An experiment was conducted in pigs to determine the source of fetal c
ortisol at 50 (n = 5) or 100 days (n = 4) of gestation (term = 114 day
s). Equilibrium concentrations of tritiated cortisol were achieved, an
d all hormonal measures were made at 110, 130, 140, and 150 min in ane
sthetized pigs. Maternal plasma cortisol did not differ (p = 0.48) bet
ween 50 (70.2 +/- 7.4 ng/ml; mean +/- SEM) and 100 days (62.4 +/- 5.8
ng/ml). Conversely, fetal cortisol increased (p = 0.048) between 50 (8
.5 +/- 2.5 ng/ml) and 100 days (24.2 +/- 4.2 ng/ml), and, at each gest
ational age, values were lower (p = 0.001) than those in maternal plas
ma. Plasma cortisone (15.1 +/- 2.3 ng/ml) did not change with gestatio
nal age (p = 0.42) in either compartment (maternal or fetal), nor did
it differ between compartments (p = 0.08). Maternal cortisol accounted
for 22.8 +/- 2.0% of fetal cortisol at 50 days of gestation, and this
contribution decreased (p < 0.001) to 5.87 +/- 0.8% at 100 days. At b
oth ages, maternal cortisol accounted for almost 50% of fetal cortison
e. Metabolism of maternal cortisol by the entire uterofetoplacental un
it was 8.4 +/- 1.7% at 50 days and 7.5 +/- 2.4% at 100 days (p = 0.76)
. The maternal metabolic clearance rate of cortisol increased 44% (p =
0.003) between 50 and 100 days (1.49 +/- 0.4 vs. 2.15 +/- 0.2 L/min).
Hence at these gestational ages, the fetus-presumably the fetal adren
al-is the primary source of fetal plasma cortisol. The major contribut
ion of maternal cortisol to fetal cortisone strongly suggests the pres
ence of porcine placental 11 beta-hydroxysteroid dehydrogenase activit
y. Further, factors constituting the placental ''barrier'' that metabo
lize maternal cortisol to cortisone and other products may be major re
gulators of porcine fetal plasma cortisol and cortisone.