Dehydroepiandrosterone decreases elevated hepatic glucose production in C57BL/KsJ-db/db mice

Life Sci. 2004 May 7;74(25):3075-84. doi: 10.1016/j.lfs.2003.10.031.

Abstract

Dehydroepiandrosterone (DHEA) is known to improve hyperglycemia in diabetic db/db mice that are obese and insulin resistant. In a previous study, we reported that DHEA suppresses the elevated hepatic gluconeogenic glucose-6-phosphatase (G6Pase) activity and gene expression in C57BL/KsJ-db/db mice. In the present study, we evaluated the total amount of gluconeogenesis using NaH[(14)C]CO(3) and hepatic glucose production using fructose as a substrate in primary cultured hepatocytes. Despite hyperinsulinemia, the glucose production of db/db mice in the total body and hepatocytes was elevated as compared to their heterozygote littermate C57BL/KsJ-db/+m mice. Administration of DHEA significantly decreased the blood glucose level and increased the plasma insulin level in db/db mice. Administration of DHEA decreased the elevated total body and hepatic glucose production in db/db mice. In addition, the glucose production in the primary cultured hepatocytes of db/db mice was decreased significantly by the direct addition of DHEA or DHEA-S to the medium. These results suggest that administration of DHEA suppresses the elevated total body and hepatic glucose production in db/db mice, and this effect on the liver is considered to result from increased plasma insulin and DHEA or DHEA-S itself.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / pharmacology*
  • Animals
  • Blood Glucose / metabolism
  • Body Weight / drug effects
  • Cells, Cultured
  • Dehydroepiandrosterone / pharmacology*
  • Diabetes Mellitus / metabolism
  • Gluconeogenesis / drug effects
  • Glucose / metabolism*
  • Hepatocytes / drug effects
  • Hepatocytes / pathology
  • Heterozygote
  • Hyperinsulinism / etiology
  • Hyperinsulinism / metabolism
  • Hyperinsulinism / pathology
  • Insulin / blood
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Organ Size / drug effects

Substances

  • Adjuvants, Immunologic
  • Blood Glucose
  • Insulin
  • Dehydroepiandrosterone
  • Glucose