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Biology of Reproduction, Vol 14, 566-571, Copyright © 1976 by Society for the Study of Reproduction
1 Department of Anatomy,
School of Medicine,
University of Oregon Health Sciences Center,
Portland, Oregon 97201 Blastocysts were collected from the uteri of normal and delayed implanting mice and
incubated with either Brinsters medium containing 3H uridine, or the same medium mixed with
material flushed from the uteri of implanting or delayed implanting animals. The rate of
embryonic RNA synthesis was estimated from the incorporation of 3H uridine by the embryos in
vitro. RNA synthesis by normal embryos incubated in Brinsters medium was linear for at least 6 h.
RNA synthesis by delayed implanting embryos in Brinsters medium was initially low and increased
to the level of normal embryos by the fourth hour in vitro. In contrast, RNA synthesis was low in
both types of embryos incubated in medium containing uterine flushings; material from the uteri
of implanting animals was as effective an inhibitor of RNA synthesis as that from delayed
implanting animals. The apparent inhibitory activity is dialyzable and heat resistant. It is not
known whether or not the inhibitory effect of uterine flushings on embryonic RNA synthesis
found in vitro has any significance in vivo.
Note:
ACKNOWLEDGMENTS
This work was carried out with the technical
assistance of Ms. J. Hodson and supported by a
research grant from the Public Health Service (HD
08496) and a Research Career Development award
(HD 00020) from the Institute of Child Health and
Human Development.
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