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PMID: 6458521 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Effect of diabetes, insulin, starvation, and refeeding on the level of rat hepatic fructose 2,6-bisphosphate.

Diabetes ·Vol. 30 ·No. 12 ·1981-12-00 ·Pages 1062-4

Neely P, El-Maghrabi MR, Pilkis SJ, Claus TH

Abstract

The influence of alloxan diabetes and starvation for 72 h on the level of rat hepatic fructose 2,6-biphosphate was investigated. Both diabetes and starvation decreased the level to 10% of the value found in livers of normal, fed rats (10 nmol/g liver). The activity of the enzyme responsible for the synthesis of fructose 2,6-bisphosphate, 6-phosphofructo 2-kinase, was also decreased in livers of diabetic rats. Insulin administration for 24 h to diabetic rats restored the level of fructose 2,6-bisphosphate to normal. Refeeding a high carbohydrate diet for 24 h to starved rats resulted in fructose, 2,6-biphosphate levels that were 2.5-fold higher than that in livers of fed rats. The level of fructose 2,6-bisphosphate in diabetes and starvation, and after refeeding correlates as well with the rate of glycolysis and gluconeogenesis in these states and thereby provides further support for its role in regulating hepatic carbohydrate metabolism.

MeSH Terms
Animals Diabetes Mellitus, Experimental/metabolism Food Fructosediphosphates/metabolism Hexosediphosphates/metabolism Insulin/pharmacology Liver/metabolism Male Phosphofructokinase-1/metabolism Rats Rats, Inbred Strains Starvation/metabolism
Chemicals
Fructosediphosphates Hexosediphosphates Insulin fructose 2,6-diphosphate Phosphofructokinase-1
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Neely P
El-Maghrabi M R
Pilkis S J
Claus T H
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
1981-12-00
Pages
1062-4
Language
English
Region
United States
NLM ID
0372763
Subset
IM
Grants
NIADDK NIH HHS · AM 18270 · United States
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