Of 48 spare human pre-embryos achieving the expanded blastocyst stage,
22 (45.6%) secreted significant amounts of human chorionic gonadotrop
hin (HCG) (>5 IU/l/day). Of these, nine remained intrazonal, seven par
tially hatched and six fully hatched. Embryonic production of HCG in v
itro appeared to be time-dependent, starting after a certain minimum t
ime (approximately 160 h post-insemination) and rising exponentially,
with maximal HCG production around day 10. Hatching was not a prerequi
site for HCG secretion, since similar amounts were produced by intrazo
nal blastocysts. Blastocysts derived from abnormally fertilized oocyte
s also began secreting HCG exponentially but secretion was delayed and
the upper limit of maximum HCG secretion rate was comparatively low.
The actual amount of HCG is thought to reflect the number of viable tr
ophectoderm cells producing the hormone. HCG doubling times for blasto
cysts in vitro were rapid when compared to implanting blastocysts of a
similar age in vivo, with 19/22 (86.4%) blastocysts having a doubling
time of < 10 h. Provided a pre-embryo can secrete HCG and maintain an
adequate doubling time, sufficient HCG should be produced for initial
stages of embryonic recognition in vivo. Since intrazonal blastocysts
are capable of fulfilling both of these criteria, the limiting factor
in realizing their full potential may be escaping from the zona pellu
cida.