Detection of functional oxytocin receptors on endometrium of pigs

• Published in: Biology of reproduction Vol. 51; no. 1; pp. 92 - 98
• Main Authors: Whiteaker, S.S, Mirando, M.A, Becker, W.C, Hostetler, C.E
• Format: Journal Article
• Language: English
• Published: Madison, WI Society for the Study of Reproduction 01.07.1994
• Subjects: Animals; Biological and medical sciences; CERDAS; CHIMIORECEPTEUR; Dinoprost - metabolism; Endometrium - chemistry; Estrus - physiology; Female; Fundamental and applied biological sciences. Psychology; Hormone metabolism and regulation; Hydrolysis; Lypressin - pharmacology; Mammalian female genital system; OCYTOCINE; OXITOCINA; Oxytocin - metabolism; Oxytocin - pharmacology; Phosphatidylinositols - metabolism; QUIMIORECEPTORS; Receptors, Oxytocin - analysis; Receptors, Oxytocin - metabolism; Swine; Tritium; TRUIE; UTERO; UTERUS; Vertebrates: reproduction; Oxytocin; Inositol phosphate; Pig; Prostaglandin F2α; Hydrolysis; Vertebrata; Mammalia; Uterus; Female genital system; Neurohypophyseal hormone; Female; Artiodactyla; Ungulata; Endometrium; Hormonal receptor
• ISSN: 0006-3363; 1529-7268
• DOI: 10.1095/biolreprod51.1.92

Oxytocin (OT) stimulates phosphoinositide (PI) hydrolysis and prostaglandin (PG) F(2 alpha) secretion from the endometrium of cyclic pigs, but the presence of specific endometrial receptors for OT has not been demonstrated in this species. Two experiments were performed to detect the presence of functional OT receptors on endometrium collected 15 days post estrus from cyclic gilts. OT receptor density and K(d) were determined by receptor assay and Scatchard analysis. Hydrolysis of PI (i.e., incorporation [(3)H] inositol into total inositol phosphates) and PGF(2 alpha) secretion were studied with use of incubations of endometrial explants. Concentrations of PGF(2 alpha) were log-transformed for analysis of variance and are expressed as means +/- standard error of log-transformed data. In experiment 1, mean density and mean K(d) of OT receptors on endometrium of gilts were 29.2 +/- 5.54 fmol/mg protein and 1.59 +/- 0.23 nM, respectively. OT receptor density was significantly correlated with the ability of 100 nM OT to stimulate PI hydrolysis (r = 0.83, p 0.05) and PGF(2 alpha) secretion (r