Fischer W, Ick M, Katz N R
Hoppe Seylers Z Physiol Chem. 1982 Apr;363(4):375-80. doi: 10.1515/bchm2.1982.363.1.375.
Glucokinase and hexokinase activities were measured in the periportal and perivenous zone of the liver acinus separated by microdissection. A microfluorimetric assay was established for the separate determination of both enzyme activities. Glucokinase activity was about 3.5-fold higher in the perivenous than in the periportal zone in fed male and female rats. after 24 h starvation this gradient was only slightly changed. Hexokinase showed an inverse gradient with about 1.5-fold higher activities in the periportal than in the perivenous zone in both fed and fasted animals. Since glucokinase is restricted to parenchymal cells and hexokinase is present predominantly or even exclusively in non-parenchymal cells, the heterogeneous distribution of glucokinase activity supports the model of a "metabolic zonation of liver parenchyma" with a predominance of glucose uptake in the perivenous and glucose release in the periportal hepatocytes.
通过显微切割分离肝腺泡的门静脉周围区和肝静脉周围区,测定其中葡萄糖激酶和己糖激酶的活性。建立了一种微量荧光测定法,用于分别测定这两种酶的活性。在喂食的雄性和雌性大鼠中,肝静脉周围区的葡萄糖激酶活性比门静脉周围区高约3.5倍。饥饿24小时后,这种梯度仅略有变化。在喂食和禁食的动物中,己糖激酶呈现相反的梯度,门静脉周围区的活性比肝静脉周围区高约1.5倍。由于葡萄糖激酶局限于实质细胞,而己糖激酶主要或甚至仅存在于非实质细胞中,葡萄糖激酶活性的不均匀分布支持了“肝实质代谢分区”模型,即肝静脉周围肝细胞以摄取葡萄糖为主,而门静脉周围肝细胞以释放葡萄糖为主。