Literature DB >> 3462741

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

M K Hellerstein, D J Greenblatt, H N Munro.   

Abstract

Recent studies have questioned the efficiency with which administered glucose generates hepatic glycogen through the direct nonrecycling route compared with the indirect route from glucose recycled through glycolysis followed by gluconeogenesis. Using fasted and refed rats, we examined the relative access of infused [1-3H]- and [U-14C]glucose by way of these two pathways to liver glycogen and to hepatic glucuronic acid, the latter recovered from the urine as the glucuronide conjugated with administered acetaminophen. In fasted animals and during early refeeding, extensive dilution of administered [3H]- and [14C]glucose recovered in glycogen showed that 60-70% of the labeled glucose had undergone recycling by the indirect route. As refeeding progressed with substantial glycogen deposition, the contribution of the recycling pathway to glycogen and glucuronic acid diminished considerably. Thus, there is a shift in pathways of hepatic glucose utilization as liver glycogen accumulates. Consequently, the ratio of 3H/14C in glucuronic acid was closely correlated with the glycogen content of the liver at sacrifice, indicating that this ratio may prove useful as a noninvasive indicator of liver glycogen concentration. Since glycogen and glucuronic acid are derived by single reactions from UDP-glucose, they should show a common labeling pattern with 3H and 14C under various nutritional conditions. However, detailed analysis of their labeling patterns showed a striking divergence, implying that there must be compartmentation of the UDP-glucose pools leading to each of these end products, either because they are made in separate compartments within the same cell or because each is made in different hepatocyte populations. We favor the former explanation because galactose secreted in glycoproteins shows 3H and 14C labeling patterns similar to those of glucuronic acid conjugated with acetaminophen, and both of these conjugations occur in the endoplasmic reticulum of the liver, whereas most glycogen is present in the cytosol.

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Year:  1986        PMID: 3462741      PMCID: PMC386649          DOI: 10.1073/pnas.83.18.7044

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  32 in total

1.  The conversion of fructose-1-C14 and sorbitol-1-C14 to liver and muscle glycogen in the rat.

Authors:  H G HERS
Journal:  J Biol Chem       Date:  1955-05       Impact factor: 5.157

Review 2.  Metabolism of hormones, drugs and other substances by the gut.

Authors:  K Hartiala
Journal:  Physiol Rev       Date:  1973-04       Impact factor: 37.312

3.  Recovery of the liver glycogen in fasted rats.

Authors:  J M Olavarria; O G Gödeken; R Sandruss; M Flawia
Journal:  Biochim Biophys Acta       Date:  1968-08-06

4.  Distribution of UDPglucuronosyltransferase in rat tissue.

Authors:  J R Chowdhury; P M Novikoff; N R Chowdhury; A B Novikoff
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

Review 5.  The glucose paradox. Is glucose a substrate for liver metabolism?

Authors:  J Katz; J D McGarry
Journal:  J Clin Invest       Date:  1984-12       Impact factor: 14.808

6.  Mechanism of liver glycogen repletion in vivo by nuclear magnetic resonance spectroscopy.

Authors:  G I Shulman; D L Rothman; D Smith; C M Johnson; J B Blair; R G Shulman; R A DeFronzo
Journal:  J Clin Invest       Date:  1985-09       Impact factor: 14.808

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

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

8.  Studies on the mechanism by which exogenous glucose is converted into liver glycogen in the rat. A direct or an indirect pathway?

Authors:  C B Newgard; L J Hirsch; D W Foster; J D McGarry
Journal:  J Biol Chem       Date:  1983-07-10       Impact factor: 5.157

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.  Active hepatic glycogen synthesis from gluconeogenic precursors despite high tissue levels of fructose 2,6-bisphosphate.

Authors:  M Kuwajima; S Golden; J Katz; R H Unger; D W Foster; J D McGarry
Journal:  J Biol Chem       Date:  1986-02-25       Impact factor: 5.157

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  15 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

2.  Effects of recombinant monokines on hepatic pyruvate dehydrogenase, pyruvate dehydrogenase kinase, lipogenesis de novo and plasma triacylglycerols. Abolition by prior fasting.

Authors:  M Blackham; D Cesar; O J Park; T C Vary; K Wu; S Kaempfer; C H Shackleton; M K Hellerstein
Journal:  Biochem J       Date:  1992-05-15       Impact factor: 3.857

3.  Interleukin-1-induced anorexia in the rat. Influence of prostaglandins.

Authors:  M K Hellerstein; S N Meydani; M Meydani; K Wu; C A Dinarello
Journal:  J Clin Invest       Date:  1989-07       Impact factor: 14.808

4.  Skeletal-muscle glycogen synthesis during the starved-to-fed transition in the rat.

Authors:  M J Holness; M J Schuster-Bruce; M C Sugden
Journal:  Biochem J       Date:  1988-09-15       Impact factor: 3.857

5.  Acetaminophen glucuronide and plasma glucose report identical estimates of gluconeogenesis and glycogenolysis for healthy and prediabetic subjects using the deuterated water method.

Authors:  Cristina Barosa; John G Jones; Robert Rizza; Ananda Basu; Rita Basu
Journal:  Magn Reson Med       Date:  2012-09-28       Impact factor: 4.668

6.  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

7.  Effect of bile acid sequestrants on glucose metabolism, hepatic de novo lipogenesis, and cholesterol and bile acid kinetics in type 2 diabetes: a randomised controlled study.

Authors:  C Beysen; E J Murphy; K Deines; M Chan; E Tsang; A Glass; S M Turner; J Protasio; T Riiff; M K Hellerstein
Journal:  Diabetologia       Date:  2011-12-02       Impact factor: 10.122

8.  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

9.  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

10.  UDP-sugar metabolism in Swarm rat chondrosarcoma chondrocytes.

Authors:  C Sweeney; D Mackintosh; R M Mason
Journal:  Biochem J       Date:  1993-03-01       Impact factor: 3.857

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