Da. Hewitt et Gcw. England, EFFECT OF PREOVULATORY ENDOCRINE EVENTS UPON MATURATION OF OOCYTES OFDOMESTIC BITCHES, Journal of Reproduction and Fertility, 1997, pp. 83-91
The effect of preovulatory endocrine changes upon oocyte maturation wa
s investigated in a combined in vivo and in vitro study. A preliminary
study was performed to investigate the effect of endocrine influences
in vivo On subsequent oocyte maturation in vitro. A hemi-ovariectomy
was performed in four bitches during pro-oestrus at the first detected
rise of plasma progesterone (mean progesterone 2.36 +/- 0.58 ng ml(-1
)) and a second performed during oestrus immediately before ovulation,
1-4 days later (mean progesterone 4.96 +/- 0.75 ng ml(-1)). The mean
numbers of high quality (grade 1) oocytes with identifiable nuclear ma
terial collected per pro-oestrous ovary was 15.5 +/- 9.88, and per oes
trous ovary was 31.75 +/- 23.76. All of the grade 1 oocytes harvested
were cultured for 96 h, after which 37% and 19% of pro-oestrous oocyte
s had matured to germinal vesicle breakdown (GVBD) and metaphase I/ana
phase I/metaphase II (MI/AI/MII), respectively, whereas 41% and 11% of
oestrous oocytes had matured to GVBD and MI/AI/MII, respectively. The
re was no significant difference in maturation between the two groups
of oocytes. In a second study, high quality grade 1 oocytes harvested
from bitches in the late luteal or anoestrous stage of the oestrous cy
cle were cultured in medium supplemented with either 1 mu g oestradiol
ml(-1) (64 oocytes), 1 mu g progesterone ml(-1) (52 oocytes), a combi
nation of oestradiol and progesterone (50 oocytes), or no supplementat
ion (55 oocytes). The mean numbers of high quality (grade I) oocytes w
ith identifiable nuclear material collected per luteal ovary was 9.7 /- 7.96, and per anoestrous ovary was 8.33 +/- 5.61. The number of ooc
ytes obtained per bitch was highly variable, and may have been affecte
d by the stage of oestrous cycle. After 48 h, maturation to GVBD was 5
6, 33, 50 and 50%, and to MI/AI/MII was 13, 17, 20 and 4% for each tre
atment respectively, and after 96 h was 45, 59, 63 and 63% and 10, 0,
4 and 0%, respectively There was no significant difference in maturati
on between the four groups. The hormonal environment in viva did not a
ffect subsequent in vitro maturation of high quality oocytes. Similarl
y, culture in steroid hormone supplemented medium did not improve matu
ration in vitro of high quality oocytes. The effects upon oocytes from
specific preovulatory follicles were not studied.