Mann G V, Newton P
Ann N Y Acad Sci. 1975 Sep 30;258:243-52. doi: 10.1111/j.1749-6632.1975.tb29285.x.
A system for measuring the rate of transport of dehydroascorbate into human red blood cells shows Michaelis-Menten type kinetics with substrate inhibition at levels above 150 muM DHA. The addition of sugars impairs this transport in the diminishing hierarchy D-glucose, D-mannose, D-xylose, D-galactose, L-lyxose, D-araboascorbate, L-sorbose and 2-deoxy-D-ribose. The effect of glucose on transport of ascorbate is marked at physiological levels. Transport of DHA is accelerated by copper ion and allows dehydroascorbate to move against a concentration gradient. The evidence supports the hypotheses proposing that hyperglycemia will impair the intracellular availability of vitamin C.
一种用于测量脱氢抗坏血酸进入人红细胞转运速率的系统显示,其具有米氏动力学特征,在脱氢抗坏血酸(DHA)浓度高于150 μM时存在底物抑制。添加糖类会损害这种转运,损害程度由高到低依次为:D - 葡萄糖、D - 甘露糖、D - 木糖、D - 半乳糖、L - 来苏糖、D - 阿拉伯抗坏血酸、L - 山梨糖和2 - 脱氧 - D - 核糖。葡萄糖对抗坏血酸转运的影响在生理水平上很显著。铜离子可加速DHA的转运,并使脱氢抗坏血酸能够逆浓度梯度移动。这些证据支持了以下假说:高血糖会损害细胞内维生素C的可利用性。