Jungermann K, Heilbronn R, Katz N, Sasse D
Eur J Biochem. 1982 Apr 1;123(2):429-36. doi: 10.1111/j.1432-1033.1982.tb19786.x.
Periportal and perivenous hepatocytes contain different activities (V) of antagonistic key enzymes such as glucokinase and glucose-6-phosphatase. In order to get an insight into the metabolism of the periportal and perivenous area the flux rates (v) of the glucose/glucose-6-phosphate cycle were calculated on the basis of the Michaelis-Menten equation using the measured zonal concentrations of glucose and glucose 6-phosphate, the zonal activities of glucokinase and glucose-6-phosphatase previously reported and the half-saturating substrate concentrations (Km) of the two enzymes found in the literature. The concentrations of glucose were obtained as a first approximation by measuring the concentrations in portal (= periportal) and hepatovenous (= perivenous) blood; those of glucose 6-phosphate were calculated from the levels determined in microdissected periportal and perivenous liver tissue. The calculations showed (a) that the overall cycling rates agreed remarkably well with those reported for intact animals and (b) that during a normal feeding rhythm the periportal zone should catalyze net glucose output and the perivenous zone should mediate net glucose uptake, as proposed by the model of 'metabolic zonation'.
汇管区和中央静脉周围的肝细胞含有不同活性(V)的拮抗关键酶,如葡萄糖激酶和葡萄糖-6-磷酸酶。为了深入了解汇管区和中央静脉周围区域的代谢情况,基于米氏方程,利用测得的葡萄糖和葡萄糖-6-磷酸的区域浓度、先前报道的葡萄糖激酶和葡萄糖-6-磷酸酶的区域活性以及文献中发现的这两种酶的半饱和底物浓度(Km),计算了葡萄糖/葡萄糖-6-磷酸循环的通量率(v)。葡萄糖浓度的初步近似值是通过测量门静脉(=汇管区)和肝静脉(=中央静脉周围)血液中的浓度获得的;葡萄糖-6-磷酸的浓度是根据在显微解剖的汇管区和中央静脉周围肝组织中测定的水平计算得出的。计算结果表明:(a)总的循环速率与完整动物报道的结果非常吻合;(b)在正常进食节律下,如“代谢分区”模型所提出的,汇管区应催化葡萄糖的净输出,而中央静脉周围区域应介导葡萄糖的净摄取。