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. 1978 Sep;188(3):423–429. doi: 10.1097/00000658-197809000-00017

Amino Acid Derangements in Patients With Sepsis: Treatment With Branched Chain Amino Acid Rich Infusions

Herbert R Freund, John A Ryan Jr, Josef E Fischer
PMCID: PMC1396972  PMID: 99098

Abstract

Sepsis is a major catabolic insult resulting in modifications in carbohydrate and fat energy metabolism, and leading to increased muscle breakdown and nitrogen loss. Insulin resistance, which develops in sepsis, decreases glucose utilization, but plasma insulin levels are sufficiently elevated to prevent lipolysis, resulting in a further energy deficit. The availability of fuels in sepsis is therefore limited, and the body resorts to muscle breakdown, gluconeogenesis, and amino acid oxidation for energy supply. Previous work has not defined, however, the exact alterations in amino acid metabolism. Therefore, the following studies were undertaken. Blood samples were drawn from fifteen patients in whom the diagnosis of sepsis was clinically established; the samples were analyzed for amino acid, β-hydroxyphenylethanolamines, glucose, insulin and glucagon concentrations. The plasma amino acid pattern observed was characterized by an increase in total amino acid content, due mainly to high levels of the aromatic amino acids (phenylalanine and tyrosine) and the sulfur-containing amino acids (taurine, cystine and methionine). Alanine, aspartic acid, glutamic acid and proline were also elevated, but to a lesser degree. The branched chain amino acids (valine, leucine and isoleucine) were within normal limits, as were glycine, serine, threonine, lysine, histidine and tryptophan. Those patients who did not survive sepsis had higher levels of aromatic and sulfur-containing amino acids as compared to those patients surviving sepsis. On the other hand, those patients surviving sepsis had higher levels of alanine and the branched chain amino acids. In a second group of five patients with overwhelming sepsis accompanied by a state of metabolic encephalopathy, a parenteral nutrition solution consisting of 23% dextrose, and an amino acid formulation enriched with branched chain amino acids was administered. In these five patients, normalization of the plasma amino acid pattern and reversal of encephalopathy was observed. The following sequence of events may be postulated: The septic patient develops insulin resistance in the peripheral tissues, primarily muscle, while the adipose tissue is much less affected. The insulin resistance and the inability to utilize fat leads to increased muscle proteolysis. Muscle breakdown results in release into the blood of enormous amounts of various amino acids; the muscle itself is able to oxidize the branched chain amino acids, supplying the muscles' own energy requirements and alanine for gluconeogenesis. The extensive muscle proteolysis coupled with relative hepatic insufficiency occurring early in sepsis results in the appearance in the plasma of high levels of most of the amino acids present in muscle, particularly the aromatic and the sulfur-containing amino acids. The outcome of patients with sepsis might be positively affected by combined therapy with glucose, insulin and branched chain amino acids.

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Selected References

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  1. ADAMS R. D., FOLEY J. M. The neurological disorder associated with liver disease. Res Publ Assoc Res Nerv Ment Dis. 1953;32:198–237. [PubMed] [Google Scholar]
  2. Clowes G. H., Jr, O'Donnell T. F., Jr, Ryan N. T., Blackburn G. L. Energy metabolism in sepsis: treatment based on different patterns in shock and high output stage. Ann Surg. 1974 May;179(5):684–696. doi: 10.1097/00000658-197405000-00023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cuthbertson D., Tilstone W. J. Metabolism during the postinjury period. Adv Clin Chem. 1969;12:1–55. doi: 10.1016/s0065-2423(08)60257-7. [DOI] [PubMed] [Google Scholar]
  4. Duke J. H., Jr, Jørgensen S. B., Broell J. R., Long C. L., Kinney J. M. Contribution of protein to caloric expenditure following injury. Surgery. 1970 Jul;68(1):168–174. [PubMed] [Google Scholar]
  5. FLECK A., MUNRO H. N. PROTEIN METABOLISM AFTER INJURY. Metabolism. 1963 Sep;12:783–789. [PubMed] [Google Scholar]
  6. Felig P. The glucose-alanine cycle. Metabolism. 1973 Feb;22(2):179–207. doi: 10.1016/0026-0495(73)90269-2. [DOI] [PubMed] [Google Scholar]
  7. Fischer J. E., Funovics J. M., Aguirre A., James J. H., Keane J. M., Wesdorp R. I., Yoshimura N., Westman T. The role of plasma amino acids in hepatic encephalopathy. Surgery. 1975 Sep;78(3):276–290. [PubMed] [Google Scholar]
  8. Fischer J. E., Rosen H. M., Ebeid A. M., James J. H., Keane J. M., Soeters P. B. The effect of normalization of plasma amino acids on hepatic encephalopathy in man. Surgery. 1976 Jul;80(1):77–91. [PubMed] [Google Scholar]
  9. HOWARD J. M. Studies of the absorption and metabolism of glucose following injury; the systemic response to injury. Ann Surg. 1955 Mar;141(3):321–326. doi: 10.1097/00000658-195503000-00005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hinshaw L. B., Peyton M. D., Archer L. T., Black M. R., Coalson J. J., Greenfield L. J. Prevention of death in endotoxin shock by glucose administration. Surg Gynecol Obstet. 1974 Dec;139(6):851–859. [PubMed] [Google Scholar]
  11. Manny J., Schiller M., Manny N., Rabinovici N., Hechtman H. B. Beneficial effects of glucose-insulin-potassium following endotoxemia. Surg Forum. 1977;28:88–90. [PubMed] [Google Scholar]
  12. Marchuk J. B., Finley R. J., Groves A. C., Wolfe L. I., Holliday R. L., Duff J. H. Catabolic hormones and substrate patterns in septic patients. J Surg Res. 1977 Sep;23(3):177–182. doi: 10.1016/0022-4804(77)90018-x. [DOI] [PubMed] [Google Scholar]
  13. Molinoff P. B., Landsberg L., Axelrod J. An enzymatic assay for octopamine and other beta-hydroxylated phenylethylamines. J Pharmacol Exp Ther. 1969 Dec;170(2):253–261. [PubMed] [Google Scholar]
  14. O'Donnel T. F., Clowes G. H., Jr, Blackburn G. L., Ryan N. T., Benotti P. N., Miller J. D. Proteolysis associated with a deficit of peripheral energy fuel substrates in septic man. Surgery. 1976 Aug;80(2):192–200. [PubMed] [Google Scholar]
  15. Odessey R., Khairallah E. A., Goldberg A. L. Origin and possible significance of alanine production by skeletal muscle. J Biol Chem. 1974 Dec 10;249(23):7623–7629. [PubMed] [Google Scholar]
  16. Ryan N. T., Blackburn G. L., Clowes H. A., Jr Differential tissue sensitivity to elevated endogenous insulin levels during experimental peritonitis in rats. Metabolism. 1974 Nov;23(11):1081–1089. doi: 10.1016/0026-0495(74)90075-4. [DOI] [PubMed] [Google Scholar]
  17. Ryan N. T., George B. C., Egdahl D. H., Egdahl R. H. Chronic tissue insulin resistance following hemorrhagic shock. Ann Surg. 1974 Oct;180(4):402–407. doi: 10.1097/00000658-197410000-00004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. UNGER R. H., EISENTRAUT A. M., McCALL M. S., MADISON L. L. Glucagon antibodies and an immunoassay for glucagon. J Clin Invest. 1961 Jul;40:1280–1289. doi: 10.1172/JCI104357. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Vaidyanath N., Oswald G., Trietley G., Weissenhofer W., Moritz E., McMenamy R. H., Birkhahn R., Yuan T. F., Border J. R. Turnover of amino acids in sepsis and starvation: Effect of glucose infusion. J Trauma. 1976 Feb;16(2):125–135. doi: 10.1097/00005373-197602000-00008. [DOI] [PubMed] [Google Scholar]
  20. Wannemacher R. W., Jr Key role of various individual amino acids in host response to infection. Am J Clin Nutr. 1977 Aug;30(8):1269–1280. doi: 10.1093/ajcn/30.8.1269. [DOI] [PubMed] [Google Scholar]
  21. Wannemacher R. W., Jr, Klainer A. S., Dinterman R. E., Beisel W. R. The significance and mechanism of an increased serum phenylalanine-tyrosine ratio during infection. Am J Clin Nutr. 1976 Sep;29(9):997–1006. doi: 10.1093/ajcn/29.9.997. [DOI] [PubMed] [Google Scholar]
  22. Wannemacher R. W., Jr, Powanda M. C., Dinterman R. E. Amino acid flux and protein synthesis after exposure of rats to either Diplococcus pneumoniae or Salmonella typhimurium. Infect Immun. 1974 Jul;10(1):60–65. doi: 10.1128/iai.10.1.60-65.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]

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