Effects of progesterone on expression of messenger RNA encoding oxytocin-neurophysin, oxytocin receptor and prostaglandin G/H synthase-1 and-2 duringthe early oestrous cycle in the ovine corpus luteum
Hy. Al-matubsi et al., Effects of progesterone on expression of messenger RNA encoding oxytocin-neurophysin, oxytocin receptor and prostaglandin G/H synthase-1 and-2 duringthe early oestrous cycle in the ovine corpus luteum, REPROD FERT, 11(7-8), 1999, pp. 435-442
This study was conducted to determine whether early progesterone treatment
plays a role in the regulation of messenger RNA (mRNA) expression for oxyto
cin-neurophysin, oxytocin receptor, prostaglandin G/H synthase (PGHS)-1 and
PGHS-2 in the ovine corpus luteum. The expression of ovarian oxytocin, oxy
tocin receptor, PGHS-1 and PGHS-2 mRNA was investigated in control, progest
erone- or RU486-treated ewes. Fifteen ewes were randomly assigned to three
groups to receive intramuscular injections of progesterone (12.5 mg; n = 5)
, RU486, (2.5 mg kg(-1) bodyweight; n = 4) or corn oil(1 mL; n = 6) twice d
aily from Day 1 to Day 3 post oestrus. On the morning of Day 4 post oestrus
, the corpora lutea were collected and analysed for oxytocin-neurophysin mR
NA by Northern blot using a labelled cDNA probe, and for the expressions of
the oxytocin receptor, PGHS-1 and PGHS-2 mRNA using the reverse transcript
ion polymerase chain reaction. Administration of progesterone or suppressio
n of progesterone activity with RU486 did not affect expression of oxytocin
-neurophysin mRNA (P>0.05). Pretreatment of the ewes with progesterone resu
lted in the enhancement of luteal oxytocin receptor mRNA expression and sup
pression of PGHS-1 and PGHS-2 mRNA (P<0,001). These results indicate that e
arly progesterone treatment does not control the expression of oxytocin-neu
rophysin mRNA in the ovine ovary but may be involved in the regulation of o
varian oxytocin receptor and PGHS expression. It is proposed, on the basis
of these results, that progesterone may play a role in premature corpus lut
eum regression through an intra-ovarian mechanism involving the induction o
f ovarian oxytocin receptor mRNA expression.