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Isolation of Leukocytes from Human Breast Milk for Use in an Antibody-dependent Cellular Phagocytosis Assay of HIV Targets
Published on: September 6, 2019
[Importance of breast-feeding in antioxidant defence]
Insights
Breast milk, rich in superoxide dismutase (SOD), enhances newborn antioxidant defense. Lower SOD in formula-fed infants and higher SOD in septic newborns highlight the critical role of breast milk enzymes for infant health.
Area of Science:
- Biochemistry
- Neonatal Physiology
- Immunology
Context:
- Newborns possess a developing antioxidant system, making them vulnerable to oxidative stress.
- Human milk, particularly colostrum, is a primary source of passive immunity and essential nutrients for neonates.
- Neonatal sepsis poses a significant threat, potentially overwhelming the immature antioxidant defenses.
Purpose:
- To investigate the activity of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in newborns.
- To analyze the role of these enzymes in antioxidant defense in human milk, gastric fluid, and plasma.
- To determine the impact of feeding method and sepsis on enzyme activity in neonates.
Summary:
- Superoxide dismutase (SOD) activity was significantly higher in colostrum than mature milk, while glutathione peroxidase (GSH-Px) showed no significant difference.
- Gastric fluid SOD activity was significantly lower in artificially-fed newborns compared to breast-fed newborns.
- Plasma SOD activity was elevated in newborns with sepsis, and a negative correlation between SOD/GSH-Px and sepsis indicated their importance in neonatal antioxidant defense.
Impact:
- Breast milk, containing vital antioxidant enzymes like SOD, is crucial for establishing adequate antioxidant defense in newborns.
- Understanding enzyme activity variations can inform strategies to support infant health and combat oxidative stress-related conditions.
- This research underscores the protective role of breastfeeding against oxidative challenges during the neonatal period.
Abstract:
We investigated the importance of two enzymes (superoxide dismutase--SOD and glutathione peroxidase--GSH-Px) in the antioxidant defence of newborns and analysed their activity in: human colostrum and milk (from 63 mothers, after normal delivery, without complications or signs of infection), gastric fluid (from 10 breast-fed newborns, 7-28 days after birth; and from 15 artificially-fed newborns, with no signs of infection, 7-28 days after birth), and plasma (from 10 newborns, 1-28 days old, with no signs of infection, and 10 newborns, 1-28 days old, with signs of neonatal sepsis). The results of the study showed that there was statistically significant increased activity of SOD (p<0.001) in colostrum compared to mature milk. There was no statistically important difference in the activity of GSH-Px between those two samples. The activity of SOD in the gastric fluid of the artificially-fed newborns was statistically significantly lower than in the breast-fed newborns (p<0.001). The same results were found for mature mother's milk. We discovered a significant increase of SOD plasma activity in the newborns with sepsis, compared to the breast-fed newborns, with no signs of infection. The negative correlation between the activities of SOD and GSH-Px in the gastric fluid samples of the breast-fed and the artificially-fed newborns and the newborns with sepsis, showed that the activities of both enzymes were important for adequate antioxidant defence during the neonatal period. Breast-feeding with both colostrum and mature human milk is probably very important for adequate antioxidant defence in newborns.
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