Gonadal effects of fetal exposure to the azo dye Congo red in mice: Infertility in female but not male offspring
The present study describes the relationship between gonadal agenesis and fertility in male and female mice exposed in utero to the diazo dye Congo red (CR). Maternal CR treatment inhibited testicular and ovarian function in the offspring after oral administration of 1 or 0.5 g/kg/day on Gestational...
Gespeichert in:
Veröffentlicht in: | Fundamental and applied toxicology 1992-10, Vol.19 (3), p.411-422 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 422 |
---|---|
container_issue | 3 |
container_start_page | 411 |
container_title | Fundamental and applied toxicology |
container_volume | 19 |
creator | Gray, L.E. Ostby, J.S. Kavlock, R.J. Marshall, R. |
description | The present study describes the relationship between gonadal agenesis and fertility in male and female mice exposed
in utero to the diazo dye Congo red (CR). Maternal CR treatment inhibited testicular and ovarian function in the offspring after oral administration of 1 or 0.5 g/kg/day on Gestational Days 8–12. The testes of male offspring from CR-exposed dams were small in size and contained hypospermatogenic seminiferous tubules. However, despite the fact that testis weight was reduced by more than 70% in some males, they displayed normal levels of fertility when mated to untreated females for over 10 months. In contrast, female offspring from CR-exposed dams produced only about half as many litters and pups as the control pairs did under longterm mating conditions. Histological examination of the ovaries revealed that subfertility was correlated with ovarian atrophy. Females lacking maturing follicles were considerably less productive (1.3 litters and 11.5 pups) than treated females with histologically normal ovaries (7.1 litters and 78.1 pups). In summary, prenatal exposure to the dye CR affects the gonads of both male and female offspring, but only the female offspring display reduced fertility. |
doi_str_mv | 10.1016/0272-0590(92)90180-P |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_16323567</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>027205909290180P</els_id><sourcerecordid>16323567</sourcerecordid><originalsourceid>FETCH-LOGICAL-e321t-f6d0a5b2562103325cac02c5483d2ecb059bcf22231fd661cc7d917025792a3e3</originalsourceid><addsrcrecordid>eNo9kUGLFDEQhYMo67j6DxRyENFDa1KZpCd7EGTQdWHBPeg5pJPKGulOxiQtjr_e7t1hT0VVfTzq1SPkJWfvOePqA4MeOiY1e6vhnWZ8x7qbR2TDmZad2gl4TDYPyFPyrNZfjHEut-yMnPGt1KKHDTlc5mS9HSmGgK5VmgMN2NbB30Ouc0HaMm0_kdp_mfoj0n1Ot5kW9DQmOkWHF_QqBSwtjrEd12HAyY5Ih7nRlBu9a3II9VBiun1OngQ7Vnxxqufkx5fP3_dfu-tvl1f7T9cdCuCtC8ozKweQCjgTAqSzjoGT253wgG5YTA0uAIDgwSvFneu95j0D2WuwAsU5eXOveyj594y1mSlWh-NoE-a5Gq4ECKn6BXx1AudhQm-WKydbjub0omX_-rS31dkxFJtcrA_YViiQepX5eI_hYupPxGKqi5gc-liWxxqfo-HMrMmZNRazxmI0mLvkzI34DzoviUA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16323567</pqid></control><display><type>article</type><title>Gonadal effects of fetal exposure to the azo dye Congo red in mice: Infertility in female but not male offspring</title><source>MEDLINE</source><source>Oxford University Press Journals Digital Archive Legacy</source><source>Alma/SFX Local Collection</source><creator>Gray, L.E. ; Ostby, J.S. ; Kavlock, R.J. ; Marshall, R.</creator><creatorcontrib>Gray, L.E. ; Ostby, J.S. ; Kavlock, R.J. ; Marshall, R.</creatorcontrib><description>The present study describes the relationship between gonadal agenesis and fertility in male and female mice exposed
in utero to the diazo dye Congo red (CR). Maternal CR treatment inhibited testicular and ovarian function in the offspring after oral administration of 1 or 0.5 g/kg/day on Gestational Days 8–12. The testes of male offspring from CR-exposed dams were small in size and contained hypospermatogenic seminiferous tubules. However, despite the fact that testis weight was reduced by more than 70% in some males, they displayed normal levels of fertility when mated to untreated females for over 10 months. In contrast, female offspring from CR-exposed dams produced only about half as many litters and pups as the control pairs did under longterm mating conditions. Histological examination of the ovaries revealed that subfertility was correlated with ovarian atrophy. Females lacking maturing follicles were considerably less productive (1.3 litters and 11.5 pups) than treated females with histologically normal ovaries (7.1 litters and 78.1 pups). In summary, prenatal exposure to the dye CR affects the gonads of both male and female offspring, but only the female offspring display reduced fertility.</description><identifier>ISSN: 0272-0590</identifier><identifier>EISSN: 1095-6832</identifier><identifier>DOI: 10.1016/0272-0590(92)90180-P</identifier><identifier>PMID: 1459372</identifier><identifier>CODEN: FAATDF</identifier><language>eng</language><publisher>Boston, MA: Elsevier Science (USA)</publisher><subject>Animals ; Biological and medical sciences ; Congo Red - toxicity ; Embryology: invertebrates and vertebrates. Teratology ; Female ; Fertility - drug effects ; Fundamental and applied biological sciences. Psychology ; Infertility, Female - chemically induced ; Infertility, Female - pathology ; Infertility, Male - chemically induced ; Infertility, Male - pathology ; Male ; Mice ; Organ Size - drug effects ; Ovarian Diseases - chemically induced ; Ovarian Diseases - pathology ; Ovary - pathology ; Pregnancy ; Prenatal Exposure Delayed Effects ; Teratology. Teratogens ; Testicular Diseases - chemically induced ; Testicular Diseases - pathology ; Testis - pathology</subject><ispartof>Fundamental and applied toxicology, 1992-10, Vol.19 (3), p.411-422</ispartof><rights>1992</rights><rights>1993 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4362597$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1459372$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gray, L.E.</creatorcontrib><creatorcontrib>Ostby, J.S.</creatorcontrib><creatorcontrib>Kavlock, R.J.</creatorcontrib><creatorcontrib>Marshall, R.</creatorcontrib><title>Gonadal effects of fetal exposure to the azo dye Congo red in mice: Infertility in female but not male offspring</title><title>Fundamental and applied toxicology</title><addtitle>Fundam Appl Toxicol</addtitle><description>The present study describes the relationship between gonadal agenesis and fertility in male and female mice exposed
in utero to the diazo dye Congo red (CR). Maternal CR treatment inhibited testicular and ovarian function in the offspring after oral administration of 1 or 0.5 g/kg/day on Gestational Days 8–12. The testes of male offspring from CR-exposed dams were small in size and contained hypospermatogenic seminiferous tubules. However, despite the fact that testis weight was reduced by more than 70% in some males, they displayed normal levels of fertility when mated to untreated females for over 10 months. In contrast, female offspring from CR-exposed dams produced only about half as many litters and pups as the control pairs did under longterm mating conditions. Histological examination of the ovaries revealed that subfertility was correlated with ovarian atrophy. Females lacking maturing follicles were considerably less productive (1.3 litters and 11.5 pups) than treated females with histologically normal ovaries (7.1 litters and 78.1 pups). In summary, prenatal exposure to the dye CR affects the gonads of both male and female offspring, but only the female offspring display reduced fertility.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Congo Red - toxicity</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Female</subject><subject>Fertility - drug effects</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Infertility, Female - chemically induced</subject><subject>Infertility, Female - pathology</subject><subject>Infertility, Male - chemically induced</subject><subject>Infertility, Male - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Organ Size - drug effects</subject><subject>Ovarian Diseases - chemically induced</subject><subject>Ovarian Diseases - pathology</subject><subject>Ovary - pathology</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects</subject><subject>Teratology. Teratogens</subject><subject>Testicular Diseases - chemically induced</subject><subject>Testicular Diseases - pathology</subject><subject>Testis - pathology</subject><issn>0272-0590</issn><issn>1095-6832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kUGLFDEQhYMo67j6DxRyENFDa1KZpCd7EGTQdWHBPeg5pJPKGulOxiQtjr_e7t1hT0VVfTzq1SPkJWfvOePqA4MeOiY1e6vhnWZ8x7qbR2TDmZad2gl4TDYPyFPyrNZfjHEut-yMnPGt1KKHDTlc5mS9HSmGgK5VmgMN2NbB30Ouc0HaMm0_kdp_mfoj0n1Ot5kW9DQmOkWHF_QqBSwtjrEd12HAyY5Ih7nRlBu9a3II9VBiun1OngQ7Vnxxqufkx5fP3_dfu-tvl1f7T9cdCuCtC8ozKweQCjgTAqSzjoGT253wgG5YTA0uAIDgwSvFneu95j0D2WuwAsU5eXOveyj594y1mSlWh-NoE-a5Gq4ECKn6BXx1AudhQm-WKydbjub0omX_-rS31dkxFJtcrA_YViiQepX5eI_hYupPxGKqi5gc-liWxxqfo-HMrMmZNRazxmI0mLvkzI34DzoviUA</recordid><startdate>19921001</startdate><enddate>19921001</enddate><creator>Gray, L.E.</creator><creator>Ostby, J.S.</creator><creator>Kavlock, R.J.</creator><creator>Marshall, R.</creator><general>Elsevier Science (USA)</general><general>Academic Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>19921001</creationdate><title>Gonadal effects of fetal exposure to the azo dye Congo red in mice: Infertility in female but not male offspring</title><author>Gray, L.E. ; Ostby, J.S. ; Kavlock, R.J. ; Marshall, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e321t-f6d0a5b2562103325cac02c5483d2ecb059bcf22231fd661cc7d917025792a3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Congo Red - toxicity</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Female</topic><topic>Fertility - drug effects</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Infertility, Female - chemically induced</topic><topic>Infertility, Female - pathology</topic><topic>Infertility, Male - chemically induced</topic><topic>Infertility, Male - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Organ Size - drug effects</topic><topic>Ovarian Diseases - chemically induced</topic><topic>Ovarian Diseases - pathology</topic><topic>Ovary - pathology</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects</topic><topic>Teratology. Teratogens</topic><topic>Testicular Diseases - chemically induced</topic><topic>Testicular Diseases - pathology</topic><topic>Testis - pathology</topic><toplevel>online_resources</toplevel><creatorcontrib>Gray, L.E.</creatorcontrib><creatorcontrib>Ostby, J.S.</creatorcontrib><creatorcontrib>Kavlock, R.J.</creatorcontrib><creatorcontrib>Marshall, 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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Fundamental and applied toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gray, L.E.</au><au>Ostby, J.S.</au><au>Kavlock, R.J.</au><au>Marshall, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gonadal effects of fetal exposure to the azo dye Congo red in mice: Infertility in female but not male offspring</atitle><jtitle>Fundamental and applied toxicology</jtitle><addtitle>Fundam Appl Toxicol</addtitle><date>1992-10-01</date><risdate>1992</risdate><volume>19</volume><issue>3</issue><spage>411</spage><epage>422</epage><pages>411-422</pages><issn>0272-0590</issn><eissn>1095-6832</eissn><coden>FAATDF</coden><abstract>The present study describes the relationship between gonadal agenesis and fertility in male and female mice exposed
in utero to the diazo dye Congo red (CR). Maternal CR treatment inhibited testicular and ovarian function in the offspring after oral administration of 1 or 0.5 g/kg/day on Gestational Days 8–12. The testes of male offspring from CR-exposed dams were small in size and contained hypospermatogenic seminiferous tubules. However, despite the fact that testis weight was reduced by more than 70% in some males, they displayed normal levels of fertility when mated to untreated females for over 10 months. In contrast, female offspring from CR-exposed dams produced only about half as many litters and pups as the control pairs did under longterm mating conditions. Histological examination of the ovaries revealed that subfertility was correlated with ovarian atrophy. Females lacking maturing follicles were considerably less productive (1.3 litters and 11.5 pups) than treated females with histologically normal ovaries (7.1 litters and 78.1 pups). In summary, prenatal exposure to the dye CR affects the gonads of both male and female offspring, but only the female offspring display reduced fertility.</abstract><cop>Boston, MA</cop><cop>San Diego, CA</cop><cop>New York, NY</cop><pub>Elsevier Science (USA)</pub><pmid>1459372</pmid><doi>10.1016/0272-0590(92)90180-P</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0272-0590 |
ispartof | Fundamental and applied toxicology, 1992-10, Vol.19 (3), p.411-422 |
issn | 0272-0590 1095-6832 |
language | eng |
recordid | cdi_proquest_miscellaneous_16323567 |
source | MEDLINE; Oxford University Press Journals Digital Archive Legacy; Alma/SFX Local Collection |
subjects | Animals Biological and medical sciences Congo Red - toxicity Embryology: invertebrates and vertebrates. Teratology Female Fertility - drug effects Fundamental and applied biological sciences. Psychology Infertility, Female - chemically induced Infertility, Female - pathology Infertility, Male - chemically induced Infertility, Male - pathology Male Mice Organ Size - drug effects Ovarian Diseases - chemically induced Ovarian Diseases - pathology Ovary - pathology Pregnancy Prenatal Exposure Delayed Effects Teratology. Teratogens Testicular Diseases - chemically induced Testicular Diseases - pathology Testis - pathology |
title | Gonadal effects of fetal exposure to the azo dye Congo red in mice: Infertility in female but not male offspring |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T16%3A20%3A01IST&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=Gonadal%20effects%20of%20fetal%20exposure%20to%20the%20azo%20dye%20Congo%20red%20in%20mice:%20Infertility%20in%20female%20but%20not%20male%20offspring&rft.jtitle=Fundamental%20and%20applied%20toxicology&rft.au=Gray,%20L.E.&rft.date=1992-10-01&rft.volume=19&rft.issue=3&rft.spage=411&rft.epage=422&rft.pages=411-422&rft.issn=0272-0590&rft.eissn=1095-6832&rft.coden=FAATDF&rft_id=info:doi/10.1016/0272-0590(92)90180-P&rft_dat=%3Cproquest_pubme%3E16323567%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=16323567&rft_id=info:pmid/1459372&rft_els_id=027205909290180P&rfr_iscdi=true |