Combination treatment of parenteral arginine and nitric oxide inhibitor NG-nitro-L-arginine methyl ester in rats with peritonitis

被引:4
作者
Lee, Chien-Hsing [1 ,2 ]
Hsiao, Chien-Chou [3 ]
Hung, Ching-Yi [1 ]
Lo, Hui-Chen [4 ]
机构
[1] Changhua Christian Hosp, Dept Surg, Div Pediat Surg, Changhua, Taiwan
[2] Chang Jung Christian Univ, Grad Inst Med Sci, Tainan, Taiwan
[3] Changhua Christian Hosp, Dept Pediat, Changhua, Taiwan
[4] Fu Jen Catholic Univ, Dept Nutr Sci, New Taipei City 24205, Taiwan
关键词
Arginine; Nitric oxide synthase; Peritonitis; Parenteral nutrition; Inflammation; L-NAME; METABOLISM; NUTRITION; LESIONS; MODEL;
D O I
10.1016/j.jss.2012.05.089
中图分类号
R61 [外科手术学];
学科分类号
摘要
Purpose: It has been shown that parenteral arginine may facilitate ureagenesis and improve leukocytic and splenocytic immunity and that the infusion of nitric oxide synthase inhibitor N-G-nitro-L-arginine methyl ester (L-NAME) may facilitate the production of arginine-associated amino acids in rats with subacute peritonitis. Herein, we investigated the effects of the combined treatment of parenteral arginine and L-NAME on arginine metabolism and inflammatory response. Methods and materials: Male Wistar rats underwent cecal puncture for induction of subacute peritonitis and were infused with conventional parenteral nutrition (arginine 0.95 g/kg/d) or parenteral nutrition supplemented with arginine (1.88 g/kg/d), L-NAME (25 mg/kg/d), or arginine plus L-NAME. Sham-operated and nonperitonitic rats with oral feeding (R group) or conventional parenteral nutrition (TPN group) were also included. Results: After 7 d of parenteral feeding, the L-NAME treatment significantly attenuated the peritonitis-induced reduction in body weight gain (1-way ANOVA, P < 0.05) and had a significant impact on decreasing body water percentage and on increasing body fat percentage and serum insulin concentrations (2-way ANOVA, P < 0.05). Parenteral arginine had a significant impact on increasing plasma arginine and ornithine and on decreasing serum glutamate oxaloacetate transaminase and plasma nitrite/nitrate in peritonitic rats. In addition, plasma interleukin-6 was significantly decreased by arginine and/or L-NAME treatment, and plasma prostaglandin E-2 was significantly decreased by arginine plus L-NAME treatment. Conclusion: These results suggest that the combination treatment of parenteral arginine and L-NAME may improve liver function and alleviate inflammatory response in rats with subacute peritonitis; however, it seems that parenteral arginine treatment is more beneficial than L-NAME. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 28 条
[1]  
Benson Renee C, 2011, J Allergy (Cairo), V2011, P736319, DOI 10.1155/2011/736319
[2]  
Chen YH, 2012, JPEN J PARE IN PRESS
[3]   Nitric oxide synthase inhibitor attenuates inflammatory lesions in the skin of zinc-deficient rats [J].
Cui, L ;
Takagi, Y ;
Sando, K ;
Wasa, M ;
Okada, A .
NUTRITION, 2000, 16 (01) :34-41
[4]   Nitric oxide synthase inhibitor attenuates intestinal damage induced by zinc deficiency in rats [J].
Cui, L ;
Takagi, Y ;
Wasa, M ;
Sando, K ;
Khan, J ;
Okada, A .
JOURNAL OF NUTRITION, 1999, 129 (04) :792-798
[5]   Pharmacokinetics of arginine and related amino acids [J].
Cynober, Luc .
JOURNAL OF NUTRITION, 2007, 137 (06) :1646S-1649S
[6]   To Give or Not to Give? Lessons from the Arginine Paradox [J].
Dioguardi, Francesco Saverio .
JOURNAL OF NUTRIGENETICS AND NUTRIGENOMICS, 2011, 4 (02) :90-98
[7]   G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences [J].
Faul, Franz ;
Erdfelder, Edgar ;
Lang, Albert-Georg ;
Buchner, Axel .
BEHAVIOR RESEARCH METHODS, 2007, 39 (02) :175-191
[8]   Inhibition of nitric oxide synthase reverses changes in peritoneal permeability in a rat model of acute peritonitis [J].
Ferrier, ML ;
Combet, S ;
van Landschoot, M ;
Stoenoiu, MS ;
Cnops, Y ;
Lameire, N ;
Devuyst, O .
KIDNEY INTERNATIONAL, 2001, 60 (06) :2343-2350
[9]   Nitric oxide inhibition decreases neutrophil adhesion at the inflammatory site, while increasing adhesion in remote organs in peritonitis [J].
Fukatsu, K ;
Saito, H ;
Han, I ;
Furukawa, S ;
Hashiguchi, Y ;
Lin, MT ;
Matsuda, T ;
Inaba, T ;
Inoue, T ;
Ikeda, S ;
Yasuhara, H ;
Muto, T .
JOURNAL OF SURGICAL RESEARCH, 1997, 68 (01) :79-86
[10]  
GEROULANOS S, 1992, LANCET, V339, P435