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Arginine metabolism in wounds
J E Albina1, C D Mills, A Barbul
1Department of Surgery, Rhode Island Hospital, Providence 02902.
The American Journal of Physiology
|April 11, 1988
Summary
Wound healing involves arginine metabolism changes, with macrophages releasing arginase after cell death. This suggests cellular cooperation for collagen synthesis during tissue repair.
Area of Science:
- Biochemistry
- Wound Healing Research
- Cellular Biology
Background:
- Arginine metabolism is crucial for wound healing.
- Understanding the source and regulation of enzymes involved in arginine breakdown is essential for optimizing tissue repair.
- Macrophages play a significant role in the inflammatory and reparative phases of wound healing.
Purpose of the Study:
- To investigate arginine metabolism in rat wound models.
- To determine the source and activity of arginase in wound environments.
- To explore the potential for cellular cooperation in providing substrates for collagen synthesis.
Main Methods:
- Utilized lambda-carrageenan-induced skeletal muscle wounds in rats.
- Employed Schilling chambers and polyvinyl alcohol sponges for wound analysis.
- Assessed arginine, ornithine, and arginase levels.
- Investigated macrophage arginase activity in vitro and in vivo.
- Measured arginase deiminase activity in macrophages using radiolabeled arginine.
Main Results:
- Wounds exhibited decreased arginine and increased ornithine levels with high arginase activity.
- Macrophages contained arginase activity, primarily after cell lysis.
- Extracellular arginase in wounds likely originates from dead macrophages.
- Wound and peritoneal macrophages demonstrated arginase deiminase activity, converting arginine to citrulline.
- This conversion was inhibited by formamidinium acetate, confirming enzymatic activity and ruling out prokaryotic contamination.
Conclusions:
- Arginase activity in wounds is linked to macrophage lysis.
- Macrophages contribute to arginine metabolism in wounds via arginase and arginase deiminase.
- Cellular cooperation among wound cells may facilitate substrate production for collagen synthesis, aiding tissue repair.