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PMID: 2205106 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

The American journal of physiology ·Vol. 259 ·No. 3 Pt 1 ·1990-09-00 ·Pages E335-41

Shulman GI, Cline G, Schumann WC, Chandramouli V, Kumaran K, Landau BR

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.

MeSH Terms
Adult Blood Glucose/metabolism Carbon Isotopes Carbon Radioisotopes Eating Fasting Humans Liver Glycogen/metabolism Magnetic Resonance Spectroscopy/methods Male Radioisotope Dilution Technique
Chemicals
Blood Glucose Carbon Isotopes Carbon Radioisotopes Liver Glycogen
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Shulman G I
Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06510.
Cline G
Schumann W C
Chandramouli V
Kumaran K
Landau B R
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1990-09-00
Pages
E335-41
Language
English
Region
United States
NLM ID
0370511
Subset
IM
Grants
NIDDK NIH HHS · R01 DK040936 · United States
NIDDK NIH HHS · DK-14507 · United States
NIDDK NIH HHS · DK-20495 · United States
NIDDK NIH HHS · DK-40936 · United States
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