Literature DB >> 1640934

Role of the rat liver in the disposal of a glucose gavage.

J Casado1, J A Fernández-López, M J Argilés, M Alemany.   

Abstract

An oral gavage of either 3, 1, or 0.1 mmoles of glucose was given to rats under standard feeding conditions or food deprived for 24 hr. The blood flow of the portal and suprahepatic veins as well as the hepatic balances for glucose, lactate, alanine and pyruvate were estimated. In fed rats, after the administration of an oral 3 mmoles load, the liver actually released 310 mumoles of glucose and 90 of lactate, amounts that could be accounted for by the uptake of alanine (148 mumoles) and small loss of glycogen (275 mumoles of glycosyl residues). In starved rats, however, the liver took a very high proportion (c. 71%) of the glucose absorbed, both as glucose (780 mumoles), lactate and pyruvate (892 mumoles) or alanine (134 mumoles). The synthesis of glycogen was considerably limited, accounting for only 205 mumoles, and leaving practically one mmol of glucose equivalent energy available for liver function and the synthesis of other compounds. Practically all glycogen was synthesized directly from glucose, since the synthesis from 3 C carriers was less than a 5%. Smaller gavages (1 or 0.1 mmoles) resulted in a much lower liver uptake activity. The strikingly different activity of the liver with respect to the available glucose and 3 C fragments could not be explained alone by the circulating levels of these compounds, suggesting a very deep influence of the intestine in hepatic function. The liver plays a very passive role in fed animals, with a very small involvement in the disposal of a glucose load, whereas it takes on an important role when the overall availability of energy is diminished.

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Year:  1992        PMID: 1640934     DOI: 10.1007/bf00230883

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  43 in total

1.  Intestinal handling of a glucose gavage by the rat.

Authors:  J A Fernández-López; J Casado; J M Argilés; M Alemany
Journal:  Mol Cell Biochem       Date:  1992-07-06       Impact factor: 3.396

2.  Changes in availability of glucogenic and ketogenic substrates and liver metabolism in fed or starved rats.

Authors:  C Rémésy; C Demigné
Journal:  Ann Nutr Metab       Date:  1983       Impact factor: 3.374

3.  Liver glycogen content decreases during meals in rats.

Authors:  W Langhans; N Geary; E Scharrer
Journal:  Am J Physiol       Date:  1982-09

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.  Hormone-fuel interrelationships during fasting.

Authors:  G F Cahill; M G Herrera; A P Morgan; J S Soeldner; J Steinke; P L Levy; G A Reichard; D M Kipnis
Journal:  J Clin Invest       Date:  1966-11       Impact factor: 14.808

6.  Influence of oral glucose ingestion on splanchnic glucose and gluconeogenic substrate metabolism in man.

Authors:  P Felig; J Wahren; R Hendler
Journal:  Diabetes       Date:  1975-05       Impact factor: 9.461

7.  Carbohydrate, fat, and protein metabolism in muscle and in the whole body after mixed meal ingestion.

Authors:  M Elia; P Folmer; A Schlatmann; A Goren; S Austin
Journal:  Metabolism       Date:  1988-06       Impact factor: 8.694

8.  Hepatic uptake of gluconeogenic substrates in late-pregnant and mid-lactating rats.

Authors:  J Casado; X Remesar; M Pastor-Anglada
Journal:  Biosci Rep       Date:  1987-07       Impact factor: 3.840

9.  Hepatic uptake of amino acids at mid-lactation in the rat.

Authors:  J Casado; M Pastor-Anglada; X Remesar
Journal:  Biochem J       Date:  1987-07-01       Impact factor: 3.857

10.  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

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  2 in total

1.  Intestinal handling of a glucose gavage by the rat.

Authors:  J A Fernández-López; J Casado; J M Argilés; M Alemany
Journal:  Mol Cell Biochem       Date:  1992-07-06       Impact factor: 3.396

2.  A Lowly Digestible-Starch Diet after Weaning Enhances Exogenous Glucose Oxidation Rate in Female, but Not in Male, Mice.

Authors:  José M S Fernández-Calleja; Lianne M S Bouwman; Hans J M Swarts; Nils Billecke; Annemarie Oosting; Jaap Keijer; Evert M van Schothorst
Journal:  Nutrients       Date:  2019-09-18       Impact factor: 5.717

  2 in total

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