Acute fructose administration improves oral glucose tolerance in adults with type 2 diabetes

Citation
Mc. Moore et al., Acute fructose administration improves oral glucose tolerance in adults with type 2 diabetes, DIABET CARE, 24(11), 2001, pp. 1882-1887
Citations number
33
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
DIABETES CARE
ISSN journal
01495992 → ACNP
Volume
24
Issue
11
Year of publication
2001
Pages
1882 - 1887
Database
ISI
SICI code
0149-5992(200111)24:11<1882:AFAIOG>2.0.ZU;2-L
Abstract
OBJECTIVE - in normal adults, a small (catalytic) dose of fructose administ ered with glucose decreases the glycemic response to a glucose load, especi ally in those with the poorest glucose tolerance. We hypothesized that an a cute catalytic dose of fructose would also improve glucose tolerance in ind ividuals With type 2 diabetes. RESEARCH DESIGN AND METHODS - Five adults with type 2 diabetes underwent an oral glucose tolerance test (OGTT) on two separate occasions, at least I w eek apart, Each OGTT consisted of 75 g glucose with or without the addition of 7.5 g fructose (OGTT + F or OGTT - R in random order. Arterialized bloo d samples were collected from a heated dorsal hand vein twice before ingest ion of the carbohydrate and every 15 min for 3 h afterward, RESULTS - The area under the curve (AUC) of the plasma glucose response was reduced by fructose administration in all subjects the mean AUC during the OGTT + F was 14% less than that during the OGTT - F (P < 0.05). The insuli n AUC was decreased 21% with fructose administration (P = 0.2). Plasma gluc agon concentrations declined similarly during OGTT- F and OGTT + F. The inc remental AUC of the blood lactate response during the OGTT - F was similar to 50% of that observed during the OGTT + F (P < 0.05). Neither nonesterifi ed fail), acid nor triglycericle concentrations differed between the two OG TTs. CONCLUSIONS - Low-close fructose improves the glycemic response to an oral glucose load in adults with type 2 diabetes, and this effect is not a resul t of stimulation of insulin secretion.