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Section: Reviews and Bibliography Download (pdf, 2.3MB )UDC612.62+612.06DOI10.17238/issn2542-1298.2019.7.1.106AuthorsViktor I. Tsirkin*/**, Svetlana I. Trukhina*, Andrey N. Trukhin**Vyatka State University (Kirov, Russian Federation) **Kazan State Medical University (Kazan, Russian Federation) AbstractVasopressin is in many respects similar to oxytocin in its structure and uterostimulating effect. This review reports on the production of vasopressin and its metabolism, as well as on three types of vasopressin receptors (V1A, V1B and V2) and their association with the corresponding G-proteins. Data are provided on the physiological effects of vasopressin depending on the receptor activated, as well as on vasopressin receptor agonists and antagonists. Further, the paper reports on the ability of oxytocin to exert a stimulating effect not only by activating oxytocin receptors of uterine myocytes, but also by activating V1A and V2 receptors. By activating V1A receptors, vasopressin, like oxytocin, increases the contractile activity of isolated myometrium in animals (rats, mice, rabbits and monkeys) and humans. In the myometrium of nonpregnant women, the uterostimulating effect of vasopressin is much greater than that of oxytocin. This gives grounds for individual authors to assert that vasopressin, activating V1A receptors, is the main cause of primary dysmenorrhea. In the myometrium of pregnant women, V1 receptors are detected starting from week 32. Their number stays unchanged until delivery, while the concentration of oxytocin receptors increases in late pregnancy, reaching the maximum values in the first hours of spontaneous delivery. This indicates that it is the oxytocin-oxytocin receptor system, not the vasopressin-vasopressin receptor system, that is directly related to labour induction. 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