Three-Generation Reproductive Toxicity Study of Dietary Bisphenol A in CD Sprague-Dawley Rats
Bisphenol A (BPA) was evaluated at concentrations of 0, 0.015, 0.3, 4.5, 75, 750, and 7500 ppm (∼ 0.001, 0.02, 0.3, 5, 50, and 500 mg/kg/day of BPA) administered in the diet ad libitum to 30 CD® Sprague-Dawley rats/sex/dose for 3 offspring generations, 1 litter/generation, through F3 adults. Adult s...
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| Veröffentlicht in: | Toxicological sciences 2002-07, Vol.68 (1), p.121-146 |
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| creator | Tyl, R. W. Myers, C. B. Marr, M. C. Thomas, B. F. Keimowitz, A. R. Brine, D. R. Veselica, M. M. Fail, P. A. Chang, T. Y. Seely, J. C. Joiner, R. L. Butala, J. H. Dimond, S. S. Cagen, S. Z. Shiotsuka, R. N. Stropp, G. D. Waechter, J. M. |
| description | Bisphenol A (BPA) was evaluated at concentrations of 0, 0.015, 0.3, 4.5, 75, 750, and 7500 ppm (∼ 0.001, 0.02, 0.3, 5, 50, and 500 mg/kg/day of BPA) administered in the diet ad libitum to 30 CD® Sprague-Dawley rats/sex/dose for 3 offspring generations, 1 litter/generation, through F3 adults. Adult systemic toxicity at 750 and 7500 ppm in all generations included: reduced body weights and body weight gains, reduced absolute and increased relative weanling and adult organ weights (liver, kidneys, adrenals, spleen, pituitary, and brain), and female slight/mild renal and hepatic pathology at 7500 ppm. Reproductive organ histopathology and function were unaffected. Ovarian weights as well as total pups and live pups/litter on postnatal day (PND) 0 were decreased at 7500 ppm, which exceeded the adult maximum tolerated dose (MTD). Mating, fertility, gestational indices; ovarian primordial follicle counts; estrous cyclicity; precoital interval; gestational length; offspring sex ratios; postnatal survival; nipple/areolae retention in preweanling males; epididymal sperm number, motility, morphology; daily sperm production (DSP), and efficiency of DSP were all unaffected. At 7500 ppm, vaginal patency (VP) and preputial separation (PPS) were delayed in F1, F2, and F3 offspring, associated with reduced body weights. Anogenital distance (AGD) on PND 0 was unaffected for F2 and F3 males and F3 females (F2 female AGD was increased at some doses, not at 7500 ppm, and was considered not biologically or toxicologically relevant). Adult systemic no observed adverse effect level (NOAEL) = 75 ppm (5 mg/kg/day); reproductive and postnatal NOAELs = 750 ppm (50 mg/kg/day). There were no treatment-related effects in the low-dose region (0.001–5 mg/kg/day) on any parameters and no evidence of nonmonotonic dose-response curves across generations for either sex. BPA should not be considered a selective reproductive toxicant, based on the results of this study. |
| doi_str_mv | 10.1093/toxsci/68.1.121 |
| format | Article |
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W. ; Myers, C. B. ; Marr, M. C. ; Thomas, B. F. ; Keimowitz, A. R. ; Brine, D. R. ; Veselica, M. M. ; Fail, P. A. ; Chang, T. Y. ; Seely, J. C. ; Joiner, R. L. ; Butala, J. H. ; Dimond, S. S. ; Cagen, S. Z. ; Shiotsuka, R. N. ; Stropp, G. D. ; Waechter, J. M.</creator><creatorcontrib>Tyl, R. W. ; Myers, C. B. ; Marr, M. C. ; Thomas, B. F. ; Keimowitz, A. R. ; Brine, D. R. ; Veselica, M. M. ; Fail, P. A. ; Chang, T. Y. ; Seely, J. C. ; Joiner, R. L. ; Butala, J. H. ; Dimond, S. S. ; Cagen, S. Z. ; Shiotsuka, R. N. ; Stropp, G. D. ; Waechter, J. M.</creatorcontrib><description>Bisphenol A (BPA) was evaluated at concentrations of 0, 0.015, 0.3, 4.5, 75, 750, and 7500 ppm (∼ 0.001, 0.02, 0.3, 5, 50, and 500 mg/kg/day of BPA) administered in the diet ad libitum to 30 CD® Sprague-Dawley rats/sex/dose for 3 offspring generations, 1 litter/generation, through F3 adults. Adult systemic toxicity at 750 and 7500 ppm in all generations included: reduced body weights and body weight gains, reduced absolute and increased relative weanling and adult organ weights (liver, kidneys, adrenals, spleen, pituitary, and brain), and female slight/mild renal and hepatic pathology at 7500 ppm. Reproductive organ histopathology and function were unaffected. Ovarian weights as well as total pups and live pups/litter on postnatal day (PND) 0 were decreased at 7500 ppm, which exceeded the adult maximum tolerated dose (MTD). Mating, fertility, gestational indices; ovarian primordial follicle counts; estrous cyclicity; precoital interval; gestational length; offspring sex ratios; postnatal survival; nipple/areolae retention in preweanling males; epididymal sperm number, motility, morphology; daily sperm production (DSP), and efficiency of DSP were all unaffected. At 7500 ppm, vaginal patency (VP) and preputial separation (PPS) were delayed in F1, F2, and F3 offspring, associated with reduced body weights. Anogenital distance (AGD) on PND 0 was unaffected for F2 and F3 males and F3 females (F2 female AGD was increased at some doses, not at 7500 ppm, and was considered not biologically or toxicologically relevant). Adult systemic no observed adverse effect level (NOAEL) = 75 ppm (5 mg/kg/day); reproductive and postnatal NOAELs = 750 ppm (50 mg/kg/day). There were no treatment-related effects in the low-dose region (0.001–5 mg/kg/day) on any parameters and no evidence of nonmonotonic dose-response curves across generations for either sex. BPA should not be considered a selective reproductive toxicant, based on the results of this study.</description><identifier>ISSN: 1096-6080</identifier><identifier>ISSN: 1096-0929</identifier><identifier>EISSN: 1096-0929</identifier><identifier>DOI: 10.1093/toxsci/68.1.121</identifier><identifier>PMID: 12075117</identifier><identifier>CODEN: TOSCF2</identifier><language>eng</language><publisher>Cary, NC: Oxford University Press</publisher><subject>Administration, Oral ; Animals ; Benzhydryl Compounds ; Biological and medical sciences ; Bisphenol A ; Body Weight - drug effects ; CAS No. 80-05-7 ; Chemical and industrial products toxicology. Toxic occupational diseases ; Diet ; dietary administration ; Dose-Response Relationship, Drug ; Estrogens, Non-Steroidal - administration & dosage ; Estrogens, Non-Steroidal - toxicity ; Female ; Lactation - drug effects ; Male ; Medical sciences ; No-Observed-Adverse-Effect Level ; OPPTS 837.3800 guidelines ; Organ Size - drug effects ; Phenols - administration & dosage ; Phenols - toxicity ; postnatal toxicity ; Pregnancy ; Prenatal Exposure Delayed Effects ; Rats ; Rats, Sprague-Dawley ; Reproduction - drug effects ; reproductive toxicity ; Sexual Maturation - drug effects ; systemic toxicity ; Toxicology ; Various organic compounds</subject><ispartof>Toxicological sciences, 2002-07, Vol.68 (1), p.121-146</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-a34b6fb4c5ececa6deb6ac046f72353352b8e41e64f8e6e30ea87a4a86e251ea3</citedby></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=13807525$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12075117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tyl, R. W.</creatorcontrib><creatorcontrib>Myers, C. B.</creatorcontrib><creatorcontrib>Marr, M. C.</creatorcontrib><creatorcontrib>Thomas, B. F.</creatorcontrib><creatorcontrib>Keimowitz, A. R.</creatorcontrib><creatorcontrib>Brine, D. R.</creatorcontrib><creatorcontrib>Veselica, M. M.</creatorcontrib><creatorcontrib>Fail, P. A.</creatorcontrib><creatorcontrib>Chang, T. Y.</creatorcontrib><creatorcontrib>Seely, J. C.</creatorcontrib><creatorcontrib>Joiner, R. L.</creatorcontrib><creatorcontrib>Butala, J. H.</creatorcontrib><creatorcontrib>Dimond, S. S.</creatorcontrib><creatorcontrib>Cagen, S. Z.</creatorcontrib><creatorcontrib>Shiotsuka, R. N.</creatorcontrib><creatorcontrib>Stropp, G. D.</creatorcontrib><creatorcontrib>Waechter, J. M.</creatorcontrib><title>Three-Generation Reproductive Toxicity Study of Dietary Bisphenol A in CD Sprague-Dawley Rats</title><title>Toxicological sciences</title><addtitle>Toxicol. Sci</addtitle><description>Bisphenol A (BPA) was evaluated at concentrations of 0, 0.015, 0.3, 4.5, 75, 750, and 7500 ppm (∼ 0.001, 0.02, 0.3, 5, 50, and 500 mg/kg/day of BPA) administered in the diet ad libitum to 30 CD® Sprague-Dawley rats/sex/dose for 3 offspring generations, 1 litter/generation, through F3 adults. Adult systemic toxicity at 750 and 7500 ppm in all generations included: reduced body weights and body weight gains, reduced absolute and increased relative weanling and adult organ weights (liver, kidneys, adrenals, spleen, pituitary, and brain), and female slight/mild renal and hepatic pathology at 7500 ppm. Reproductive organ histopathology and function were unaffected. Ovarian weights as well as total pups and live pups/litter on postnatal day (PND) 0 were decreased at 7500 ppm, which exceeded the adult maximum tolerated dose (MTD). Mating, fertility, gestational indices; ovarian primordial follicle counts; estrous cyclicity; precoital interval; gestational length; offspring sex ratios; postnatal survival; nipple/areolae retention in preweanling males; epididymal sperm number, motility, morphology; daily sperm production (DSP), and efficiency of DSP were all unaffected. At 7500 ppm, vaginal patency (VP) and preputial separation (PPS) were delayed in F1, F2, and F3 offspring, associated with reduced body weights. Anogenital distance (AGD) on PND 0 was unaffected for F2 and F3 males and F3 females (F2 female AGD was increased at some doses, not at 7500 ppm, and was considered not biologically or toxicologically relevant). Adult systemic no observed adverse effect level (NOAEL) = 75 ppm (5 mg/kg/day); reproductive and postnatal NOAELs = 750 ppm (50 mg/kg/day). There were no treatment-related effects in the low-dose region (0.001–5 mg/kg/day) on any parameters and no evidence of nonmonotonic dose-response curves across generations for either sex. BPA should not be considered a selective reproductive toxicant, based on the results of this study.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Benzhydryl Compounds</subject><subject>Biological and medical sciences</subject><subject>Bisphenol A</subject><subject>Body Weight - drug effects</subject><subject>CAS No. 80-05-7</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Diet</subject><subject>dietary administration</subject><subject>Dose-Response Relationship, Drug</subject><subject>Estrogens, Non-Steroidal - administration & dosage</subject><subject>Estrogens, Non-Steroidal - toxicity</subject><subject>Female</subject><subject>Lactation - drug effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>No-Observed-Adverse-Effect Level</subject><subject>OPPTS 837.3800 guidelines</subject><subject>Organ Size - drug effects</subject><subject>Phenols - administration & dosage</subject><subject>Phenols - toxicity</subject><subject>postnatal toxicity</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reproduction - drug effects</subject><subject>reproductive toxicity</subject><subject>Sexual Maturation - drug effects</subject><subject>systemic toxicity</subject><subject>Toxicology</subject><subject>Various organic compounds</subject><issn>1096-6080</issn><issn>1096-0929</issn><issn>1096-0929</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0FFP2zAQB3Br2jQY45k35JfxltaOHcd5ZC2DTcAQFAlNmqyLexne0qTYztZ--xk1gidb9u9Od39CjjibcFaJaew3wbqp0hM-4Tl_Q_bTs8pYlVdvx7timu2RDyH8Zoxzxar3ZI_nrCw4L_fJz8WjR8zOsUMP0fUdvcW175eDje4v0kW_cdbFLb2Lw3JL-4bOHUbwW_rZhfUjdn1LT6nr6GxO79Yefg2YzeFfi1t6CzF8JO8aaAMejucBuf9ytphdZJffz7_OTi8zK6sqZiBkrZpa2gItWlBLrBVYJlVT5qIQoshrjZKjko1GhYIh6BIkaIV5wRHEATnZ9U2jPw0Yolm5YLFtocN-CIZrKblSIsHpDlrfh-CxMWvvVmkfw5l5TtTsEjVKG25SoqnieGw91CtcvvoxwgQ-jQCChbbx0FkXXp3QCeZFctnOuRBx8_IP_o9RpSgLc_HwwyjxTVxf3cxNJf4DNOeP5Q</recordid><startdate>20020701</startdate><enddate>20020701</enddate><creator>Tyl, R. W.</creator><creator>Myers, C. B.</creator><creator>Marr, M. C.</creator><creator>Thomas, B. F.</creator><creator>Keimowitz, A. R.</creator><creator>Brine, D. R.</creator><creator>Veselica, M. M.</creator><creator>Fail, P. A.</creator><creator>Chang, T. Y.</creator><creator>Seely, J. C.</creator><creator>Joiner, R. L.</creator><creator>Butala, J. H.</creator><creator>Dimond, S. S.</creator><creator>Cagen, S. Z.</creator><creator>Shiotsuka, R. N.</creator><creator>Stropp, G. D.</creator><creator>Waechter, J. M.</creator><general>Oxford University Press</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>20020701</creationdate><title>Three-Generation Reproductive Toxicity Study of Dietary Bisphenol A in CD Sprague-Dawley Rats</title><author>Tyl, R. W. ; Myers, C. B. ; Marr, M. C. ; Thomas, B. F. ; Keimowitz, A. R. ; Brine, D. R. ; Veselica, M. M. ; Fail, P. A. ; Chang, T. Y. ; Seely, J. C. ; Joiner, R. L. ; Butala, J. H. ; Dimond, S. S. ; Cagen, S. Z. ; Shiotsuka, R. N. ; Stropp, G. D. ; Waechter, J. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-a34b6fb4c5ececa6deb6ac046f72353352b8e41e64f8e6e30ea87a4a86e251ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Benzhydryl Compounds</topic><topic>Biological and medical sciences</topic><topic>Bisphenol A</topic><topic>Body Weight - drug effects</topic><topic>CAS No. 80-05-7</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Diet</topic><topic>dietary administration</topic><topic>Dose-Response Relationship, Drug</topic><topic>Estrogens, Non-Steroidal - administration & dosage</topic><topic>Estrogens, Non-Steroidal - toxicity</topic><topic>Female</topic><topic>Lactation - drug effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>No-Observed-Adverse-Effect Level</topic><topic>OPPTS 837.3800 guidelines</topic><topic>Organ Size - drug effects</topic><topic>Phenols - administration & dosage</topic><topic>Phenols - toxicity</topic><topic>postnatal toxicity</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reproduction - drug effects</topic><topic>reproductive toxicity</topic><topic>Sexual Maturation - drug effects</topic><topic>systemic toxicity</topic><topic>Toxicology</topic><topic>Various organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tyl, R. W.</creatorcontrib><creatorcontrib>Myers, C. B.</creatorcontrib><creatorcontrib>Marr, M. C.</creatorcontrib><creatorcontrib>Thomas, B. F.</creatorcontrib><creatorcontrib>Keimowitz, A. R.</creatorcontrib><creatorcontrib>Brine, D. R.</creatorcontrib><creatorcontrib>Veselica, M. M.</creatorcontrib><creatorcontrib>Fail, P. A.</creatorcontrib><creatorcontrib>Chang, T. Y.</creatorcontrib><creatorcontrib>Seely, J. C.</creatorcontrib><creatorcontrib>Joiner, R. L.</creatorcontrib><creatorcontrib>Butala, J. H.</creatorcontrib><creatorcontrib>Dimond, S. S.</creatorcontrib><creatorcontrib>Cagen, S. Z.</creatorcontrib><creatorcontrib>Shiotsuka, R. N.</creatorcontrib><creatorcontrib>Stropp, G. D.</creatorcontrib><creatorcontrib>Waechter, J. M.</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>Toxicological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tyl, R. W.</au><au>Myers, C. B.</au><au>Marr, M. C.</au><au>Thomas, B. F.</au><au>Keimowitz, A. R.</au><au>Brine, D. R.</au><au>Veselica, M. M.</au><au>Fail, P. A.</au><au>Chang, T. Y.</au><au>Seely, J. C.</au><au>Joiner, R. L.</au><au>Butala, J. H.</au><au>Dimond, S. S.</au><au>Cagen, S. Z.</au><au>Shiotsuka, R. N.</au><au>Stropp, G. D.</au><au>Waechter, J. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Three-Generation Reproductive Toxicity Study of Dietary Bisphenol A in CD Sprague-Dawley Rats</atitle><jtitle>Toxicological sciences</jtitle><addtitle>Toxicol. Sci</addtitle><date>2002-07-01</date><risdate>2002</risdate><volume>68</volume><issue>1</issue><spage>121</spage><epage>146</epage><pages>121-146</pages><issn>1096-6080</issn><issn>1096-0929</issn><eissn>1096-0929</eissn><coden>TOSCF2</coden><abstract>Bisphenol A (BPA) was evaluated at concentrations of 0, 0.015, 0.3, 4.5, 75, 750, and 7500 ppm (∼ 0.001, 0.02, 0.3, 5, 50, and 500 mg/kg/day of BPA) administered in the diet ad libitum to 30 CD® Sprague-Dawley rats/sex/dose for 3 offspring generations, 1 litter/generation, through F3 adults. Adult systemic toxicity at 750 and 7500 ppm in all generations included: reduced body weights and body weight gains, reduced absolute and increased relative weanling and adult organ weights (liver, kidneys, adrenals, spleen, pituitary, and brain), and female slight/mild renal and hepatic pathology at 7500 ppm. Reproductive organ histopathology and function were unaffected. Ovarian weights as well as total pups and live pups/litter on postnatal day (PND) 0 were decreased at 7500 ppm, which exceeded the adult maximum tolerated dose (MTD). Mating, fertility, gestational indices; ovarian primordial follicle counts; estrous cyclicity; precoital interval; gestational length; offspring sex ratios; postnatal survival; nipple/areolae retention in preweanling males; epididymal sperm number, motility, morphology; daily sperm production (DSP), and efficiency of DSP were all unaffected. At 7500 ppm, vaginal patency (VP) and preputial separation (PPS) were delayed in F1, F2, and F3 offspring, associated with reduced body weights. Anogenital distance (AGD) on PND 0 was unaffected for F2 and F3 males and F3 females (F2 female AGD was increased at some doses, not at 7500 ppm, and was considered not biologically or toxicologically relevant). Adult systemic no observed adverse effect level (NOAEL) = 75 ppm (5 mg/kg/day); reproductive and postnatal NOAELs = 750 ppm (50 mg/kg/day). There were no treatment-related effects in the low-dose region (0.001–5 mg/kg/day) on any parameters and no evidence of nonmonotonic dose-response curves across generations for either sex. BPA should not be considered a selective reproductive toxicant, based on the results of this study.</abstract><cop>Cary, NC</cop><pub>Oxford University Press</pub><pmid>12075117</pmid><doi>10.1093/toxsci/68.1.121</doi><tpages>26</tpages><oa>free_for_read</oa></addata></record> |
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| subjects | Administration, Oral Animals Benzhydryl Compounds Biological and medical sciences Bisphenol A Body Weight - drug effects CAS No. 80-05-7 Chemical and industrial products toxicology. Toxic occupational diseases Diet dietary administration Dose-Response Relationship, Drug Estrogens, Non-Steroidal - administration & dosage Estrogens, Non-Steroidal - toxicity Female Lactation - drug effects Male Medical sciences No-Observed-Adverse-Effect Level OPPTS 837.3800 guidelines Organ Size - drug effects Phenols - administration & dosage Phenols - toxicity postnatal toxicity Pregnancy Prenatal Exposure Delayed Effects Rats Rats, Sprague-Dawley Reproduction - drug effects reproductive toxicity Sexual Maturation - drug effects systemic toxicity Toxicology Various organic compounds |
| title | Three-Generation Reproductive Toxicity Study of Dietary Bisphenol A in CD Sprague-Dawley Rats |
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