Skip to main content

The effect of branched-chain amino acids on body protein breakdown and synthesis in patients with chronic liver disease

  • Chapter
Advances in Clinical Nutrition
  • 174 Accesses

Abstract

Abnormal patterns of plasma amino acids are common in patients with liver disease1–5 and can be corrected by the administration of both branched-chain enriched amino-acid solutions6–9 or the three branched-chain amino acids (BCAA) alone10,11. These solutions have been reported as valuable in hepatic encephalopathy6,7,9 in restoring the profile of plasma amino acids towards normal6,8–11 and improving nitrogen balance6,7,11. There is also evidence that nitrogen losses are reduced following injury in patients or animals with normal liver function given branched-chain amino acids. The effect recorded appears to be out of proportion to the nitrogen content of the infusions13. O’Keefe et al.15 investigated the effect of oral BCAA on body protein metabolism in liver disease and reported that turnover, breakdown and synthesis were diminished.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Iber, F. L., Rosen, H., Levenson, S. M. and Chalmers, T. C. (1957). The plasma amino acids in patients with liver failure. J. Lab. Clin. Med., 50, 417

    CAS  Google Scholar 

  2. Richmond, J. and Girdwood, R. H. (1962). Observations on amino acid absorption. Clin. Sci., 22, 301

    CAS  Google Scholar 

  3. Iob, V., Coon, W. W. and Sloan, M. (1967). Free amino acids in liver, plasma and muscle of patients with cirrhosis of the liver. J. Surg. Res., 7, 41

    Article  CAS  Google Scholar 

  4. Fischer, J. E., Yoshimura, N., Aguirre, A., James, J. H., Cummings, M. G., Abel, R. M. and Diendorfer, F. (1974). Plasma amino acids in patients with hepatic encephalopathy. Am. J. Surg., 127, 40

    Article  CAS  Google Scholar 

  5. Rosen, H. M., Yoshimura, N., Hodgman, J. H. and Fischer, J. E. (1977). Plasma amino acid patterns in hepatic encephalopathy of differing etiology. Gastroenterology, 72, 483

    CAS  Google Scholar 

  6. Fischer, J. E., Rosen, H. M., Ebeid, A. M., James, J. H., Keane, J. M. and Soeters, P. B. (1976). The effect of normalisation of plasma amino acids on hepatic encephalopathy in man. Surgery, 80, 77

    CAS  Google Scholar 

  7. Fischer, J. E. (1981). The etiology of hepatic encephalopathy. Acta Chir. Scand. Suppl., 507, 50

    CAS  Google Scholar 

  8. Egberts, E. H., Hamster, W., Jurgens, P., Schumacher, H., Fondalinski, G., Reinhard, U. and Schomerus, H. (1981). Effect of branched chain amino acids on latent portal-systemic encephalopathy. In Walser, M. and Williamson, J. R. (eds.) Metabolism and Clinical Implications of Branched Chain Amino and Keto Acids. pp. 453–463. ( Amsterdam: Elsevier—North Holland )

    Google Scholar 

  9. Okada, A., Kamata, S., Kim, C. W. and Kawashima, Y. (1981). Treatment of hepatic encephalopathy with BCAA-rich amino acid mixture. In Walser, M. and Williamson, J. R. (eds.) Metabolism and Clinical Implications of Branched Chain Amino and Keto Acids. pp. 447–452. ( Amsterdam: Elsevier—North Holland )

    Google Scholar 

  10. Wahren, J., Eriksson, S. and Hagenfeldt, L. (1981). The influence of branched chain amino acids and keto acids on arterial concentration and brain exchange of amino acids in man. In Walser, M. and Williams, J. R. (eds.) Metabolism and Clinical Implications of Branched Chain Amino and Keto Acids. pp. 471–488. (Amsterdam: Elsevier—North Holland)

    Google Scholar 

  11. Okita, M., Watanabe, A. and Nagashima, H. (1981). Treatment of liver cirrhosis with branched chain amino acid supplemented diet. Gastroenterol. Jap., 16, 389

    CAS  Google Scholar 

  12. Freund, H., Hoover, H. C., Atamian, S. and Fischer, J. E. (1979). Infusion of the branched chain amino acids in postoperative patients. Ann. Surg., 190, 18

    Article  CAS  Google Scholar 

  13. Blackburn, G. L., Moldawer, L. L., Usui, S., Bothe, A., O’Keefe, S. J. D. and Bistrian, B. R. (1979). Branched chain amino acid administration and metabolism during starvation, injury and infection. Surgery, 86, 307

    CAS  Google Scholar 

  14. Freund, H., Yoshimura, N. and Fischer, J. E. (1980). The effect of branched chain amino acids and hypertonic glucose infusions on post injury catabolism in the rat. Surgery, 87, 401

    CAS  Google Scholar 

  15. O’Keefe, S. J. D., Abraham, R. R., Davis, M. and Williams, R. (1981). Protein turnover in acute and chronic liver disease. Acta Chir. Scand. Suppl., 507, 99

    Google Scholar 

  16. Waterlow, J. C., Garlick, P. J. and Millward, D. J. (1978). Summary of methods of measuring total protein turnover. In Protein Turnover in Mammalian Tissues and in the Whole Body. pp. 327–338. ( Amsterdam: Elsevier—North Holland )

    Google Scholar 

  17. Clague, M. B. and Keir, M. J. (1982). A modified technique for measuring whole body protein metabolism in surgical patients using L(14C)leucine. Clin. Sci. Mol. Med.,(in press)

    Google Scholar 

  18. Clague, M. B., Keir, M. J. and Wright, P. D. (1981). Determination of the oxidation rate of 14C-labelled substances in surgical patients by assessment of 14CO2 production without the need to collect expired air. Clin. Sci. Mol. Med., 60, 233

    CAS  Google Scholar 

  19. Pugh, R. N. H., Murray-Lyon, I. M., Dawson, J. L., Pietroni, M. C. and Williams, R. (1973). Transection of the oesophagus for bleeding oesophageal varices. Br. J. Surg., 60, 646

    Article  CAS  Google Scholar 

  20. Block, R. J. and Weiss, K. W. (1956). Amino Acid Handbook. ( Illinois: Charles C. Thomas )

    Google Scholar 

  21. Desai, S. P., Moldawer, L. L., Bistrian, B. R., Blackburn, G. L., Bothe, A. and Schulte, R. D. (1981). Amino acid and protein in humans using L(U 14C)tyrosine and 1.(114C)leucine. In Walser, M. and Williamson, J. R. (eds.) Metabolism and Clinical Implications of Branched Chain Amino and Keto Acids. pp. 307–312. ( Amsterdam: Elsevier—North Holland )

    Google Scholar 

  22. Sherwin, R. S. (1978). Effect of starvation on the turnover and metabolic response to leucine. J. Clin. Invest., 61, 1471

    Article  CAS  Google Scholar 

  23. Buse, M. G. and Reid, S. S. (1975). Leucine; a possible regulator of protein turnover in muscle. J. Clin. Invest., 56, 1250

    Article  CAS  Google Scholar 

  24. Goldberg, A. L. and Chang, T. W. (1978). Regulation and significance of amino acid metabolism in skeletal muscle. Fed. Proc., 37, 2301

    CAS  Google Scholar 

  25. Kirsch, R. E., Frith, L. O. and Saunders, S. J. (1976). Stimulation of albumin synthesis by keto analogues of amino acids. Biochim. Biophys. Acta, 442, 437

    CAS  Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1983 MTP Press Limited

About this chapter

Cite this chapter

Holdsworth, J.D., Clague, M.B., Wright, P.D., Johnston, I.D.A. (1983). The effect of branched-chain amino acids on body protein breakdown and synthesis in patients with chronic liver disease. In: Johnston, I.D.A. (eds) Advances in Clinical Nutrition. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-5918-0_8

Download citation

  • DOI: https://doi.org/10.1007/978-94-011-5918-0_8

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-011-5920-3

  • Online ISBN: 978-94-011-5918-0

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics