Divergent changes in plasma ACTH and pituitary POMC mRNA after cortisol administration to late-gestation ovine fetus

Am J Physiol. 1998 Mar;274(3):E417-25. doi: 10.1152/ajpendo.1998.274.3.E417.

Abstract

Plasma concentrations of cortisol and adrenocorticotropic hormone (ACTH) rise in the late-gestation sheep fetus at approximately the same time as there is an increase in the plasma levels of corticosteroid-binding globulin (CBG). We hypothesized that intrafetal cortisol infusion during late pregnancy would stimulate an increase in fetal plasma CBG, which in turn would bind cortisol and diminish glucocorticoid negative-feedback regulation of the fetal pituitary, leading to an increase in plasma ACTH concentrations. Cortisol was infused into chronically catheterized fetal sheep beginning at 126.1 +/- 0.5 days of gestation and continued for 96 h. Control fetuses were infused with saline. In cortisol-infused fetuses, the plasma cortisol concentrations rose significantly from control levels (4.4 +/- 0.6 ng/ml) to 19.3 +/- 3.1 ng/ml within 24 h and remained significantly elevated throughout the infusion period. Plasma immunoreactive (i.r.) ACTH concentrations were significantly elevated in cortisol-infused fetuses within 24-48 h and remained significantly higher than in controls throughout the 96-h experimental period. Plasma free cortisol concentrations increased 10-fold and remained significantly elevated in cortisol-infused animals, despite a rise in plasma corticosteroid-binding capacity. Levels of pituitary proopiomelanocortin (POMC) mRNA in the fetal pars distalis and pars intermedia were 96 and 38% lower, respectively, after 96 h of cortisol infusion. Therefore physiological elevations of plasma cortisol, in the late-gestation ovine fetus, lead to increases in mean plasma irACTH concentrations, but this is not associated with increases in fetal pituitary POMC mRNA levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenocorticotropic Hormone / blood*
  • Animals
  • Blood Gas Analysis
  • Carrier Proteins / biosynthesis
  • Female
  • Gestational Age
  • Hydrocortisone / blood
  • Hydrocortisone / pharmacology*
  • Liver / drug effects
  • Liver / embryology
  • Liver / metabolism
  • Pituitary Gland / drug effects
  • Pituitary Gland / embryology*
  • Pituitary Gland / metabolism
  • Pregnancy
  • Pregnancy, Animal / blood*
  • Pro-Opiomelanocortin / biosynthesis
  • Pro-Opiomelanocortin / genetics*
  • RNA, Messenger / metabolism*
  • Sheep

Substances

  • Carrier Proteins
  • RNA, Messenger
  • cortisol binding globulin
  • Pro-Opiomelanocortin
  • Adrenocorticotropic Hormone
  • Hydrocortisone