Human mitochondrial oxidative capacity is acutely impaired after burn trauma

American Journal of Surgery

Volumn 196, Issue 2, 2008, Pages 234-239

  Cree, Melanie G ^a,b   Fram, Ricki Y ^a,b   Herndon, David N ^a,b   Qian, Ting ^a   Angel, Carlos ^a   Green, Justin M ^a   Mlcak, Ronald ^b   Aarsland, Asle ^b,c   Wolfe, Robert R ^a,b,d  

^a University of Texas Medical Branch School of Medicine   (United States)

^b SHRINERS HOSPITALS FOR CHILDREN   (United States)

^c UNIVERSITY OF TEXAS MEDICAL BRANCH   (United States)

^d UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

Author keywords

Burn; Mitochondria; Muscle; Trauma

Indexed keywords

ADENOSINE TRIPHOSPHATE; CITRATE SYNTHASE; PALMITIC ACID; PALMITOYL COENZYME A; PYRUVIC ACID;

ARTICLE; BODY SURFACE; BURN; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; ENERGY YIELD; ENZYME ACTIVITY; FEMALE; HUMAN; HUMAN TISSUE; MALE; MITOCHONDRIAL RESPIRATION; MUSCLE BIOPSY; MUSCLE METABOLISM; MUSCLE MITOCHONDRION; PRIORITY JOURNAL; WOUND HEALING;

ADENOSINE TRIPHOSPHATE; BIOPSY; BURNS; CASE-CONTROL STUDIES; CHILD; CROSS-SECTIONAL STUDIES; FEMALE; HUMANS; MALE; MITOCHONDRIA; MUSCLE, SKELETAL; OXIDATION-REDUCTION; PALMITATES; PROSPECTIVE STUDIES; PYRUVIC ACID;

EID: 47049089794     PISSN: 00029610     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjsurg.2007.09.048     Document Type: Article

References (30)

1. Howard J.M. Studies of the absorption and metabolism of glucose following injury; the systemic response to injury. Ann Surg 141 (1955) 321-326
2. Frayn K.N. Effects of burn injury on insulin secretion and on sensitivity to insulin in the rat in vivo. Eur J Clin Invest 5 (1975) 331-337
3. Wolfe R.R. Glucose metabolism in burn injury: a review. J Burn Care Rehabil 6 (1985) 408-418
4. Wilmore D.W., Long J.M., Mason Jr. A.D., et al. Catecholamines: mediator of the hypermetabolic response to thermal injury. Ann Surg 180 (1974) 653-669
5. Wolfe R.R., Herndon D.N., Jahoor F., et al. Effect of severe burn injury on substrate cycling by glucose and fatty acids. N Engl J Med 317 (1987) 403-408
6. Wolfe R.R., Klein S., Herndon D.N., et al. Substrate cycling in thermogenesis and amplification of net substrate flux in human volunteers and burned patients. J Trauma 30 Suppl (1990) S6-S9
7. Gore D.C., Rinehart A., and Asimakis G. Temporal changes in cellular energy following burn injury 31 (2005) 998-1002
8. Huang Y.S., Yang Z.C., Liu X.S., et al. Serial experimental and clinical studies on the pathogenesis of multiple organ dysfunction syndrome (MODS) in severe burns. Burns 24 (1998) 706-716
9. Padfield K.E., Astrakas L.G., Zhang Q., et al. Burn injury causes mitochondrial dysfunction in skeletal muscle. Proc Natl Acad Sci U S A 102 (2005) 5368-5373
10. Liang W.Y., Tang L.X., Yang Z.C., et al. Calcium induced the damage of myocardial mitochondrial respiratory function in the early stage after severe burns. Burns 28 (2002) 143-146
11. Yasuhara S., Perez M.E., Kanakubo E., et al. Skeletal muscle apoptosis after burns is associated with activation of proapoptotic signals. Am J Physiol Endocrinol Metab 279 (2000) E1114-E1121
12. Wang X.M., Chen K.M., Wang Y., et al. Functional changes in rat-liver mitochondria during the early phase of burn injury. Burns Incl Therm Inj 12 (1986) 461-464
13. Vanhorebeek I., De Vos R., Mesotten D., et al. Protection of hepatocyte mitochondrial ultrastructure and function by strict blood glucose control with insulin in critically ill patients. Lancet 365 (2005) 53-59
14. Pereira C., Murphy K., Jeschke M., et al. Post burn muscle wasting and the effects of treatments. Int J Biochem Cell Biol 37 (2005) 1948-1961
15. Chance B., and Williams G.R. The respiratory chain and oxidative phosphorylation. Adv Enzymol Relat Subj Biochem 17 (1956) 65-134
16. Veksler V.I., Kuznetsov A.V., Sharov V.G., et al. Mitochondrial respiratory parameters in cardiac tissue: a novel method of assessment by using saponin-skinned fibers. Biochim Biophys Acta 892 (1987) 191-196
17. Alp P.R., Newsholme E.A., and Zammit V.A. Activities of citrate synthase and NAD+-linked and NADP+-linked isocitrate dehydrogenase in muscle from vertebrates and invertebrates. Biochem J 154 (1976) 689-700
18. Lowry O.H., Rosebrough N.J., Farr A.L., et al. Protein measurement with the Folin phenol reagent. J Biol Chem 193 (1951) 265-275
19. Champe P., and Harvey R. Lippincott's Illustrated Reviews. 2nd ed. (1994), Lippincott Williams and Wilkins, Philadelphia
20. Wolfe R.R., Jahoor F., Herndon D.N., et al. Isotopic evaluation of the metabolism of pyruvate and related substrates in normal adult volunteers and severely burned children: effect of dichloroacetate and glucose infusion. Surgery 110 (1991) 54-67
21. Ferrando A.A., Chinkes D.L., Wolf S.E., et al. Acute dichloroacetate administration increases skeletal muscle free glutamine concentrations after burn injury. Ann Surg 228 (1998) 249-256
22. Yu Y.M., Tompkins R.G., Ryan C.M., et al. The metabolic basis of the increase of the increase in energy expenditure in severely burned patients. JPEN J Parenter Enteral Nutr 23 (1999) 160-168
23. Nubel T., and Ricquier D. Respiration under control of uncoupling proteins: clinical perspective. Horm Res 65 (2006) 300-310
24. Kelley D.E., He J., Menshikova E.V., et al. Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes. Diabetes 51 (2002) 2944-2950
25. Petersen K.F., Befroy D., Dufour S., et al. Mitochondrial dysfunction in the elderly: possible role in insulin resistance. Science 300 (2003) 1140-1142
26. Veening M.A., Van Weissenbruch M.M., and Delemarre-Van De Waal H.A. Glucose tolerance, insulin sensitivity, and insulin secretion in children born small for gestational age. J Clin Endocrinol Metab 87 (2002) 4657-4661
27. Magalhaes J., Ascensao A., Soares J.M., et al. Acute and severe hypobaric hypoxia increases oxidative stress and impairs mitochondrial function in mouse skeletal muscle. J Appl Physiol 99 (2005) 1247-1253
28. Oliveira C.P., Coelho A.M., Barbeiro H.V., et al. Liver mitochondrial dysfunction and oxidative stress in the pathogenesis of experimental nonalcoholic fatty liver disease. Braz J Med Biol Res 39 (2006) 189-194
29. Kim J.K., Fillmore J.J., Sunshine M.J., et al. PKC-theta knockout mice are protected from fat-induced insulin resistance. J Clin Invest 114 (2004) 823-827
30. Li Y.P., Atkins C.M., Sweatt J.D., et al. Mitochondria mediate tumor necrosis factor-alpha/NF-kappaB signaling in skeletal muscle myotubes. Antioxid Redox Signal 1 (1999) 97-104