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. 1983 Feb;197(2):163–171. doi: 10.1097/00000658-198302000-00007

Response of protein and urea kinetics in burn patients to different levels of protein intake.

R R Wolfe, R D Goodenough, J F Burke, M H Wolfe
PMCID: PMC1353104  PMID: 6824370

Abstract

The effects of two levels of protein intake on protein metabolism in six severely burned adult patients were studied (means of 70% BSA burned). A crossover experimental design enabled the authors to study each patient at the end of two three-day dietary regimens. All diets were isocaloric and provided approximately 25% more calories than the measured energy expenditure (means = 40.8 Kcal/kg X day). In one regimen, each patient received 2.2 g protein/kg X day, while during the other treatment period they received 1.4 g protein/kg X day. The patients were studied in the fed state and after 10 to 12 hours of fasting. Leucine kinetics were determined by means of the primed-constant infusion of [1--13C]--leucine. The authors were able to distinguish the oxidation of plasma leucine from the oxidation of leucine derived from intracellular protein at the site of the deamination of leucine (predominantly muscle) by simultaneously determining both leucine and alpha-ketoisocaproic acid enrichment. Also, rates of whole-body protein synthesis and catabolism were calculated from the leucine flux and oxidation data. Net protein synthesis was also calculated by means of another stable-isotope technique involving the infusion of [15N2]--urea. Finally, a third means of estimating net protein catabolism based on urinary N-excretion data was used at the same time that the isotopic studies were performed. The 13C leucine-data and the N-excretion data indicated that a balance between protein synthesis and catabolism could be achieved with a protein intake of 1.4 protein/kg X day. When protein intake was increased to 2.2 g protein/kg X day, neither isotopic method indicated a further beneficial effect on net protein synthesis, although the absolute rates of protein synthesis and catabolism were stimulated. The N-excretion data, on the other hand, indicated a significant improvement in net protein synthesis with higher protein intake. Regardless of the level of protein intake, the underlying alterations in protein metabolism that occurred as a response to burn injury persisted.

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Selected References

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  1. Adams R. F. Determination of amino acid profiles in biological samples by gas chromatography. J Chromatogr. 1974 Aug 14;95(2):189–212. doi: 10.1016/s0021-9673(00)84078-9. [DOI] [PubMed] [Google Scholar]
  2. Alexander J. W., MacMillan B. G., Stinnett J. D., Ogle C. K., Bozian R. C., Fischer J. E., Oakes J. B., Morris M. J., Krummel R. Beneficial effects of aggressive protein feeding in severely burned children. Ann Surg. 1980;192(4):505–517. doi: 10.1097/00000658-198010000-00009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Allsop J. R., Wolfe R. R., Burke J. F. Tracer priming the bicarbonate pool. J Appl Physiol Respir Environ Exerc Physiol. 1978 Jul;45(1):137–139. doi: 10.1152/jappl.1978.45.1.137. [DOI] [PubMed] [Google Scholar]
  4. Aulick L. H., Wilmore D. W. Increased peripheral amino acid release following burn injury. Surgery. 1979 May;85(5):560–565. [PubMed] [Google Scholar]
  5. Blackburn G. L. Nutritional assessment and support during infection. Am J Clin Nutr. 1977 Sep;30(9):1493–1497. doi: 10.1093/ajcn/30.9.1493. [DOI] [PubMed] [Google Scholar]
  6. EDWARDS L. C., DUNPHY J. E. Wound healing. II. Injury and abnormal repair. N Engl J Med. 1958 Aug 7;259(6):275–285. doi: 10.1056/NEJM195808072590605. [DOI] [PubMed] [Google Scholar]
  7. Giordano C., De Pascale C., Balestrieri C., Cittadini D., Crescenzi A. Incorporation of urea 15N in amino acids of patients with chronic renal failure on low nitrogen diet. Am J Clin Nutr. 1968 May;21(5):394–404. doi: 10.1093/ajcn/21.5.394. [DOI] [PubMed] [Google Scholar]
  8. Goodenough R. D., Royle G. T., Nadel E. R., Wolfe M. H., Wolfe R. R. Leucine and urea metabolism in acute human cold exposure. J Appl Physiol Respir Environ Exerc Physiol. 1982 Aug;53(2):367–372. doi: 10.1152/jappl.1982.53.2.367. [DOI] [PubMed] [Google Scholar]
  9. Hegsted D. M. Assessment of nitrogen requirements. Am J Clin Nutr. 1978 Sep;31(9):1669–1677. doi: 10.1093/ajcn/31.9.1669. [DOI] [PubMed] [Google Scholar]
  10. Kien C. L., Young V. R., Rohrbaugh D. K., Burke J. F. Increased rates of whole body protein synthesis and breakdown in children recovering from burns. Ann Surg. 1978 Apr;187(4):383–391. doi: 10.1097/00000658-197804000-00007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Long J. M., 3rd, Wilmore D. W., Mason A. D., Jr, Pruitt B. A., Jr Effect of carbohydrate and fat intake on nitrogen excretion during total intravenous feeding. Ann Surg. 1977 Apr;185(4):417–422. doi: 10.1097/00000658-197704000-00008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. MacLean L. D. Host resistance in surgical patients. J Trauma. 1979 May;19(5):297–304. doi: 10.1097/00005373-197905000-00001. [DOI] [PubMed] [Google Scholar]
  13. Motil K. J., Matthews D. E., Bier D. M., Burke J. F., Munro H. N., Young V. R. Whole-body leucine and lysine metabolism: response to dietary protein intake in young men. Am J Physiol. 1981 Jun;240(6):E712–E721. doi: 10.1152/ajpendo.1981.240.6.E712. [DOI] [PubMed] [Google Scholar]
  14. Newsholme E. A. Substrate cycles: their metabolic, energetic and thermic consequences in man. Biochem Soc Symp. 1978;(43):183–205. [PubMed] [Google Scholar]
  15. Odessey R., Goldberg A. L. Leucine degradation in cell-free extracts of skeletal muscle. Biochem J. 1979 Feb 15;178(2):475–489. doi: 10.1042/bj1780475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Shizgal H. M., Forse R. A. Protein and calorie requirements with total parenteral nutrition. Ann Surg. 1980;192(4):562–569. doi: 10.1097/00000658-198010000-00014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Wilmore D. W., Long J. M., Mason A. D., Jr, Skreen R. W., Pruitt B. A., Jr Catecholamines: mediator of the hypermetabolic response to thermal injury. Ann Surg. 1974 Oct;180(4):653–669. doi: 10.1097/00000658-197410000-00031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Wolfe R. R., Allsop J. R., Burke J. F. Glucose metabolism in man: responses to intravenous glucose infusion. Metabolism. 1979 Mar;28(3):210–220. doi: 10.1016/0026-0495(79)90066-0. [DOI] [PubMed] [Google Scholar]
  19. Wolfe R. R., Durkot M. J., Allsop J. R., Burke J. F. Glucose metabolism in severely burned patients. Metabolism. 1979 Oct;28(10):1031–1039. doi: 10.1016/0026-0495(79)90007-6. [DOI] [PubMed] [Google Scholar]
  20. Wolfe R. R., Goodenough R. D., Wolfe M. H., Royle G. T., Nadel E. R. Isotopic analysis of leucine and urea metabolism in exercising humans. J Appl Physiol Respir Environ Exerc Physiol. 1982 Feb;52(2):458–466. doi: 10.1152/jappl.1982.52.2.458. [DOI] [PubMed] [Google Scholar]
  21. Wolfe R. R. Measurement of urea kinetics in vivo by means of a constant tracer infusion of di-15N-urea. Am J Physiol. 1981 Apr;240(4):E428–E434. doi: 10.1152/ajpendo.1981.240.4.E428. [DOI] [PubMed] [Google Scholar]

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