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Abstract
Developmental exposure to estrogenic chemicals induces
morphological, functional and behavioral anomalies
associated with reproduction. Humans are routinely exposed
to bisphenol-A (BPA), an estrogenic compound that leaches
from dental materials and plastic food and beverage
containers. The aim of the present study was to determine
the effects of in utero exposure to low, environmentally
relevant doses of BPA on the development of female
reproductive tissues in CD-1 mice. In previous
publications, we have shown that this treatment alters the
morphology of the mammary gland and affects estrous
cyclicity. Here we report that in utero exposure to 25 and
250 ng BPA/kg body weight/day via osmotic pumps implanted
into pregnant dams at gestational day 9 induces
alterations in the genital tract of female offspring that
are revealed during adulthood. They include: decreased wet
weight of the vagina, decreased volume of the endometrial
lamina propria, increased incorporation of
bromodeoxyuridine into the DNA of endometrial gland
epithelial cells, and increased expression of estrogen
receptor-
(ER
) and progesterone receptor
in the luminal
epithelium of the endometrium and subepithelial stroma.
Since ER
is known to be expressed in these
estrogen-target organs at the time of BPA exposure, it is
plausible that BPA may directly affect the expression of
ER controlled genes involved in the morphogenesis of these
organs. In addition, BPA-induced alterations that
specifically affect hypothalamic-pituitary-gonadal axis
function may further contribute to the anomalies observed
at three months of age, long after the cessation of BPA
exposure.
Key words:
Environment
Toxicology
Early development
Estradiol receptor
Progesterone receptor
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