β-glucan protects against burn-induced oxidative organ damage in rats

被引:83
作者
Toklu, HZ
Sener, G [1 ]
Jahovic, N
Uslu, B
Arbak, S
Yegen, BÇ
机构
[1] Marmara Univ, Sch Pharm, Dept Pharmacol, TR-34668 Istanbul, Turkey
[2] Marmara Univ, Sch Med, Dept Physiol, Istanbul, Turkey
[3] Marmara Univ, Dept Histol & Embryol, Istanbul, Turkey
关键词
glucan; burn; thermal injury; oxidative; antioxidant;
D O I
10.1016/j.intimp.2005.07.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thermal injury may lead to systemic inflammatory response, and multiple organ failure. Generation of reactive oxygen radicals and lipid peroxidation play important roles in burn-induced remote organ injury. In the present study, we investigated the putative protective effect of local or systemic beta-glucan treatment on burn-induced remote organ injury. Wistar albino rats were exposed to 90 degrees C bath for 10 s to induce thermal trauma. beta-glucan (3.75 mg/rat locally or 50 mg/kg orally) or saline was administered immediately after the trauma and were repeated twice daily in 48 h groups. Rats were decapitated either 6 or 48 h after burn injury and the skin, lung, liver, ileum and kidney tissues were taken for the measurement of malondialdehyde (MDA) - an index of lipid peroxidation - and glutathione (GSH) - a key antioxidant - levels. Neutrophil infiltration was evaluated by the measurement of tissue myeloperoxidase (MPO) activity, while the tumor necrosis factor-alpha (TNF-alpha) levels were measured in serum samples. Skin tissues were also examined microscopically. Severe skin scald injury (30% of total body surface area) caused significant decreases in GSH levels of the liver and intestinal tissues (p < 0.01-< 0.001), while MDA levels were significantly (p < 0.01-p < 0.001) increased at post-burn 6 and 48 h. Both local and systemic P-glucan treatments significantly reversed (p < 0.01-p < 0.001) the elevations in MDA levels, while reduced GSH levels were reversed back to control levels (p < 0.01-p < 0.001); and the raised MPO levels were significantly decreased (p < 0.05-p < 0.001). The results indicate that both systemic and local administration of beta-glucan were effective against burn-induced oxidative tissue damage in the rat. beta-glucans, besides their immunomodulatory effects, have additional antioxidant properties. Therefore, beta-glucans merit consideration as therapeutic agents in the treatment of burn injuries. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 169
页数:14
相关论文
共 61 条
[1]  
Babincova M., 2002, Journal of Medicinal Food, V5, P79, DOI 10.1089/109662002760178159
[2]   Effect of β-glucan from oats and yeast on serum lipids [J].
Bell, S ;
Goldman, VM ;
Bistrian, BR ;
Arnold, AH ;
Ostroff, G ;
Forse, RA .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1999, 39 (02) :189-202
[3]  
Beuge J.A., 1978, METHOD ENZYMOL, V52, P302
[4]  
BEUTLER E, 1975, GLUTATHIONE RED BLOO, V112
[5]   Dectin-1 is a major β-glucan receptor on macrophages [J].
Brown, GD ;
Taylor, PR ;
Reid, DM ;
Willment, JA ;
Williams, DL ;
Martinez-Pomares, L ;
Wong, SYC ;
Gordon, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (03) :407-412
[6]   Dectin-1 mediates the biological effects of β-glucans [J].
Brown, GD ;
Herre, J ;
Williams, DL ;
Willment, JA ;
Marshall, ASJ ;
Gordon, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (09) :1119-1124
[7]   Fungal β-glucans and mammalian immunity [J].
Brown, GD ;
Gordon, S .
IMMUNITY, 2003, 19 (03) :311-315
[8]   Leptin ameliorates burn-induced multiple organ damage and modulates postburn immune response in rats [J].
Çakir, B ;
Çevik, H ;
Contuk, G ;
Ercan, F ;
Eksioglu-Demiralp, E ;
Yegen, BÇ .
REGULATORY PEPTIDES, 2005, 125 (1-3) :135-144
[9]  
Carrow DJ, 1996, TOWNSEND LETT, P86
[10]   Inflammatory reaction and sepsis in severely burned patients. [J].
Carsin, H ;
Bargues, L ;
Stéphanazzi, J ;
Paris, A ;
Aubert, P ;
Le Béver, H .
PATHOLOGIE BIOLOGIE, 2002, 50 (02) :93-101