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. 1989 Jan;209(1):63–72. doi: 10.1097/00000658-198901000-00010

An integrated analysis of glucose, fat, and protein metabolism in severely traumatized patients. Studies in the basal state and the response to total parenteral nutrition.

J H Shaw 1, R R Wolfe 1
PMCID: PMC1493884  PMID: 2491939

Abstract

A series of isotopic infusions were performed in 43 severely ill patients suffering from blunt trauma (mean injury severity score of 31). The patient data have been compared with data obtained from 32 normal volunteers, and in addition the metabolic response of the trauma patient to total nutritional support (TPN) has been assessed. The rate of VO2 was elevated in the trauma patients compared with that of the volunteers (160 mumol/kg/minute vs. 103 mumol/kg/minute). Glucose production was significantly increased in the patients compared with the volunteers (21 +/- 2 mumol/kg/minute vs. 14 +/- 1 mumol/kg/minute), but the trauma patients had an impaired capacity to directly oxidize plasma glucose. The percentage of glucose uptake oxidized in the volunteers was 36 +/- 2%, and the percentage of glucose uptake recycled was 10 +/- 1%. By contrast, in the trauma patients, 23 +/- 4% of the glucose uptake was directly oxidized, and 29 +/- 11% was recycled. The rate of glycerol turnover in the trauma patients (5.3 +/- 0.3 mumol/kg/minute) was significantly elevated compared with the volunteer value (2.2 +/- 0.1 mumol/kg/minute), and the basal rate of fat oxidation was twice as high in the patients as in the volunteers (2 mg/kg/minute vs. 1 mg/kg/minute). The rate of whole body protein catabolism was significantly higher in the patients (5.8 +/- 0.7 g/kg/day vs. 4.3 +/- 0.3 g/kg/day), and as a result, the rate of net protein catabolism was significantly elevated in the patients. The response to TPN (amino acids and a 50:50 mixture of glucose and fat) included an increase in the percentage of glucose uptake oxidized (up to 45 +/- 12%), a decrease in the oxidation of fat (up to 0.8 mg/kg/minute), and a significant increase in whole body protein synthesis (up to 6.1 +/- 1.1 g/kg/day) so that the rate of net protein loss was minimized but not prevented. (The rate of net protein catabolism during TPN was 1.3 +/- 0.5 g/kg/day.) There was no correlation between the injury severity score (ISS) and the degree of metabolic abnormality. The rate of NPC in the patients with ISS less than 20 was higher than in the volunteers (ISS = 0), but the values for NPC in patients with ISS 21-40, and ISS greater than 40 were virtually identical to the corresponding values in patients with ISS less than 20. It is concluded from these studies that: 1) Trauma patients have a high rate of VO2.(ABSTRACT TRUNCATED AT 250 WORDS)

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Selected References

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  1. ARMSTRONG D. T., STEELE R., ALTSZULER N., DUNN A., BISHOP J. S., DE BODO R. C. Regulation of plasma free fatty acid turnover. Am J Physiol. 1961 Jul;201:9–15. doi: 10.1152/ajplegacy.1961.201.1.9. [DOI] [PubMed] [Google Scholar]
  2. 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]
  3. Albano J. D., Ekins R. P., Maritz G., Turner R. C. A sensitive, precise radioimmunoassay of serum insulin relying on charcoal separation of bound and free hormone moieties. Acta Endocrinol (Copenh) 1972 Jul;70(3):487–509. doi: 10.1530/acta.0.0700487. [DOI] [PubMed] [Google Scholar]
  4. 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]
  5. Birke G., Carlson L. A., Liljedahl S. O. Lipid metabolism and trauma. 3. Plasma lipids and lipoproteins in burns. Acta Med Scand. 1965 Sep;178(3):337–350. [PubMed] [Google Scholar]
  6. Birkhahn R. H., Long C. L., Fitkin D., Geiger J. W., Blakemore W. S. Effects of major skeletal trauma on whole body protein turnover in man measured by L-[1,14C]-leucine. Surgery. 1980 Aug;88(2):294–300. [PubMed] [Google Scholar]
  7. Crane C. W., Picou D., Smith R., Waterlow J. C. Protein turnover in patients before and after elective orthopaedic operations. Br J Surg. 1977 Feb;64(2):129–133. doi: 10.1002/bjs.1800640212. [DOI] [PubMed] [Google Scholar]
  8. Heath D. F., Stoner H. B. Studies on the mechanism of shock. Non-esterified fatty acid metabolism in normal and injured rats. Br J Exp Pathol. 1968 Apr;49(2):160–169. [PMC free article] [PubMed] [Google Scholar]
  9. 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]
  10. Long C. L., Kinney J. M., Geiger J. W. Nonsuppressability of gluconeogenesis by glucose in septic patients. Metabolism. 1976 Feb;25(2):193–201. doi: 10.1016/0026-0495(76)90049-4. [DOI] [PubMed] [Google Scholar]
  11. MOORE F. D. Bodily changes in surgical convalescence. I. The normal sequence observations and interpretations. Ann Surg. 1953 Mar;137(3):289–315. doi: 10.1097/00000658-195303000-00001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. MOORE F. D. THE EFFECTS OF HEMORRHAGE ON BODY COMPOSITION. N Engl J Med. 1965 Sep 9;273:567–577. doi: 10.1056/NEJM196509092731101. [DOI] [PubMed] [Google Scholar]
  13. Newsholme E. A., Crabtree B. Substrate cycles in metabolic regulation and in heat generation. Biochem Soc Symp. 1976;(41):61–109. [PubMed] [Google Scholar]
  14. O'Keefe S. J., Sender P. M., James W. P. "Catabolic" loss of body nitrogen in response to surgery. Lancet. 1974 Nov 2;2(7888):1035–1038. doi: 10.1016/s0140-6736(74)92149-7. [DOI] [PubMed] [Google Scholar]
  15. Robinson K. M., Miller H. I. Free fatty acid turnover and oxidation after burn shock in guinea pigs. Circ Shock. 1981;8(3):283–290. [PubMed] [Google Scholar]
  16. STEELE R. Influences of glucose loading and of injected insulin on hepatic glucose output. Ann N Y Acad Sci. 1959 Sep 25;82:420–430. doi: 10.1111/j.1749-6632.1959.tb44923.x. [DOI] [PubMed] [Google Scholar]
  17. Shaw J. H., Galler L., Holdaway I. M., Holdaway C. M. The effect of extradural blockage upon glucose and urea kinetics in surgical patients. Surg Gynecol Obstet. 1987 Sep;165(3):260–266. [PubMed] [Google Scholar]
  18. Shaw J. H., Klein S., Wolfe R. R. Assessment of alanine, urea, and glucose interrelationships in normal subjects and in patients with sepsis with stable isotopic tracers. Surgery. 1985 May;97(5):557–568. [PubMed] [Google Scholar]
  19. Shaw J. H., Wolfe R. R. Determinations of glucose turnover and oxidation in normal volunteers and septic patients using stable and radio-isotopes: the response to glucose infusion and total parenteral feeding. Aust N Z J Surg. 1986 Oct;56(10):785–791. doi: 10.1111/j.1445-2197.1986.tb02327.x. [DOI] [PubMed] [Google Scholar]
  20. Shaw J. H., Wolfe R. R. Fatty acid and glycerol kinetics in septic patients and in patients with gastrointestinal cancer. The response to glucose infusion and parenteral feeding. Ann Surg. 1987 Apr;205(4):368–376. doi: 10.1097/00000658-198704000-00005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Shaw J. H., Wolfe R. R. Glucose and urea kinetics in patients with early and advanced gastrointestinal cancer: the response to glucose infusion, parenteral feeding, and surgical resection. Surgery. 1987 Feb;101(2):181–191. [PubMed] [Google Scholar]
  22. Shaw J. H., Wolfe R. R. Glucose, fatty acid, and urea kinetics in patients with severe pancreatitis. The response to substrate infusion and total parenteral nutrition. Ann Surg. 1986 Dec;204(6):665–672. doi: 10.1097/00000658-198612000-00008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Shizgal H. M., Spanier A. H., Kurtz R. S. Effect of parenteral nutrition on body composition in the critically ill patient. Am J Surg. 1976 Feb;131(2):156–161. doi: 10.1016/0002-9610(76)90089-1. [DOI] [PubMed] [Google Scholar]
  24. Streat S. J., Hill G. L. Nutritional support in the management of critically ill patients in surgical intensive care. World J Surg. 1987 Apr;11(2):194–201. doi: 10.1007/BF01656402. [DOI] [PubMed] [Google Scholar]
  25. WEIR J. B. DE B. New methods for calculating metabolic rate with special reference to protein metabolism. J Physiol. 1949 Aug;109(1-2):1–9. doi: 10.1113/jphysiol.1949.sp004363. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Wilmore D. W., Aulick L. H., Mason A. D., Pruitt B. A., Jr Influence of the burn wound on local and systemic responses to injury. Ann Surg. 1977 Oct;186(4):444–458. doi: 10.1097/00000658-197710000-00006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Wilmore D. W. Hormonal responses and their effect on metabolism. Surg Clin North Am. 1976 Oct;56(5):999–1018. doi: 10.1016/s0039-6109(16)41029-7. [DOI] [PubMed] [Google Scholar]
  28. Wilmore D. W., Mason A. D., Jr, Pruitt B. A., Jr Insulin response to glucose in hypermetabolic burn patients. Ann Surg. 1976 Mar;183(3):314–320. doi: 10.1097/00000658-197603000-00018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Wilmore D. W. Nutrition and metabolism following thermal injury. Clin Plast Surg. 1974 Oct;1(4):603–619. [PubMed] [Google Scholar]
  30. 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]
  31. Wolfe R. R., Durkot M. J. Evaluation of the role of the sympathetic nervous system in the response of substrate kinetics and oxidation to burn injury. Circ Shock. 1982;9(4):395–406. [PubMed] [Google Scholar]
  32. Wolfe R. R., Durkot M. J., Wolfe M. H. Effect of thermal injury on energy metabolism, substrate kinetics, and hormonal concentrations. Circ Shock. 1982;9(4):383–394. [PubMed] [Google Scholar]
  33. Wolfe R. R., Evans J. E., Mullany C. J., Burke J. F. Measurement of plasma free fatty acid turnover and oxidation using [1-13C]palmitic acid. Biomed Mass Spectrom. 1980 Apr;7(4):168–171. doi: 10.1002/bms.1200070407. [DOI] [PubMed] [Google Scholar]
  34. 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]
  35. Wolfe R. R., Miller H. I. Cardiovascular and metabolic responses during burn shock in the guinea pig. Am J Physiol. 1976 Sep;231(3):892–897. doi: 10.1152/ajplegacy.1976.231.3.892. [DOI] [PubMed] [Google Scholar]
  36. Wolfe R. R., O'Donnell T. F., Jr, Stone M. D., Richmand D. A., Burke J. F. Investigation of factors determining the optimal glucose infusion rate in total parenteral nutrition. Metabolism. 1980 Sep;29(9):892–900. doi: 10.1016/0026-0495(80)90130-4. [DOI] [PubMed] [Google Scholar]
  37. Wolfe R. R., Peters E. J. Lipolytic response to glucose infusion in human subjects. Am J Physiol. 1987 Feb;252(2 Pt 1):E218–E223. doi: 10.1152/ajpendo.1987.252.2.E218. [DOI] [PubMed] [Google Scholar]
  38. Wolfe R. R., Shaw J. H., Durkot M. J. Energy metabolism in trauma and sepsis: the role of fat. Prog Clin Biol Res. 1983;111:89–109. [PubMed] [Google Scholar]
  39. Wolfe R. R., Wolfe M. H., Nadel E. R., Shaw J. H. Isotopic determination of amino acid-urea interactions in exercise in humans. J Appl Physiol Respir Environ Exerc Physiol. 1984 Jan;56(1):221–229. doi: 10.1152/jappl.1984.56.1.221. [DOI] [PubMed] [Google Scholar]

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