Prepubertal tamoxifen treatment affects development of heifer reproductive tissues and related signaling pathways
Prepubertal exposure of the developing ovaries and reproductive tract (RT) to estrogen or xenoestrogens can have acute and long-term consequences that compromise the reproductive performance of cattle. This research examined effects of the selective estrogen receptor modulator tamoxifen (TAM) on gen...
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Veröffentlicht in: | Journal of dairy science 2016-07, Vol.99 (7), p.5780-5792 |
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container_title | Journal of dairy science |
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creator | Al Naib, A. Tucker, H.L.M. Xie, G. Keisler, D.H. Bartol, F.F. Rhoads, R.P. Akers, R.M. Rhoads, M.L. |
description | Prepubertal exposure of the developing ovaries and reproductive tract (RT) to estrogen or xenoestrogens can have acute and long-term consequences that compromise the reproductive performance of cattle. This research examined effects of the selective estrogen receptor modulator tamoxifen (TAM) on gene and protein abundance in prepubertal ovaries and RT, with a particular focus on signaling pathways that affect morphology. Tamoxifen was administered to Holstein heifer calves (n=8) daily (0.3mg/kg subcutaneously) from 28 to 120 d of age, when tissues were collected. Control calves (n=7) received an equal volume of excipient. Weight, gross measurements, and samples of reproductive tissues were collected, and protein and mRNA were extracted from snap-frozen samples of vagina, cervix, uterus, oviduct, ovary, and liver. Neither estradiol nor insulin-like growth factor I (IGFI) concentrations in the serum were affected by TAM treatment. Tamoxifen treatment reduced ovarian weight independently from effects on antral follicle populations, as there was no difference in visible antral follicle numbers on the day of collection. Estrogen receptor α (ESR1) and β (ESR2) mRNA, ESR1 protein, IGFI, progesterone receptor, total growth hormone receptor, WNT4, WNT5A, and WNT7A mRNA, in addition to mitogen-activated protein kinase (MAPK) and phosphorylated MAPK proteins were affected differently depending on the tissue examined. However, neither IGFI receptor mRNA nor protein abundance were affected by TAM treatment. Results indicate that reproductive development in prepubertal Holstein heifer calves is TAM-sensitive, and that bovine RT and ovarian development are supported, in part, by estrogen receptor-dependent mechanisms during the period studied here. Potential long-term consequences of such developmental disruption remain to be defined. |
doi_str_mv | 10.3168/jds.2015-10679 |
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This research examined effects of the selective estrogen receptor modulator tamoxifen (TAM) on gene and protein abundance in prepubertal ovaries and RT, with a particular focus on signaling pathways that affect morphology. Tamoxifen was administered to Holstein heifer calves (n=8) daily (0.3mg/kg subcutaneously) from 28 to 120 d of age, when tissues were collected. Control calves (n=7) received an equal volume of excipient. Weight, gross measurements, and samples of reproductive tissues were collected, and protein and mRNA were extracted from snap-frozen samples of vagina, cervix, uterus, oviduct, ovary, and liver. Neither estradiol nor insulin-like growth factor I (IGFI) concentrations in the serum were affected by TAM treatment. Tamoxifen treatment reduced ovarian weight independently from effects on antral follicle populations, as there was no difference in visible antral follicle numbers on the day of collection. Estrogen receptor α (ESR1) and β (ESR2) mRNA, ESR1 protein, IGFI, progesterone receptor, total growth hormone receptor, WNT4, WNT5A, and WNT7A mRNA, in addition to mitogen-activated protein kinase (MAPK) and phosphorylated MAPK proteins were affected differently depending on the tissue examined. However, neither IGFI receptor mRNA nor protein abundance were affected by TAM treatment. Results indicate that reproductive development in prepubertal Holstein heifer calves is TAM-sensitive, and that bovine RT and ovarian development are supported, in part, by estrogen receptor-dependent mechanisms during the period studied here. Potential long-term consequences of such developmental disruption remain to be defined.</description><identifier>ISSN: 0022-0302</identifier><identifier>EISSN: 1525-3198</identifier><identifier>DOI: 10.3168/jds.2015-10679</identifier><identifier>PMID: 27085397</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Cattle - physiology ; Estradiol - pharmacology ; estrogen ; Female ; Insulin-Like Growth Factor I - metabolism ; Mitogen-Activated Protein Kinases - metabolism ; ovary ; Ovary - drug effects ; prepubertal ; Receptors, Estrogen - metabolism ; Tamoxifen ; uterus</subject><ispartof>Journal of dairy science, 2016-07, Vol.99 (7), p.5780-5792</ispartof><rights>2016 American Dairy Science Association</rights><rights>Copyright © 2016 American Dairy Science Association. Published by Elsevier Inc. 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This research examined effects of the selective estrogen receptor modulator tamoxifen (TAM) on gene and protein abundance in prepubertal ovaries and RT, with a particular focus on signaling pathways that affect morphology. Tamoxifen was administered to Holstein heifer calves (n=8) daily (0.3mg/kg subcutaneously) from 28 to 120 d of age, when tissues were collected. Control calves (n=7) received an equal volume of excipient. Weight, gross measurements, and samples of reproductive tissues were collected, and protein and mRNA were extracted from snap-frozen samples of vagina, cervix, uterus, oviduct, ovary, and liver. Neither estradiol nor insulin-like growth factor I (IGFI) concentrations in the serum were affected by TAM treatment. Tamoxifen treatment reduced ovarian weight independently from effects on antral follicle populations, as there was no difference in visible antral follicle numbers on the day of collection. Estrogen receptor α (ESR1) and β (ESR2) mRNA, ESR1 protein, IGFI, progesterone receptor, total growth hormone receptor, WNT4, WNT5A, and WNT7A mRNA, in addition to mitogen-activated protein kinase (MAPK) and phosphorylated MAPK proteins were affected differently depending on the tissue examined. However, neither IGFI receptor mRNA nor protein abundance were affected by TAM treatment. Results indicate that reproductive development in prepubertal Holstein heifer calves is TAM-sensitive, and that bovine RT and ovarian development are supported, in part, by estrogen receptor-dependent mechanisms during the period studied here. Potential long-term consequences of such developmental disruption remain to be defined.</description><subject>Animals</subject><subject>Cattle - physiology</subject><subject>Estradiol - pharmacology</subject><subject>estrogen</subject><subject>Female</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Mitogen-Activated Protein Kinases - metabolism</subject><subject>ovary</subject><subject>Ovary - drug effects</subject><subject>prepubertal</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Tamoxifen</subject><subject>uterus</subject><issn>0022-0302</issn><issn>1525-3198</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kDlPxDAQRi0EYpejpUQuabLYTmInJUJc0kpQQG35mIBXOXZtZ4F_j_eAjsoaz5tPMw-hC0pmOeXV9cKGGSO0zCjhoj5AU1qyMstpXR2iKSGMZSQnbIJOQlikkjJSHqMJE6Qq81pM0erFw3LU4KNqcVTd8OUa6HH0oGIHfcSqacDEgC2soR2W27-hwR-QOI_TsB_saKJbA44uhBECVr1NjVZFsDi49161rn_HSxU_PtV3OENHjWoDnO_fU_R2f_d6-5jNnx-ebm_mmcmrImYlr21BiNbC2EoVFefCaKp1zZuSckpZOkAUYAqilWKW5iRnmhuqaJHaROSn6GqXmzZcpbWi7Fww0Laqh2EMkopapFTO64TOdqjxQwgeGrn0rlP-W1IiN5pl0iw3muVWcxq43GePugP7h_96TUC1AyBduHbgZTAOegPW-aRT2sH9l_0DKICNtg</recordid><startdate>201607</startdate><enddate>201607</enddate><creator>Al Naib, A.</creator><creator>Tucker, H.L.M.</creator><creator>Xie, G.</creator><creator>Keisler, D.H.</creator><creator>Bartol, F.F.</creator><creator>Rhoads, R.P.</creator><creator>Akers, R.M.</creator><creator>Rhoads, M.L.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope></search><sort><creationdate>201607</creationdate><title>Prepubertal tamoxifen treatment affects development of heifer reproductive tissues and related signaling pathways</title><author>Al Naib, A. ; Tucker, H.L.M. ; Xie, G. ; Keisler, D.H. ; Bartol, F.F. ; Rhoads, R.P. ; Akers, R.M. ; Rhoads, M.L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-569d400bb7cd8a48667cb1bb96f51611285374ec40baa2d13032b6c1a14161073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Cattle - physiology</topic><topic>Estradiol - pharmacology</topic><topic>estrogen</topic><topic>Female</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Mitogen-Activated Protein Kinases - metabolism</topic><topic>ovary</topic><topic>Ovary - drug effects</topic><topic>prepubertal</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Tamoxifen</topic><topic>uterus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Al Naib, A.</creatorcontrib><creatorcontrib>Tucker, H.L.M.</creatorcontrib><creatorcontrib>Xie, G.</creatorcontrib><creatorcontrib>Keisler, D.H.</creatorcontrib><creatorcontrib>Bartol, F.F.</creatorcontrib><creatorcontrib>Rhoads, R.P.</creatorcontrib><creatorcontrib>Akers, R.M.</creatorcontrib><creatorcontrib>Rhoads, M.L.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dairy science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al Naib, A.</au><au>Tucker, H.L.M.</au><au>Xie, G.</au><au>Keisler, D.H.</au><au>Bartol, F.F.</au><au>Rhoads, R.P.</au><au>Akers, R.M.</au><au>Rhoads, M.L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prepubertal tamoxifen treatment affects development of heifer reproductive tissues and related signaling pathways</atitle><jtitle>Journal of dairy science</jtitle><addtitle>J Dairy Sci</addtitle><date>2016-07</date><risdate>2016</risdate><volume>99</volume><issue>7</issue><spage>5780</spage><epage>5792</epage><pages>5780-5792</pages><issn>0022-0302</issn><eissn>1525-3198</eissn><abstract>Prepubertal exposure of the developing ovaries and reproductive tract (RT) to estrogen or xenoestrogens can have acute and long-term consequences that compromise the reproductive performance of cattle. This research examined effects of the selective estrogen receptor modulator tamoxifen (TAM) on gene and protein abundance in prepubertal ovaries and RT, with a particular focus on signaling pathways that affect morphology. Tamoxifen was administered to Holstein heifer calves (n=8) daily (0.3mg/kg subcutaneously) from 28 to 120 d of age, when tissues were collected. Control calves (n=7) received an equal volume of excipient. Weight, gross measurements, and samples of reproductive tissues were collected, and protein and mRNA were extracted from snap-frozen samples of vagina, cervix, uterus, oviduct, ovary, and liver. Neither estradiol nor insulin-like growth factor I (IGFI) concentrations in the serum were affected by TAM treatment. Tamoxifen treatment reduced ovarian weight independently from effects on antral follicle populations, as there was no difference in visible antral follicle numbers on the day of collection. Estrogen receptor α (ESR1) and β (ESR2) mRNA, ESR1 protein, IGFI, progesterone receptor, total growth hormone receptor, WNT4, WNT5A, and WNT7A mRNA, in addition to mitogen-activated protein kinase (MAPK) and phosphorylated MAPK proteins were affected differently depending on the tissue examined. However, neither IGFI receptor mRNA nor protein abundance were affected by TAM treatment. Results indicate that reproductive development in prepubertal Holstein heifer calves is TAM-sensitive, and that bovine RT and ovarian development are supported, in part, by estrogen receptor-dependent mechanisms during the period studied here. Potential long-term consequences of such developmental disruption remain to be defined.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27085397</pmid><doi>10.3168/jds.2015-10679</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cattle - physiology Estradiol - pharmacology estrogen Female Insulin-Like Growth Factor I - metabolism Mitogen-Activated Protein Kinases - metabolism ovary Ovary - drug effects prepubertal Receptors, Estrogen - metabolism Tamoxifen uterus |
title | Prepubertal tamoxifen treatment affects development of heifer reproductive tissues and related signaling pathways |
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