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The Great Endocrine Disruptor: How Bisphenol A Influences Sexual Development and Behavior
Melissa-Marie Marks
Browsing many grocery and department stores today, one will find quite a few plastic
products labeled “Bisphenol-A Free” or “BPA Free”. On television and commercials, there are
advertisements exclaiming the wonders of a new plastic toy that is safe for children because it
does not contain harmful BPA. But despite the “BPA Free” campaign, most consumers still
have no idea what Bisphenol-A actually is, where it is found, and what it does to the
environment and the human body. Due to numerous government-funded studies declaring the
potential danger of BPA, it has been banned from baby products in Canada, Japan, Denmark, and
France, but only a handful of states in the US have followed suit. In order for a world-wide ban
on the estrogen-mimic BPA to be enacted, it is more important now than ever to inform the
What is Bisphenol-A?
now, has been one of the highest-volume chemicals in worldwide production; it has an annual
production capacity in excess of six-billion pounds (vom Saal et al 2006). According to the
polycarbonate plastics and epoxy resins.” BPA is found in the linings of food cans, dental
sealants, polyvinyl chloride plastic products (such as shower curtain liners and vinyl pool toys),
polycarbonate plastic products (such as plastic children’s toys, baby formula bottles, and sports
bottles) (vom Saal et al 2006), and also in thermal printer paper taking the form of cash register
THE GREAT ENDOCRINE DISRUPTOR: HOW BISPHENOL A INFLUENCES SEXUAL DEVELOPMENT AND BEHAVIOR 3
receipts (Biedermann 2010). Unless a plastic product is specifically labeled “BPA Free” or
The ester bonds in BPA-based polymers are subject to hydrolysis and, therefore, BPA
leaches into food and drinks from their storage containers. Heat and/or acids speed up the
leaching process, and “repeated washing of polycarbonate products have all been shown to result
in an increase in the rate of leaching of BPA” (vom Saal et al 2005). Drinking and bathing water
are another potential source of human exposure, and studies conducted in Japan and the US have
shown that BPA leaches from landfills into the surrounding ecosystem (vom Saal et al 2005).
Unborn fetuses are exposed to BPA through their mothers’ contact with the chemical.
Measurable amounts of BPA have been found in the human umbilical cord (Kubo et al 2003),
amniotic fluid, maternal and fetal plasma, and placental tissue at birth. BPA has also been found
The safe or reference dose of BPA for human exposure is 50 µg/kg/day. However, over
30 publications utilizing vertebrate and invertebrate animal studies state that “significant effects
occurred below the predicted ‘safe’ or reference dose…” How do these animal studies pertain to
humans? Recent reports state that the median BPA level in human blood (including fetal blood)
and tissues is actually higher than the level that causes harmful effects in mice. Indeed, “…rate
of growth and sexual maturation, hormone levels in blood, reproductive organ function, fertility,
immune function, enzyme activity, brain structure, brain chemistry, and behavior are all affected
One study conducted in the United States on 394 humans found that BPA was present in
the urine of 95% of the population. These findings were similar to those observed in other
human populations (Calafat et al 2005). A similar study was later conducted on 1,469 humans to
see how quickly BPA was cleared from the body, under the hypothesis that BPA levels in the
urine of fasting humans should decrease with increased fasting time. The findings of these
studies showed that BPA levels did not decrease with increased fasting time, suggesting that
either there was a substantial nonfood exposure to BPA, it accumulated in body fat, or both
(Stahlhut et al 2009).
doses results in morphological and functional alterations of the male and female genital tract and
mammary glands that may predispose the tissue to earlier onset of disease, reduced fertility, and
In one study conducted in 1999, female mice were exposed prenatally to low doses of
BPA and subsequently displayed first estrus (sexual maturity) at a significantly earlier age than
mice that were not exposed. Female mice exposed to environmentally relevant doses of BPA
also displayed morphological and functional alterations in their reproductive tracts including
decreased weight of the vagina and endometrial lamina propria and increased proliferation of
In two separate studies involving female mice, Bisphenol-A was found to cause meiotic
aneuploidy, or an abnormal amount of chromosomes in oocytes (germ cells that turn into eggs or
THE GREAT ENDOCRINE DISRUPTOR: HOW BISPHENOL A INFLUENCES SEXUAL DEVELOPMENT AND BEHAVIOR 5
ovums when fertilized) (Hunt et al 2003 and Susiarjo et al 2007). About 40-70% of spontaneous
abortions in humans are linked to aneuploidy, and according to a study involving 77 human
women, 45 of whom had a history of three or more consecutive first-trimester miscarriages and
32 of whom had no history of live birth or infertility, Bisphenol-A levels were significantly
2005).
When female mice pregnant with male fetuses were exposed to levels of BPA at doses
below the range of exposure by pregnant human women, their male offspring showed increased
prostate size and malformations of the urethra, specifically constriction where it enters the
Male germ cells are also at risk of harmful effects due to BPA exposure. At an infertility
clinic in Boston, urine and semen samples were collected from 190 human males. 89% of these
men had measurable amounts of BPA in their urine, and those with the highest levels were more
likely to produce sperm with decreased motility and morphology and increased sperm DNA
to low levels of BPA from day 8 of pregnancy through day 16 of lactation resulted in permanent
effects on the brains of the offspring, including demasculinization of males and defeminization
of females. Sex differences (of behavior) observed in control groups of mice were not observed
in the offspring of the BPA-exposed mothers. The study concluded “These data indicate that
THE GREAT ENDOCRINE DISRUPTOR: HOW BISPHENOL A INFLUENCES SEXUAL DEVELOPMENT AND BEHAVIOR 6
BPA may be capable of altering important events during critical periods of brain development.”
(Rubin et al 2006).
Though there have been over 100 government-funded studies done indicating the harmful
effects of BPA, no industry-funded studies have shown statistically significant harm to humans
from exposure to BPA. BPA is used extensively worldwide in the production of thousands of
different products that are in great demand by consumers. Until a substitute of equal or cheaper
value is put on the market, it can be hypothesized that there will never be any industry-funded
studies showing the great dangers of BPA, and therefore BPA will continue to be in production.
For now, consumers and parents can take small steps towards reducing their exposure to
• Use glass, ceramic, or stainless steel drinking bottles, storage containers, dishes, and
cutlery instead of plastic. If you must use plastic, be sure to avoid #7 plastics, and avoid
• Reduce or eliminate the consumption of canned foods or choose canned foods packaged
in cans that do not contain BPA (such as the brand “Eden Organics”).
• Reduce exposure to cash register receipts and when you must handle them, wash hands
• Buy wooden or cloth toys for your children, or make sure that the plastic toys you buy do
• Breastfeed. All liquid infant formula and some powdered infant formula cans are lined
• Before getting dental sealants or fillings, make sure your dentist does not use products
• Become an activist. Write to your local, state, and federal government officials and tell
them about your concern over the harmful effects of BPA. Ask them to work toward
legislation to ban BPA from all products that can leach the chemical into food and drinks.
Write to your favorite canned good and/or storage container companies and ask them to
people stop demanding harmful products, companies will stop supplying them.
THE GREAT ENDOCRINE DISRUPTOR: HOW BISPHENOL A INFLUENCES SEXUAL DEVELOPMENT AND BEHAVIOR 8
References
Biedermann, S., et al. (2010). Transfer of Bisphenol A from thermal printer paper to the skin.
Correspondence. (2007). Chapel Hill bisphenol A expert panel consensus statement: Integration
of mechanisms, effects in animals and potential to impact human health at current levels
Hunt, P.A., et al. (2003). Bisphenol A exposure causes meiotic aneuploidy in the female mouse.
Kubo, K., et al. (2003). Low dose effects of bisphenol A on sexual differentiation of the brain
Maffini, M.V., et al. (2006). Endocrine disruptors and reproductive health: The case of
Meeker, J.D., et al. (2010). Semen quality and sperm DNA damage in relation to urinary
Murray, T.J., et al. (2007). Induction of mammary gland ductal hyperplasias and carcinoma in
Newbold, R.R., et al. (2007). Long-term adverse effects of neonatal exposure to Bisphenol A on
Rubin, B.S., et al. (2006). Evidence of altered brain sexual differentiation in mice exposed
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Sharpe, R.M. (2010). Is it time to end concerns over the estrogenic effects of bisphenol A.
Stahlhut, R.W., et al. (2009). Bisphenol A data in NHANES suggest longer than expected half-
784-789.
Susiarjo, M., et al. (2007). Bisphenol A exposure in utero disrupts early oogenesis in the mouse.
Timms, B.G., et al. (2005). Estrogenic chemicals in plastic and oral contraceptives disrupt
development of the fetal mouse prostate and urethra. PNAS, 102(19), 7014-7019.
148(1): 1-24.
THE GREAT ENDOCRINE DISRUPTOR: HOW BISPHENOL A INFLUENCES SEXUAL DEVELOPMENT AND BEHAVIOR 10
Vom Saal, F.S. & Hughes, C. (2005). An extensive new literature concerning low-dose effects of
bisphenol A shows the need for a new risk assessment. Environmental Health
Vom Saal, F.S. & Welshons, W.V. (2006). Large effects from small exposures. II. The