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Fundacíon Jiménez Díaz, Madrid, Spain (J.C., P.G.P., M.L.V., I.V.)
Laboratory of Experimental Hormonology, Brussels Free University, Brussels, Belgium (W.J.M.)
Address reprint requests to: W.J. Malaisse, MD, PhD, FACN, Laboratory of Experimental Hormonology, Brussels Free University (CP 626), 808 Route de Lennik, B-1070 Brussels, BELGIUM. E-mail: malaisse{at}ulb.ac.be
Objective: To assess whether oral D-fructose modifies the plasma D-glucose and insulin responses to oral D-glucose administration in normal rats.
Design: Oral D-glucose (1.7, 3.5, 6.9 or 13.9 µmol/g body weight), D-fructose (6.9 µmol/g), both D-glucose and D-fructose (1.7 or 3.5 µmol/g of each hexose) or sucrose (3.7 µmol/g) were administered intragastrically to overnight fasted rats and the plasma concentration of D-glucose, D-fructose and insulin measured over the ensuing 120 minutes. Control experiments were conducted after oral administration of H2O or saline.
Results: The administration of D-fructose, given as the free hexose or as sucrose, instead of augmenting the plasma D-glucose concentration evoked by the concomitant administration of D-glucose, tended both to improve the insulin response of the pancreatic B-cell and to minimize hyperglycemia, when compared to the results of experiments including the administration of equimolar amounts of D-glucose alone. For instance, the area under the plasma D-glucose curve was comparable in the rats receiving both D-glucose and D-fructose (3.5 µmol/g of each hexose) and the rats receiving only D-glucose (3.5 µmol/g), averaging respectively 836 ± 32 and 850 ± 34 mM · min each. Likewise, the paired ratio between the areas under the plasma insulin and D-glucose curves, when corrected for the threshold concentration for the insulinotropic action of the hexose (2.05 ± 0.10 mM), averaged 44.3 ± 3.0 nmol/mol in the 16 rats receiving D-fructose alone, sucrose alone or both D-glucose and D-fructose, as compared to 37.7 ± 2.9 nmol/mol in the 22 rats receiving increasing amounts of D-glucose alone.
Conclusions: The intake of D-fructose, as the free hexose or as sucrose, favours D-glucose homeostasis. This is likely to be attributable to the reciprocal effects of the aldose and ketose upon their respective phosphorylation by glucokinase in both hepatocytes and insulin-producing pancreatic islet cells.
Key words: D-glucose, D-fructose, sucrose, plasma insulin, normal rats
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