Literature DB >> 2205106

Quantitative comparison of pathways of hepatic glycogen repletion in fed and fasted humans.

G I Shulman1, G Cline, W C Schumann, V Chandramouli, K Kumaran, B R Landau.   

Abstract

The effect of fasting vs. refeeding on hepatic glycogen repletion by the direct pathway, i.e., glucose----glucose 6-phosphate (G-6-P)----glycogen, was determined. Acetaminophen was administered during an infusion of glucose labeled with [1-13C]- and [6-14C]glucose into four healthy volunteers after an overnight fast and into the same subjects 4 h after breakfast. 13C enrichments in C-1 and C-6 of glucose formed from urinary acetaminophen glucuronide compared with enrichments in C-1 and C-6 of plasma glucose provided an estimate of glycogen formation by the direct pathway. The specific activity of glucose from the glucuronide compared with the specific activity of the plasma glucose, along with the percentages of 14C in C-1 and C-6 of the glucose from the glucuronide, also provided an estimate of the amount of glycogen formed by the direct pathway. The estimates were similar. Those from [6-14C]glucose would have been higher than from [1-13C]glucose if the pentose cycle contribution to overall glucose utilization had been significant. After an overnight fast, during the last hour of infusion, 49 +/- 3% of the glycogen formed was formed via the direct pathway. After breakfast, at similar plasma glucose and insulin concentrations, the percentage increased to 69 +/- 7% (P less than 0.02). Thus the contributions of the pathways to hepatic glycogen formation depend on the dietary state of the individual. For a dietary regimen in which individuals consume multiple meals per day containing at least a moderate amount of carbohydrates most glycogen synthesis occurs by the direct pathway.

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Year:  1990        PMID: 2205106     DOI: 10.1152/ajpendo.1990.259.3.E335

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


  24 in total

1.  Hepatic gluconeogenic fluxes and glycogen turnover during fasting in humans. A stable isotope study.

Authors:  M K Hellerstein; R A Neese; P Linfoot; M Christiansen; S Turner; A Letscher
Journal:  J Clin Invest       Date:  1997-09-01       Impact factor: 14.808

Review 2.  The use of magnetic resonance methods in translational cardiovascular research.

Authors:  Arthur H L From; Kamil Ugurbil
Journal:  J Cardiovasc Transl Res       Date:  2009-01-13       Impact factor: 4.132

3.  Mechanism by which glucose and insulin inhibit net hepatic glycogenolysis in humans.

Authors:  K F Petersen; D Laurent; D L Rothman; G W Cline; G I Shulman
Journal:  J Clin Invest       Date:  1998-03-15       Impact factor: 14.808

4.  Impaired hepatic glycogen synthesis in glucokinase-deficient (MODY-2) subjects.

Authors:  G Velho; K F Petersen; G Perseghin; J H Hwang; D L Rothman; M E Pueyo; G W Cline; P Froguel; G I Shulman
Journal:  J Clin Invest       Date:  1996-10-15       Impact factor: 14.808

5.  Loss of Par-1a/MARK3/C-TAK1 kinase leads to reduced adiposity, resistance to hepatic steatosis, and defective gluconeogenesis.

Authors:  Jochen K Lennerz; Jonathan B Hurov; Lynn S White; Katherine T Lewandowski; Julie L Prior; G James Planer; Robert W Gereau; David Piwnica-Worms; Robert E Schmidt; Helen Piwnica-Worms
Journal:  Mol Cell Biol       Date:  2010-08-23       Impact factor: 4.272

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.  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

8.  Sources of carbon for hepatic glycogen synthesis in the conscious dog.

Authors:  M C Moore; A D Cherrington; G Cline; M J Pagliassotti; E M Jones; D W Neal; C Badet; G I Shulman
Journal:  J Clin Invest       Date:  1991-08       Impact factor: 14.808

9.  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

10.  Comparison of the time courses of insulin and the portal signal on hepatic glucose and glycogen metabolism in the conscious dog.

Authors:  M J Pagliassotti; L C Holste; M C Moore; D W Neal; A D Cherrington
Journal:  J Clin Invest       Date:  1996-01-01       Impact factor: 14.808

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