Developmental patterns of antioxidant defense mechanisms in human erythrocytes

Pediatr Res. 1989 Oct;26(4):366-9. doi: 10.1203/00006450-198910000-00016.


To obtain a profile of erythrocyte antioxidant defense potential during late fetal development, we studied selected antioxidant parameters in blood samples from 65 neonates with birth wt between 520 and 4210 g and from 12 healthy adults. Erythrocyte superoxide dismutase activity did not change significantly with maturation and no significant differences were observed among preterm infants grouped in increasing birth wt categories, term neonates, and adults. Erythrocyte catalase and glutathione peroxidase, as well as plasma vitamin E levels, showed highly significant positive correlations (p less than 0.001) with increasing fetal wt and gestational age; by term, CAT activity reached a level similar to the adult control group, but glutathione peroxidase activity, as well as plasma vitamin E levels, were markedly lower in all the preterm and in the term groups than in adults (p less than 0.01). Erythrocyte glutathione S-transferase activity showed a negative correlation with increasing gestational age (p less than 0.01) and the adult values were considerably lower than any of the neonatal levels (p less than 0.001). The role of glutathione S-transferase in erythrocyte metabolism remains obscure. Maturational changes in the activity of the red cell enzymes that were studied and in the plasma vitamin E level were apparent from about 31-36 wk of gestation, suggesting that the stimulation for these changes may have commenced from about 28-31 wk.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aging / blood*
  • Catalase / blood
  • Erythrocytes / metabolism*
  • Fetal Blood / metabolism
  • Gestational Age
  • Glutathione Peroxidase / blood
  • Humans
  • Infant, Newborn / blood*
  • Infant, Premature / blood*
  • Oxygen / blood*
  • Superoxide Dismutase / blood
  • Vitamin E / blood


  • Vitamin E
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Oxygen