Kurland I J, Pilkis S J
Department of Physiology and Biophysics, State University of New York, Stony Brook 11794.
FASEB J. 1989 Sep;3(11):2277-81. doi: 10.1096/fasebj.3.11.2673899.
During refeeding after a brief period of starvation, glucose carbon is deposited into hepatic glycogen by both a direct and an indirect route. In the indirect route glucose is first metabolized to 3-carbon precursors, which then transverse the gluconeogenic pathway before being deposited into glycogen. Recent studies have yielded widely different estimates of the percentage of glucose carbon that follows the indirect route. Work summarized here demonstrates that the relative contributions of glucose carbon to hepatic glycogen formation by the indirect and direct pathways are greatly dependent on experimental design, and at least in vitro, are possibly dependent on the extent of glycogen/glucose 1-P recycling. Under physiological refeeding conditions in vivo, both pathways are used, each contributing approximately 50% of the amount of carbon appearing in glycogen. The level of glucokinase activity does not appear to be responsible for poor glucose utilization in liver. Poor glucose utilization in isolated liver preparations may result from the absence of a neurophysiological feedback loop that senses the arterial/portal glucose gradient and then regulates whole liver glucose uptake.
在短期饥饿后的再喂养过程中,葡萄糖碳通过直接和间接途径沉积到肝糖原中。在间接途径中,葡萄糖首先代谢为三碳前体,然后这些前体在进入糖原沉积之前先经过糖异生途径。最近的研究对通过间接途径的葡萄糖碳的百分比得出了差异很大的估计值。此处总结的研究表明,葡萄糖碳通过间接和直接途径对肝糖原形成的相对贡献在很大程度上取决于实验设计,并且至少在体外,可能取决于糖原/葡萄糖-1-磷酸循环的程度。在体内生理再喂养条件下,两条途径都会被利用,每条途径对糖原中出现的碳量的贡献约为50%。葡萄糖激酶活性水平似乎不是肝脏中葡萄糖利用不良的原因。分离的肝脏制剂中葡萄糖利用不良可能是由于缺乏一种神经生理反馈回路,该回路能感知动脉/门静脉葡萄糖梯度,进而调节整个肝脏的葡萄糖摄取。