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Transfusion of packed red blood cells reduces selenium levels and increases lipid peroxidation in an in vivo ovine model
Author(s) -
McDonald C. I.,
Fraser J. F.,
Shekar K.,
Dunster K. R.,
Thom O.,
Fung Y. L.
Publication year - 2014
Publication title -
transfusion medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.471
H-Index - 59
eISSN - 1365-3148
pISSN - 0958-7578
DOI - 10.1111/tme.12087
Subject(s) - lipid peroxidation , oxidative stress , tbars , packed red blood cells , selenium , thiobarbituric acid , antioxidant , glutathione peroxidase , red blood cell , medicine , chemistry , biochemistry , immunology , blood transfusion , catalase , organic chemistry
SUMMARY Background Oxidative stress from surgery or critically illness has been shown to adversely contribute to morbidity and mortality. Recent studies record that oxidative stress is heightened following packed red blood cell ( PRBC ) transfusions and that products of oxidative stress accumulate as the PRBC ages. However, there are no studies that investigate if transfusion of aged PRBC actually increases the recipient's oxidative stress profile more than fresh PRBC . Objective To compare the effect of fresh vs aged PRBC transfusions on the recipient's oxidative stress using an ovine model. Materials and methods Male sheep were transfused with either fresh ( n = 6) or aged ( n = 6) ovine PRBC , and serial blood samples taken. Plasma samples were analysed for lipid peroxidation using the thiobarbituric acid reactive substances ( TBARS ) assay. This served as an indicator of oxidative injury. Antioxidant function and trace element levels were also measured. Results Like human PRBC , the ovine PRBC had negligible selenium levels. Irrespective of age, PRBC transfusion was associated with reduced selenium levels and antioxidant function, which correlated with increased markers of lipid peroxidation. Conclusion Transfusion of selenium poor PRBC can dilute selenium levels and compromise glutathione peroxidase antioxidant activity and thereby allow lipid peroxidation. As there was no evidence that aged PRBC induced more severe oxidative injury this suggests that selenium dilution is a key underlying mechanism. Further studies are needed to assess the impact of transfusion‐related oxidative stress in massive transfusions.