Abstract:Endocrine disruptors and their possible impact on human and animal health have become a topic of discussion and an area of active research in toxicology. A focus has been on xenoestrogens, i.e., environmental chemicals with estrogenic activity. In principle, there is agreement that such compounds, in high doses, may cause developmental, reproductive and tumorigenic effects ("hazard"). A matter of controversy is the question of risks associated with xenoestrogens under realistic (low) exposure scenarios; this i… Show more
“…Based upon numerous previous studies, xenoestrogens, also called "environmental estrogens or hormones" or "Endocrine Disrupting Compounds (EDC)", are considered as serious environmental hazards that have hormone disruptive effects on human and wildlife health [5,6]. Studies have found that fetuses and young children exposed to BPA are at risk for secondary sexual developmental changes, brain and behavior changes and immune disorders [7].…”
Section: Environmental Estrogen-biphenol a (Bpa)mentioning
“…Based upon numerous previous studies, xenoestrogens, also called "environmental estrogens or hormones" or "Endocrine Disrupting Compounds (EDC)", are considered as serious environmental hazards that have hormone disruptive effects on human and wildlife health [5,6]. Studies have found that fetuses and young children exposed to BPA are at risk for secondary sexual developmental changes, brain and behavior changes and immune disorders [7].…”
Section: Environmental Estrogen-biphenol a (Bpa)mentioning
“…The availability of funds in areas of political preference may have a higher impact on the choice of a particular research field than scientific considerations. A now classical example for such a development is the global wave of publications on ''endocrine disruptors'' (Degen and Bolt 2000).…”
“…Xenoestrogens as environmental contaminants have sparked much debate as a public health concern, because significant levels are present in the environment (Degen and Bolt, 2000). The industrial chemical bisphenol A (BPA; used to make polycarbonate plastics and epoxy resins), naturally occurring plant estrogens (e.g., zearalenone), and the potent synthetic pharmaceutical estrogen diethylstilbestrol (DES) are some examples of the more prevalent environmental xenoestrogens of toxicological interest (Degen and Bolt, 2000;Juberg, 2000;Safe, 2000).…”
mentioning
confidence: 99%
“…The industrial chemical bisphenol A (BPA; used to make polycarbonate plastics and epoxy resins), naturally occurring plant estrogens (e.g., zearalenone), and the potent synthetic pharmaceutical estrogen diethylstilbestrol (DES) are some examples of the more prevalent environmental xenoestrogens of toxicological interest (Degen and Bolt, 2000;Juberg, 2000;Safe, 2000). Although the potential hazard to human health from exposure to environmental xenoestrogens has not been conclusively determined (Degen and Bolt, 2000;Juberg, 2000;Safe, 2000), significant reproductive and associated anomalies in wildlife have been attributed to their exposure to xenoestrogens (Juberg, 2000), raising a significant health concern for humans.…”
mentioning
confidence: 99%
“…Much of the focus on xenoestrogens has been on the disruption of reproductive function (Degen and Bolt, 2000;Juberg, 2000;Safe, 2000). However, as noted above, sex hormones also have well documented physiological effects on nonreproductive tissues such as the kidney, which contain receptors for both testosterone and estrogen (DeVries et al, 1972;Stefani et al, 1994).…”
The sex steroid hormone estrogen down-regulates renal organic cation (OC) transport in animals, and it may contribute to sex-related differences in xenobiotic accumulation and excretion. Also, the presence of various endocrine-disrupting chemicals, i.e., environmental chemicals that possess estrogenic activity (e.g., xenoestrogens) may down-regulate various transporters involved in renal accumulation and excretion of xenobiotics. The present study characterizes the mechanism by which long-term (6-day) incubation with physiological concentrations of 17-estradiol (E 2 ) or the xenoestrogens diethylstilbestrol (DES) and bisphenol A (BPA) regulates the basolateral membrane transport of the OC tetraethylammonium (TEA) in opossum kidney (OK) cell renal cultures. Both 17-E 2 and the xenoestrogen DES produced a dose-and time-dependent inhibition of basolateral TEA uptake in OK cell cultures, whereas the weakly estrogenic BPA had no effect on TEA uptake. Treatment for 6 days with either 1 nM 17-E 2 or DES reduced TEA uptake by ϳ30 and 40%, respectively. These effects were blocked completely by the estrogen receptor antagonist ICI 182780 (Faslodex, fulvestrant), suggesting that these estrogens regulate OC transport through the estrogen receptor, which was detected (estrogen receptor ␣) in OK cell cultures by reverse transcription-polymerase chain reaction. The J max value for TEA uptake in 17-E 2 -and DES-treated OK cell cultures was ϳ40 to 50% lower than for ethanol-treated cultures, whereas K t was unaffected. This reduction in transport capacity was correlated with a reduction in OC transporter OCT1 protein expression following treatment with both agents.
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