Effect of oxytocin antagonists on the activation of human myometrium in vitro: Atosiban prevents oxytocin-induced desensitization

• Published in: American journal of obstetrics and gynecology Vol. 171; no. 6; pp. 1627 - 1634
• Main Authors: Phaneuf, S., Asbóth, G., MacKenzie, I.Z., Melin, P., López Bernal, A.
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA Elsevier Inc 01.12.1994; Elsevier
• Subjects: Biological and medical sciences; Calcium - metabolism; Cell receptors; Cell structures and functions; Culture Techniques; Female; Fundamental and applied biological sciences. Psychology; Hormone receptors. Growth factor receptors. Cytokine receptors. Prostaglandin receptors; human myometrium; Humans; inositol phosphates; Inositol Phosphates - biosynthesis; intracellular calcium; Intracellular Membranes - metabolism; Molecular and cellular biology; Myometrium - cytology; Myometrium - drug effects; Myometrium - physiology; Oxytocin - antagonists & inhibitors; Oxytocin - metabolism; Oxytocin antagonists; oxytocin receptors; Time Factors; Vasotocin - analogs & derivatives; Vasotocin - pharmacology; Oxytocin antagonists; human myometrium; intracellular calcium; inositol phosphates; oxytocin receptors; Human; Myometrium; Desensitization; Oxytocin; Peptide hormone; Neuropeptide; In vitro; Prevention; Sensitivity resistance; Neurohypophyseal hormone; Delivery disorders; Antagonist; Hormonal receptor
• ISSN: 0002-9378; 1097-6868
• DOI: 10.1016/0002-9378(94)90414-6

Objective: Our purpose was to investigate whether the sensitivity of myometrial cells to oxytocin is affected by prolonged exposure to oxytocin antagonists. Study Design: Tissue slices or cultured myometrial cells were exposed to peptides in vitro. Myometrial activation was studied by measuring the formation of inositol phosphates and the changes in intracellular calcium. Oxytocin binding was measured by saturation analysis. Results: Atosiban and related peptides inhibited oxytocin-induced myometrial activation as pure antagonists (inhibition constant 10 nmol/L) but had no effect on prostaglandin E2 induced activation. Long-term (≥ 24 hours) exposure to atosiban had no residual effect on oxytocin sensitivity. However, long-term exposure to oxytocin resulted in homologous desensitization and loss of oxytocin receptors. Oxytocin-induced desensitization was prevented by coincubation with atosiban. Conclusions: Atosiban is a pure oxytocin antagonist and has a specific, reversible effect on myometrial cells in vitro. Its potential use for the management or even prevention of idiopathic preterm labor or to reverse uterine hypertony during oxytocin-induced labor should be tested in controlled clinical trials.