Kuwajima M, Newgard C B, Foster D W, McGarry J D
J Clin Invest. 1984 Sep;74(3):1108-11. doi: 10.1172/JCI111479.
The time course of changes in hepatic fructose-2,6-bisphosphate (F-2,6-P2) and glycogen content was examined in fasted rats infused with glucose intragastrically or allowed to eat a chow diet ad lib. Initial values for the two parameters were approximately 0.4 nmol/g and 2 mg/g of tissue, respectively. Contrary to what might have been expected on the basis of reported studies with hepatocytes exposed to glucose (i.e., a rapid elevation of F-2,6-P2), the rise in F-2,6-P2 levels in vivo was a late event. It began only 4-5 h after glucose administration or refeeding, at which time glycogen content had reached approximately 35 mg/g of tissue. Thereafter, [F-2,6-P2] climbed rapidly, attaining fed values in the region of 10 nmol/g as glycogen stores became maximal (approximately 60 mg/g of tissue). Although the biochemical basis for these changes is still unclear, the delayed increase in [F-2,6-P2] is entirely consistent with the fact that much of the glycogen deposited in liver in the early postprandial phase is gluconeogenic in origin. The later rise in [F-2,6-P2] likely represents a key signal for the attenuation of gluconeogenic carbon flow into glycogen as the latter approaches repletion levels.
在禁食大鼠中,通过胃内输注葡萄糖或随意给予普通饲料,研究了肝果糖-2,6-二磷酸(F-2,6-P2)和糖原含量的变化时间进程。这两个参数的初始值分别约为0.4 nmol/g和2 mg/g组织。与基于报道的肝细胞暴露于葡萄糖的研究可能预期的情况(即F-2,6-P2迅速升高)相反,体内F-2,6-P2水平的升高是一个后期事件。它仅在给予葡萄糖或重新喂食后4-5小时开始,此时糖原含量已达到约35 mg/g组织。此后,[F-2,6-P2]迅速攀升,随着糖原储备达到最大值(约60 mg/g组织),达到进食状态下约10 nmol/g的水平。尽管这些变化的生化基础仍不清楚,但[F-2,6-P2]的延迟增加与餐后早期肝脏中沉积的大部分糖原起源于糖异生这一事实完全一致。[F-2,6-P2]的后期升高可能代表了一个关键信号,即随着糖原接近充盈水平,糖异生碳流入糖原的过程减弱。