Mammary gland morphology and responsiveness to regulatory molecules following prenatal exposure to diethylstilbestrol
Female ACI rats were exposed to diethylstilbestrol (DES) in utero to evaluate the effects on the peri‐pubertal mammary gland with respect to 1) mammary gland morphology, 2) sensitivity to natural and synthetic estrogens, and 3) sensitivity to endogenous epidermal growth factor (EGF). Pregnant rats w...
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Veröffentlicht in: | Teratogenesis, carcinogenesis, and mutagenesis carcinogenesis, and mutagenesis, 1993, Vol.13 (2), p.59-74 |
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description | Female ACI rats were exposed to diethylstilbestrol (DES) in utero to evaluate the effects on the peri‐pubertal mammary gland with respect to 1) mammary gland morphology, 2) sensitivity to natural and synthetic estrogens, and 3) sensitivity to endogenous epidermal growth factor (EGF). Pregnant rats were injected with vehicle (sesame oil) or DES (total dose, 8.0 μg) on days 15 and 18 of gestation. DES‐exposed and control offspring were ovariectomized at 34 days of age and sacrificed at day 53 to ascertain the morphology of the mammary glands in peri‐pubertal rats. Elvax pellets containing 5 or 11 ng 17 β‐estradiol (E2) or DES were implanted subcutaneously adjacent to the third mammary gland pair. Furthermore, additional groups of rats were subjected to bilateral sialoadenectomy at the day of ovariectomy to remove the major source of endogenous EGF. A significant proportion of mammary glands of DES‐exposed animals exhibited atypical mammary gland morphology, with approximately 25% displaying hypo‐differentiation, and about 5% with aberrant hyper‐proliferation. From the pellet implantation experiments, the DES‐exposed glands were found to be refractory to stimulation by 5 and 11 ng DES; however, there was no significant difference in the degree of local stimulation elicited by either dose of E2. Sialoadenectomy at d34 had no apparent effect on mammary gland morphology in either the DES‐exposed or vehicle‐exposed groups. These data support the premise that the mammary gland of the peri‐pubertal ACI rat is morphologically and physiologically aberrant as a function of transplacental exposure to DES, with a significant percentage hypo‐differentiated and refractory to subsequent hormonal stimulation. ©1993 Wiley‐Liss, Inc. |
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Pregnant rats were injected with vehicle (sesame oil) or DES (total dose, 8.0 μg) on days 15 and 18 of gestation. DES‐exposed and control offspring were ovariectomized at 34 days of age and sacrificed at day 53 to ascertain the morphology of the mammary glands in peri‐pubertal rats. Elvax pellets containing 5 or 11 ng 17 β‐estradiol (E2) or DES were implanted subcutaneously adjacent to the third mammary gland pair. Furthermore, additional groups of rats were subjected to bilateral sialoadenectomy at the day of ovariectomy to remove the major source of endogenous EGF. A significant proportion of mammary glands of DES‐exposed animals exhibited atypical mammary gland morphology, with approximately 25% displaying hypo‐differentiation, and about 5% with aberrant hyper‐proliferation. From the pellet implantation experiments, the DES‐exposed glands were found to be refractory to stimulation by 5 and 11 ng DES; however, there was no significant difference in the degree of local stimulation elicited by either dose of E2. Sialoadenectomy at d34 had no apparent effect on mammary gland morphology in either the DES‐exposed or vehicle‐exposed groups. These data support the premise that the mammary gland of the peri‐pubertal ACI rat is morphologically and physiologically aberrant as a function of transplacental exposure to DES, with a significant percentage hypo‐differentiated and refractory to subsequent hormonal stimulation. ©1993 Wiley‐Liss, Inc.</description><identifier>ISSN: 0270-3211</identifier><identifier>EISSN: 1520-6866</identifier><identifier>DOI: 10.1002/tcm.1770130203</identifier><identifier>PMID: 8102210</identifier><identifier>CODEN: TCMUD8</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>ACI rat ; Animals ; Biological and medical sciences ; Diethylstilbestrol - toxicity ; Drug toxicity and drugs side effects treatment ; Elvax pellet ; epidermal growth factor ; Estradiol - pharmacology ; estrogen ; Female ; Fetus - drug effects ; Mammary Glands, Animal - drug effects ; Mammary Glands, Animal - pathology ; mammary tumor ; Medical sciences ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Pharmacology. Drug treatments ; Pregnancy ; Prenatal Exposure Delayed Effects ; Rats ; Rats, Inbred ACI ; sialoadenectomy ; Submandibular Gland - surgery</subject><ispartof>Teratogenesis, carcinogenesis, and mutagenesis, 1993, Vol.13 (2), p.59-74</ispartof><rights>Copyright © 1993 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1993 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4383-cf6d387b3dd0de28ebb93a099bd29e08cef9601c0d13c732539a2da5e1a1674e3</citedby><cites>FETCH-LOGICAL-c4383-cf6d387b3dd0de28ebb93a099bd29e08cef9601c0d13c732539a2da5e1a1674e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Ftcm.1770130203$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Ftcm.1770130203$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27900,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4806984$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8102210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vassilacopoulou, Dido</creatorcontrib><creatorcontrib>Boylan, Elizabeth S.</creatorcontrib><title>Mammary gland morphology and responsiveness to regulatory molecules following prenatal exposure to diethylstilbestrol</title><title>Teratogenesis, carcinogenesis, and mutagenesis</title><addtitle>Teratog. Carcinog. Mutagen</addtitle><description>Female ACI rats were exposed to diethylstilbestrol (DES) in utero to evaluate the effects on the peri‐pubertal mammary gland with respect to 1) mammary gland morphology, 2) sensitivity to natural and synthetic estrogens, and 3) sensitivity to endogenous epidermal growth factor (EGF). Pregnant rats were injected with vehicle (sesame oil) or DES (total dose, 8.0 μg) on days 15 and 18 of gestation. DES‐exposed and control offspring were ovariectomized at 34 days of age and sacrificed at day 53 to ascertain the morphology of the mammary glands in peri‐pubertal rats. Elvax pellets containing 5 or 11 ng 17 β‐estradiol (E2) or DES were implanted subcutaneously adjacent to the third mammary gland pair. Furthermore, additional groups of rats were subjected to bilateral sialoadenectomy at the day of ovariectomy to remove the major source of endogenous EGF. A significant proportion of mammary glands of DES‐exposed animals exhibited atypical mammary gland morphology, with approximately 25% displaying hypo‐differentiation, and about 5% with aberrant hyper‐proliferation. From the pellet implantation experiments, the DES‐exposed glands were found to be refractory to stimulation by 5 and 11 ng DES; however, there was no significant difference in the degree of local stimulation elicited by either dose of E2. Sialoadenectomy at d34 had no apparent effect on mammary gland morphology in either the DES‐exposed or vehicle‐exposed groups. These data support the premise that the mammary gland of the peri‐pubertal ACI rat is morphologically and physiologically aberrant as a function of transplacental exposure to DES, with a significant percentage hypo‐differentiated and refractory to subsequent hormonal stimulation. ©1993 Wiley‐Liss, Inc.</description><subject>ACI rat</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Diethylstilbestrol - toxicity</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Elvax pellet</subject><subject>epidermal growth factor</subject><subject>Estradiol - pharmacology</subject><subject>estrogen</subject><subject>Female</subject><subject>Fetus - drug effects</subject><subject>Mammary Glands, Animal - drug effects</subject><subject>Mammary Glands, Animal - pathology</subject><subject>mammary tumor</subject><subject>Medical sciences</subject><subject>Miscellaneous (drug allergy, mutagens, teratogens...)</subject><subject>Pharmacology. Drug treatments</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects</subject><subject>Rats</subject><subject>Rats, Inbred ACI</subject><subject>sialoadenectomy</subject><subject>Submandibular Gland - surgery</subject><issn>0270-3211</issn><issn>1520-6866</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEGP0zAQRi0EWsrClRtSDohbythO4viIKthF2gWBijhajj3pGpw42Am7_fe4alXEiZNlz3sz44-QlxTWFIC9nc2wpkIA5cCAPyIrWjMom7ZpHpMVMAElZ5Q-Jc9S-gFAgVJ2QS5aCoxRWJHlVg-Djvti5_VoiyHE6S74sNsXh2vENIUxud84YkrFHPLLbvF6DtkYgkezeExFH7wP927cFVPEUc_aF_gwhbREPDjW4Xy392l2vsM0x-Cfkye99glfnM5L8u3D--3murz5fPVx8-6mNBVveWn6xvJWdNxasMha7DrJNUjZWSYRWoO9bIAasJQbwVnNpWZW10g1bUSF_JK8OfadYvi15NlqcMmgz3_FsCRFm1ryWtQZXB9BE0NKEXs1RXfIRVFQh5xVzln9zTkLr06dl25Ae8ZPweb661NdJ6N9H_VoXDpjVQuNbKuMySN27zzu_zNUbTe3_6xQHl2XZnw4uzr-VI3golbfP12p7fUXud18rZTkfwDceak_</recordid><startdate>1993</startdate><enddate>1993</enddate><creator>Vassilacopoulou, Dido</creator><creator>Boylan, Elizabeth S.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>1993</creationdate><title>Mammary gland morphology and responsiveness to regulatory molecules following prenatal exposure to diethylstilbestrol</title><author>Vassilacopoulou, Dido ; Boylan, Elizabeth S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4383-cf6d387b3dd0de28ebb93a099bd29e08cef9601c0d13c732539a2da5e1a1674e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>ACI rat</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Diethylstilbestrol - toxicity</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Elvax pellet</topic><topic>epidermal growth factor</topic><topic>Estradiol - pharmacology</topic><topic>estrogen</topic><topic>Female</topic><topic>Fetus - drug effects</topic><topic>Mammary Glands, Animal - drug effects</topic><topic>Mammary Glands, Animal - pathology</topic><topic>mammary tumor</topic><topic>Medical sciences</topic><topic>Miscellaneous (drug allergy, mutagens, teratogens...)</topic><topic>Pharmacology. Drug treatments</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects</topic><topic>Rats</topic><topic>Rats, Inbred ACI</topic><topic>sialoadenectomy</topic><topic>Submandibular Gland - surgery</topic><toplevel>online_resources</toplevel><creatorcontrib>Vassilacopoulou, Dido</creatorcontrib><creatorcontrib>Boylan, Elizabeth S.</creatorcontrib><collection>Istex</collection><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Teratogenesis, carcinogenesis, and mutagenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vassilacopoulou, Dido</au><au>Boylan, Elizabeth S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mammary gland morphology and responsiveness to regulatory molecules following prenatal exposure to diethylstilbestrol</atitle><jtitle>Teratogenesis, carcinogenesis, and mutagenesis</jtitle><addtitle>Teratog. Carcinog. Mutagen</addtitle><date>1993</date><risdate>1993</risdate><volume>13</volume><issue>2</issue><spage>59</spage><epage>74</epage><pages>59-74</pages><issn>0270-3211</issn><eissn>1520-6866</eissn><coden>TCMUD8</coden><abstract>Female ACI rats were exposed to diethylstilbestrol (DES) in utero to evaluate the effects on the peri‐pubertal mammary gland with respect to 1) mammary gland morphology, 2) sensitivity to natural and synthetic estrogens, and 3) sensitivity to endogenous epidermal growth factor (EGF). Pregnant rats were injected with vehicle (sesame oil) or DES (total dose, 8.0 μg) on days 15 and 18 of gestation. DES‐exposed and control offspring were ovariectomized at 34 days of age and sacrificed at day 53 to ascertain the morphology of the mammary glands in peri‐pubertal rats. Elvax pellets containing 5 or 11 ng 17 β‐estradiol (E2) or DES were implanted subcutaneously adjacent to the third mammary gland pair. Furthermore, additional groups of rats were subjected to bilateral sialoadenectomy at the day of ovariectomy to remove the major source of endogenous EGF. A significant proportion of mammary glands of DES‐exposed animals exhibited atypical mammary gland morphology, with approximately 25% displaying hypo‐differentiation, and about 5% with aberrant hyper‐proliferation. From the pellet implantation experiments, the DES‐exposed glands were found to be refractory to stimulation by 5 and 11 ng DES; however, there was no significant difference in the degree of local stimulation elicited by either dose of E2. Sialoadenectomy at d34 had no apparent effect on mammary gland morphology in either the DES‐exposed or vehicle‐exposed groups. These data support the premise that the mammary gland of the peri‐pubertal ACI rat is morphologically and physiologically aberrant as a function of transplacental exposure to DES, with a significant percentage hypo‐differentiated and refractory to subsequent hormonal stimulation. ©1993 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8102210</pmid><doi>10.1002/tcm.1770130203</doi><tpages>16</tpages></addata></record> |
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subjects | ACI rat Animals Biological and medical sciences Diethylstilbestrol - toxicity Drug toxicity and drugs side effects treatment Elvax pellet epidermal growth factor Estradiol - pharmacology estrogen Female Fetus - drug effects Mammary Glands, Animal - drug effects Mammary Glands, Animal - pathology mammary tumor Medical sciences Miscellaneous (drug allergy, mutagens, teratogens...) Pharmacology. Drug treatments Pregnancy Prenatal Exposure Delayed Effects Rats Rats, Inbred ACI sialoadenectomy Submandibular Gland - surgery |
title | Mammary gland morphology and responsiveness to regulatory molecules following prenatal exposure to diethylstilbestrol |
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