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Published on: July 12, 2024
The effect of chronic stress on prenatal development of the central nervous system
L N Giordana1, A A Bozzo, D S Cots
1Cell Biology and Embryology, Animal Anatomy Department, School of Agronomy and Veterinary, National University of Rio Cuarto.
Insights
Chronic stress during pregnancy in rats reduced embryonic brain cell proliferation by day 21, particularly in the cortex and dentate gyrus. This neurodevelopmental impact was linked to hormonal changes, affecting offspring
Area of Science:
- Neuroscience
- Developmental Biology
- Endocrinology
Background:
- Embryonic development relies on homeostasis.
- Maternal stress can negatively impact fetal neurodevelopment.
- Chronic immobilization stress during pregnancy is a potential disruptor.
Purpose of the Study:
- To investigate the effects of chronic maternal stress on embryonic brain cell proliferation.
- To examine specific brain regions: forebrain, hippocampus, dentate gyrus, and cortex.
- To assess these effects at different gestational ages (12, 17, and 21 days).
Main Methods:
- Utilized a rat model of chronic immobilization stress during pregnancy.
- Examined embryonic brain sections at 12, 17, and 21 days of gestation.
- Employed anti-PCNA immunolabeling and stereological analysis on 540 images.
Main Results:
- No significant differences in cell proliferation were observed at 12 and 17 days of gestation.
- A statistically significant decrease in cell proliferation was found in the cortex and dentate gyrus by day 21 of gestation in stressed embryos.
- These proliferative changes correlated with decreased plasma prolactin and increased corticosterone levels.
Conclusions:
- Chronic maternal stress can impair embryonic neurodevelopment, specifically affecting cell proliferation in later gestation.
- Hormonal alterations (prolactin and corticosterone) are implicated in mediating the stress-induced effects on fetal brain development.
- Findings suggest potential long-term implications for offspring susceptibility to psychiatric disorders.
Abstract:
The survival of developing embryos depends on the control and maintenance of homeostasis. Stress caused by chronic immobilization during pregnancy in rats may alter the normal development of the nervous system and increase susceptibility to psychiatric disorders. We investigated the effects of chronic stress on cell proliferation in the forebrains of embryos at 12 days of gestation, and in the hippocampus, dentate gyrus and cortex in embryos at 17 and 21 days of gestation. We examined serial sections of the embryonic brains of control and stressed rats at days 12, 17 and 21 of gestation. Brain sections were immunolabeled with anti-PCNA and stereological analysis was performed on 540 images. The results showed no statistical differences on days 12 and 17 of gestation in the proliferation area of the structures studied, whereas on day 21 of gestation, proliferation decreased in the cortex and dentate gyrus of embryos of the stressed group. These changes were related to decreased prolactin and increased corticosterone concentrations in the plasma.
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