Early wound healing occurs during a period of negative energy balance and negative bodily balance of most constituents. In addition, a continuously open wound impairs host protein anabolism and restoration of lost body composition. These findings suggest a biological priority of healing wounds and the transmission of a message from the wound to the host. Glucose, amino acid and energy metabolism are altered in wound tissue. These alterations in wound metabolism could be caused by 1) neural stimulation; 2) hormonal and substrate alterations following wounding; or 3) local changes in the wound. A perfused wound model, developed in our laboratory, has demonstrated characteristically altered wound metabolism occurs in the absence of hormones and with perfusate substrate concentrations which mimic the plasma of normal fed rats. These findings suggest that metabolic changes observed in wounded muscle are local and may proceed in the absence of the hormonal and substrate environment that follow wounding thus confirming biological priority. The relationship between this environment in response to wounding and convalescence, and the local changes in a healing wound will be explored using this isolated perfused rat hindlimb model. The hormone and substrate milieu, present in control animals and at various intervals following wounding, will be determined and reproduced in the perfusate. Since the wound model is denervated, this approach allows evaluation of the other non-local variable (i.e., the hormone and substrate milieu) on wound amino acid and glucose metabolism and on collagen synthesis. Wounded tissue has accelerated glycolysis with the concomitant production of many gluconeogenic substrates. We have shown glycolysis in wounded tissue to be aerobic suggesting impairment of shuttle mechanisms for oxidation of NADH. The involvement of these shuttle mechanisms will be evaluated. Since there is no obvious flux-generating step in wounded muscle for glycolysis, it is most likely this step is one of glucose production external to the wound. As a consequence, it is proposed to evaluate the effect of substrate supply from the wound and the hormonal milieu on glucose production in the liver. In addition, the effect of glucose supply on glycolysis and glucose disposal in the wound will be examined. The effect of exogenous amino acid supply on collagen synthesis in wounded tissue will be investigated. This is a comprehensive proposal which seeks to understand many of the important processes that bestow biological priority to healing wounds.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM032224-03
Application #
3280861
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Project Start
1984-12-01
Project End
1988-02-29
Budget Start
1986-12-01
Budget End
1988-02-29
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Rhode Island Hospital (Providence, RI)
Department
Type
DUNS #
161202122
City
Providence
State
RI
Country
United States
Zip Code
02903
Ulland, A E; Shearer, J D; Coulter, C et al. (1997) Altered wound arginine metabolism by corticosterone and retinoic acid. J Surg Res 70:84-8
Shearer, J D; Richards, J R; Mills, C D et al. (1997) Differential regulation of macrophage arginine metabolism: a proposed role in wound healing. Am J Physiol 272:E181-90
Shearer, J D; Coulter, C F; Engeland, W C et al. (1997) Insulin is degraded extracellularly in wounds by insulin-degrading enzyme (EC 3.4.24.56). Am J Physiol 273:E657-64
Caldwell, M D; Mastrofrancesco, B; Shearer, J et al. (1991) The temporal change in amino acid concentration within wound fluid--a putative rationale. Prog Clin Biol Res 365:205-22
Mills, C D; Pricolo, V E; Albina, J E et al. (1991) Concomitant macrophage activation and fibroblast/lymphocyte inhibition by wound fluid: the ""arginine-deficiency of inflammation"" is a partial explanation. Prog Clin Biol Res 365:193-203
Daley, J M; Shearer, J D; Mastrofrancesco, B et al. (1990) Glucose metabolism in injured tissue: a longitudinal study. Surgery 107:187-92
Falcone, P A; Caldwell, M D (1990) Wound metabolism. Clin Plast Surg 17:443-56
Albina, J E; Caldwell, M D; Henry Jr, W L et al. (1989) Regulation of macrophage functions by L-arginine. J Exp Med 169:1021-9
Albina, J E; Mills, C D; Henry Jr, W L et al. (1989) Regulation of macrophage physiology by L-arginine: role of the oxidative L-arginine deiminase pathway. J Immunol 143:3641-6
Forster, J; Morris, A S; Shearer, J D et al. (1989) Glucose uptake and flux through phosphofructokinase in wounded rat skeletal muscle. Am J Physiol 256:E788-97

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