EFFECT OF THE OXYTOCIN ANTAGONIST ATOSIBAN (1-DEAMINO-2-D-TYR(OET)-4-THR-8-ORN-VASOTOCIN OXYTOCIN) ON NOCTURNAL MYOMETRIAL CONTRACTIONS, MATERNAL CARDIOVASCULAR FUNCTION, TRANSPLACENTAL PASSAGE, AND FETAL OXYGENATION IN THE PREGNANT BABOON DURING THE LAST 3RD OF GESTATION/
Pw. Nathanielsz et al., EFFECT OF THE OXYTOCIN ANTAGONIST ATOSIBAN (1-DEAMINO-2-D-TYR(OET)-4-THR-8-ORN-VASOTOCIN OXYTOCIN) ON NOCTURNAL MYOMETRIAL CONTRACTIONS, MATERNAL CARDIOVASCULAR FUNCTION, TRANSPLACENTAL PASSAGE, AND FETAL OXYGENATION IN THE PREGNANT BABOON DURING THE LAST 3RD OF GESTATION/, Biology of reproduction, 57(2), 1997, pp. 320-324
The oxytocin antagonist, atosiban amino-2-D-tyr(OET)4-thr-8-orn-vasoto
cin/oxytocin), was infused i.v. to chronically instrumented pregnant b
aboons in the last third of pregnancy. Atosiban (6 mu g/kg per min) in
hibited myometrial electromyographic activity associated with spontane
ous myometrial contractions that occurred around the onset of darkness
between 134 and 162 days gestation (term 180 days gestation). The eff
ect of atosiban on maternal heart rate was minimal. Maternal blood pre
ssure remained unaltered during atosiban infusion. Fetal carotid arter
ial PO2 was unchanged during a 2-h infusion of atosiban. Transplacenta
l passage of atosiban from mother to fetus was assessed at cesarean se
ction under halothane anesthesia in four baboons and in two chronicall
y instrumented fetuses in the absence of anesthesia. The maternal:feta
l concentration gradient ranged from 9.2 to 22.8. Maternal atosiban cl
earance rates were 9.2-16.9 ml/kg per min. In conclusion, atosiban was
very effective at inhibiting spontaneously occurring nocturnal myomet
rial contractions during the last third of gestation in the pregnant b
aboon. Although atosiban crosses the placenta relatively freely, there
was no effect on fetal oxygenation.