Enteral nutrition affects nitric oxide production in peripheral blood and liver after a postoperative lipopolysaccharide-induced endotoxemia in rats

Nutrition

Volumn 23, Issue 7-8, 2007, Pages 575-581

  Kolios, George ^a   Kotzampassi, Katerina ^b   Manousou, Pinelopi ^a   Paramythiotis, Daniel ^b   Papanastasiou, Helen ^b   Drygiannakis, Ioannis ^a   Notas, George ^a   Tsagarakis, Nikos ^a   Eleftheriadis, Efthimios ^b   Kouroumalis, Elias ^a  

^a UNIVERSITY OF CRETE   (Greece)

^b ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

Author keywords

Enteral nutrition; Lipopolysaccharide endotoxemia; Nitric oxide; Postoperative sepsis; Rats

Indexed keywords

LIPOPOLYSACCHARIDE; MESSENGER RNA; NITRIC OXIDE; NITRIC OXIDE SYNTHASE; SODIUM CHLORIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BLOOD; CONTROLLED STUDY; ENTERIC FEEDING; ENZYME ACTIVITY; FEEDING; GENE EXPRESSION; LAPAROTOMY; LIVER; LIVER HOMOGENATE; MALE; NITROSATIVE STRESS; NONHUMAN; POSTOPERATIVE COMPLICATION; PRIORITY JOURNAL; RAT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEPSIS; STOMACH TUBE; SURGICAL STRESS;

ANIMALS; ENDOTOXEMIA; ENTERAL NUTRITION; GASTROSTOMY; LIPOPOLYSACCHARIDES; LIVER; MALE; NITRIC OXIDE; NITRIC OXIDE SYNTHASE; NITRIC OXIDE SYNTHASE TYPE II; NITRIC OXIDE SYNTHASE TYPE III; NITRITES; OXIDATIVE STRESS; POSTOPERATIVE PERIOD; RATS; RATS, WISTAR; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER;

RATTUS;

EID: 34347221901     PISSN: 08999007     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nut.2007.04.010     Document Type: Article

References (40)

1. Heyland D.K., Cook D.J., and Guyatt G.H. Enteral nutrition in the critically ill patient: a critical review of the evidence. Intensive Care Med 19 (1993) 435-442
2. Eleftheriadis E. Role of enteral nutrition-induced splanchnic hyperemia in ameliorating splanchnic ischemia. Nutrition 15 (1999) 247-248
3. Sigalet D.L., Mackenzie S.L., and Hameed S.M. Enteral nutrition and mucosal immunity: implications for feeding strategies in surgery and trauma. Can J Surg 47 (2004) 109-116
4. Kazamias P., Kotzampassi K., Koufogiannis D., and Eleftheriadis E. Influence of enteral nutrition-induced splanchnic hyperemia on the septic origin of splanchnic ischemia. World J Surg 22 (1998) 6-11
5. Gianotti L., Alexander J.W., Nelson J.L., Fukushima R., Pyles T., and Chalk C.L. Role of early enteral feeding and acute starvation on postburn bacterial translocation and host defense: prospective, randomized trials. Crit Care Med 22 (1994) 265-272
6. Delogu G., Antonucci A., Moretti S., Marandola M., Tellan G., Signore M., and Famularo G. Oxidative stress and mitochondrial glutathione in human lymphocytes exposed to clinically relevant anesthetic drug concentrations. J Clin Anesth 16 (2004) 189-194
7. Thomas S., and Balasubramanian K.A. Role of intestine in postsurgical complications: involvement of free radicals. Free Radic Biol Med 36 (2004) 745-756
8. Satoi S., Kamiyama Y., Kitade H., Kwon A.H., Takahashi K., Wei T., et al. Nitric oxide production and hepatic dysfunction in patients with postoperative sepsis. Clin Exp Pharmacol Physiol 27 (2000) 197-201
9. Dhainaut J.F., Marin N., Mignon A., and Vinsonneau C. Hepatic response to sepsis: interaction between coagulation and inflammatory processes. Crit Care Med 29 (2001) S42-S47
10. Hon W.M., Lee K.H., and Khoo H.E. Nitric oxide in liver diseases: friend, foe, or just passerby?. Ann N Y Acad Sci 962 (2002) 275-295
11. Ceppi E.D., Smith F.S., and Titheradge M.A. Nitric oxide, sepsis and liver metabolism. Biochem Soc Trans 25 (1997) 929-934
12. Taylor B.S., Alarcon L.H., and Billiar T.R. Inducible nitric oxide synthase in the liver: regulation and function. Biochemistry (Moscow) 63 (1998) 766-781
13. Razavi H.M., Wang L., Weicker S., Quinlan G.J., Mumby S., McCormack D.G., and Mehta S. Pulmonary oxidant stress in murine sepsis is due to inflammatory cell nitric oxide. Crit Care Med 33 (2005) 1333-1339
14. Linehan J.D., Kolios G., Valatas V., Robertson D.A., and Westwick J. Effect of corticosteroids on nitric oxide production in inflammatory bowel disease: are leukocytes the site of action?. Am J Physiol Gastrointest Liver Physiol 288 (2005) G261-G267
15. Matrella E., Valatas V., Notas G., Roumpaki H., Xidakis C., Hadzidakis A., et al. Bolus somatostatin but not octreotide reduces hepatic sinusoidal pressure by a NO-independent mechanism in chronic liver disease. Aliment Pharmacol Ther 15 (2001) 857-864
16. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72 (1976) 248-254
17. Kolios G., Wright K.L., Linehan J.D., Robertson D.A., and Westwick J. Interleukin-13 inhibits nitric oxide production in human colonic mucosa. Hepatogastroenterology 47 (2000) 714-717
18. Johnson M.L., and Billiar T.R. Roles of nitric oxide in surgical infection and sepsis. World J Surg 22 (1998) 187-196
19. Jourd'Heuil D., Gray L., and Grisham M.B. S-nitrosothiol formation in blood of lipopolysaccharide-treated rats. Biochem Biophys Res Commun 273 (2000) 22-26
20. Ochoa J.B., Udekwu A.O., Billiar T.R., Curran R.D., Cerra F.B., Simmons R.L., and Peitzman A.B. Nitrogen oxide levels in patients after trauma and during sepsis. Ann Surg 214 (1991) 621-626
21. Wong H.R., Carcillo J.A., Burckart G., Shah N., and Janosky J.E. Increased serum nitrite and nitrate concentrations in children with the sepsis syndrome. Crit Care Med 23 (1995) 835-842
22. Hersch M., Scott J.A., Izbicki G., McCormack D., Cepinkas G., Ostermann M., and Sibbald W.J. Differential inducible nitric oxide synthase activity in circulating neutrophils vs. mononuclears of septic shock patients. Intensive Care Med 31 (2005) 1132-1135
23. Gladwin M.T., Schechter A.N., Kim-Shapiro D.B., Patel R.P., Hogg N., Shiva S., et al. The emerging biology of the nitrite anion. Nat Chem Biol 1 (2005) 308-314
24. Lu P., Liu F., Yao Z., Wang C.Y., Chen D.D., Tian Y., et al. Nitrite-derived nitric oxide by xanthine oxidoreductase protects the liver against ischemia-reperfusion injury. Hepatobiliary Pancreat Dis Int 4 (2005) 350-355
25. Houdijk A.P., Visser J.J., Rijnsburger E.R., Teerlink T., and van Leeuwen P.A. Dietary glutamine supplementation reduces plasma nitrate levels in rats. Clin Nutr 17 (1998) 11-14
26. Arnal J.F., Munzel T., Venema R.C., James N.L., Bai C.L., Mitch W.E., and Harrison D.G. Interactions between L-arginine and L-glutamine change endothelial NO production. An effect independent of NO synthase substrate availability. J Clin Invest 95 (1995) 2565-2572
27. Sessa W.C., Hecker M., Mitchell J.A., and Vane J.R. The metabolism of L-arginine and its significance for the biosynthesis of endothelium-derived relaxing factor: L-glutamine inhibits the generation of L-arginine by cultured endothelial cells. Proc Natl Acad Sci U S A 87 (1990) 8607-8611
28. Roth E. L-argine-nitric oxide metabolism. Glutamine: a new player in this metabolic game?. Clin Nutr 17 (1998) 1-2
29. Wu G., Jaeger L.A., Bazer F.W., and Rhoads J.M. Arginine deficiency in preterm infants: biochemical mechanisms and nutritional implications. J Nutr Biochem 15 (2004) 442-451
30. Hecker M., Mitchell J.A., Swierkosz T.A., Sessa W.C., and Vane J.R. Inhibition by L-glutamine of the release of endothelium-derived relaxing factor from cultured endothelial cells. Br J Pharmacol 101 (1990) 237-239
31. Chamulitrat W., Skrepnik N.V., and Spitzer J.J. Endotoxin-induced oxidative stress in the rat small intestine: role of nitric oxide. Shock 5 (1996) 217-222
32. Pastor C.M., Losser M.R., and Payen D. Nitric oxide donor prevents hepatic and systemic perfusion decrease induced by endotoxin in anesthetized rabbits. Hepatology 22 (1995) 1547-1553
33. Thiemermann C., Ruetten H., Wu C.C., and Vane J.R. The multiple organ dysfunction syndrome caused by endotoxin in the rat: attenuation of liver dysfunction by inhibitors of nitric oxide synthase. Br J Pharmacol 116 (1995) 2845-2851
34. Kolios G., Brown Z., Robson R.L., Robertson D.A.F., and Westwick J. Inducible nitric oxide synthase activity and expression in a human colonic epithelial cell line, HT-29. Br J Pharmacol 116 (1995) 2866-2872
35. Valatas V., Kolios G., Manousou P., Xidakis C., Notas G., Ljumovic D., and Kouroumalis E.A. Secretion of inflammatory mediators by isolated rat Kupffer cells: the effect of octreotide. Regul Pept 120 (2004) 215-225
36. Luiking Y.C., Poeze M., Dejong C.H., Ramsay G., and Deutz N.E. Sepsis: an arginine deficiency state?. Crit Care Med 32 (2004) 2135-2145
37. Luiking Y.C., Poeze M., Ramsay G., and Deutz N.E. The role of arginine in infection and sepsis. JPEN 29 (2005) S70-S74
38. Mojena M., Hortelano S., Castrillo A., Diaz-Guerra M.J., Garcia-Barchino M.J., Saez G.T., and Bosca L. Protection by nitric oxide against liver inflammatory injury in animals carrying a nitric oxide synthase-2 transgene. FASEB J 15 (2001) 583-585
39. Diez-Fernandez C., Sanz N., Alvarez A.M., Zaragoza A., and Cascales M. Influence of aminoguanidine on parameters of liver injury and regeneration induced in rats by a necrogenic dose of thioacetamide. Br J Pharmacol 125 (1998) 102-108
40. Gardner C.R., Heck D.E., Yang C.S., Thomas P.E., Zhang X.J., DeGeorge G.L., et al. Role of nitric oxide in acetaminophen-induced hepatotoxicity in the rat. Hepatology 27 (1998) 748-754