The hypermetabolic response to injury causes muscle wasting through increased protein breakdown relative to protein synthesis. This muscle wasting increases morbidity and mortality by prolonging healing and delaying time to full functional recovery. Recent studies done by our group indicate that anabolic agents such as insulin decrease protein catabolism when used over short terms in the severely burned. However, continuous anabolic agent treatment throughout hospitalization on clinical parameters of body composition and functional recovery have not been systematically studied. The goal of our studies is to show that muscle wasting with injury can be attenuated with insulin to improve clinical outcomes. In this proposal, we will investigate these aims: 1. To determine the effect of euglycemic hyperinsulinemia throughout the hospital course on net muscle protein synthesis, and to relate continued muscle anabolism to improved lean body mass and improved functional recovery in severely burned patients. 2. To assess the relationship of insulin's physiologic and molecular effects on skeletal muscle in severely burned patients. We will test the hypotheses that: a) the acute effects of insulin on net protein synthesis are sustained throughout the hospital course, and b) continued stimulation of net muscle protein synthesis with euglycemic hyperinsulinemia throughout the hospital course will be associated with identifiable molecular changes. With completion of this proposal, we will demonstrate, for the first time, that prolonged treatment with the anabolic agent, insulin, will not only result in improved physiologic measurements, but will also improve lean body mass, muscular function, and clinical outcomes. We will also demonstrate mechanisms by which these changes take place, to provide further basis for anabolic agent therapy during catabolism associated with severe injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM063120-01A2
Application #
6680125
Study Section
Special Emphasis Panel (ZRG1-SSS-W (01))
Program Officer
Somers, Scott D
Project Start
2003-09-02
Project End
2004-08-31
Budget Start
2003-09-02
Budget End
2004-08-31
Support Year
1
Fiscal Year
2003
Total Cost
$324,650
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Surgery
Type
Schools of Medicine
DUNS #
800771149
City
Galveston
State
TX
Country
United States
Zip Code
77555
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Xiao, Yufei; Hsiao, Tzu-Hung; Suresh, Uthra et al. (2014) A novel significance score for gene selection and ranking. Bioinformatics 30:801-7
Wade, Charles E; Baer, Lisa A; Wu, Xiaowu et al. (2013) Severe burn and disuse in the rat independently adversely impact body composition and adipokines. Crit Care 17:R225
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Wade, Charles E; Mora, Alejandra G; Shields, Beth A et al. (2013) Signals from fat after injury: plasma adipokines and ghrelin concentrations in the severely burned. Cytokine 61:78-83
Shields, Beth A; Doty, Kevin A; Chung, Kevin K et al. (2013) Determination of resting energy expenditure after severe burn. J Burn Care Res 34:e22-8
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Mann, Elizabeth A; Jones, John A; Wolf, Steven E et al. (2011) Computer decision support software safely improves glycemic control in the burn intensive care unit: a randomized controlled clinical study. J Burn Care Res 32:246-55
Farhy, Leon S; Ortiz, Edward A; Kovatchev, Boris P et al. (2011) Average daily risk range as a measure of glycemic risk is associated with mortality in the intensive care unit: a retrospective study in a burn intensive care unit. J Diabetes Sci Technol 5:1087-98

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