Influence of structurally different lipid emulsions on human neutrophil oxygen radical production

European Journal of Clinical Investigation

Volumn 29, Issue 4, 1999, Pages 357-363

  Wanten, G J A ^a   Naber, A H J ^a   Kruimel, J W ^a   Tool, A T J ^b   Roos, D ^b   Jansen, J B M J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

Chemiluminescence; Lipid emulsion; Neutrophil; Oxygen radical; Respiratory burst

Indexed keywords

HYDROGEN PEROXIDE; INTRALIPID; LIPID EMULSION; LIPOFUNDIN; OXYGEN RADICAL; PHORBOL 13 ACETATE 12 MYRISTATE; SUPEROXIDE; ZYMOSAN;

ADULT; ARTICLE; CHEMOLUMINESCENCE; CONTROLLED STUDY; FEMALE; HUMAN; HUMAN CELL; IMMUNOMODULATION; MALE; NEUTROPHIL; NORMAL HUMAN; OXYGEN CONSUMPTION; PARENTERAL NUTRITION; PRIORITY JOURNAL; RESPIRATORY BURST;

ADULT; CHEMILUMINESCENT MEASUREMENTS; EMULSIONS; FEMALE; HUMANS; HYDROGEN PEROXIDE; INDICATORS AND REAGENTS; LIPIDS; LUMINOL; MALE; MIDDLE AGED; NEUTROPHILS; RESPIRATORY BURST; SUPEROXIDES;

EID: 0032895176     PISSN: 00142972     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2362.1999.00486.x     Document Type: Article

References (24)

1. 1 Freeman J, Goldmann DA, Smith NE, Sidebottom DG, Epstein MF, Platt R. Association of intravenous fat emulsions and coagulase-negative staphylococcal bacteremia in neonatal intensive care units. N Engl J Med 1990; 323: 301-8.
2. 2 Snydman DR, Murray SA, Kornfeld SJ, Majka JA, Ellis CA. Total parenteral nutrition-related infections. Prospective epidemiological study using semiquantitative methods. Am J Med 1982; 73: 695-9.
3. 3 The Veterans Affairs Total Parenteral Nutrition Cooperative Study Group. Perioperative total parenteral nutrition in surgical patients. N Engl J Med 1991; 325: 525-32.
4. 4 Fisher GW, Hunter KW, Wilson SR, Mease AD. Diminished bacterial defence with Intralipid. Lancet 1980; 2: 819-20.
5. 5 English D, Roloff JS, Lukens JN, Parker P, Greene HL, Ghishan FK. Intravenous lipid emulsions and human neutrophil function. J Pediatr 1981; 99: 913-6.
6. 6 Wiernick A, Jarstrand C, Julander I. The effect of Intralipid on mononuclear and polymorphonuclear phagocytes. Am J Clin Nutr 1983; 37: 256-61.
7. 7 Jarstrand C, Rasool O. Intralipid decreases the bacterial lipopolysaccharide induced release of oxygen radicals and lysozyme from human neutrophils. Scand J Infect Dis 1991; 23: 481-7.
8. 8 Wheeler JG, Boyle RJ, Abramson JS. Intralipid infusion in neonates: effects on polymorphonuclear leukocyte function. J Paediatr Gastroenterol Nutr 1985; 4: 453-6.
9. 9 Bellinati-Pires Waitzberg DL, Salgado MM, Carneiro-Sampaio MMS. Effect of medium-and long-chain triglycerides on human neutrophil migration. Braz J Med Biol Res 1992; 25: 369-73.
10. 10 Palmblad J, Brostrom O, Lahnborg G, Voen AM, Venizelos N. Neutrophil functions during total parenteral nutrition and Intralipid infusion. Am J Clin Nutr 1982; 35: 1430-6.
11. 11 Rasmussen A, Hessov I, Segel E. The effect of Intralipid on polymorphonuclear leukocytes. Clin Nutr 1988; 7: 37-41.
12. 12 Robin AP, Arain I, Phuangsab A, Holian O, Roccaforte P, Barrett JA. Intravenous fat emulsion acutely suppresses neutrophil chemiluminescence. J Parent Ent Nutr 1989; 13: 608-13.
13. 13 Waitzberg DL, Bellinati-Pires R, Salgado MM et al. Effect of total parenteral nutrition with different lipid emulsions on human monocyte and neutrophil functions. Nutrition 1997; 13: 128-32.
14. 2 generating system in a cell-free preparation from neutrophils. J Biol Chem 1988; 263: 13670-6.
15. 15 Bellinati-Pires R, Waitzberg DL, Salgado MM, Carneiro-Sampaio. Functional alterations of human neutrophils by medium-chain triglyceride emulsions: evaluation of phagocytosis, bacterial killing, and oxidative activity. J Leuk Biol 1993; 53: 404-10.
16. 16 Kruimel JW, Naber AHJ, van der Vliet JA, Carneheim C, Katan MB, Jansen JBMJ. Parenteral administration of structured triglycerides improves nitrogen balance in post-operative patients. J Parent Ent Nutr 1997; 21(1):S34.
17. 17 Goldstein IM, Roos D, Kaplan HB, Weissmann G. Complement and immunoglobulins stimulate superoxide production by human leukocytes independently of phagocytosis. J Clin Invest 1975; 56: 1155.
18. 18 Kuijpers TW, Tool ATJ, van der School CE, et al. Membrane surface antigen expression on neutrophils: a reappraisal of the use of surface markers for neutrophil activation. Blood 1991; 4: 1105-11.
19. 19 Weening RS, Roos D, Loos JA. Oxygen consumption of phagocytizing cells in human leukocyte and granulocyte preparations: a comparative study. J Lab Clin Med 1974; 83: 570.
20. 20 Kessels GCR, Krause K, Verhoeven AJ. Protein kinase C activity is not involved in N-formylmethionyl-leucylphenylalanine induced phospholipase D activation in human neutrophils, but is essential for concomitant NADPH oxidase activation. Biochem J 1993; 292: 781.
21. 21 Van Gelder BF, Slater EC. The extinction coefficient of cytochrome c. Biochim Biophys Acta 1962; 58: 593-5.
22. 2 production by macrophages and neutrophils with homovanillic acid and horse-radish peroxidase. J Immunol Methods 1983; 63: 347-57.
23. 23 Lundqvist H, Dahlgren C. Isoluminol-enhanced chemiluminescence: a sensitive method to study the release of super-oxide anion from human neutrophils. Free Rad Biol Med 1996; 20 (6):785-92.
24. 24 Kruimel JW, Wenker MAM, Naber AHJ, et al. Influence of the emulsifier in parenteral lipid emulsions on polymorphonuclear leukocyte function. Neth J Med 1995; 46: A18.