F. Hulten et al., Determining ovulation frequency in individually penned lactating sows using a faecal 'Progestin' assay, REPROD DOM, 34(2), 1999, pp. 71-76
Trials were performed to evaluate the validity of a modified faecal 'proges
tin' assay for monitoring ovarian activity (Trial 1) and to determine the o
ccurrence of ovulation among individually housed lactating sows by repealed
measurements of faecal 'progestins' (Trial 2). In trial 1 faecal and plasm
a samples were collected from six multiparous sows, from the day after wean
ing until oestrus occurred in the third oestrous cycle. A progesterone radi
oimmunoassay was applied to skimmed milk extracts of the faecal samples, an
d plasma progesterone concentrations were determined with a chemiluminescen
t assay. In addition, high performance liquid chromatography (HPLC) analysi
s was performed on faecal extracts and the immunoreactivity in the differen
t fractions was determined. In Trial 2, faecal samples were collected from
88 multiparous sows at weekly intervals from the day of farrowing until 2 w
eeks after breeding. Samples were subjected to 'progestin' analysis. Trial
showed that the excretion patterns of faecal 'progestins' and plasma proges
terone were significantly correlated (r = 0.79, p < 0.05) during the oestro
us cycles. Parallelism was obtained in the assay, but recovery was low(11.4
%). The HPLC analysis revealed one major peak of immunoreactivity in a frac
tion; which corresponded with progesterone. This finding suggests that inta
ct progesterone was a source for immunoreactivity in the assay. In Trial 2,
a 10-fold decrease in mean 'progestin' concentrations was noted from the d
ay of farrowing to day 7 of lactation. The mean 'progestin' values remained
low throughout lactation and started to increase 2 weeks after breeding. L
arge individual variations in luteal phase values were noted. Only 1.1% (on
e) of the sows ovulated during lactation.