Literature DB >> 17190974

Gestational exposure to nonylphenol causes precocious mammary gland development in female rat offspring.

Hyun Ju Moon1, Soon Young Han, Jae-Ho Shin, Il Hyun Kang, Tae Sung Kim, Jin Hwan Hong, Seung-Hee Kim, Suzanne E Fenton.   

Abstract

This study examined whether or not exposure to 4-nonylphenol (NP) during late gestation affects reproductive and mammary development in the offspring of female rats. Time pregnant Long Evans rats were gavaged with NP (10 or 100 mg/kg), atrazine (ATR, 100 mg/kg), or corn oil on gestation days 15-19. The uterus weights of the NP (100 mg/kg/d)-exposed pups were higher than those of the controls but the weights of the other organs were unchanged. Delayed mammary gland (MG) development was detected in the ATR pups on PND 4 and persisted through to PND 66. The high dose NP pups had advanced lobular development of their MG on PND 22, while the glands from the low dose NP pups were no different morphologically from the controls. Immunohistochemical comparisons of the mammary sections from PND 41 demonstrated low levels of estrogen receptor (ER) staining in the control gland stroma and epithelium but higher levels in the tissue of the pups exposed to NP and ATR. ATR also elevated ER in the stroma surrounding the epithelial layer of the terminal end buds. The level of progesterone receptor (PR) staining was markedly lower in the epithelium of the 100 mg/kg NP glands vs. the control glands. However, PR was present at high levels in the epithelium of the 10 mg/kg NP glands and was even more prominent in the ATR-exposed ductal epithelium and fat cell nuclei. The level of prolactin staining was only elevated in glands containing lobule areas (NP-exposed) compared with the control levels. These results suggest that NP and ATR have opposite effects on the development of MG after gestational exposure. Exposure to them during the critical period of epithelial outgrowth altered the receptor levels of mammary progesterone and prolactin and might contribute to the differences in the mammary morphology at PND 41.

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Year:  2006        PMID: 17190974     DOI: 10.1262/jrd.18055

Source DB:  PubMed          Journal:  J Reprod Dev        ISSN: 0916-8818            Impact factor:   2.214


  11 in total

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4.  Self-reported chemicals exposure, beliefs about disease causation, and risk of breast cancer in the Cape Cod Breast Cancer and Environment Study: a case-control study.

Authors:  Ami R Zota; Ann Aschengrau; Ruthann A Rudel; Julia Green Brody
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Review 5.  The epigenetic lorax: gene-environment interactions in human health.

Authors:  Keith E Latham; Carmen Sapienza; Nora Engel
Journal:  Epigenomics       Date:  2012-08       Impact factor: 4.778

6.  The mammary gland: a tissue sensitive to environmental exposures.

Authors:  Suzanne E Fenton
Journal:  Rev Environ Health       Date:  2009 Oct-Dec       Impact factor: 3.458

7.  Combinations of physiologic estrogens with xenoestrogens alter ERK phosphorylation profiles in rat pituitary cells.

Authors:  Yow-Jiun Jeng; Cheryl S Watson
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Review 8.  Environmental exposures and mammary gland development: state of the science, public health implications, and research recommendations.

Authors:  Ruthann A Rudel; Suzanne E Fenton; Janet M Ackerman; Susan Y Euling; Susan L Makris
Journal:  Environ Health Perspect       Date:  2011-06-22       Impact factor: 9.031

9.  Alkylphenol xenoestrogens with varying carbon chain lengths differentially and potently activate signaling and functional responses in GH3/B6/F10 somatomammotropes.

Authors:  Mikhail Y Kochukov; Yow-Jiun Jeng; Cheryl S Watson
Journal:  Environ Health Perspect       Date:  2008-12-31       Impact factor: 9.031

10.  Exogenous hormonal regulation in breast cancer cells by phytoestrogens and endocrine disruptors.

Authors:  A Albini; C Rosano; G Angelini; A Amaro; A I Esposito; S Maramotti; D M Noonan; U Pfeffer
Journal:  Curr Med Chem       Date:  2014       Impact factor: 4.530

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