Low glucose-6-phosphate dehydrogenase (G-6-PD) activity in red blood cells and susceptibility to copper-induced oxidative damage.

@article{Calabrese1980LowGD,
  title={Low glucose-6-phosphate dehydrogenase (G-6-PD) activity in red blood cells and susceptibility to copper-induced oxidative damage.},
  author={Edward J. Calabrese and Gary S. Moore and S C Ho},
  journal={Environmental research},
  year={1980},
  volume={21 2},
  pages={
          366-72
        }
}
Predictive models for human glucose-6-phosphate dehydrogenase deficiency.
TLDR
The present paper has discussed available test systems for determination of the response of G-6-PD-deficient human erythrocytes to environmental agents and the results of research using each model have been presented.
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Abstract An in vitro test system was established to determine the oxidant Stressor effects of various agents on erythrocytes having low Superoxide dismutase (SOD) activity. The compound,
An evaluation of the dorset sheep as a predictive animal model for the response of G-6-PD deficient human erythrocytes to a proposed systemic toxic ozone intermediate, methyl oleate hydroperoxide.
TLDR
The results suggest a qualitative difference in the response of sheep erythrocytes and human G-6-PD deficient ery Throcytes to MOHP that seriously questions the value of the sheep ERYthrocyte as a quantitatively accurate predictive model.
The effects of ascorbic acid on copper‐induced oxidative changes in human erythrocytes: Example of a biphasic dose‐response relationship
TLDR
In an in vitro study, ascorbic acid reduced the occurrence of copper acetate‐induced oxidative stress in human erythrocytes at biologically relevant concentrations while enhancing oxidative changes at higher levels of exposure.
Molecular study of ovine glucose 6-phosphate dehydrogenase gene expression in respect to different energy intake.
Use of a bioactivation system to screen for hemolytic response to environmental agents: Evaluation of six pesticides
TLDR
The pesticides, zineb and parathion, incubated without the microsomal enzyme system, did exert statistically significant oxidizing effects on the G‐6‐PD deficient erythrocytes, in vitro.
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