Literature DB >> 8380985

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.

L Agius1, D Tosh, M Peak.   

Abstract

1. During conversion of [6-3H,U-14C]glucose to glycogen in liver, loss of 6-3H can occur either by cycling via pyruvate (between glycolysis and gluconeogenesis) or by other mechanisms. We used mercaptopicolinate, an inhibitor of phosphoenolpyruvate carboxykinase, to determine the extent to which pyruvate cycling contributes to loss of 6-3H during glucose conversion to glycogen in hepatocytes. 2. Mercaptopicolinate increased the 3H/14C ratio in glycogen during incubation of rat, guinea pig, pig and human hepatocytes with [6-3H,U-14C]glucose. The increase in the 3H/14C ratio in glycogen caused by mercaptopicolinate was greater in periportal than in perivenous rat hepatocytes, indicating that cycling of glucose via pyruvate is more prominent in cells with a higher gluconeogenic relative to glycolytic capacity. 3. The effect of mercaptopicolinate on the 3H/14C ratio in glycogen was observed both in the absence and in the presence of insulin, indicating that stimulation of glycogen synthesis by insulin is not associated with inhibition of pyruvate cycling. In rat and guinea pig but not in pig hepatocytes, the effects of mercaptopicolinate on the 3H/14C ratio in glycogen were greater at 10-15 mM glucose than at 30 mM glucose, suggesting diminished cycling via pyruvate at high glucose concentrations. 4. Insulin increased the loss of 6-3H during stimulation of conversion of glucose to glycogen in hepatocytes from all species. This was due in part to an increase in pyruvate cycling and in part to other mechanisms that are not inhibited by mercaptopicolinate. 5. These results suggest that pyruvate cycling is a significant, but not exclusive, component of the loss of 6-3H in the hepatocyte during glucose conversion to glycogen. The extent of pyruvate cycling is dependent on the acinar origin of the hepatocytes and on the glucose concentration and presence of insulin.

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Year:  1993        PMID: 8380985      PMCID: PMC1132158          DOI: 10.1042/bj2890255

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  41 in total

1.  Futile cycles in isolated perfused rat liver and in isolated rat liver parenchymal cells.

Authors:  D Clark; D Lee; R Rognstad; J Katz
Journal:  Biochem Biophys Res Commun       Date:  1975-11-03       Impact factor: 3.575

2.  The effect of 3-mercaptopicolinic acid on phosphoenolpyruvate carboxykinase (GTP) in the rat and guinea pig.

Authors:  V Kostos; N W DiTullio; J Rush; L Cieslinski; H L Saunders
Journal:  Arch Biochem Biophys       Date:  1975-12       Impact factor: 4.013

3.  Futile cycles in the metabolism of glucose.

Authors:  J Katz; R Rognstad
Journal:  Curr Top Cell Regul       Date:  1976

4.  Effect of mercaptopicolinic acid and of transaminase inhibitors on glycogen synthesis by rat hepatocytes.

Authors:  F Okajima; J Katz
Journal:  Biochem Biophys Res Commun       Date:  1979-03-15       Impact factor: 3.575

5.  Control of glycogen synthesis in isolated rat hepatocytes by insulin, glucagon & acetylcholine.

Authors:  A C Beynen; M J Geelen
Journal:  Indian J Exp Biol       Date:  1981-01       Impact factor: 0.818

6.  Regulation of glycogen synthesis and glycolysis by insulin, pH and cell volume. Interactions between swelling and alkalinization in mediating the effects of insulin.

Authors:  M Peak; M al-Habori; L Agius
Journal:  Biochem J       Date:  1992-03-15       Impact factor: 3.857

7.  Estimation of glucose turnover and recycling in rabbits using various [3H, 14C]glucose labels.

Authors:  A Dunn; J Katz; S Golden; M Chenoweth
Journal:  Am J Physiol       Date:  1976-04

8.  Measurement of glucose recycling and liver glycogen synthesis in mice using doubly labeled substrates.

Authors:  N Baker
Journal:  Fed Proc       Date:  1977-02

9.  In vitro reversal of the fasting state of liver metabolism in the rat. Reevaluation of the roles of insulin and glucose.

Authors:  M E Boyd; E B Albright; D W Foster; J D McGarry
Journal:  J Clin Invest       Date:  1981-07       Impact factor: 14.808

10.  Influence of insulin, glucocorticoids and glucose on glycogen synthase activity in hepatocyte cultures.

Authors:  C Schudt
Journal:  Biochim Biophys Acta       Date:  1980-05-22
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  5 in total

1.  The control of hepatic glycogen metabolism in an in vitro model of sepsis.

Authors:  Jennifer Wallington; Jian Ning; Michael Alan Titheradge
Journal:  Mol Cell Biochem       Date:  2007-10-13       Impact factor: 3.396

2.  Fatty acid and amino acid modulation of glucose cycling in isolated rat hepatocytes.

Authors:  L A Gustafson; M Neeft; D J Reijngoud; F Kuipers; H P Sauerwein; J A Romijn; A W Herling; H J Burger; A J Meijer
Journal:  Biochem J       Date:  2001-09-15       Impact factor: 3.857

3.  Direct assessment of liver glycogen storage by 13C nuclear magnetic resonance spectroscopy and regulation of glucose homeostasis after a mixed meal in normal subjects.

Authors:  R Taylor; I Magnusson; D L Rothman; G W Cline; A Caumo; C Cobelli; G I Shulman
Journal:  J Clin Invest       Date:  1996-01-01       Impact factor: 14.808

4.  Intracellular binding of glucokinase in hepatocytes and translocation by glucose, fructose and insulin.

Authors:  L Agius; M Peak
Journal:  Biochem J       Date:  1993-12-15       Impact factor: 3.857

5.  Glycogen synthesis in amphibian oocytes: evidence for an indirect pathway.

Authors:  E Kessi; V Guixé; A Preller; T Ureta
Journal:  Biochem J       Date:  1996-04-15       Impact factor: 3.857

  5 in total

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