Literature DB >> 3343346

Role of the direct and indirect pathways for glycogen synthesis in rat liver in the postprandial state.

M T Huang1, R L Veech.   

Abstract

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.

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Year:  1988        PMID: 3343346      PMCID: PMC442539          DOI: 10.1172/JCI113397

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  24 in total

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Journal:  J Appl Physiol       Date:  1975-02       Impact factor: 3.531

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Journal:  Biochem J       Date:  1974-07       Impact factor: 3.857

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Journal:  J Neurochem       Date:  1973-06       Impact factor: 5.372

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Journal:  Biochem Biophys Res Commun       Date:  1980-03-13       Impact factor: 3.575

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Journal:  Physiol Behav       Date:  1981-03

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Journal:  Biochemistry       Date:  1967-01       Impact factor: 3.162

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Journal:  Eur J Biochem       Date:  1975-12-01

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Journal:  Biochem J       Date:  1978-02-15       Impact factor: 3.857

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  20 in total

Review 1.  Fuel selection and carbon flux during the starved-to-fed transition.

Authors:  M C Sugden; M J Holness; T N Palmer
Journal:  Biochem J       Date:  1989-10-15       Impact factor: 3.857

2.  Role of the rat liver in the disposal of a glucose gavage.

Authors:  J Casado; J A Fernández-López; M J Argilés; M Alemany
Journal:  Mol Cell Biochem       Date:  1992-07-06       Impact factor: 3.396

3.  Intestinal handling of a glucose gavage by the rat.

Authors:  J A Fernández-López; J Casado; J M Argilés; M Alemany
Journal:  Mol Cell Biochem       Date:  1992-07-06       Impact factor: 3.396

4.  Pyruvate dehydrogenase activities during the fed-to-starved transition and on re-feeding after acute or prolonged starvation.

Authors:  M J Holness; M C Sugden
Journal:  Biochem J       Date:  1989-03-01       Impact factor: 3.857

5.  Comparison of tissue pyruvate dehydrogenase activities on re-feeding rats fed ad libitum or meal-fed rats with a chow-diet meal.

Authors:  M J Holness; M C Sugden
Journal:  Biochem J       Date:  1989-08-15       Impact factor: 3.857

6.  Skeletal-muscle glycogen synthesis during the starved-to-fed transition in the rat.

Authors:  M J Holness; M J Schuster-Bruce; M C Sugden
Journal:  Biochem J       Date:  1988-09-15       Impact factor: 3.857

Review 7.  Mammalian glucokinase and its gene.

Authors:  P B Iynedjian
Journal:  Biochem J       Date:  1993-07-01       Impact factor: 3.857

8.  Initial glucose kinetics and hormonal response to a gastric glucose load in unrestrained post-absorptive and starved rats.

Authors:  C Smadja; J Morin; P Ferré; J Girard
Journal:  Biochem J       Date:  1990-09-01       Impact factor: 3.857

9.  Rapid switch of hepatic fatty acid metabolism from oxidation to esterification during diurnal feeding of meal-fed rats correlates with changes in the properties of acetyl-CoA carboxylase, but not of carnitine palmitoyltransferase I.

Authors:  A M Moir; V A Zammit
Journal:  Biochem J       Date:  1993-04-01       Impact factor: 3.857

10.  Predominant role of gluconeogenesis in the hepatic glycogen repletion of diabetic rats.

Authors:  A Giaccari; L Rossetti
Journal:  J Clin Invest       Date:  1992-01       Impact factor: 14.808

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