Dm. Sheehan et al., No threshold dose for estradiol-induced sex reversal of turtle embryos: How little is too much?, ENVIR H PER, 107(2), 1999, pp. 155-159
Risk assessments for nongenotoxic chemicals assume a threshold below which
no adverse outcomes are seen. However, when an endogenous chemical, such as
17 beta-estradiol (E-2), occurs at a concentration sufficient to cause an
effect, the threshold is already exceeded. Under these circumstances, exoge
nous estradiol is not expected to provide a threshold dose. This principle
is demonstrated for E-2 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 en
dogenous estrogens is not an adverse effect, exogenous estrogens can sex re
verse presumptive males, which can be an adverse effect. A large dose-respo
nse study was conducted using seven doses and a vehicle control (starting n
= 300/group); a single E-2 dose was applied to the eggshell of recently la
id eggs. Animals were sexed after hatching. The incubation temperature chos
en, 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 th
ere is endogenous estrogen and that it generates an irreversible response.
The lowest E-2 dose tested, 400 pg/egg (40 ng/kg), sex reversed 14.4% of th
e 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 (35% confidence limits), of which 1.7 ng/egg was endogenous estr
adiol and 3.3 ng/egg came from the applied estradiol. There was no apparent
threshold dose for E-2. A smaller replication confirmed these results. The
se results provide a simple biologically based dose-response model and sugg
est that chemicals which act mechanistically like E-2 may also show no thre
shold dose. If so, even low environmental concentrations of such chemicals
may carry risk for sex reversal.