502d888b7413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Abnormalities, Drug-Induced</topic><topic>Animals</topic><topic>Blood Substitutes</topic><topic>Embryo Culture Techniques</topic><topic>Embryonic Development - drug effects</topic><topic>Female</topic><topic>Fetal Death - etiology</topic><topic>Gestational Age</topic><topic>Hemoglobin-based oxygen carrier</topic><topic>Hemoglobins - administration & dosage</topic><topic>Hemoglobins - toxicity</topic><topic>Histiotrophic</topic><topic>Infant, Low Birth Weight</topic><topic>Models, Animal</topic><topic>Placenta</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Species Specificity</topic><topic>Visceral yolk sac</topic><topic>Whole embryo culture</topic><topic>Yolk Sac - drug effects</topic><topic>Yolk Sac - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stump, D.G.</creatorcontrib><creatorcontrib>Holson, J.F.</creatorcontrib><creatorcontrib>Harris, C.</creatorcontrib><creatorcontrib>Pearce, L.B.</creatorcontrib><creatorcontrib>Watson, R.E.</creatorcontrib><creatorcontrib>DeSesso, J.M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Reproductive toxicology (Elmsford, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stump, D.G.</au><au>Holson, J.F.</au><au>Harris, C.</au><au>Pearce, L.B.</au><au>Watson, R.E.</au><au>DeSesso, J.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental toxicity in rats of a hemoglobin-based oxygen carrier results from impeded function of the inverted visceral yolk sac</atitle><jtitle>Reproductive toxicology (Elmsford, N.Y.)</jtitle><addtitle>Reprod Toxicol</addtitle><date>2015-04-01</date><risdate>2015</risdate><volume>52</volume><spage>108</spage><epage>117</epage><pages>108-117</pages><issn>0890-6238</issn><eissn>1873-1708</eissn><abstract>•Infusion HBOC into pregnant rats causes developmental toxicity.•Sensitive from GD 7 to 11 when inverted yolk sac placenta (invYSP) supplies nutrition.•Controls for protein content, oncotic properties and Hb show effects are due to Hb.•Whole embryo culture verified HBOC interference with invYSP function.•Humans lack invYSP and are unlikely to be affected by HBOC.
HBOC-201 is a bovine-derived, cross-linked, and stabilized hemoglobin (250kDa) in physiological saline. Daily intravenous infusions of HBOC (1.95, 3.90, or 5.85g/kg/day) during gestational days (GDs) 6–18 in Sprague-Dawley rats caused fetal mortality, reduced birth weight, and malformations. Subsequent single-day infusions (5.85g/kg/day) showed that developmental toxicity was limited to GDs 7–9 when histiotrophic nutrition via the inverted visceral yolk sac (invVYS) is essential. Histiotrophic nutrition is receptor-mediated endocytosis of bulk maternal proteins and subsequent lysosomal degradation providing amino acids and other nutrients for embryonic growth. Controls for protein content, oncotic properties, and hemoglobin content indicated that toxicity was due to hemoglobin. Rat whole embryo cultures verified HBOC interference with invVYS transport capacity and resultant deficient embryonic nutrition. These mechanisms of action are not expected to impact human development based on differences in VYS morphology and function, although a complete understanding of early human embryonic nutrition is lacking.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25617809</pmid><doi>10.1016/j.reprotox.2015.01.005</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0890-6238 |
ispartof | Reproductive toxicology (Elmsford, N.Y.), 2015-04, Vol.52, p.108-117 |
issn | 0890-6238 1873-1708 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7127137 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Abnormalities, Drug-Induced Animals Blood Substitutes Embryo Culture Techniques Embryonic Development - drug effects Female Fetal Death - etiology Gestational Age Hemoglobin-based oxygen carrier Hemoglobins - administration & dosage Hemoglobins - toxicity Histiotrophic Infant, Low Birth Weight Models, Animal Placenta Pregnancy Rats Rats, Sprague-Dawley Species Specificity Visceral yolk sac Whole embryo culture Yolk Sac - drug effects Yolk Sac - physiology |
title | Developmental toxicity in rats of a hemoglobin-based oxygen carrier results from impeded function of the inverted visceral yolk sac |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T15%3A03%3A02IST&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=Developmental%20toxicity%20in%20rats%20of%20a%20hemoglobin-based%20oxygen%20carrier%20results%20from%20impeded%20function%20of%20the%20inverted%20visceral%20yolk%20sac&rft.jtitle=Reproductive%20toxicology%20(Elmsford,%20N.Y.)&rft.au=Stump,%20D.G.&rft.date=2015-04-01&rft.volume=52&rft.spage=108&rft.epage=117&rft.pages=108-117&rft.issn=0890-6238&rft.eissn=1873-1708&rft_id=info:doi/10.1016/j.reprotox.2015.01.005&rft_dat=%3Cproquest_pubme%3E1732809860%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=1732809860&rft_id=info:pmid/25617809&rft_els_id=S0890623815000064&rfr_iscdi=true |