Abstract
The aim of our in vitro experiments was to study the role of oxytocin (OT), cAMP/protein kinase A (PKA),
and mitogen-activated protein kinase (ERKs MAP-kinase) in the control of ovarian cell
functions as well as the role of PKA and MAPK in mediating OT effects on these processes.
The whole porcine ovarian follicles were cultured in the presence or absence of OT
(1, 10, 100 ng/ml), PKA inhibitor Rp-cAMPS (10 nM), MAP-kinase inhibitor PD98059 (1
μg/ml), or their combination. The release of prostaglandins F (PGF) and E (PGE) were
determined by RIA, PKA (α-cat subunit), the proliferation-associated peptide PCNA
and ERK-1, -2 expression in cell lyzates were analysed by Western-blotting.
OT stimulated the release of PGF and PGE, and accumulation of PKA, ERK-1/-2, and PCNA
in cell lysate. PD98059 decreased the basal PGF and PGE output, as well as reduced
both ERK-1 and ERK-2 accumulation in cell lysates. Rp-cAMPS decreased PKA accumulation
in cell lysates. Rp-cAMPS prevented the OT-induced stimulation of PKA, ERK-1, ERK-2,
PGF, and PGE, PD98059 did so for PKA, PGF, and PGE. However, PD98059 reduced either
basal or OT-induced p-ERK level. OT-stimulated PCNA accumulation was only slightly
modified by these blockers.
These observations suggest that OT, PKA, and ERKs MAPK can be involved in the control
of PGs release and proliferation of ovarian cells. The influence of OT on both PKA
and MAPK, and the ability of PKA and MAPK blockers to prevent completely or partially
OT effects suggest, that effects of OT on PGF and PGE can be mediated by both PKA
and MAPK. The role of MAPK and PKA in mediating the proliferative effects of OT seems
to be minor assuming the involvement of other intracellular messengers.
Key words
Porcine - ovarian follicle - oxytocin - prostaglandin - MAPK/ERKs - protein kinase
A
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Dr. Ph.D. A. V. Makarevich
Laboratory of Endocrinology
Research Institute of Animal Production
Hlohovska 2
94992 Nitra
Slovak Republic
Phone: + 421376546335
Fax: + 42 13 76 54 63 61
Email: makarev@vuzv.sk