Acute effects of insulin-like growth factor I on inter-organ amino acid flux in protein-catabolic dogs

E Roth, L Valentini, T Hölzenbein, S Winkler, T Sautner, H Hörtnagl, J Karner, E Roth, L Valentini, T Hölzenbein, S Winkler, T Sautner, H Hörtnagl, J Karner

Abstract

The effects of acute administration of human recombinant insulin-like growth factor-I (rhIGF-I) on amino acid (AA) flux between hindlimbs, liver and gut were investigated in anaesthetized post-operative dogs. rhIGF-I produced about a 10-fold increase in plasma IGF-I concentrations above baseline values (P < 0.001), increased the plasma levels of glucagon and adrenaline (P < 0.05), and evoked a fall in plasma glucose (-55 +/- 8%; (P < 0.001) and plasma total AA levels (-23 +/- 8%; P < 0.05). AA flux in post-absorptive dogs under NaCl infusions was characterized by an efflux of AA from the hindlimbs (as a result of the protein-catabolic situation), an equal AA balance across the gut and an AA uptake by the liver. The administration of rhIGF-I increased hepatic AA uptake in the NaCl group from 3.51 +/- 0.8 to 7.5 +/- 0.4 mumol/min per kg (P < 0.01) and in the AA-infused group from 16.8 +/- 0.6 to 22.4 +/- 1.5 mumol/min per kg (P < 0.05), but did not influence the AA balance across hindlimbs and gut. Glucose infusions normalized the plasma concentrations of counter-regulatory hormones without influencing the inter-organ AA balances. We conclude that hypoaminoacidaemia caused by rhIGF-I infusions is the result of a stimulated AA uptake by the liver, but is unrelated to alterations of AA exchange across the hindlimbs.

References

    1. Physiol Rev. 1971 Jan;51(1):23-65
    1. Am J Physiol. 1989 Aug;257(2 Pt 1):E228-34
    1. Surgery. 1979 Sep;86(3):409-22
    1. Nature. 1982 Mar 18;296(5854):252-3
    1. Clin Chem. 1982 Mar;28(3):527-31
    1. Metabolism. 1982 May;31(5):463-70
    1. Experientia. 1982 Aug 15;38(8):979-81
    1. Diabetes. 1983 May;32(5):392-7
    1. Endocrinology. 1985 Jun;116(6):2578-82
    1. Diabetologia. 1985 Aug;28(8):485-93
    1. Nature. 1986 Sep 11-17;323(6084):169-71
    1. Pediatr Res. 1986 Sep;20(9):825-7
    1. J Clin Chem Clin Biochem. 1986 Sep;24(9):651-8
    1. Clin Sci (Lond). 1988 Dec;75(6):641-8
    1. Proc Natl Acad Sci U S A. 1989 Apr;86(8):2868-72
    1. J Clin Invest. 1989 May;83(5):1717-23
    1. Surgery. 1989 Nov;106(5):893-900
    1. Am J Physiol. 1990 Jun;258(6 Pt 1):E907-17
    1. Surgery. 1990 Aug;108(2):161-4
    1. Am J Physiol. 1990 Sep;259(3 Pt 1):E342-50
    1. Clin Sci (Lond). 1991 Jun;80(6):625-31
    1. Am J Physiol. 1991 Nov;261(5 Pt 1):E606-12
    1. J Clin Endocrinol Metab. 1992 Jul;75(1):234-8
    1. J Clin Endocrinol Metab. 1992 Nov;75(5):1192-7
    1. Am J Physiol. 1978 Aug;235(2):E238-47

Source: PubMed

3
Prenumerera