Metabolism - Clinical and Experimental
Volume 47, Issue 6 , Pages 681-685, June 1998

Leucine metabolism in rat liver after a bolus injection of endotoxin

  • Milan Holeček

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Milan Holeček, MD, Department of Physiology, Charles University School of Medicine, Šimkova 870, 500 01 Hradec Králové, Czech Republic.
    • Department of Physiology, Charles University School of Medicine, Hradec Králové, Czech Republic
    • Department of Medicine, Charles University School of Medicine, Hradec Králové, Czech Republic
    • University Hospital Motol, Prague, Czech Republic
  • ,
  • Luděk Šprongl

      Affiliations

    • Department of Physiology, Charles University School of Medicine, Hradec Králové, Czech Republic
    • Department of Medicine, Charles University School of Medicine, Hradec Králové, Czech Republic
    • University Hospital Motol, Prague, Czech Republic
  • ,
  • Miloslav Tichý

      Affiliations

    • Department of Physiology, Charles University School of Medicine, Hradec Králové, Czech Republic
    • Department of Medicine, Charles University School of Medicine, Hradec Králové, Czech Republic
    • University Hospital Motol, Prague, Czech Republic
  • ,
  • Miroslav Pecka

      Affiliations

    • Department of Physiology, Charles University School of Medicine, Hradec Králové, Czech Republic
    • Department of Medicine, Charles University School of Medicine, Hradec Králové, Czech Republic
    • University Hospital Motol, Prague, Czech Republic

Received 1 July 1997; accepted 3 December 1997.

Abstract 

To evaluate the contribution of hepatic tissue to alterations in the metabolism of proteins and the branched-chain amino acids (BCAA) leucine, isoleucine, and valine in systemic inflammatory response syndrome, we studied the changes of leucine metabolism in isolated perfused liver (IPL) of endotoxin-treated rats. Male albino rats were injected with the endotoxin of Salmonella enteritidis (5 mg · kg−1) or saline (control). Four hours later, leucine and ketoisocaproate (KIC) oxidation and incorporation into liver proteins were determined in IPL using the single-pass liver perfusion technique. l-[1-14C]leucine and α-keto[1-14C]isocaproic acid were used as a tracer in two separate experiments. Endotoxin treatment resulted in a decrease of plasma BCAA levels, an increase of leucine oxidation, and a decrease of KIC oxidation by IPL. Leucine incorporation into liver proteins was lower in endotoxin-treated rats, and we did not find measurable incorporation of the labeled carbon of KIC in liver proteins in either group of animals. The sum of individual amino acid concentrations in the effluent perfusate was higher in endotoxin-treated animals, although only leucine and phenylalanine increased significantly. The decrease in KIC oxidation indicates a decreased capacity of hepatic tissue to oxidize branched-chain ketoacids (BCKA). The increase in leucine oxidation by IPL of endotoxin-treated rats indicates an increase in BCAA aminotransferase activity. These changes demonstrate an important response of the body that enables the resynthesis of essential BCAA from their ketoanalogs delivered to the liver from peripheral tissues, particularly muscle.

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 Supported by grants from the Grant Agency of the Czech Republic (306/94/1873), the Internal Grant Agency of the Ministry of Health of the Czech Republic (3772-3), and Charles University (258).

PII: S0026-0495(98)90030-0

Metabolism - Clinical and Experimental
Volume 47, Issue 6 , Pages 681-685, June 1998