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Dehydroepiandrosterone suppresses elevated hepatic glucose-6-phosphatase mRNA level in C57BL/KsJ-db/db mice: comparison with troglitazone.

Abstract
Dehydroepiandrosterone (DHEA) is known to improve hyperglycemia of diabetic C57BL/KsJ-db/db mice that are obese and insulin resistant. In a previous study, we reported that DHEA as well as troglitazone suppresses the elevated hepatic gluconeogenic enzymes, glucose-6-phosphatase (G6Pase) and fructose-1,6-bisphosphatase (FBPase) activities in C57BL/KsJ-db/db mice. In the present study, we evaluated the changes in mRNA of G6Pase and FBPase in db/db mice. Despite hyperinsulinemia, the G6Pase mRNA level of db/db mice was elevated as compared to their heterozygote littermate db/+m mice. In contrast, the FBPase mRNA level was not elevated in db/db mice. Administration of DHEA for two weeks significantly decreased the blood glucose level and the elevated G6Pase mRNA level in db/db mice. No significant changes were seen in the FBPase mRNA level after the administration of DHEA. Administration of troglitazone also decreased the blood glucose and G6Pase mRNA level in db/db mice although no changes were seen in the FBPase mRNA level. These results suggest that the elevation of G6Pase mRNA is important in elucidating the cause of insulin resistance, and that the G6Pase gene is at least one target for the hypoglycemic effects of DHEA as an insulin sensitizing agent in db/db mice.
AuthorsK Aoki, T Kikuchi, K Mukasa, S Ito, A Nakajima, S Satoh, A Okamura, H Sekihara
JournalEndocrine journal (Endocr J) Vol. 47 Issue 6 Pg. 799-804 (Dec 2000) ISSN: 0918-8959 [Print] Japan
PMID11228057 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Blood Glucose
  • Chromans
  • Hypoglycemic Agents
  • Insulin
  • RNA, Messenger
  • Thiazoles
  • Thiazolidinediones
  • Dehydroepiandrosterone
  • Glucose-6-Phosphatase
  • Troglitazone
Topics
  • Animals
  • Blood Glucose (metabolism)
  • Blotting, Northern
  • Body Weight
  • Chromans (pharmacology)
  • Dehydroepiandrosterone (pharmacology)
  • Diabetes Mellitus (enzymology, pathology)
  • Glucose-6-Phosphatase (genetics)
  • Hypoglycemic Agents (pharmacology)
  • Insulin (blood)
  • Insulin Resistance
  • Liver (drug effects, enzymology, pathology)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Organ Size
  • RNA, Messenger (analysis)
  • Thiazoles (pharmacology)
  • Thiazolidinediones
  • Troglitazone

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