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Biology of Reproduction, Vol 23, 88-91, Copyright © 1980 by Society for the Study of Reproduction
1 Department of Obstetrics and Gynecology,
Michael Reese Hospital and Medical Center
and
The Pritzker School of Medicine,
University of Chicago,
Chicago, Illinois 60616 It has been suggested that estradiol-induced specific uterine protein is required for blastocyst
implantation in laboratory rodents. Estriol has an anti-implantation effect which can be overcome
by administration of estradiol. Recent data indicate, however, that the biological differences
between estriol and estradiol are the result of the relatively short nuclear retention time of receptor-estriol complexes which can be overcome by repeated injections. To determine whether estriol
administered repeatedly in small doses can be as effective as estradiol in inducing delayed nidation,
several delayed implantation experiments in the rat have been performed. Termination of delayed
implantation was observed in all oophorectomized, progesterone-treated rats following administration of 0.1 µg of estradiol in a single dose. Estriol, when administered as a single injection in doses
ranging between 0.1 and 1.0 µg was significantly (P<0.01) less effective. However, if 0.8 µg of
estriol was administered in eight divided doses over a period of 24 h, its effectiveness was comparable to that of estradiol. A similar implantation-promoting effect was achieved when estriol was
released continuously from a s.c. capsule in a dose of 1.25 µg/24 h. When 1.0 µg of estriol was
administered 1 h before 0.1 µg of estradiol was given, no antagonistic effect was observed. These
data are consistent with recent reports indicating that the difference in biologic activity between
estradiol and estriol is related to the brief nuclear retention time of the receptor-estriol complexes.
Accepted on April 22, 1980
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