Jl. Cavilla et al., The effects of meiosis activating sterol on in-vitro maturation and fertilization of human oocytes from stimulated and unstimulated ovaries, HUM REPR, 16(3), 2001, pp. 547-555
The object of this study was to assess functional maturation in vitro by ob
taining data on the fertilization and embryonic competence of human oocytes
with or without exposure to meiosis activating sterol (MAS) during maturat
ion in vitro. Immature oocytes were either collected from unstimulated pati
ents with polycystic ovaries (PCO) during gynaecological surgery, or were d
onated by patients undergoing a cycle of intracytoplasmic sperm injection (
ICSI) treatment including ovarian stimulation with gonadotrophins, PCO oocy
tes had variable cumulus cover, which was retained during culture while tho
se from ICSI patients were cultured without cumulus. The study included 119
oocytes from PCO patients and 72 from ICSI patients. The oocytes were allo
wed to mature in vitro for up to 46 h in the presence or absence of MAS. Ma
ture oocytes were inseminated by ICSI with fertile donor spermatozoa and em
bryo development was monitored in vitro. MAS (30 mug/ml) significantly incr
eased the survival of oocytes from PCO patients (P < 0.01) but did not sign
ificantly affect the proportion completing maturation in vitro. For the ICS
I patients, >90 % of oocytes survived in all culture groups, regardless of
MAS addition, however MAS (10 or 30 mug/ml) significantly increased the pro
portion of oocytes maturing in vitro (P < 0.05). The apparent tendency towa
rds improved subsequent development in vitro will require larger numbers of
oocytes for evaluation. Oocytes from ICSI patients matured more rapidly in
vitro than those from PCO patients. Our results show positive effects of M
AS on human oocytes, confirming previous data in mice. This work may have i
mplications for the future clinical application of IVM.