The hCG induced ovulation in sows was studied by use of ultrasonography, an
d an investigation of the development and diversity of the zygotes/embryos
was performed at 24 h after ovulation. Crossbred sows (N=48) were weaned (d
ay 0) and checked for heat twice daily from day 3 onwards. From day 4, the
ovaries were transrectally scanned twice daily. On day 4, the sows were giv
en an injection of 750 iu hCG im and inseminated 27 +/- 2 h (X +/- SD) and
38 +/- 1 h later. From 38 to 48 h after the hCG injection, the ovaries were
scanned at 60 to 90 min intervals. At 24 h after ovulation the oviducts we
re surgically flushed in 18 sows. Out of the 48 sows, 34 showed heat at 12-
36 h after the hCG-treatment and 14 showed heat before the hCG treatment. I
n the former group of sows, 20 (59%) ovulated within the interval of 38 to
48 h after the hCG treatment, and the follicular size immediately before ov
ulation was 7.8 +/- 0.6 mm. Among the sows which showed heat before hCG tre
atment only 7 (50%) ovulated within the above interval and the preovulatory
follicle size was larger (8.3 +/- 0.5, p<0.05) than in the former group of
sows, which showed heat after the hCG treatment. The flushing of 18 sows y
ielded a total of 243 ova, 70 (29%) 1-cell stages, 160 (66%) 2-cell stages
and 13 (5%) 4-cell stages. A pronounced difference in the degree of variati
on in embryonic development was seen between sows: 4 animals yielded 1- to
4-cell stages, one exclusively 2-cell stage. In conclusion, the control of
ovulation in sows by hCG treatment will affect the follicular growth and th
e exact timing of ovulation can not always be relied on. It is strongly rec
ommended to use ultrasonography to monitor the time of ovulation if this pa
rameter is important. Ova recovered at 24+/-1 h after the median time of ov
ulation revealed a pronounced diversity (1- to 4- cell stage) within sows.
No obvious relation with this embryonic diversity and the follicular size a
t ovulation was seen in these data.