Literature DB >> 6421171

Metabolic effects of oral glucose in the liver of fasted rats.

C B Niewoehner, D P Gilboe, F Q Nuttall.   

Abstract

Twenty-four-hour-fasted rats were given glucose (4 g/kg) by gavage. Glucose absorption and portal and peripheral plasma glucose, lactate, and insulin concentrations, as well as liver glucose, UDPglucose, glucose-6-P, lactate, ATP, and inorganic phosphate (Pi), and % glycogen synthase I and % phosphorylase a were measured at 10, 20, 30, 40, 60, and 120 min after the glucose was given. Liver and muscle glycogen also were measured. Ninety-one percent of the glucose load had disappeared from the gut in 2 h. Despite increased plasma glucose and insulin levels the liver continued to produce glucose. Lactate produced in the periphery was the major substrate for gluconeogenesis, and lactate utilization could account for the hepatic glycogen synthesized. Glucose ingestion did not affect lactate production by the splanchnic bed. In the liver glucose-6-P was transiently increased; UDP glucose decreased after glucose administration. ATP and Pi were unchanged. Glycogen synthase was activated by 20 min without a significant change in phosphorylase a. Hepatic glycogen increased linearly after 20 min. Total glucose storage as glycogen was similar in liver (20%) and muscle (19%). We could account for 41% of the glucose absorbed as glycogen, unmetabolized glucose, or glucose metabolites. Most of the remainder probably was oxidized.

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Year:  1984        PMID: 6421171     DOI: 10.1152/ajpendo.1984.246.1.E89

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


  14 in total

Review 1.  Fuel selection and carbon flux during the starved-to-fed transition.

Authors:  M C Sugden; M J Holness; T N Palmer
Journal:  Biochem J       Date:  1989-10-15       Impact factor: 3.857

2.  In vitro study on the contribution of the rat intestine-pancreas to glucose homeostasis.

Authors:  M A Tormo; M A Zubeldia; J L Montero; J E Campillo
Journal:  Diabetologia       Date:  1988-12       Impact factor: 10.122

3.  Simultaneous synthesis and degradation of rat liver glycogen. An in vivo nuclear magnetic resonance spectroscopic study.

Authors:  M David; W A Petit; M R Laughlin; R G Shulman; J E King; E J Barrett
Journal:  J Clin Invest       Date:  1990-08       Impact factor: 14.808

Review 4.  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

5.  Post-oral infusion sites that support glucose-conditioned flavor preferences in rats.

Authors:  Karen Ackroff; Yeh-Min Yiin; Anthony Sclafani
Journal:  Physiol Behav       Date:  2009-12-21

6.  Acute inhibition by ethanol of intestinal absorption of glucose and hepatic glycogen synthesis on glucose refeeding after starvation in the rat.

Authors:  E B Cook; J A Preece; S D Tobin; M C Sugden; D J Cox; T N Palmer
Journal:  Biochem J       Date:  1988-08-15       Impact factor: 3.857

7.  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

8.  Comparison of the flux of carbon to hepatic glycogen deposition and fatty acid and cholesterol synthesis on refeeding rats fed ad libitum or meal-fed rats with a chow-diet meal.

Authors:  F V Pallardo; D H Williamson
Journal:  Biochem J       Date:  1989-01-15       Impact factor: 3.857

9.  Effect of insulin and gliclazide on glucose utilization by a perfused intestine-pancreas preparation isolated from diabetic and non-diabetic rats.

Authors:  M A Tormo; M A Gomez-Zubeldia; F Ropero; J E Campillo
Journal:  Acta Diabetol       Date:  1994-09       Impact factor: 4.280

10.  Evidence that the stimulation of lipogenesis in the mammary glands of starved lactating rats re-fed with a chow diet is dependent on continued hepatic gluconeogenesis during the absorptive period. Effects of a gluconeogenic inhibitory, mercaptopicolinic acid, in vivo.

Authors:  D H Williamson; V Ilic; R G Jones
Journal:  Biochem J       Date:  1985-06-15       Impact factor: 3.857

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