FASEB J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Van Schaftingen, E.
Right arrow Articles by Davies, D. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Van Schaftingen, E.
Right arrow Articles by Davies, D. R.

The FASEB Journal, Vol 5, 326-330, Copyright © 1991 by The Federation of American Societies for Experimental Biology


RESEARCH COMMUNICATIONS

Fructose administration stimulates glucose phosphorylation in the livers of anesthetized rats

E Van Schaftingen and DR Davies
Laboratory of Physiological Chemistry, International Institute of Cellular and Molecular Pathology, Brussels, Belgium.

A method allowing one to measure the rate of glucose phosphorylation in the livers of anesthetized rats is described. Upon injection of [2- 3H]glucose into the portal vein, about 90% of the radioactivity remained in the liver for approximately 30 s. The proportion of radioactivity accounted for by tritiated water increased linearly at a rate of about 5%/min in control animals. Fructose injected into the penile vein stimulated this rate up to 2.2- and 2.7-fold in fed and overnight starved rats respectively, a maximal effect being observed at a dose of 50 mg/kg under both conditions. Fructose was also active when administered by intragastric infusion. The ketose caused increases in the concentration of fructose 1-phosphate, which reached values known to relieve the inhibition exerted on glucokinase by its regulatory protein.


This article has been cited by other articles:


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
M. E. Bizeau, J. S. Thresher, and M. J. Pagliassotti
A high-sucrose diet increases gluconeogenic capacity in isolated periportal and perivenous rat hepatocytes
Am J Physiol Endocrinol Metab, May 1, 2001; 280(5): E695 - E702.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. Burcelin, C. Mrejen, J. F. Decaux, S. H. De Mouzon, J. Girard, and M. J. Charron
In Vivo and in Vitro Regulation of Hepatic Glucagon Receptor mRNA Concentration by Glucose Metabolism
J. Biol. Chem., April 3, 1998; 273(14): 8088 - 8093.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
D. Mitanchez, B. Doiron, R. Chen, and A. Kahn
Glucose-Stimulated Genes and Prospects of Gene Therapy for Type I Diabetes
Endocr. Rev., August 1, 1997; 18(4): 520 - 540.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1991 by The Federation of American Societies for Experimental Biology.