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Prenatal stress causes gender-dependent neuronal loss and oxidative stress in rat hippocampus
Zhongliang Zhu1, Xia Li, Weina Chen
1Department of Physiology, Xi'an Jiaotong University Medical College, Xi'an, China. zlzhu@mail.xjtu.edu.cn
Insights
Prenatal stress in rats increased neuronal nitric oxide synthase (nNOS) expression. It also caused hippocampal neuron loss in female offspring, suggesting prenatal stress-induced oxidative stress damages developing neurons.
Area of Science:
- Neuroscience
- Developmental Biology
- Toxicology
Background:
- Prenatal stress is a known environmental factor impacting offspring neurodevelopment.
- Oxidative stress plays a role in various neurological disorders.
- The hippocampus is crucial for learning and memory and is vulnerable to stress.
Purpose of the Study:
- To investigate the impact of prenatal stress on hippocampal neuronal changes in female and male rat offspring.
- To explore the role of oxidative stress in mediating these prenatal stress-induced effects.
Main Methods:
- Pregnant rats were subjected to restraint stress during middle (MS) or later (LS) stages of gestation.
- One-month-old offspring were assessed for hippocampal neuron number and neuronal nitric oxide synthase (nNOS) expression.
- Calcium content and oxidant generation were measured in the hippocampal CA3 region of female offspring.
Main Results:
- Both MS and LS increased nNOS-positive neurons in the hippocampus of both sexes.
- MS and LS significantly decreased hippocampal neuron numbers in female offspring, but not males.
- LS exposure led to increased calcium and oxidant generation in the female offspring hippocampus.
Conclusions:
- Prenatal stress can induce oxidative stress in the developing hippocampus.
- This oxidative stress contributes to neuronal damage and loss, particularly in female offspring.
- These findings highlight the long-term neurodevelopmental consequences of prenatal stress.
Abstract:
Our purpose was to investigate the effects of prenatal stress on neuronal changes in the hippocampus and the possible involvement of oxidative stress in female and male rats. Female and male offspring (1-month-old), whose dams were restrained in middle or later pregnant stage (MS or LS), were studied to observe changes in the number of hippocampal neurons and the expression of neuronal nitric oxide synthase (nNOS) in the hippocampus. Both MS and LS induced an increase in the number of nNOS-positive expression in female and male offspring in the hippocampus; however, both MS and LS caused a significant decrease in the number of hippocampal neurons in the female, but not in the male offspring. In addition, significant increases in calcium content and oxidant generation were induced by LS in the hippocampal CA3 region in female rats. These data suggest that prenatal stress can cause oxidative stress and consequent damage to neurons, leading to neuronal loss in the brain of offspring during development.
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