Dehydroepiandrosterone suppresses the elevated hepatic glucose-6-phosphatase and fructose-1,6-bisphosphatase activities in C57BL/Ksj-db/db mice: comparison with troglitazone

Diabetes. 1999 Aug;48(8):1579-85. doi: 10.2337/diabetes.48.8.1579.

Abstract

The effect of dehydroepiandrosterone (DHEA) on the hepatic and muscle glucose metabolizing enzymes and on blood glucose were investigated in insulin-resistant diabetic C57BL/KsJ-db/db mice and their heterozygote littermates (db/+m). The results were compared with those after troglitazone administration under the same conditions. Despite hyperinsulinemia, hepatic glucose-6-phosphatase (G6Pase) and fructose-1,6-bisphosphatase (FBPase) activities are higher in db/db than in db/+m mice. Dietary administration of DHEA and that of troglitazone for 15 days to respective groups of five mice each significantly decreased blood glucose in db/db mice and hepatic G6Pase and FBPase activities in both db/db and db/+m mice. Hepatic G6Pase and FBPase activities showed a linear relationship with blood glucose in all groups of mice, suggesting that the activities of G6Pase and FBPase are closely related to blood glucose levels. Because androstenedione, a DHEA metabolite, barely affected either of these enzyme activities or blood glucose in db/db mice, the actions of DHEA, which are similar to those of troglitazone, are presumed to be caused by DHEA itself. DHEA is considered to be a modulating agent for the activities of hepatic gluconeogenic enzymes in db/db mice.

Publication types

  • Comparative Study

MeSH terms

  • Androstenedione / pharmacology
  • Animals
  • Blood Glucose / analysis
  • Body Composition / drug effects
  • Chromans / pharmacology*
  • Dehydroepiandrosterone / blood
  • Dehydroepiandrosterone / pharmacology*
  • Diabetes Mellitus / enzymology*
  • Diabetes Mellitus / genetics
  • Eating / drug effects
  • Fructose-Bisphosphatase / metabolism*
  • Glucose-6-Phosphatase / metabolism*
  • Hypoglycemic Agents / pharmacology*
  • Insulin / blood
  • Insulin / pharmacology
  • Insulin Resistance / genetics
  • Insulin Resistance / physiology*
  • Liver / enzymology*
  • Male
  • Mice
  • Mice, Inbred C57BL / genetics
  • Thiazoles / pharmacology*
  • Thiazolidinediones*
  • Troglitazone

Substances

  • Blood Glucose
  • Chromans
  • Hypoglycemic Agents
  • Insulin
  • Thiazoles
  • Thiazolidinediones
  • Androstenedione
  • Dehydroepiandrosterone
  • Fructose-Bisphosphatase
  • Glucose-6-Phosphatase
  • Troglitazone