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Inflammatory disturbances in preeclampsia: relationship between maternal and umbilical cord blood
Cristina Catarino1, Alice Santos-Silva, Luís Belo
1Serviço de Bioquímica, Faculdade de Farmácia da Universidade do Porto (FFUP), 4050-313 Porto, Portugal; Instituto de Biologia Molecular e Celular (IBMC), Universidade do Porto, 4150-180 Porto, Portugal. cristinacatarino@ff.up.pt
Insights
Preeclampsia (PE) involves increased inflammation and oxidative stress in mothers, affecting fetal circulation. Markers like IL-6 and CRP are elevated in PE pregnancies, indicating endothelial dysfunction.
Area of Science:
- Obstetrics and Gynecology
- Perinatology
- Maternal-Fetal Medicine
Background:
- Preeclampsia (PE) is a leading cause of maternal and fetal mortality.
- PE is characterized by maternal inflammatory and oxidative stress states.
Purpose of the Study:
- To compare oxidative stress and inflammatory markers in maternal and umbilical cord blood (UCB) between normal and PE pregnancies.
- To investigate the relationship between maternal inflammation and fetal circulation markers.
Main Methods:
- Measured acute-phase proteins (CRP, α1-antitrypsin), cytokines (IL-6, TNF-α), leukocyte activation markers, total antioxidant status (TAS), thiobarbituric acid reactive substances (TBARS), and uric acid.
- Studied 42 healthy pregnant women, 46 PE women, and their neonates.
Main Results:
- PE mothers showed higher IL-6, TNF-α, α1-antitrypsin, CRP, sVCAM, uric acid, and TBARS; lower sL-selectin compared to controls.
- Newborns from PE pregnancies had higher uric acid, α1-antitrypsin, CRP; lower leukocyte count, sL-selectin, lactoferrin, and elastase/α1-antitrypsin ratio.
Conclusions:
- PE pregnancies exhibit heightened maternal inflammation reflected in fetal circulation.
- The inflammatory state in PE is linked to endothelial dysfunction and cytokine synthesis, not primarily neutrophil activation.
Abstract:
Preeclampsia (PE) is one of the main causes of maternal and fetal mortality and morbidity. PE is associated with an inflammatory state and with oxidative stress, in maternal circulation. Our aim was to evaluate and compare the levels of oxidative stress and inflammatory markers in maternal and umbilical cord blood (UCB), in normal and PE pregnancies. We measured acute-phase proteins (CRP and α1-antitrypsin), proinflammatory cytokines (IL-6 and TNF-α), leukocyte activation (elastase, lactoferrin, sL-selectin, sVCAM, sPECAM), total antioxidant status (TAS), thiobarbituric acid reactive substances (TBARS), and uric acid levels. We studied 42 healthy pregnant women, 46 PE women, and their neonates. The concentrations of IL-6, TNF-α, α1-antitrypsin, CRP, sVCAM, uric acid, and TBARS were significantly higher, and sL-selectin was significantly lower in PE pregnant women as compared with normotensive pregnant women. In newborns uric acid, α1-antitrypsin, and CRP values were significantly higher in PE; leukocyte count, sL-selectin, lactoferrin, and the ratio elastase/α1-antitrypsin were significantly lower. Our data suggest that PE pregnancy is associated with an enhanced maternal inflammatory condition, which is reflected in fetal circulation. This enhanced inflammatory state seems to be related to endothelial dysfunction and increased cytokine synthesis, rather than with neutrophil activation.
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