Insulin and glucagon during the perinatal period: secretion and metabolic effects on the liver

Biol Neonate. 1985;48(4):204-20. doi: 10.1159/000242173.

Abstract

Insulin and glucagon are detected in the plasma of most species early in gestation. In the fetus at term, insulin and glucagon secretion can be modified by long-term changes in glucose concentration but the responsiveness of A and B cells to glucose is lower than in the adult. The plasma insulin/glucagon molar ratio is high in the fetus at term, then decreases dramatically immediately after birth and remains low during the first hours of extrauterine life. This situation results in favored hepatic glycogen storage and prevented gluconeogenesis in utero, and sharp glycogen breakdown and active gluconeogenesis during the early postnatal period.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Animals
  • Animals, Newborn / physiology*
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Experimental / physiopathology
  • Fasting
  • Female
  • Fetal Blood / metabolism
  • Fetus / physiology*
  • Gestational Age
  • Glucagon / metabolism*
  • Glucagon / pharmacology
  • Gluconeogenesis
  • Glucose / metabolism
  • Glucose / pharmacology
  • Glycogen / metabolism
  • Humans
  • In Vitro Techniques
  • Infant, Newborn*
  • Insulin / metabolism*
  • Insulin / pharmacology
  • Insulin Secretion
  • Islets of Langerhans / embryology
  • Islets of Langerhans / growth & development
  • Islets of Langerhans / metabolism
  • Liver / drug effects
  • Liver / embryology
  • Liver / metabolism
  • Pancreas / drug effects
  • Pancreas / embryology
  • Pancreas / metabolism
  • Phosphoenolpyruvate Carboxykinase (GTP) / metabolism
  • Pregnancy
  • Pregnancy in Diabetics / physiopathology
  • Receptor, Insulin / metabolism
  • Receptors, Cell Surface / metabolism
  • Receptors, Glucagon
  • Theophylline / pharmacology

Substances

  • Blood Glucose
  • Insulin
  • Receptors, Cell Surface
  • Receptors, Glucagon
  • Glycogen
  • Glucagon
  • Theophylline
  • Receptor, Insulin
  • Phosphoenolpyruvate Carboxykinase (GTP)
  • Glucose