The prenatal development and glucocorticoid control of brush-border hydrolases in the pig small intestine

Pediatr Res. 1995 Feb;37(2):207-12. doi: 10.1203/00006450-199502000-00014.

Abstract

The development of brush-border enzymes and the possible regulatory role of cortisol were investigated in the small intestine of the fetal and neonatal pig. With the sows under pentobarbitone anesthesia, osmotic minipumps containing either saline or cortisol were inserted s.c. into 25 fetuses from 10 pregnant sows (82-96 d gestation). Six d later, the infused fetuses were removed by cesarean section and samples of the proximal, middle, and distal intestine taken for analysis. Samples were also obtained from 48 piglets that did not undergo an operation (controls) and that were removed at intervals from 82 d gestation until term (114 +/- 2 d). In the proximal and middle intestine, the mean levels of lactase-phlorizin hydrolase (EC 3.2.1.23-62), maltaseglucoamylase (EC 3.2.1.20), aminopeptidase N (EC 3.4.11.2), and aminopeptidase A (EC 3.4.11.7) increased during the last 10-15 d before term, correlated positively with log10 plasma cortisol values, and were higher in cortisol-infused than in saline-infused fetuses (p < 0.05). Activity of sucrase-isomaltase (EC 3.2.1.48-10) was low in fetal pigs, and this enzyme and dipeptidyl peptidase IV (EC 3.4.14.5) were not significantly affected by fetal age or exogenous cortisol. Maltase (EC 3.2.1.48-10 and EC 3.2.1.20) activity was significantly decreased in the middle and distal intestine of cortisol-infused fetuses. The results suggest that the prepartum rise in endogenous cortisol secretion stimulates the prenatal expression of certain brush-border enzymes in the pig small intestine at this critical time. However, the effects of cortisol on the developing intestine were highly idiosyncratic for particular enzymes and intestinal regions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminopeptidases / biosynthesis*
  • Animals
  • Animals, Newborn
  • Body Weight
  • Dipeptidyl Peptidase 4 / biosynthesis*
  • Disaccharidases / biosynthesis*
  • Enzyme Induction / drug effects
  • Hydrocortisone / blood
  • Hydrocortisone / pharmacology*
  • Intestine, Small / embryology
  • Intestine, Small / enzymology*
  • Intestine, Small / ultrastructure
  • Microvilli / enzymology
  • Organ Size
  • Swine

Substances

  • Disaccharidases
  • Aminopeptidases
  • Dipeptidyl Peptidase 4
  • Hydrocortisone