Cargando…

Effects of Developmental Exposure to 2,2′,4,4′,5-Pentabromodiphenyl Ether (PBDE-99) on Sex Steroids, Sexual Development, and Sexually Dimorphic Behavior in Rats

Increasing concentrations of polybrominated flame retardants, including polybrominated diphenyl ethers (PBDEs), in breast milk cause concern about possible developmental effects in nursed babies. Because previous studies in rats have indicated effects on sex steroids and sexually dimorphic behavior...

Descripción completa

Detalles Bibliográficos
Autores principales: Lilienthal, Hellmuth, Hack, Alfons, Roth-Härer, Astrid, Grande, Simone Wichert, Talsness, Chris E.
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1367831/
https://www.ncbi.nlm.nih.gov/pubmed/16451854
http://dx.doi.org/10.1289/ehp.8391
_version_ 1782126753868677120
author Lilienthal, Hellmuth
Hack, Alfons
Roth-Härer, Astrid
Grande, Simone Wichert
Talsness, Chris E.
author_facet Lilienthal, Hellmuth
Hack, Alfons
Roth-Härer, Astrid
Grande, Simone Wichert
Talsness, Chris E.
author_sort Lilienthal, Hellmuth
collection PubMed
description Increasing concentrations of polybrominated flame retardants, including polybrominated diphenyl ethers (PBDEs), in breast milk cause concern about possible developmental effects in nursed babies. Because previous studies in rats have indicated effects on sex steroids and sexually dimorphic behavior after maternal exposure to polychlorinated biphenyls (PCBs), our goal in the present study was to determine if developmental exposure to 2,2′,4,4′,5-pentabromodiphenyl ether (PBDE-99) induces similar endocrine-mediated effects. Pregnant rats were exposed to vehicle or PBDE-99 (1 or 10 mg/kg body weight, daily during gestational days 10–18). For comparison, we also included a group exposed to the technical PCB mixture Aroclor 1254 (30 mg/kg body weight, daily). PBDE exposure resulted in pronounced decreases in circulating sex steroids in male offspring at weaning and in adulthood. Female offspring were less affected. Anogenital distance was reduced in male offspring. Puberty onset was delayed in female offspring at the higher dose level, whereas a slight acceleration was detected in low-dose males. The number of primordial/primary ovarian follicles was reduced in females at the lower dose, whereas decline of secondary follicles was more pronounced at the higher dose. Sweet preference was dose-dependently increased in PBDE-exposed adult males, indicating a feminization of this sexually dimorphic behavior. Aroclor 1254 did not alter sweet preference and numbers of primordial/primary and secondary follicles but it did affect steroid concentrations in males and sexual development in both sexes. PBDE concentrations in tissues of dams and offspring were highest on gestational day 19. These results support the hypothesis that PBDEs are endocrine-active compounds and interfere with sexual development and sexually dimorphic behavior.
format Text
id pubmed-1367831
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher National Institute of Environmental Health Sciences
record_format MEDLINE/PubMed
spelling pubmed-13678312006-02-22 Effects of Developmental Exposure to 2,2′,4,4′,5-Pentabromodiphenyl Ether (PBDE-99) on Sex Steroids, Sexual Development, and Sexually Dimorphic Behavior in Rats Lilienthal, Hellmuth Hack, Alfons Roth-Härer, Astrid Grande, Simone Wichert Talsness, Chris E. Environ Health Perspect Research Increasing concentrations of polybrominated flame retardants, including polybrominated diphenyl ethers (PBDEs), in breast milk cause concern about possible developmental effects in nursed babies. Because previous studies in rats have indicated effects on sex steroids and sexually dimorphic behavior after maternal exposure to polychlorinated biphenyls (PCBs), our goal in the present study was to determine if developmental exposure to 2,2′,4,4′,5-pentabromodiphenyl ether (PBDE-99) induces similar endocrine-mediated effects. Pregnant rats were exposed to vehicle or PBDE-99 (1 or 10 mg/kg body weight, daily during gestational days 10–18). For comparison, we also included a group exposed to the technical PCB mixture Aroclor 1254 (30 mg/kg body weight, daily). PBDE exposure resulted in pronounced decreases in circulating sex steroids in male offspring at weaning and in adulthood. Female offspring were less affected. Anogenital distance was reduced in male offspring. Puberty onset was delayed in female offspring at the higher dose level, whereas a slight acceleration was detected in low-dose males. The number of primordial/primary ovarian follicles was reduced in females at the lower dose, whereas decline of secondary follicles was more pronounced at the higher dose. Sweet preference was dose-dependently increased in PBDE-exposed adult males, indicating a feminization of this sexually dimorphic behavior. Aroclor 1254 did not alter sweet preference and numbers of primordial/primary and secondary follicles but it did affect steroid concentrations in males and sexual development in both sexes. PBDE concentrations in tissues of dams and offspring were highest on gestational day 19. These results support the hypothesis that PBDEs are endocrine-active compounds and interfere with sexual development and sexually dimorphic behavior. National Institute of Environmental Health Sciences 2006-02 2005-10-06 /pmc/articles/PMC1367831/ /pubmed/16451854 http://dx.doi.org/10.1289/ehp.8391 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Lilienthal, Hellmuth
Hack, Alfons
Roth-Härer, Astrid
Grande, Simone Wichert
Talsness, Chris E.
Effects of Developmental Exposure to 2,2′,4,4′,5-Pentabromodiphenyl Ether (PBDE-99) on Sex Steroids, Sexual Development, and Sexually Dimorphic Behavior in Rats
title Effects of Developmental Exposure to 2,2′,4,4′,5-Pentabromodiphenyl Ether (PBDE-99) on Sex Steroids, Sexual Development, and Sexually Dimorphic Behavior in Rats
title_full Effects of Developmental Exposure to 2,2′,4,4′,5-Pentabromodiphenyl Ether (PBDE-99) on Sex Steroids, Sexual Development, and Sexually Dimorphic Behavior in Rats
title_fullStr Effects of Developmental Exposure to 2,2′,4,4′,5-Pentabromodiphenyl Ether (PBDE-99) on Sex Steroids, Sexual Development, and Sexually Dimorphic Behavior in Rats
title_full_unstemmed Effects of Developmental Exposure to 2,2′,4,4′,5-Pentabromodiphenyl Ether (PBDE-99) on Sex Steroids, Sexual Development, and Sexually Dimorphic Behavior in Rats
title_short Effects of Developmental Exposure to 2,2′,4,4′,5-Pentabromodiphenyl Ether (PBDE-99) on Sex Steroids, Sexual Development, and Sexually Dimorphic Behavior in Rats
title_sort effects of developmental exposure to 2,2′,4,4′,5-pentabromodiphenyl ether (pbde-99) on sex steroids, sexual development, and sexually dimorphic behavior in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1367831/
https://www.ncbi.nlm.nih.gov/pubmed/16451854
http://dx.doi.org/10.1289/ehp.8391
work_keys_str_mv AT lilienthalhellmuth effectsofdevelopmentalexposureto22445pentabromodiphenyletherpbde99onsexsteroidssexualdevelopmentandsexuallydimorphicbehaviorinrats
AT hackalfons effectsofdevelopmentalexposureto22445pentabromodiphenyletherpbde99onsexsteroidssexualdevelopmentandsexuallydimorphicbehaviorinrats
AT rothharerastrid effectsofdevelopmentalexposureto22445pentabromodiphenyletherpbde99onsexsteroidssexualdevelopmentandsexuallydimorphicbehaviorinrats
AT grandesimonewichert effectsofdevelopmentalexposureto22445pentabromodiphenyletherpbde99onsexsteroidssexualdevelopmentandsexuallydimorphicbehaviorinrats
AT talsnesschrise effectsofdevelopmentalexposureto22445pentabromodiphenyletherpbde99onsexsteroidssexualdevelopmentandsexuallydimorphicbehaviorinrats