Immunomodulatory Effects of Estradiol and Cadmium in Adult Female Rats
A wide range of toxic effects has been associated with cadmium (Cd) exposure in mammals. However, the physiological factors that modulate these effects have received limited attention. We have previously demonstrated that neonatal exposure of rats to Cd during lactation results in sex-specific immun...
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Veröffentlicht in: | Toxicological sciences 2006-08, Vol.92 (2), p.423-432 |
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creator | Pillet, Stéphane D'Elia, Michele Bernier, Jacques Bouquegneau, Jean-Marie Fournier, Michel Cyr, Daniel G. |
description | A wide range of toxic effects has been associated with cadmium (Cd) exposure in mammals. However, the physiological factors that modulate these effects have received limited attention. We have previously demonstrated that neonatal exposure of rats to Cd during lactation results in sex-specific immunotoxic effects in both juvenile and adult rats. The objectives of this study were to determine the effects of 17β-estradiol (E2) on the immunotoxicity of Cd in female rats. We compared the effects of 28 days of exposure to 0, 5, and 25 ppm cadmium chloride (CdCl2) through drinking water on ovariectomized Sprague-Dawley rats and on ovariectomized rats with E2 implant which mimicked the physiological level of E2 in female rat. Our results clarify the control of important immune functions by E2 at physiological level and demonstrate significant interactions between Cd and E2 effects on the cytotoxic activity of natural killer cells and phagocytosis of splenic cells as well as on the total number of thymocytes and of the four subpopulations of the thymocytes as defined by the expression of the cell-surface markers CD4 and CD8. Cd and E2 share several mechanisms of action that may account for these interactions. The estrogenic potential of Cd could also account for some of the observed effects. These interactions have to be taken into consideration in evaluating the risk of Cd immunotoxicity and the possible interactions with hormonal treatments. |
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However, the physiological factors that modulate these effects have received limited attention. We have previously demonstrated that neonatal exposure of rats to Cd during lactation results in sex-specific immunotoxic effects in both juvenile and adult rats. The objectives of this study were to determine the effects of 17β-estradiol (E2) on the immunotoxicity of Cd in female rats. We compared the effects of 28 days of exposure to 0, 5, and 25 ppm cadmium chloride (CdCl2) through drinking water on ovariectomized Sprague-Dawley rats and on ovariectomized rats with E2 implant which mimicked the physiological level of E2 in female rat. Our results clarify the control of important immune functions by E2 at physiological level and demonstrate significant interactions between Cd and E2 effects on the cytotoxic activity of natural killer cells and phagocytosis of splenic cells as well as on the total number of thymocytes and of the four subpopulations of the thymocytes as defined by the expression of the cell-surface markers CD4 and CD8. Cd and E2 share several mechanisms of action that may account for these interactions. The estrogenic potential of Cd could also account for some of the observed effects. These interactions have to be taken into consideration in evaluating the risk of Cd immunotoxicity and the possible interactions with hormonal treatments.</description><identifier>ISSN: 1096-6080</identifier><identifier>EISSN: 1096-0929</identifier><identifier>DOI: 10.1093/toxsci/kfl005</identifier><identifier>PMID: 16675514</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animals ; cadmium ; Cadmium - toxicity ; Cell Line, Tumor ; Drug Synergism ; estradiol ; Estradiol - administration & dosage ; Estrogens - toxicity ; Female ; Immunologic Factors - toxicity ; immunotoxic effects ; Killer Cells, Natural - drug effects ; Killer Cells, Natural - immunology ; Mice ; ovariectomized rats ; Phagocytosis - drug effects ; Rats ; Rats, Sprague-Dawley ; Spleen - drug effects ; Spleen - immunology ; T-Lymphocyte Subsets - drug effects ; T-Lymphocyte Subsets - immunology ; T-Lymphocytes - drug effects ; T-Lymphocytes - immunology</subject><ispartof>Toxicological sciences, 2006-08, Vol.92 (2), p.423-432</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-789166a50d2b0805bb4997359978ef5c77b0c709d7a96d621b512fb995e5c6043</citedby><cites>FETCH-LOGICAL-c399t-789166a50d2b0805bb4997359978ef5c77b0c709d7a96d621b512fb995e5c6043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16675514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pillet, Stéphane</creatorcontrib><creatorcontrib>D'Elia, Michele</creatorcontrib><creatorcontrib>Bernier, Jacques</creatorcontrib><creatorcontrib>Bouquegneau, Jean-Marie</creatorcontrib><creatorcontrib>Fournier, Michel</creatorcontrib><creatorcontrib>Cyr, Daniel G.</creatorcontrib><title>Immunomodulatory Effects of Estradiol and Cadmium in Adult Female Rats</title><title>Toxicological sciences</title><addtitle>Toxicol. Sci</addtitle><description>A wide range of toxic effects has been associated with cadmium (Cd) exposure in mammals. However, the physiological factors that modulate these effects have received limited attention. We have previously demonstrated that neonatal exposure of rats to Cd during lactation results in sex-specific immunotoxic effects in both juvenile and adult rats. The objectives of this study were to determine the effects of 17β-estradiol (E2) on the immunotoxicity of Cd in female rats. We compared the effects of 28 days of exposure to 0, 5, and 25 ppm cadmium chloride (CdCl2) through drinking water on ovariectomized Sprague-Dawley rats and on ovariectomized rats with E2 implant which mimicked the physiological level of E2 in female rat. Our results clarify the control of important immune functions by E2 at physiological level and demonstrate significant interactions between Cd and E2 effects on the cytotoxic activity of natural killer cells and phagocytosis of splenic cells as well as on the total number of thymocytes and of the four subpopulations of the thymocytes as defined by the expression of the cell-surface markers CD4 and CD8. Cd and E2 share several mechanisms of action that may account for these interactions. The estrogenic potential of Cd could also account for some of the observed effects. These interactions have to be taken into consideration in evaluating the risk of Cd immunotoxicity and the possible interactions with hormonal treatments.</description><subject>Animals</subject><subject>cadmium</subject><subject>Cadmium - toxicity</subject><subject>Cell Line, Tumor</subject><subject>Drug Synergism</subject><subject>estradiol</subject><subject>Estradiol - administration & dosage</subject><subject>Estrogens - toxicity</subject><subject>Female</subject><subject>Immunologic Factors - toxicity</subject><subject>immunotoxic effects</subject><subject>Killer Cells, Natural - drug effects</subject><subject>Killer Cells, Natural - immunology</subject><subject>Mice</subject><subject>ovariectomized rats</subject><subject>Phagocytosis - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Spleen - drug effects</subject><subject>Spleen - immunology</subject><subject>T-Lymphocyte Subsets - drug effects</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocytes - drug effects</subject><subject>T-Lymphocytes - immunology</subject><issn>1096-6080</issn><issn>1096-0929</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM9LwzAUx4Mobk6PXiUnb3VJ2yTLceyHGw7EqSBeQpofUNc0s0lh---tdOjlvUfy4fseHwBuMXrAiGfj6A9BleOdrRAiZ2DYPdIE8ZSfn2aKJmgArkL4QghjivglGGBKGSE4H4Ll2rm29s7rtpLRN0e4sNaoGKC3cBFiI3XpKyhrDWdSu7J1sKzhtKMjXBonKwO3MoZrcGFlFczNqY_A-3LxNlslm-fH9Wy6SVTGeUzYhHerJUE6LbqzSFHknLOMdGViLFGMFUgxxDWTnGqa4oLg1BacE0MURXk2Avd97r7x360JUbgyKFNVsja-DQLznGDUeRmBpAdV40NojBX7pnSyOQqMxK840YsTvbiOvzsFt4Uz-p8-mfoPLEM0h79_2ewEZRkjYvXxKZ7m6Zy-brl4yX4AxPB5WA</recordid><startdate>200608</startdate><enddate>200608</enddate><creator>Pillet, Stéphane</creator><creator>D'Elia, Michele</creator><creator>Bernier, Jacques</creator><creator>Bouquegneau, Jean-Marie</creator><creator>Fournier, Michel</creator><creator>Cyr, Daniel G.</creator><general>Oxford University Press</general><scope>BSCLL</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>200608</creationdate><title>Immunomodulatory Effects of Estradiol and Cadmium in Adult Female Rats</title><author>Pillet, Stéphane ; D'Elia, Michele ; Bernier, Jacques ; Bouquegneau, Jean-Marie ; Fournier, Michel ; Cyr, Daniel G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-789166a50d2b0805bb4997359978ef5c77b0c709d7a96d621b512fb995e5c6043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>cadmium</topic><topic>Cadmium - toxicity</topic><topic>Cell Line, Tumor</topic><topic>Drug Synergism</topic><topic>estradiol</topic><topic>Estradiol - administration & dosage</topic><topic>Estrogens - toxicity</topic><topic>Female</topic><topic>Immunologic Factors - toxicity</topic><topic>immunotoxic effects</topic><topic>Killer Cells, Natural - drug effects</topic><topic>Killer Cells, Natural - immunology</topic><topic>Mice</topic><topic>ovariectomized rats</topic><topic>Phagocytosis - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Spleen - drug effects</topic><topic>Spleen - immunology</topic><topic>T-Lymphocyte Subsets - drug effects</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocytes - drug effects</topic><topic>T-Lymphocytes - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pillet, Stéphane</creatorcontrib><creatorcontrib>D'Elia, Michele</creatorcontrib><creatorcontrib>Bernier, Jacques</creatorcontrib><creatorcontrib>Bouquegneau, Jean-Marie</creatorcontrib><creatorcontrib>Fournier, Michel</creatorcontrib><creatorcontrib>Cyr, Daniel G.</creatorcontrib><collection>Istex</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>Toxicological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pillet, Stéphane</au><au>D'Elia, Michele</au><au>Bernier, Jacques</au><au>Bouquegneau, Jean-Marie</au><au>Fournier, Michel</au><au>Cyr, Daniel G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunomodulatory Effects of Estradiol and Cadmium in Adult Female Rats</atitle><jtitle>Toxicological sciences</jtitle><addtitle>Toxicol. Sci</addtitle><date>2006-08</date><risdate>2006</risdate><volume>92</volume><issue>2</issue><spage>423</spage><epage>432</epage><pages>423-432</pages><issn>1096-6080</issn><eissn>1096-0929</eissn><abstract>A wide range of toxic effects has been associated with cadmium (Cd) exposure in mammals. However, the physiological factors that modulate these effects have received limited attention. We have previously demonstrated that neonatal exposure of rats to Cd during lactation results in sex-specific immunotoxic effects in both juvenile and adult rats. The objectives of this study were to determine the effects of 17β-estradiol (E2) on the immunotoxicity of Cd in female rats. We compared the effects of 28 days of exposure to 0, 5, and 25 ppm cadmium chloride (CdCl2) through drinking water on ovariectomized Sprague-Dawley rats and on ovariectomized rats with E2 implant which mimicked the physiological level of E2 in female rat. Our results clarify the control of important immune functions by E2 at physiological level and demonstrate significant interactions between Cd and E2 effects on the cytotoxic activity of natural killer cells and phagocytosis of splenic cells as well as on the total number of thymocytes and of the four subpopulations of the thymocytes as defined by the expression of the cell-surface markers CD4 and CD8. Cd and E2 share several mechanisms of action that may account for these interactions. The estrogenic potential of Cd could also account for some of the observed effects. These interactions have to be taken into consideration in evaluating the risk of Cd immunotoxicity and the possible interactions with hormonal treatments.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>16675514</pmid><doi>10.1093/toxsci/kfl005</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals cadmium Cadmium - toxicity Cell Line, Tumor Drug Synergism estradiol Estradiol - administration & dosage Estrogens - toxicity Female Immunologic Factors - toxicity immunotoxic effects Killer Cells, Natural - drug effects Killer Cells, Natural - immunology Mice ovariectomized rats Phagocytosis - drug effects Rats Rats, Sprague-Dawley Spleen - drug effects Spleen - immunology T-Lymphocyte Subsets - drug effects T-Lymphocyte Subsets - immunology T-Lymphocytes - drug effects T-Lymphocytes - immunology |
title | Immunomodulatory Effects of Estradiol and Cadmium in Adult Female Rats |
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