Literature DB >> 3535533

Plasma glucose concentration determines direct versus indirect liver glycogen synthesis.

C H Lang, G J Bagby, H L Blakesley, J L Johnson, J J Spitzer.   

Abstract

In the present study hepatic glycogenesis by the direct versus indirect pathway was determined as a function of the glucose infusion rate. Glycogen synthesis was examined in catheterized conscious rats that had been fasted 48 h before receiving a 3-h infusion (iv) of glucose. Glucose, containing tracer quantities of [U-14C]- and [6-3H]glucose, was infused at rates ranging from 0 to 230 mumol X min-1 X kg-1. Plasma concentrations of glucose, lactate, and insulin were positively correlated with the glucose infusion rate. Despite large changes in plasma glucose, lactate, and insulin concentrations, the rate of hepatic glycogen deposition (0.46 +/- 0.03 mumol X min-1 X g-1) did not vary significantly between glucose infusion rates of 20 and 230 mumol X min-1 X kg-1. However, the percent contribution of the direct pathway to glycogen repletion gradually increased from 13 +/- 2 to 74 +/- 4% in the lowest to the highest glucose infusion rates, with prevailing plasma glucose concentrations from 9.4 +/- 0.5 to 21.5 +/- 2.1 mM. Endogenous glucose production was depressed (by up to 40%), but not abolished by the glucose infusions. Only a small fraction (7-14%) of the infused glucose load was incorporated into liver glycogen via the direct pathway irrespective of the glucose infusion rate. Our data indicate that the relative contribution of the direct and indirect pathways of hepatic glycogen synthesis are dependent on the glucose load or plasma glucose concentration and emphasize the predominance of the indirect pathway of glycogenesis at plasma glucose concentrations normally observed after feeding.

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Year:  1986        PMID: 3535533     DOI: 10.1152/ajpendo.1986.251.5.E584

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


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

Authors:  M T Huang; R L Veech
Journal:  J Clin Invest       Date:  1988-03       Impact factor: 14.808

5.  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

6.  Determination of pathways of glycogen synthesis and the dilution of the three-carbon pool with [U-13C]glucose.

Authors:  J Katz; P A Wals; W N Lee
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-15       Impact factor: 11.205

7.  Activation of basal gluconeogenesis by coactivator p300 maintains hepatic glycogen storage.

Authors:  Ling He; Jia Cao; Shumei Meng; Anlin Ma; Sally Radovick; Fredric E Wondisford
Journal:  Mol Endocrinol       Date:  2013-06-14

8.  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

9.  Hepatic carbon flux after re-feeding. Hyperthyroidism blocks glycogen synthesis and the suppression of glucose output observed in response to carbohydrate re-feeding.

Authors:  M J Holness; M C Sugden
Journal:  Biochem J       Date:  1987-11-01       Impact factor: 3.857

10.  The contribution of pyruvate cycling to loss of [6-3H]glucose during conversion of glucose to glycogen in hepatocytes: effects of insulin, glucose and acinar origin of hepatocytes.

Authors:  L Agius; D Tosh; M Peak
Journal:  Biochem J       Date:  1993-01-01       Impact factor: 3.857

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