Production of carbon dioxide in vitro by blastocysts from intact and ovariectomized mice

'Normal' and 'delayed implanting' mouse blastocysts were incubated in non-radioactive culture medium for various lengths of time (preincubation), and then placed in culture medium with (14-C)-glucose for 2 hr. The rate of embryonic CO-2 given off by the blastocysts. Normal embryos were unaffected by the length of preincubation. By contrast, 'delayed implantating' embryos had a low level of CO-2 production with short preincubations (i.e. less than 2 hr), but approached the normal range with longer preincubations (i.e. more than 8 hr) and thus, were 'activated ' in vitro. Incubation of the 'delayed implanting' embryos with actinomycin D prevented the expected increase in CO-2 production, indicating that synthesis of new RNA is necessary for their activation. Preincubation of normal and 'delayed implanting' blastocysts with oestradiol-17 beta and/ or progesterone had no effect on the level of CO-2 production, suggesting that the hormones do not directly stimulate or inhibit carbohydrate metabolism in the embryos.