Anita Franczak1. 1. Department of Animal Physiology, University of Warmia and Mazury in Olsztyn, Oczapowski 1A, 10-718 Olsztyn, Poland. anitaf@uwm.edu.pl
Abstract
UNLABELLED: Previously, we found that in addition to embryos, the uterine tissues may be a source of estradiol-17beta (E(2)) during early pregnancy in the pig. The aim of the present study was to determine whether porcine endometrium and myometrium secrete androgens - androstenedione (A(4)), testosterone (T) and estrone (E(1)) during early pregnancy and luteolysis (Days 14-16) in pigs. Individual endometrial and myometrial slices (200 mg) were first pre-incubated (24 h) and then incubated (6 h, 37 degrees C in an atmosphere of 95% O(2) and 5% CO(2)) in the presence or absence of progesterone (P(4); 10(-5) M), oxytocin (OT; 10(-7) M) or OT plus P(4). Basal endometrial and myometrial secretion of A(4) and T did not differ between pregnant and cyclic gilts. Endometrial secretion of E(1) was higher in pregnant than cyclic gilts (p<0.05) while myometrial secretion of E(1) did not differ between the two groups of the examined pigs (p>0.05). Progesterone significantly increased A(4) and T secretion (p<0.001) by uterine tissues regardless of the reproductive status. In the presence of P(4), endometrial and myometrial secretion of E(1) was increased only during luteolysis (p<0.001). In both tissues, OT did not affect the examined steroid secretion and did not change the effect of P(4). IN CONCLUSION: 1) porcine endometrium and myometrium was found to produce A(4), T and E(1) in vitro; 2) basal endometrial and myometrial production of A(4) and T did not differ between the examined reproductive periods; 3) the endometrium released more E(1) during early pregnancy than luteolysis; 4) in the presence of substrate (P(4)), uterine tissues increased secretion of A(4) and T during early pregnancy and luteolysis; and 5) P(4) increased uterine production of E(1) only during luteolysis. These data demonstrated the presence of the active steroid pathway in porcine endometrium and myometrium which may serve as an alternative source of androgens and estrogens in pigs.
UNLABELLED: Previously, we found that in addition to embryos, the uterine tissues may be a source of estradiol-17beta (E(2)) during early pregnancy in the pig. The aim of the present study was to determine whether porcine endometrium and myometrium secrete androgens - androstenedione (A(4)), testosterone (T) and estrone (E(1)) during early pregnancy and luteolysis (Days 14-16) in pigs. Individual endometrial and myometrial slices (200 mg) were first pre-incubated (24 h) and then incubated (6 h, 37 degrees C in an atmosphere of 95% O(2) and 5% CO(2)) in the presence or absence of progesterone (P(4); 10(-5) M), oxytocin (OT; 10(-7) M) or OT plus P(4). Basal endometrial and myometrial secretion of A(4) and T did not differ between pregnant and cyclic gilts. Endometrial secretion of E(1) was higher in pregnant than cyclic gilts (p<0.05) while myometrial secretion of E(1) did not differ between the two groups of the examined pigs (p>0.05). Progesterone significantly increased A(4) and T secretion (p<0.001) by uterine tissues regardless of the reproductive status. In the presence of P(4), endometrial and myometrial secretion of E(1) was increased only during luteolysis (p<0.001). In both tissues, OT did not affect the examined steroid secretion and did not change the effect of P(4). IN CONCLUSION: 1) porcine endometrium and myometrium was found to produce A(4), T and E(1) in vitro; 2) basal endometrial and myometrial production of A(4) and T did not differ between the examined reproductive periods; 3) the endometrium released more E(1) during early pregnancy than luteolysis; 4) in the presence of substrate (P(4)), uterine tissues increased secretion of A(4) and T during early pregnancy and luteolysis; and 5) P(4) increased uterine production of E(1) only during luteolysis. These data demonstrated the presence of the active steroid pathway in porcine endometrium and myometrium which may serve as an alternative source of androgens and estrogens in pigs.