Transuteroplacental Metabolism of Cortisol and Cortisone during Mid- and Late Gestation in the Baboon*
- 1 November 1984
- journal article
- research article
- Published by The Endocrine Society in Endocrinology
- Vol. 115 (5) , 1946-1951
- https://doi.org/10.1210/endo-115-5-1946
Abstract
Uterine extraction (i.e., metabolism) and transuteroplacental interconversion of cortisol (F) and cortisone (E) to determine whether metabolism across the uterus changes during pregnancy and contributes to the MCR [metabolic clearance rate] of these corticosteroids. On day 100 (n = 4) or 170 (n = 3) or pregnancy (term = day 184), baboons (P. anubis; 14-18 kg) were sedated with ketamine, and a constant infusion (0.38 ml/min) of 8-12 .mu.Ci [3H]F and 9-15 .mu.Ci [14C]E in 80 ml 0.9% NaCl-1% ethanol was initiated (time zero) via a maternal antecubital vein. At 60 min, animals were laparotomized, and at 70, 80, and 90 min, blood samples were obtained from right and left uterine veins and from a maternal saphenous vein. At 95 min, a transverse incision was made in the uterus, the fetus was isolated, and blood samples were obtained from the umbilical vein and artery. The cord was then clamped, and the fetus was delivered. Radiolabeled F and E were extracted from serum and purified by sequential paper chromatography, and metabolic parameters were calculated. Endogenous F and E levels were determined by radioimmunoassay. In the mother, the percent conversions of E to F at midgestation (mean .+-. SE; 72 .+-. 4) and late gestation (65 .+-. 3) were similar and exceeded (P < 0.01) respective values for oxidation of F to E (51 .+-. 7 and 46 .+-. 7, respectively), indicating that maternal corticosteroid metabolism favors F formation and is unchanged during the second half of gestation. Corticosteroid metabolism across the uterus and placenta (transuteroplacental) was altered during pregnancy. At midgestation, transuteroplacental conversion of E to F (37 .+-. 9) exceeded (P < 0.05) the reverse reaction (18 .+-. 3), whereas oxidation of F to E at term (28 .+-. 4) was 7-fold greater (P < 0.05) than reduction of E to F (4 .+-. 1). At midgestation, essentially all of the F and E in umbilical vein was derived from maternal F. This contrasts with that observed in near-term baboons in which only 41 .+-. 9% of the F and 64 .+-. 8% of the E entering the fetal circulation was of maternal origin. As a result of uterine, placental, and fetal metabolism, 30% of the F and 15% of the E in maternal circulation were extracted by the uterus at both mid- and late gestation. Transuteroplacental corticosteroid metabolism changes from reduction at midgestation to oxidation at term. Corticosteroid metabolism by the uterus and its contents is significant during the second half of baboon pregnancy and contributes to the overall clearance of F and the quantity of F and E measured in the fetal circulation.This publication has 12 references indexed in Scilit:
- The utilization of placental substrates for cortisol synthesis by the baboon fetus near termSteroids, 1980
- A role for estrogen in progesterone production during baboon pregnancyAmerican Journal of Obstetrics and Gynecology, 1980
- The production and secretion of cortisol by baboon neonatesSteroids, 1979
- STRESS-INDUCED DECREASES IN THE SERUM CONCENTRATION OF PROGESTERONE IN THE PREGNANT BABOONJournal of Endocrinology, 1978
- Increasing Fetal Adrenal Formation of Cortisol from Pregnenolone During Baboon (Papio papio) GestationBiology of Reproduction, 1977
- Serum cortisol levels affect the metabolic clearance rate of progesterone in female baboonsSteroids, 1977
- Catabolic regulation of blood cortisol in premature and term baboon neonatesThe Journal of Steroid Biochemistry and Molecular Biology, 1977
- The Metabolic Clearance Rates and Interconversion of Cortisol and Cortisone in Pregnant and Nonpregnant BaboonsEndocrinology, 1976
- Physiological Disposition of 4-C14-Cortisol During Late Pregnancy1Journal of Clinical Investigation, 1957
- A QUANTITATIVE COLOR REACTION FOR CORTISONE AND RELATED 17,21-DIHYDROXY-20-KETOSTEROIDSJournal of Biological Chemistry, 1950