AI Article Synopsis

  • * A study revealed that while certain antioxidant levels in the placenta remained stable, infected mothers showed a decrease in serum antioxidant capacity and catalase activity, along with increased markers of oxidative stress.
  • * The research found that COVID-19 infection led to changes in placental iron-related proteins, suggesting a complex relationship between COVID-19, oxidative stress, and iron metabolism during pregnancy, indicating a need for further investigation into these effects on maternal and infant health.

Article Abstract

COVID-19 has reached pandemic proportions worldwide, with considerable consequences for both health and the economy. In pregnant women, COVID-19 can alter the metabolic environment, iron metabolism, and oxygen supply of trophoblastic cells, and therefore have a negative influence on essential mechanisms of fetal development. The purpose of this study was to investigate, for the first time, the effects of COVID-19 infection during pregnancy with regard to the oxidative/antioxidant status in mothers' serum and placenta, together with placental iron metabolism. Results showed no differences in superoxide dismutase activity and placental antioxidant capacity. However, antioxidant capacity decreased in the serum of infected mothers. Catalase activity decreased in the COVID-19 group, while an increase in 8-hydroxy-2'-deoxyguanosine, hydroperoxides, 15-FT-isoprostanes, and carbonyl groups were recorded in this group. Placental vitamin D, E, and Coenzyme-Q10 also showed to be increased in the COVID-19 group. As for iron-related proteins, an up-regulation of placental DMT1, ferroportin-1, and ferritin expression was recorded in infected women. Due to the potential role of iron metabolism and oxidative stress in placental function and complications, further research is needed to explain the pathogenic mechanism of COVID-19 that may affect pregnancy, so as to assess the short-term and long-term outcomes in mothers' and infants' health.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868249PMC
http://dx.doi.org/10.3390/antiox11020184DOI Listing

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