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No threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much?

Risk assessments for nongenotoxic chemicals assume a threshold below which no adverse outcomes are seen. However, when an endogenous chemical, such as 17ss-estradiol (E2), occurs at a concentration sufficient to cause an effect, the threshold is already exceeded. Under these circumstances, exogenous...

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Detalles Bibliográficos
Autores principales: Sheehan, D M, Willingham, E, Gaylor, D, Bergeron, J M, Crews, D
Formato: Texto
Lenguaje:English
Publicado: 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566346/
https://www.ncbi.nlm.nih.gov/pubmed/9924012
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author Sheehan, D M
Willingham, E
Gaylor, D
Bergeron, J M
Crews, D
author_facet Sheehan, D M
Willingham, E
Gaylor, D
Bergeron, J M
Crews, D
author_sort Sheehan, D M
collection PubMed
description Risk assessments for nongenotoxic chemicals assume a threshold below which no adverse outcomes are seen. However, when an endogenous chemical, such as 17ss-estradiol (E2), occurs at a concentration sufficient to cause an effect, the threshold is already exceeded. Under these circumstances, exogenous estradiol is not expected to provide a threshold dose. This principle is demonstrated for E2 in the red-eared slider, a turtle with temperature-dependent sex determination. In this species, gonadal sex is determined by egg incubation temperature; female development requires endogenous estrogen produced by elevated temperature. While normal production of females by endogenous estrogens is not an adverse effect, exogenous estrogens can sex reverse presumptive males, which can be an adverse effect. A large dose-response study was conducted using seven doses and a vehicle control (starting n = 300/group); a single E2 dose was applied to the eggshell of recently laid eggs. Animals were sexed after hatching. The incubation temperature chosen, 28.6 degrees C, generates a minority of females. Thus, the criteria for testing the threshold hypothesis were met, i.e., there is evidence that there is endogenous estrogen and that it generates an irreversible response. The lowest E2 dose tested, 400 pg/egg (40 ng/kg), sex reversed 14.4% of the animals, demonstrating very low dose sensitivity. The data were fit with a modified Michaelis-Menten equation, which provided an estimate of 1.7 ng/egg for endogenous estradiol. The median effective dose (ED50) was 5.0 +/- 2.0 ng/egg (95% confidence limits), of which 1.7 ng/egg was endogenous estradiol and 3.3 ng/egg came from the applied estradiol. There was no apparent threshold dose for E2. A smaller replication confirmed these results. These results provide a simple biologically based dose-response model and suggest that chemicals which act mechanistically like E2 may also show no threshold dose. If so, even low environmental concentrations of such chemicals may carry risk for sex reversal.
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spelling pubmed-15663462006-09-19 No threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much? Sheehan, D M Willingham, E Gaylor, D Bergeron, J M Crews, D Environ Health Perspect Research Article Risk assessments for nongenotoxic chemicals assume a threshold below which no adverse outcomes are seen. However, when an endogenous chemical, such as 17ss-estradiol (E2), occurs at a concentration sufficient to cause an effect, the threshold is already exceeded. Under these circumstances, exogenous estradiol is not expected to provide a threshold dose. This principle is demonstrated for E2 in the red-eared slider, a turtle with temperature-dependent sex determination. In this species, gonadal sex is determined by egg incubation temperature; female development requires endogenous estrogen produced by elevated temperature. While normal production of females by endogenous estrogens is not an adverse effect, exogenous estrogens can sex reverse presumptive males, which can be an adverse effect. A large dose-response study was conducted using seven doses and a vehicle control (starting n = 300/group); a single E2 dose was applied to the eggshell of recently laid eggs. Animals were sexed after hatching. The incubation temperature chosen, 28.6 degrees C, generates a minority of females. Thus, the criteria for testing the threshold hypothesis were met, i.e., there is evidence that there is endogenous estrogen and that it generates an irreversible response. The lowest E2 dose tested, 400 pg/egg (40 ng/kg), sex reversed 14.4% of the animals, demonstrating very low dose sensitivity. The data were fit with a modified Michaelis-Menten equation, which provided an estimate of 1.7 ng/egg for endogenous estradiol. The median effective dose (ED50) was 5.0 +/- 2.0 ng/egg (95% confidence limits), of which 1.7 ng/egg was endogenous estradiol and 3.3 ng/egg came from the applied estradiol. There was no apparent threshold dose for E2. A smaller replication confirmed these results. These results provide a simple biologically based dose-response model and suggest that chemicals which act mechanistically like E2 may also show no threshold dose. If so, even low environmental concentrations of such chemicals may carry risk for sex reversal. 1999-02 /pmc/articles/PMC1566346/ /pubmed/9924012 Text en
spellingShingle Research Article
Sheehan, D M
Willingham, E
Gaylor, D
Bergeron, J M
Crews, D
No threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much?
title No threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much?
title_full No threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much?
title_fullStr No threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much?
title_full_unstemmed No threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much?
title_short No threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much?
title_sort no threshold dose for estradiol-induced sex reversal of turtle embryos: how little is too much?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566346/
https://www.ncbi.nlm.nih.gov/pubmed/9924012
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