Ap. Beard et Mg. Hunter, EFFECTS OF EXOGENOUS OXYTOCIN AND PROGESTERONE ON GNRH-INDUCED SHORT LUTEAL PHASES IN ANESTROUS EWES, Journal of Reproduction and Fertility, 106(1), 1996, pp. 55-61
Two experiments investigate the effects of oxytocin and progesterone o
n premature luteolysis in ewes. In Expt 1, 20 anoestrous ewes were ind
uced to ovulate by multiple injections of GnRH (250 ng i.v. every 2 h
for 24 h) followed by a bolus injection of GnRH (125 mu g, i.v.). Ten
ewes received a continuous infusion of oxytocin from the day after the
GnRH bolus injection and the other ten ewes were infused with saline.
Oxytocin infusion had no significant effect on the proportion of ewes
with short luteal phases (P > 0.05). All ewes that had luteal phases
of normal duration from either group (n = 9) exhibited a transient inc
rease in plasma concentrations of progesterone 2 h after insertion of
the pump. In Expt 2, 25 anoestrous ewes were treated with GnRH as in E
xpt 1. Five ewes were pretreated with progestagen for 11 days and ten
ewes received progesterone (12 mg, i.m.) 24 h after the bolus injectio
n of GnRH. All animals received an oxytocin injection (1 mu g, i.v.) o
n day 4 after the GnRH bolus. All five ewes that were pretreated with
progestagen had normal luteal function and none exhibited a 13, 14-dih
ydro-15-keto PGF(2 alpha) (PGFM) response to oxytocin. None of the ten
ewes injected with progesterone had a normal luteal phase and six ewe
s exhibited a PGFM response to oxytocin. Four ewes in the control, gro
up had normal luteal function and three had short luteal phases. It is
concluded that (1) administration of oxytocin from about the time of
ovulation does not prevent premature luteal regression; (2) a transien
t increase in progesterone at about the time of ovulation is associate
d with luteal phases of normal duration; (3) a more extended exposure
to progesterone at about the time of ovulation prevents normal luteal
function and may inhibit luteinization and (4) pretreatment with proge
sterone prevents luteolysis by reducing the uterine response to oxytoc
in early in the luteal phase.