Malaisse-Lagae F, Sterling I, Sener A, Malaisse W J
Laboratory of Experimental Medicine, Brussels Free University, Brussels, Belgium.
Clin Chim Acta. 1988 Mar 15;172(2-3):223-31. doi: 10.1016/0009-8981(88)90327-0.
The metabolism of D-[5-3H]glucose and D-[U-14C]glucose displays anomeric specificity in human erythrocytes. At close-to-physiological hexose concentrations, pure beta-D-[5-3H]glucose is metabolized at a higher rate than the corresponding pure alpha-anomer in most, but not all, subjects. This situation represents a mirror image of that found in rat erythrocytes. The anomeric preference is modulated by the extracellular concentration of D-glucose and may differ for distinct metabolic variables. The anomeric specificity of D-glucose metabolism remains operative, whether at low or normal temperature, even in erythrocytes exposed to equilibrated D-glucose.