Role of arginine in superficial wound healing in man

被引:76
作者
Debats, I. B. J. G. [1 ]
Wolfs, T. G. A. M. [2 ]
Gotoh, T. [3 ]
Cleutjens, J. P. M. [4 ]
Peutz-Kootstra, C. J. [4 ]
van der Hulst, R. R. W. J. [1 ]
机构
[1] Univ Hosp Maastricht, Dept Plast Reconstruct & Handsurg, NL-6202 AZ Maastricht, Netherlands
[2] Univ Hosp Maastricht, Dept Gen Surg, NL-6202 AZ Maastricht, Netherlands
[3] Kumamoto Univ, Grad Sch Med Sci, Dept Mol Genet, Kumamoto 8608556, Japan
[4] Univ Hosp Maastricht, Dept Pathol, NL-6202 AZ Maastricht, Netherlands
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2009年 / 21卷 / 3-4期
关键词
Nitric oxide; Arginine; Wound healing; Human; Acute wounds; Arginase; NOS; NITRIC-OXIDE SYNTHASE; ARGINASE-I EXPRESSION; ENDOTHELIAL-CELLS; AMINO-ACID; ACTIVATED MACROPHAGES; HUMAN-NEUTROPHILS; IMMUNE-RESPONSES; NO PRODUCTION; RAT SKIN; METABOLISM;
D O I
10.1016/j.niox.2009.07.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Arginine supplementation has been identified as advantageous in experimental wound healing. However, the mechanisms underlying this beneficial effect in tissue repair remain unresolved. Animal studies suggest that the beneficial role of arginine supplementation is mediated, at least in part through NO. The latter component mediates processes involved in tissue repair, including angiogenesis, epithelialization and collagen formation. This prospective study is performed to investigate arginine metabolism in acute surgical wounds in man. Expression of enzymes, known to be involved in arginine metabolism, was studied in donor sites of skin grafts of 10 hospitalized patients undergoing skin transplantation. Plasma and wound fluid levels of arginine metabolites (ornithine, citrulline, nitrate and nitrite = NOx) were measured using High Performance Liquid Chromatography. Expression of iNOS, eNOS, arginase-1 and arginase-2 was studied by immunohistochemistry in paraffin sections of skin tissue. Arginase-1 concentration was measured in plasma and wound fluid using ELISA. Arginase-2 was determined using Western blot analysis. We observed increased levels of citrulline, ornithine, NOx and arginase-1 in wound fluid when compared with plasma. Arginase-2 was expressed in both plasma and wound fluid and seemed higher in plasma. iNOS was expressed by neutrophils, macrophages, fibroblasts, keratinocytes and endothelial cells upon wounding, whereas eNOS reactivity was observed in endothelial cells and fibroblasts. Arginase-1 was expressed in neutrophils post-wounding, while arginase-2 staining was observed in endothelial cells, keratinocytes, fibroblasts, macrophages and neutrophils. For the first time, human data support previous animal studies suggesting arginine metabolism for an NO- as well as arginase-mediated reparation of injured skin. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:175 / 183
页数:9
相关论文
共 82 条
[1]  
Abd-El-Aleem SA, 2000, J PATHOL, V191, P434, DOI 10.1002/1096-9896(2000)9999:9999<::AID-PATH654>3.0.CO
[2]  
2-S
[3]   METABOLISM OF PROLINE AND THE HYDROXYPROLINES [J].
ADAMS, E ;
FRANK, L .
ANNUAL REVIEW OF BIOCHEMISTRY, 1980, 49 :1005-1061
[4]   ROLE OF ORNITHINE AS A PROLINE PRECURSOR IN HEALING WOUNDS [J].
ALBINA, JE ;
ABATE, JA ;
MASTROFRANCESCO, B .
JOURNAL OF SURGICAL RESEARCH, 1993, 55 (01) :97-102
[5]   ARGININE METABOLISM IN WOUNDS [J].
ALBINA, JE ;
MILLS, CD ;
BARBUL, A ;
THIRKILL, CE ;
HENRY, WL ;
MASTROFRANCESCO, B ;
CALDWELL, MD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (04) :E459-E467
[6]  
ALBINA JE, 1990, J IMMUNOL, V144, P3877
[7]   Nitric oxide donor improves healing if applied on inflammatory and proliferative phase [J].
Amadeu, Thais P. ;
Seabra, Amedea. B. ;
de Oliveira, Marcelo G. ;
Monte-Alto-Costa, Andrea .
JOURNAL OF SURGICAL RESEARCH, 2008, 149 (01) :84-93
[8]   Early effects of exogenous arginine after the implantation of prosthetic material into the rat abdominal wall [J].
Arbós, MA ;
Ferrando, JM ;
Vidal, J ;
Quiles, MT ;
Huguet, P ;
Castells, J ;
Segarra, A ;
Armengol, M ;
Schwartz, S .
LIFE SCIENCES, 2000, 67 (20) :2493-2512
[9]   Arginase pathway in human endothelial cells in pathophysiological conditions [J].
Bachetti, T ;
Comini, L ;
Francolini, G ;
Bastianon, D ;
Valetti, B ;
Cadei, M ;
Grigolato, PG ;
Suzuki, H ;
Finazzi, D ;
Albertini, A ;
Curello, S ;
Ferrari, R .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2004, 37 (02) :515-523
[10]   Arginine availability, arginase, and the immune response [J].
Bansal, V ;
Ochoa, JB .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2003, 6 (02) :223-228