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Inhibition of uterine contractions of premature labour with an oxytocin analogue. Results from a pilot study
Author(s) -
ÅKERLUND MATS,
STRÖMBERG PER,
HAUKSSON ARNAR,
ANDERSEN LARS FRANCH,
LYNDRUP JENS,
TROJNAR JERZY,
MELIN PER
Publication year - 1987
Publication title -
bjog: an international journal of obstetrics and gynaecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.157
H-Index - 164
eISSN - 1471-0528
pISSN - 1470-0328
DOI - 10.1111/j.1471-0528.1987.tb02287.x
Subject(s) - oxytocin , cardiotocography , antagonist , uterus , oxytocin receptor , medicine , endocrinology , tocolytic , fetus , pregnancy , receptor , preterm labor , biology , genetics
Summary. A competitive inhibitor of the action of oxytocin on the uterus, l‐deamino‐2‐D‐Tyr‐(OEt)‐4‐Thr‐8‐Orn‐oxytocin, was studied for the first time in 13 patients with established, uncomplicated premature labour. Intravenous infusion of 10–100 μg/min of the analogue was given for 1–10 h and the effect was monitored by external cardiotoco‐graphy. In all women an inhibition of uterine activity was observed, and in the majority of patients infused with 25 μg/min and a total dose of about 5 mg or more of the drug total inhibition of uterine contractions was achieved. There were no effects on the maternal and fetal pulse rates, nor were there any other side‐effects. The results of this preliminary study support the concept of an increased concentration of uterine oxytocin receptors being aetiologically important in uncomplicated premature labour. They also suggest that the present oxytocin antagonist could be an interesting therapeutic alternative in the condition, primarily because of the marked selectivity of its effect.