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Environmental toxicology and pharmacology2006; 23(3); 340-346; doi: 10.1016/j.etap.2006.12.002

In vitro effects of oxygen on physico-chemical properties of horse erythrocyte membrane.

Abstract: Whether direct exposure to different concentrations (0%, 13%, 100%) of oxygen may affect horse erythrocyte membrane fluidity (EMF) and fatty acid (FA) composition was studied during 1 (T60) and 2h (T120) exposure. EMF was investigated at the head group level and hydrophobic core thanks to phosphorus nucleus 31 ((31)P) nuclear magnetic resonance ((31)P NMR) and electronic paramagnetic resonance (EPR) using two spin probes: 5-nitroxydestearic acid and 16-doxylstearic acid. Lipid structure of the membranes was studied by gas liquid chromatography. 4-Hydroxy-2E-nonenal was also analyzed as a marker of lipid peroxidation. It increased at T120 13% and 100% oxygen whereas there were no significant changes in membrane dynamic or structure. Correlation was demonstrated between EMF and partial pressure of oxygen in the blood ( [Formula: see text] ). In vitro high rate of oxygenation was efficient to induce lipid peroxidation but did not change membrane dynamics. This may be due to a low free radical production in vitro or to the high red blood cells antioxidant properties.
Publication Date: 2006-12-27 PubMed ID: 21783778DOI: 10.1016/j.etap.2006.12.002Google Scholar: Lookup
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  • Journal Article

Summary

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The research article investigates the impacts of varied oxygen exposure levels on the properties of horse erythrocyte membranes, particularly their fluidity and fatty acid composition, during one and two-hour exposure periods. It finds that high oxygen concentration tends to increase lipid peroxidation but doesn’t change the fluid dynamics of the membrane.

Research Setup

  • The experiment was set up to study the effects of varying oxygen concentrations (0%, 13%, 100%) on the fluidity and fatty acid composition of horse erythrocyte membranes over 1 and 2-hour exposure periods.
  • The fluidity of the erythrocyte membrane was analyzed at the head group level and the hydrophobic core using phosphorus nucleus 31 (31P) via nuclear magnetic resonance (31P NMR) and electronic paramagnetic resonance (EPR). Two spin probes, namely 5-nitroxydestearic acid and 16-doxylstearic acid, were used.
  • The lipid structure of the membranes was studied via gas-liquid chromatography, while 4-Hydroxy-2E-nonenal served as a marker of lipid peroxidation.

Findings

  • The level of 4-Hydroxy-2E-nonenal increased during two-hour exposure at 13% and 100% oxygen concentrations, indicating increased lipid peroxidation.
  • Despite this increase, there were no significant changes observed in the membrane dynamics or structure.
  • There was a correlation found between erythrocyte membrane fluidity and the partial pressure of oxygen in the blood.

Conclusion

  • High levels of oxygen were found to induce lipid peroxidation, but they did not alter the membrane dynamics according to this study.
  • The unaltered membrane dynamics could be attributed to a low production of free radicals in vitro or to the strong antioxidant properties of red blood cells.

Cite This Article

APA
Portier K, Guichardant M, Debouzy JC, Crouzier D, Geraud I, Kirschvink N, Lekeux P, Fellmann N, Coudert J. (2006). In vitro effects of oxygen on physico-chemical properties of horse erythrocyte membrane. Environ Toxicol Pharmacol, 23(3), 340-346. https://doi.org/10.1016/j.etap.2006.12.002

Publication

ISSN: 1382-6689
NlmUniqueID: 9612020
Country: Netherlands
Language: English
Volume: 23
Issue: 3
Pages: 340-346

Researcher Affiliations

Portier, Karine
  • Equine Department, National Veterinary School of Lyon, Lyon, France.
Guichardant, Michel
    Debouzy, Jean-Claude
      Crouzier, David
        Geraud, Ingrid
          Kirschvink, Nathalie
            Lekeux, Pierre
              Fellmann, Nicole
                Coudert, Jean

                  Citations

                  This article has been cited 1 times.
                  1. Garrido D, Rubin T, Poidevin M, Maroni B, Le Rouzic A, Parvy JP, Montagne J. Fatty acid synthase cooperates with glyoxalase 1 to protect against sugar toxicity.. PLoS Genet 2015 Feb;11(2):e1004995.
                    doi: 10.1371/journal.pgen.1004995pubmed: 25692475google scholar: lookup