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Pregnancy alters the pattern of maternal cortisol (F) metabolism and increases the maternal serum cortisol-binding capacity (CBC) of baboons. To determine whether these changes are associated with alterations in F clearance,the metabolic clearance rate (MCR) and interconversion (p) of F and cortisone (E) were measured by continuous infusion of (3H)F and (14C)E in 9 regularly menstruating and 7 pregnant baboons (Papio papio). In nonpregnant animals, the values (X +/- SE) for MCR-E (488 +/- 48 1/day) were greater (P less than 0.001) than those for MCR-F (214 +/- 22 1/day). The p value for the conversion of E leads to F (62.8 +/- 4.7%) was greater (P less than 0.001) than that for the reaction F leads to E (41.6 +/- 3.7%), indicating that F formation is favored. Consistent with MCR-E greater than MCR-F, the per cent of F bound to proteins other than albumin (75 +/- 2) was greater (P less than 0.001) than the per cent of E bound (52 +/-3). The production rate (MCR x peripheral concentration; mug/min) of F (55.1 +/- 7.9) was greater (P less than 0.001) than that of E (28.5 +/-3.9) with essentially all of the F being secreted directly (secretion rate 51.2 +/- 7.9 mug/min). Essentially all of the E produced was derived from circulating F, vitually none being secreted directly (secretion rate 4.6 +/- 3.9 mug/min). Pregnancy did not alter the MCR-F (190 +/- 23 1/day), MCR-E 525+/- 51 1/day), per cent of F (79 +/- 3), or per cent of E (49 +/-3) bound,or F (57.2 +/- 9.2 mug/min) or E (35.5 +/- 4.9 mug/min) production rates. CBC (mug F/100 ml) was significantly (P less than 0.01) elevated (25.3 +/- 2.3, nonpregnant vs 35.1 +/- u.6, pregnant). In addition, p E leads to F was increased (75.5 +/- 1.8%) as was p F leads to E (54.3 +/- 3.7%; P less than 0.01). We have concluded that the MCR-F during pregnancy is more dependent on alterations in maternal metabolism than on the increased serum CBC characteristic of gestation. We suggest that the latter factor may be important in regulating the physiologic levels of the other steroids which bind to it.
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
July 1972,
The Journal of clinical endocrinology and metabolism,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
November 1976,
Endocrinology,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
May 1973,
Pediatric research,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
January 1988,
Endocrinology,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
July 1985,
The American journal of physiology,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
November 1968,
Experientia,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
October 1977,
Steroids,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
September 1985,
Journal of steroid biochemistry,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
September 1994,
American journal of obstetrics and gynecology,
G J Pepe, and
R A Ehrenkranz, and
J D Townsley
June 1977,
Biology of reproduction,
