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L-arginine: a unique amino acid for improving depressed wound immune function following hemorrhage.

AbstractOBJECTIVE:
To determine whether L-arginine has any salutary effects on wound immune cell function following trauma-hemorrhage.
BACKGROUND:
Depressed wound immune function contributes to an increased incidence of wound infections following hemorrhage. Although administration of L-arginine has been shown to restore depressed cell-mediated immune responses following hemorrhage potentially by maintaining organ blood flow, it remains unknown whether L-arginine has any salutary effects on the depressed local immune response at the wound site.
METHODS:
Male mice were subjected to a midline laparotomy and polyvinyl sponges were implanted subcutaneously in the abdominal wound prior to hemorrhage (35 +/- 5 mm Hg for 90 min and resuscitation) or sham operation. During resuscitation mice received 300 mg/kg body weight L-arginine or saline (vehicle). Sponges were harvested 24 h thereafter, wound fluid collected and wound immune cells cultured for 24 h in the presence of LPS. Pro- (IL-1 beta, IL-6) and anti-inflammatory (IL-10) cytokines were determined in the supernatants and the wound fluid. In addition, wounds were stained for IL-6 immunohistochemically. In a separate set of animals, skin and muscle blood flow was determined by microspheres.
RESULTS:
The capacity of wound immune cells to release IL-1 beta and IL-6 in vitro was significantly depressed in hemorrhaged mice receiving vehicle. Administration of L-arginine, however, improved wound immune cell function. In contrast, in vivo the increased IL-6 release at the wound site was decreased in L-arginine-treated mice following hemorrhage. Moreover, IL-10 levels were significantly increased in the wound fluid in hemorrhaged animals receiving L-arginine compared to vehicle-treated mice. In addition, the depressed skin and muscle blood flow after hemorrhage was restored by L-arginine.
CONCLUSIONS:
Thus, L-arginine might improve local wound cell function by decreasing the inflammatory response at the wound site. Since L-arginine protected wound immune cell function this amino acid might represent a novel and useful adjunct to fluid resuscitation for decreasing wound complications following hemorrhage.
AuthorsMartin K Angele, Stefan M Nitsch, Rudolf A Hatz, Peter Angele, Thomas Hernandez-Richter, Mathias W Wichmann, Irshad H Chaudry, Fredrich W Schildberg
JournalEuropean surgical research. Europaische chirurgische Forschung. Recherches chirurgicales europeennes (Eur Surg Res) 2002 Jan-Apr Vol. 34 Issue 1-2 Pg. 53-60 ISSN: 0014-312X [Print] Switzerland
PMID11867902 (Publication Type: Journal Article)
CopyrightCopyright 2002 S. Karger AG, Basel
Chemical References
  • Interleukin-1
  • Interleukin-6
  • Interleukin-10
  • Arginine
Topics
  • Animals
  • Arginine (pharmacology)
  • Bacterial Infections (immunology, prevention & control)
  • Exudates and Transudates (chemistry, immunology)
  • Interleukin-1 (analysis, metabolism)
  • Interleukin-10 (analysis, metabolism)
  • Interleukin-6 (analysis, metabolism)
  • Macrophages (cytology, metabolism)
  • Male
  • Mice
  • Mice, Inbred C3H
  • Muscle, Skeletal (blood supply)
  • Neutrophils (cytology, metabolism)
  • Regional Blood Flow (immunology)
  • Shock, Hemorrhagic (immunology)
  • Skin (blood supply)
  • Wound Healing (drug effects, immunology)
  • Wounds and Injuries (drug therapy, immunology)

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