R. Garciavillar et al., EVIDENCE FOR THE PRESENCE OF AH 13205-SENSITIVE EP(2)-PROSTANOID RECEPTORS IN THE PREGNANT BABOON BUT NOT IN THE PREGNANT SHEEP MYOMETRIUM NEAR-TERM, Journal of the Society for Gynecologic Investigation, 2(1), 1995, pp. 6-12
OBJECTIVE: Our purposes were to assess the effects of prostaglandin (P
G) E(2) and PGF(2 alpha) on myometrial contractility in pregnant sheep
and baboons in an in vitro superfusion study, and to characterize fur
ther the PGE-sensitive (EP) receptor subtype involved in the myometria
l response to PGE(2) by using the selective prostanoid EP(2) agonist A
H 13205. METHODS: Strip preparations of uterine muscle from 15 sheep (
107-145 days' gestational age) and ten baboons (158-185 days' gestatio
n) were studied. Cumulative concentration-response curves (CRC) were c
onstructed to oxytocin (4.2 pmol/L to 0.42 mu mol/L, PGE(2) (0.1 nmol/
L to 1 mu mol/L), and PGF(2 alpha) (1 nmol/L to 100 mu mol/L), and 50%
effective concentration (EC50) values (mean and 95% confidence interv
al) were calculated. We also tested the hypothesis that PGE(2)-induced
myometrial relaxation in pregnant baboons could be mediated by EP(2)-
prostanoid receptors. Myometrial strips were stimulated by oxytacin (0
.42 nmol/L), and CRCs to the EP(2)-agonist AH 13205 (0.1 nmol/L to 10
mu mol/L) were constructed. RESULTS: Prostaglandin F-2 alpha stimulate
d myometrial activity in a concentration-related fashion in all prepar
ations from both sheep and baboons. The EC50 in the sheep myometrium P
GF(2 alpha) (52 nmol/L, 95% confidence interval [CI] 25-110) was signi
ficantly (P <.05) lower than that in baboon myometrium (183 nmol/L, 95
% CI 93-355). Oxytocin stimulated myometrial activity in preparations
of both sheep (EC50 = 0.29 nmol/L, 95% CI 0.11-0.71) and baboon (EC50
= 0.31 nmol/L, 95% CI 0.18-0.52). In contrast, responses to PGE(2) wer
e species-related: PGE, caused concentration-related stimulation of my
ometrial activity in sheep tissue (EC50 = 3.2 nmol/L, 95% CI 2.0-5.0),
but induced concentration-related inhibition of activity in baboon my
ometrium (50% inhibitory concentration [IC50] = 21 nmol/L, 95% CI 2.2-
203). A concentration-related inhibitory response to AH 13205 (IC50 =
3.56 nmol/L, 95% CI 1.28-5.99) was obtained in the baboon. In contrast
, AH 13205 failed to inhibit comparable myometrial strip preparations
from pregnant sheep. CONCLUSIONS: The present studies suggest that bot
h sheep and baboon myometrium contain prostanoid receptors that mediat
e stimulation. In addition, baboon myometrium, like that from the huma
n, contains AH 13205-sensitive EP receptors (EP(2) receptors), which m
ediate inhibition. The pregnant baboon may therefore represent a suita
ble animal model for investigations into the use of EP(2) agonists for
the prevention of premature labor in humans.