Literature DB >> 4019452

Quantitative estimation of the pathways followed in the conversion to glycogen of glucose administered to the fasted rat.

R F Scofield, K Kosugi, W C Schumann, K Kumaran, B R Landau.   

Abstract

When [6-3H,6-14C]glucose was given in glucose loads to fasted rats, the average 3H/14C ratios in the glycogens deposited in their livers, relative to that in the glucoses administered, were 0.85 and 0.88. When [3-3H,3-14C]lactate was given in trace quantity along with unlabeled glucose loads, the average 3H/14C ratio in the glycogens deposited was 0.08. This indicates that a major fraction of the carbons of the glucose loads was converted to liver glycogen without first being converted to lactate. When [3-3H,6-14C]glucose was given in glucose loads, the 3H/14C ratios in the glycogens deposited averaged 0.44. This indicates that a significant amount of H bound to carbon 3, but not carbon 6, of glucose is removed within liver in the conversion of the carbons of the glucose to glycogen. This can occur in the pentose cycle and by cycling of glucose-6-P via triose phosphates: glucose----glucose-6-P----triose phosphates----glucose-6-P----glycogen. The contributions of these pathways were estimated by giving glucose loads labeled with [1-14C]glucose, [2-14C]glucose, [5-14C]glucose, and [6-14C]glucose and degrading the glucoses obtained by hydrolyzing the glycogens that deposited. Only a few per cent of the glucose carbons deposited in glycogen were deposited in liver via glucose-6-P conversion to triose phosphates. Between 4 and 9% of the glucose utilized by the liver was utilized in the pentose cycle. While these are relatively small percentages, since three NADP3H molecules are formed from each molecule of [3-3H]glucose-6-P utilized in the cycle, a major portion of the difference between the ratios obtained with [3-3H]glucose and with [6-3H]glucose is attributable to metabolism in the pentose cycle. Because 3H of [3-3H]glucose is extensively removed during the conversion of the glucose to glycogen within liver the extent of incorporation of the 3H into liver glycogen is not the measure of glucose's metabolism in other tissues before its carbons are deposited in liver glycogen. The distributions of 14C from the 14C-labeled glucoses into the carbons of the liver glycogens mean that at a minimum about 30% of the carbons of the glucose deposited in the glycogen were first converted to lactate or its metabolic equivalent.

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Year:  1985        PMID: 4019452

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  13 in total

1.  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

2.  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

3.  Hormone and substrate regulation of glycogen accumulation in primary cultures of rat hepatocytes.

Authors:  A I Salhanick; C L Chang; J M Amatruda
Journal:  Biochem J       Date:  1989-08-01       Impact factor: 3.857

4.  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

5.  Quantitative analysis of glycogen repletion by nuclear magnetic resonance spectroscopy in the conscious rat.

Authors:  G I Shulman; L Rossetti; D L Rothman; J B Blair; D Smith
Journal:  J Clin Invest       Date:  1987-08       Impact factor: 14.808

6.  Quantitation of the pathways of hepatic glycogen formation on ingesting a glucose load.

Authors:  I Magnusson; V Chandramouli; W C Schumann; K Kumaran; J Wahren; B R Landau
Journal:  J Clin Invest       Date:  1987-12       Impact factor: 14.808

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.  Carcass glycogen repletion on carbohydrate re-feeding after starvation.

Authors:  D J Cox; T N Palmer
Journal:  Biochem J       Date:  1987-08-01       Impact factor: 3.857

9.  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

10.  Glycoconjugates as noninvasive probes of intrahepatic metabolism: pathways of glucose entry into compartmentalized hepatic UDP-glucose pools during glycogen accumulation.

Authors:  M K Hellerstein; D J Greenblatt; H N Munro
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

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