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Prenatal Stress Induces Changes in Behavior, HPA Axis, Inflammation, and Oxidative Stress in Adult Rats Offspring
Jorge M Aguiar-Geraldo1, Jefté Peper-Nascimento1, José Henrique Cararo1
1Translational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, SC, Brazil.
Insights
Prenatal stress in rats caused lasting behavioral and biochemical changes, including inflammation and oxidative stress. Lithium treatment helped reduce these harmful effects in offspring.
Area of Science:
- Neuroscience
- Psychiatry
- Endocrinology
Background:
- Prenatal stress is linked to psychiatric disorders.
- These disorders involve inflammation, oxidative stress, and HPA axis dysregulation.
Purpose of the Study:
- To investigate prenatal stress effects on behavior, inflammation, oxidative stress, and HPA axis in dams and offspring.
- To evaluate lithium's therapeutic potential.
Main Methods:
- A prenatal chronic unpredictable stress model was used in Wistar rats.
- Offspring were treated with lithium or saline postnatally.
- Behavioral tests (open field), and biochemical analyses (oxidative stress, inflammation, HPA axis) were performed.
Main Results:
- Prenatal stress induced hyperactivity and increased pro-inflammatory cytokines, oxidative damage, and HPA axis hormones in female offspring.
- Lithium administration mitigated these biochemical alterations.
Conclusions:
- Prenatal stress induces persistent behavioral, inflammatory, oxidative, and HPA axis changes in offspring.
- These alterations may contribute to psychiatric disorder development.
- Lithium shows potential in ameliorating stress-induced biochemical changes.
Abstract:
Prenatal stress is related to the development of psychiatric disorders involving inflammation, oxidative stress, and hypothalamic-pituitary-adrenal (HPA) axis. Therefore, the aim of the present study was to evaluate the effects of prenatal stress on behavior, inflammation, oxidative stress, and the HPA-axis in the dams and their offspring treated with lithium. Thirteen pregnant Wistar rats were exposed to a prenatal chronic unpredictable stress protocol from the 14th day of gestation until birth. At the 60th postnatal day (PND), a treatment protocol was carried out in the offspring with lithium (intraperitoneally - 47.5 mg/kg) or saline for seven days (twice a day). The behavior was assessed in the open field test to evaluate free movements. The dams (21 PND) and offspring (after open field) were euthanized, their brains were dissected in frontal cortex, hippocampus, and striatum, and the serum was collected. In the brain and/or serum, the levels of oxidative stress, inflammation, and HPA axis parameters were evaluated. Female offspring from stressed dams showed hyperactivity. Besides behavior alterations, offspring brain and serum showed an increase in pro-inflammatory cytokines, oxidative damage markers, and HPA axis hormones levels. Lithium administration only reduced the biochemical alterations. The prenatal stress protocol induced long-lasting behavior, inflammatory, oxidative stress, and HPA-axis alterations in the offspring which could underlie the development of psychiatric disorders.
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