Tissue repairis accompanied by an ordered sequence of cellular responses which leads to a clearly defined sequence of alterations in the context and function of the wound fluid comprising the extracellular environment. There is a gradual accumulation of all amino acids with the exception of arginine, a decrease in glucose, and an increase in lactate concentration. Specific temporal alterations occur in the expression of message for peptide growth factors, and classical endocrine hormones accumulate to reach concentrations far exceeding those found in plasma. Previous studies support the concept that wound metabolism and wound cell function are independent of circulating hormone and substrate alterations. Yet several of the more common clinical examples of impaired wound healing involve systemic hormonal, and substrate changes. This proposal will examine this apparent controversy, attempt to understand the lack of hormonal responsiveness in normal wound healing, and investigate the underlying mechanisms where pathological alterations of hormone and substrate concentrations are associated with poor repair. Two hypotheses are presented: first, that under normal circumstances the wound environment is insensitive to circulating hormone concentrations; second, that the impaired wound healing associated with pathologic changes in systemic hormonal substrate concentrations is due to nonclassical effects of these hormones or substrates.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM032224-11
Application #
2176479
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Project Start
1990-09-01
Project End
1997-06-30
Budget Start
1994-07-01
Budget End
1995-06-30
Support Year
11
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Surgery
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
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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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