Cremer J E, Cunningham V J
Biochem J. 1979 Jun 15;180(3):677-9. doi: 10.1042/bj1800677.
The inhibition of D-glucose transport into brain by several hexose analogues has been investigated in adult anaesthetized rats. D-Glucose was transported with apparent Vmax. = 1.22 mumol/g per min, Km = 11.12 mM and Kd = 0.008 ml/g per min. 6-Chloro-6-deoxyglucose was transported with corresponding values of Vmax. = 1.33 mumol/g per min, Km = 5.5 mM and Kd = 0.0155 ml/g per min and inhibited D-glucose transport with apparent Ki = 3.01 mM. 6-Chloro-6-deoxymannose, 6-chloro-6-deoxygalactose and 6-tosyl-6-deoxygalactose also inhibited D-glucose transport, but 6-chloro-6-deoxyfructose was without effect. The results were consistent with a model for glucose transport at the blood/brain interface that involves a hydrophobic site on the transport protein at or near the 6-position of bound glucose.
在成年麻醉大鼠中研究了几种己糖类似物对脑内D-葡萄糖转运的抑制作用。D-葡萄糖的转运表现出表观最大转运速率(Vmax)= 1.22 μmol/g每分钟,米氏常数(Km)= 11.12 mM,解离常数(Kd)= 0.008 ml/g每分钟。6-氯-6-脱氧葡萄糖的转运对应值为Vmax = 1.33 μmol/g每分钟,Km = 5.5 mM,Kd = 0.0155 ml/g每分钟,并且以表观抑制常数(Ki)= 3.01 mM抑制D-葡萄糖的转运。6-氯-6-脱氧甘露糖、6-氯-6-脱氧半乳糖和6-甲苯磺酰基-6-脱氧半乳糖也抑制D-葡萄糖的转运,但6-氯-6-脱氧果糖没有作用。这些结果与血脑界面葡萄糖转运模型一致,该模型涉及转运蛋白上结合葡萄糖6位或其附近的疏水位点。