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Prenatal stress perturbs fetal iron homeostasis in a sex-specific manner

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 Added by Martin Frasch
 Publication date 2021
  fields Biology
and research's language is English




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What is the influence of chronic maternal prenatal stress (PS) on fetal iron homeostasis? In a prospective case-control study in 164 pregnant women, we show that cord blood transferrin saturation is lower in male stressed neonates. The total effect of PS exposure on fetal ferritin revealed a decrease of 15.4% compared with controls. Electrocardiogram-based Fetal Stress Index (FSI) identified affected fetuses non-invasively during the third trimester of gestation. FSI-based timely detection of fetuses affected by PS can support early individualized iron supplementation and neurodevelopmental follow-up to prevent long-term sequelae due to PS-exacerbated impairment of the iron homeostasis.



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Functional development of affective and reward circuits, cognition and response inhibition later in life exhibits vulnerability periods during gestation and early childhood. Extensive evidence supports the model that exposure to stressors in the gestational period and early postnatal life increases an individuals susceptibility to future impairments of functional development. Rece
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102 - Xin Yang , Xu Wang , Yi Wang 2020
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The two classic theories for the existence of sexual replication are that sex purges deleterious mutations from a population, and that sex allows a population to adapt more rapidly to changing environments. These two theories have often been presented as opposing explanations for the existence of sex. Here, we develop and analyze evolutionary models based on the asexual and sexual replication pathways in Saccharomyces cerevisiae (Bakers yeast), and show that sexual replication can both purge deleterious mutations in a static environment, as well as lead to faster adaptation in a dynamic environment. This implies that sex can serve a dual role, which is in sharp contrast to previous theories.
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