Huang M T, Veech R L
Laboratory of Metabolism, National Institute on Alcohol Abuse, Rockville, Maryland 20852.
J Clin Invest. 1988 Mar;81(3):872-8. doi: 10.1172/JCI113397.
The pathway for hepatic glycogen synthesis in the postprandial state was studied in meal-fed rats chronically cannulated in the portal vein. Plasma glucose concentration in the portal vein was found to be 4.50 +/- 1.01 mM (mean +/- SE; n = 3) before a meal and 11.54 +/- 0.70 mM (mean +/- SE; n = 4) after a meal in rats meal-fed a diet consisting of 100% commercial rat chow for 7 d. The hepatic-portal difference of plasma glucose concentration showed that liver released glucose in the fasted state and either extracted or released glucose after feeding depending on plasma glucose concentration in the portal vein. The concentration of portal vein glucose at which liver changes from glucose releasing to glucose uptake was 8 mM, the Km of glucokinase [E.C. 2.7.1.12]. The rate of glycogen synthesis in liver during meal-feeding was found to be approximately 1 mumol glucosyl U/g wet wt/min in rats meal-fed a 50% glucose supplemented chow diet. The relative importance of the direct vs. indirect pathway for the replenishment of hepatic glycogen was determined by the incorporation of [3-3H,U-14C]glucose into liver glycogen. Labeled glucose was injected into the portal vein at the end of meal-feeding. The ratio of 3H/14C in the glucosyl units of glycogen was found to be 83-92% of the ratio in liver free glucose six minutes after the injection, indicating that the majority of exogenous glucose incorporated into glycogen did not go through glycolysis. The percent contribution of the direct versus indirect pathway was quantitated from the difference in the relative specific activity (RSA) of [3H] and [14C]-glycogen in rats infused with [3-3H,U-14C]glucose. No significant difference was found between the RSA of [3H]glycogen and [14C]glycogen, indicating further that the pathway for glycogen synthesis in liver from exogenous glucose is from the direct pathway. Our results do not support the thesis that the majority of liver glycogen is synthesized from glucose-6-phosphate derived from gluconeogenesis. Reasons for the discrepancy between current findings and other reports supporting the indirect pathway for glycogen synthesis in the liver are discussed.
对长期经门静脉插管的进食大鼠餐后肝糖原合成途径进行了研究。给大鼠喂食由100%市售大鼠饲料组成的日粮7天,发现进食前门静脉血浆葡萄糖浓度为4.50±1.01 mM(平均值±标准误;n = 3),进食后为11.54±0.70 mM(平均值±标准误;n = 4)。血浆葡萄糖浓度的肝门静脉差值表明,肝脏在禁食状态下释放葡萄糖,进食后根据门静脉血浆葡萄糖浓度摄取或释放葡萄糖。肝脏从释放葡萄糖转变为摄取葡萄糖时的门静脉葡萄糖浓度为8 mM,即葡萄糖激酶[E.C. 2.7.1.12]的米氏常数。给喂食50%葡萄糖补充饲料日粮的大鼠喂食期间,肝脏中糖原合成速率约为1 μmol葡萄糖基U/g湿重/分钟。通过将[3-³H,U-¹⁴C]葡萄糖掺入肝糖原中,确定了肝糖原补充的直接途径与间接途径的相对重要性。在进食结束时将标记葡萄糖注入门静脉。注射后6分钟,糖原葡萄糖基单位中³H/¹⁴C的比率为肝脏游离葡萄糖中该比率的83 - 92%,这表明掺入糖原的大部分外源葡萄糖未经过糖酵解。根据注射[3-³H,U-¹⁴C]葡萄糖的大鼠中[³H]和[¹⁴C]糖原相对比活性(RSA)的差异,对直接途径与间接途径的贡献百分比进行了定量。[³H]糖原和[¹⁴C]糖原的RSA之间未发现显著差异,进一步表明肝脏中外源葡萄糖合成糖原的途径是直接途径。我们的结果不支持大多数肝糖原由糖异生衍生的6-磷酸葡萄糖合成这一论点。讨论了当前研究结果与支持肝脏糖原合成间接途径的其他报告之间存在差异的原因。