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Rapid Quantification of Oxidized and Reduced Forms of Glutathione Using Ortho -phthalaldehyde in Cultured Mammalian Cells In Vitro
Published on: June 28, 2024
Labor augmentation with oxytocin decreases glutathione level
Naomi Schneid-Kofman1, Tali Silberstein, Oshra Saphier
1Department of Obstetrics and Gynecology, Faculty of Health Sciences, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer-sheva, Israel.
Oxytocin augmentation during labor may increase oxidative stress, indicated by lower glutathione (GSH) levels in umbilical cord blood. However, key markers of cell damage did not differ between groups, suggesting a nuanced impact.
Area of Science:
- Obstetrics and Gynecology
- Biochemistry
- Perinatal Medicine
Background:
- Oxidative stress is a concern in childbirth.
- Oxytocin is commonly used for labor augmentation.
- Understanding its impact on neonatal oxidative status is crucial.
Purpose of the Study:
- To compare oxidative stress markers in neonates from spontaneous vaginal deliveries versus oxytocin-augmented deliveries.
- To investigate the effect of oxytocin on glutathione levels and lipid peroxidation in cord blood.
Main Methods:
- A comparative study of 98 women (57 spontaneous, 41 oxytocin-augmented deliveries).
- Analysis of arterial cord blood for glutathione (GSH), malondialdehyde (MDA), and red blood cell (RBC) phenol red uptake.
- Exclusion of complicated deliveries and high-risk pregnancies.
Main Results:
- Significantly lower cord blood GSH levels were observed in the oxytocin-augmented group (P = .01).
- No significant differences in plasma or RBC malondialdehyde (MDA) levels were found between groups.
- Red blood cell (RBC) uptake of phenol red did not differ, indicating no change in cell penetrability.
Conclusions:
- Lower GSH levels in the oxytocin group suggest increased oxidative stress.
- Despite reduced GSH, specific markers of cell damage (MDA, phenol red uptake) showed no significant difference.
- Oxytocin augmentation may induce oxidative stress without causing detectable cellular damage in neonates.
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