Cargando…

Gestational and Chronic Low-Dose PFOA Exposures and Mammary Gland Growth and Differentiation in Three Generations of CD-1 Mice

Background: Prenatal exposure to perfluorooctanoic acid (PFOA), a ubiquitous industrial surfactant, has been reported to delay mammary gland development in female mouse offspring (F(1)) and the treated lactating dam (P(0)) after gestational treatments at 3 and 5 mg PFOA/kg/day. Objective: We investi...

Descripción completa

Detalles Bibliográficos
Autores principales: White, Sally S., Stanko, Jason P., Kato, Kayoko, Calafat, Antonia M., Hines, Erin P., Fenton, Suzanne E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237341/
https://www.ncbi.nlm.nih.gov/pubmed/21501981
http://dx.doi.org/10.1289/ehp.1002741
_version_ 1782218875921760256
author White, Sally S.
Stanko, Jason P.
Kato, Kayoko
Calafat, Antonia M.
Hines, Erin P.
Fenton, Suzanne E.
author_facet White, Sally S.
Stanko, Jason P.
Kato, Kayoko
Calafat, Antonia M.
Hines, Erin P.
Fenton, Suzanne E.
author_sort White, Sally S.
collection PubMed
description Background: Prenatal exposure to perfluorooctanoic acid (PFOA), a ubiquitous industrial surfactant, has been reported to delay mammary gland development in female mouse offspring (F(1)) and the treated lactating dam (P(0)) after gestational treatments at 3 and 5 mg PFOA/kg/day. Objective: We investigated the consequences of gestational and chronic PFOA exposure on F(1) lactational function and subsequent development of F(2) offspring. Methods: We treated P(0) dams with 0, 1, or 5 mg PFOA/kg/day on gestation days 1–17. In addition, a second group of P(0) dams treated with 0 or 1 mg/kg/day during gestation and their F(1) and F(2) offspring received continuous PFOA exposure (5 ppb) in drinking water. Resulting adult F(1) females were bred to generate F(2) offspring, whose development was monitored over postnatal days (PNDs) 1–63. F(1) gland function was assessed on PND10 by timed-lactation experiments. Mammary tissue was isolated from P(0), F(1), and F(2) females throughout the study and histologically assessed for age-appropriate development. Results: PFOA-exposed F(1) dams exhibited diminished lactational morphology, although F(1) maternal behavior and F(2) offspring body weights were not significantly affected by P(0) treatment. In addition to reduced gland development in F(1) females under all exposures, F(2) females with chronic low-dose drinking-water exposures exhibited visibly slowed mammary gland differentiation from weaning onward. F(2) females derived from 5 mg/kg PFOA-treated P(0) dams displayed gland morphology similar to F(2) chronic water exposure groups on PNDs 22–63. Conclusions: Gestational PFOA exposure induced delays in mammary gland development and/or lactational differentiation across three generations. Chronic, low-dose PFOA exposure in drinking water was also sufficient to alter mammary morphological development in mice, at concentrations approximating those found in contaminated human water supplies.
format Online
Article
Text
id pubmed-3237341
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher National Institute of Environmental Health Sciences
record_format MEDLINE/PubMed
spelling pubmed-32373412011-12-15 Gestational and Chronic Low-Dose PFOA Exposures and Mammary Gland Growth and Differentiation in Three Generations of CD-1 Mice White, Sally S. Stanko, Jason P. Kato, Kayoko Calafat, Antonia M. Hines, Erin P. Fenton, Suzanne E. Environ Health Perspect Research Background: Prenatal exposure to perfluorooctanoic acid (PFOA), a ubiquitous industrial surfactant, has been reported to delay mammary gland development in female mouse offspring (F(1)) and the treated lactating dam (P(0)) after gestational treatments at 3 and 5 mg PFOA/kg/day. Objective: We investigated the consequences of gestational and chronic PFOA exposure on F(1) lactational function and subsequent development of F(2) offspring. Methods: We treated P(0) dams with 0, 1, or 5 mg PFOA/kg/day on gestation days 1–17. In addition, a second group of P(0) dams treated with 0 or 1 mg/kg/day during gestation and their F(1) and F(2) offspring received continuous PFOA exposure (5 ppb) in drinking water. Resulting adult F(1) females were bred to generate F(2) offspring, whose development was monitored over postnatal days (PNDs) 1–63. F(1) gland function was assessed on PND10 by timed-lactation experiments. Mammary tissue was isolated from P(0), F(1), and F(2) females throughout the study and histologically assessed for age-appropriate development. Results: PFOA-exposed F(1) dams exhibited diminished lactational morphology, although F(1) maternal behavior and F(2) offspring body weights were not significantly affected by P(0) treatment. In addition to reduced gland development in F(1) females under all exposures, F(2) females with chronic low-dose drinking-water exposures exhibited visibly slowed mammary gland differentiation from weaning onward. F(2) females derived from 5 mg/kg PFOA-treated P(0) dams displayed gland morphology similar to F(2) chronic water exposure groups on PNDs 22–63. Conclusions: Gestational PFOA exposure induced delays in mammary gland development and/or lactational differentiation across three generations. Chronic, low-dose PFOA exposure in drinking water was also sufficient to alter mammary morphological development in mice, at concentrations approximating those found in contaminated human water supplies. National Institute of Environmental Health Sciences 2011-04-18 2011-08 /pmc/articles/PMC3237341/ /pubmed/21501981 http://dx.doi.org/10.1289/ehp.1002741 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
White, Sally S.
Stanko, Jason P.
Kato, Kayoko
Calafat, Antonia M.
Hines, Erin P.
Fenton, Suzanne E.
Gestational and Chronic Low-Dose PFOA Exposures and Mammary Gland Growth and Differentiation in Three Generations of CD-1 Mice
title Gestational and Chronic Low-Dose PFOA Exposures and Mammary Gland Growth and Differentiation in Three Generations of CD-1 Mice
title_full Gestational and Chronic Low-Dose PFOA Exposures and Mammary Gland Growth and Differentiation in Three Generations of CD-1 Mice
title_fullStr Gestational and Chronic Low-Dose PFOA Exposures and Mammary Gland Growth and Differentiation in Three Generations of CD-1 Mice
title_full_unstemmed Gestational and Chronic Low-Dose PFOA Exposures and Mammary Gland Growth and Differentiation in Three Generations of CD-1 Mice
title_short Gestational and Chronic Low-Dose PFOA Exposures and Mammary Gland Growth and Differentiation in Three Generations of CD-1 Mice
title_sort gestational and chronic low-dose pfoa exposures and mammary gland growth and differentiation in three generations of cd-1 mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237341/
https://www.ncbi.nlm.nih.gov/pubmed/21501981
http://dx.doi.org/10.1289/ehp.1002741
work_keys_str_mv AT whitesallys gestationalandchroniclowdosepfoaexposuresandmammaryglandgrowthanddifferentiationinthreegenerationsofcd1mice
AT stankojasonp gestationalandchroniclowdosepfoaexposuresandmammaryglandgrowthanddifferentiationinthreegenerationsofcd1mice
AT katokayoko gestationalandchroniclowdosepfoaexposuresandmammaryglandgrowthanddifferentiationinthreegenerationsofcd1mice
AT calafatantoniam gestationalandchroniclowdosepfoaexposuresandmammaryglandgrowthanddifferentiationinthreegenerationsofcd1mice
AT hineserinp gestationalandchroniclowdosepfoaexposuresandmammaryglandgrowthanddifferentiationinthreegenerationsofcd1mice
AT fentonsuzannee gestationalandchroniclowdosepfoaexposuresandmammaryglandgrowthanddifferentiationinthreegenerationsofcd1mice