Enteral nutritional supplementation prevents mesenteric lymph node T-cell suppression in burn injury

被引:27
作者
Choudhry, MA [1 ]
Haque, F [1 ]
Khan, M [1 ]
Fazal, N [1 ]
Al-Ghoul, W [1 ]
Ravindranath, T [1 ]
Gamelli, RL [1 ]
Sayeed, MM [1 ]
机构
[1] Loyola Univ Chicago Med Ctr, Burn & Shock Trauma Inst, Crit Care Res Labs, Dept Surg, Maywood, IL 60153 USA
关键词
rat; T lymphocyte; interleukin-2; prostaglandin; signaling molecule; IMPACT; immune-enhancing diet;
D O I
10.1097/01.CCM.0000063053.31485.DF
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: To determine the effects of an immune-enhancing diet supplemented with glutamine, arginine, fish oil, and dietary nucleotides on mesenteric lymph node T-cell functional disturbances encountered after burn injury in rats. Design: A prospective animal study. Setting: University medical center research laboratory. Subjects. Adult male Sprague-Dawley rats. Interventions. Rats received a 30%, total body surface, full-thickness burn. Burn-injury rats received the IMPACT diet supplemented with glutamine, arginine, fish oil, and nucleotides or arginine, fish oil, and nucleotides, or an isocaloric/isonitrogenous diet without supplementation with glutamine, arginine, fish oil, or nucleotides. Measurements and Main Results., Two days after injury, we found a significant decrease in the proliferation and interleukin-2 production by mesenteric lymph node T cells derived from rats fed on conventional chow compared with sham rats. The burn-related suppression of mesenteric lymph node T-cell proliferation and interleukin-2 production was prevented when the rats were fed on a high-protein diet rich in glutamine, arginine, fish oil, and nucleotides. We found that the immunostimulatory effects of the enriched diet are dependent on the presence of glutamine, arginine, fish oil, and nucleotides as feeding of rats on the isocaloric/isonitrogenous diet deficient in glutamine, arginine, fish oil, and nucleotides did not prevent the burn-related suppression of mesenteric lymph node T-cell dysfunction. Finally, our studies suggested that immunostimulatory effects of the diet are mediated by prostaglandin E-2 regulation of T-cell activation signaling molecule P59(fyn). Conclusion. These results suggest that a diet rich in arginine, fish oil, and nucleotides, with and without glutamine, can effectively prevent T-cell dysfunction encountered after burn injury.
引用
收藏
页码:1764 / 1770
页数:7
相关论文
共 49 条
[1]   Glutamine: essential for immune nutrition in the critically ill [J].
Andrews, FJ ;
Griffiths, RD .
BRITISH JOURNAL OF NUTRITION, 2002, 87 :S3-S8
[2]   DEFECTIVE T-CELL RECEPTOR SIGNALING IN MICE LACKING THE THYMIC ISOFORM OF P59(FYN) [J].
APPLEBY, MW ;
GROSS, JA ;
COOKE, MP ;
LEVIN, SD ;
QIAN, X ;
PERLMUTTER, RM .
CELL, 1992, 70 (05) :751-763
[3]  
Bahrami S, 1996, CURR TOP MICROBIOL, V216, P239
[4]   Lymphocyte activation in health and disease [J].
Berridge, MJ .
CRITICAL REVIEWS IN IMMUNOLOGY, 1997, 17 (02) :155-178
[5]   Sir Isaac Newton, sepsis, SIRS, and CARS [J].
Bone, RC .
CRITICAL CARE MEDICINE, 1996, 24 (07) :1125-1128
[6]   EARLY ENTERAL ADMINISTRATION OF A FORMULA (IMPACT((R))) SUPPLEMENTED WITH ARGININE, NUCLEOTIDES, AND FISH-OIL IN INTENSIVE-CARE UNIT PATIENTS - RESULTS OF A MULTICENTER, PROSPECTIVE, RANDOMIZED, CLINICAL-TRIAL [J].
BOWER, RH ;
CERRA, FB ;
BERSHADSKY, B ;
LICARI, JJ ;
HOYT, DB ;
JENSEN, GL ;
VANBUREN, CT ;
ROTHKOPF, MM ;
DALY, JM ;
ADELSBERG, BR .
CRITICAL CARE MEDICINE, 1995, 23 (03) :436-449
[7]  
Braga M, 1996, ARCH SURG-CHICAGO, V131, P1257
[8]   PGE2 suppresses mitogen-induced Ca2+ mobilization in T cells [J].
Choudhry, MA ;
Hockberger, PE ;
Sayeed, MM .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 277 (06) :R1741-R1748
[9]   PGE2-mediated inhibition of T cell p59fyn is independent of cAMP [J].
Choudhry, MA ;
Ahmed, Z ;
Sayeed, MM .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 277 (02) :C302-C309
[10]   ROLE OF CA2+ IN PROSTAGLANDIN E(2)-INDUCED T-LYMPHOCYTE PROLIFERATIVE SUPPRESSION IN SEPSIS [J].
CHOUDHRY, MA ;
AHMAD, S ;
SAYEED, MM .
INFECTION AND IMMUNITY, 1995, 63 (08) :3101-3105