Literature DB >> 2688436

Influence of the route of glucose administration on hepatic glycogen repletion.

G I Shulman1, L Rossetti.   

Abstract

To delineate the role of the route of glucose administration on liver glycogen synthesis, we administered [1-13C]glucose either by intravenous or intraduodenal infusion to chronically catheterized 24-h fasted rats and performed 1) intravenous-hyperglycemic clamp (group I, n = 9), portal vein plasma glucose and insulin concentrations were 216 +/- 6 mg/dl and 23.9 +/- 4.2 ng/ml; 2) intraduodenal-hyperglycemic infusion (group II, n = 8), portal vein glucose and insulin concentrations were 219 +/- 6 mg/dl and 17.5 +/- 2.7 ng/ml; and 3) intravenous-hyperglycemic-suprahyperinsulinemic clamp (group III, n = 5), portal vein glucose and insulin concentrations were 203 +/- 12 mg/dl and 44.6 +/- 5.0 ng/ml. The mean glucose infusion rates (mumol.kg-1.min-1) and glycogenic rates (mumol.g liver-1.min-1) were 201 +/- 8, 0.34 +/- 0.05; 129 +/- 3, 0.73 +/- 0.11; and 269 +/- 19, 0.38 +/- 0.08 in groups I-III, respectively. The percent of glycogen synthesized by the direct pathway was group I = 43 +/- 6%, group II = 44 +/- 6%, and group III = 46 +/- 7%. In conclusion, despite similar or lower portal vein insulin and glucose concentrations, the intraduodenal route of glucose administration (group II), compared with the intravenous route (groups I and III), markedly increased the total amount of liver glycogen synthesized without altering the percent of the direct vs. indirect pathways by which liver glycogen was repleted.

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Year:  1989        PMID: 2688436     DOI: 10.1152/ajpendo.1989.257.5.E681

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


  6 in total

Review 1.  Regulation of glycogen synthase activation in isolated hepatocytes.

Authors:  S Pugazhenthi; R L Khandelwal
Journal:  Mol Cell Biochem       Date:  1995 Aug-Sep       Impact factor: 3.396

2.  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

3.  Enhancement of the gluconeogenic flux of hepatic glycogen repletion by a phenacyl imidazolium compound in vivo.

Authors:  G W Cline; K Greenawalt; G I Shulman
Journal:  Acta Diabetol       Date:  1993       Impact factor: 4.280

4.  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

5.  Effect of intraportal glucose infusion on hepatic glycogen content and degradation, and outcome of liver transplantation.

Authors:  R Cywes; P D Greig; J R Sanabria; P A Clavien; G A Levy; P R Harvey; S M Strasberg
Journal:  Ann Surg       Date:  1992-09       Impact factor: 12.969

6.  Portal vein glucose entry triggers a coordinated cellular response that potentiates hepatic glucose uptake and storage in normal but not high-fat/high-fructose-fed dogs.

Authors:  Katie C Coate; Guillaume Kraft; Jose M Irimia; Marta S Smith; Ben Farmer; Doss W Neal; Peter J Roach; Masakazu Shiota; Alan D Cherrington
Journal:  Diabetes       Date:  2012-10-01       Impact factor: 9.461

  6 in total

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