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Journal of Intensive Care Medicine
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Increased Oxidants and Reduced Antioxidants in Irradiated Parenteral Nutrition Solutions May Contribute to the Inflammatory Response

Guy A. Richards, MBBCh, PhD, FCP SA

Intensive Care Unit, Johannesburg Hospital and University of the Witwatersrand, Johannesburg, South Africa, guy.richards{at}wits.ac.za

Hayden White, MBBCh, FCP SA

South African Breweries, Sandton, South Africa

Heidi Grimmer, MSc

National Institute for Occupational Health, Johannesburg, South Africa

Caiphus Ramoroka, MSc

National Institute for Occupational Health, Johannesburg, South Africa

Kalavati Channa, MSc

National Institute for Occupational Health, Johannesburg, South Africa

Mark Hopley, MBBCh, FCP SA

Departments of Medicine and Pulmonology, Baragwanath Hospital and University of the Witwatersrand Johannesburg, South Africa

Heidi Fickl

Medical Research Council Unit for Inflammation and Immunity, Department of Immunology, Tshwane Academic Division of the National Health Laboratory Service and Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa

Mary Gulumian, PhD

Haematology and Molecular Medicine Department, School of Health Sciences, Parktown, Johannesburg, South Africa

Background/Objectives: To measure reactive oxidant production and the decline in antioxidant potential in commercially available, irradiated parenteral nutrition (PN) solutions and the effect that these have on oxidant production in patients in the intensive care unit. Subjects and Methods: Vitamin E and malondialdehyde in irradiated and nonirradiated commercially available, PN solutions were measured. The PBN ({alpha}-phenyl-n-test-butylnitrone (PBN) spin trap was used to measure free radicals and TEMPOL (2,2,6,6-tetramethyl-4-hydroxy-piperidine-oxyl) was used to assess antioxidant capacity. The irradiated PN was administered (as per unit protocol) to 10 patients with gut failure and plasma and urinary isoprostanes and interleukin-6 (IL-6) were measured 1 hour preadministration, at the time of, and 1 and 2 hours postadministration of PN. Results: Irradiation reduced vitamin E significantly (P < .0025). Malondialdehyde products were present in both samples, but more so in irradiated samples (P < .0001), as were free radicals measured by PBN spin trapping. Irradiated samples had a higher scavenging capacity of TEMPOL free radical due to depletion of antioxidants in irradiated samples. Urinary isoprostanes increased at time 2 by 6.3 units relative to time 0 and by 5.23 units relative to time 1(Friedman ANOVA: P < .01413). Conclusions: Lipid hydroperoxides are formed in PN solutions and increase further following irradiation. This is associated with a significant reduction in vitamin E and antioxidant potential. The increase in urinary isoprostanes indicates a potentially proinflammatory effect of irradiated PN.

Key Words: oxidants • parenteral nutrition • irradiation • inflammation • isoprostanes

This version was published on July 1, 2009

Journal of Intensive Care Medicine, Vol. 24, No. 4, 252-260 (2009)
DOI: 10.1177/0885066609332744


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