# Sex-Dependent Effects of Prenatal Stress on Seizure Susceptibility and Neurodegeneration in Neonatal Rats

**Authors:** Daniel Antonio Cruz-Rojas, Luis Beltrán-Parrazal, Consuelo Morgado-Valle, Grecia Herrera-Meza, Aleph A. Corona-Morales, Joel Martínez-Quiroz, Brenda Martínez-Rojas, María-Leonor López-Meraz

PMC · DOI: 10.3390/brainsci15111220 · 2025-11-13

## TL;DR

Prenatal stress in rats leads to sex-specific effects on seizure susceptibility and brain damage in newborns, mainly impacting males.

## Contribution

This study reveals sex-dependent effects of prenatal stress on neonatal seizure susceptibility and neurodegeneration in rats.

## Key findings

- Maternal restraint stress reduced maternal weight gain and offspring body weight and size.
- Male neonates from stressed mothers had shorter seizure latency and hippocampal neurodegeneration.
- Female neonates showed minimal effects from maternal stress exposure.

## Abstract

Background: Prenatal stress affects fetal neurodevelopment and may increase the risk of seizures. This study aimed to analyze the impact of maternal restraint stress during pregnancy on neonatal status epilepticus (SE) in rats. Methods: Pregnant Wistar rats were subjected to restraint stress from gestation days 12 to 20. Offspring were assessed for body weight, size, and corticosterone levels. SE was induced in postnatal day 7 rats using the lithium–pilocarpine model. Neurodegeneration was analyzed using Fluoro-Jade C staining. Results: Maternal restraint stress resulted in reduced weight gain for the mothers and lower body weight and size for their offspring. Stressed neonates exhibited higher levels of serum corticosterone. Male neonates exhibited shorter latency to stage 1 seizures and increased hippocampal neurodegeneration compared with control males, whereas female neonates were largely unaffected. Conclusions: Maternal restraint stress produced only mild, sex-dependent effects on neonatal seizure susceptibility, affecting males but not females, suggesting a limited yet selective influence of prenatal stress on early brain vulnerability.

## Linked entities

- **Chemicals:** corticosterone (PubChem CID 5753), lithium (PubChem CID 28486), pilocarpine (PubChem CID 4819)

## Full-text entities

- **Diseases:** Seizure (MESH:D012640), Neurodegeneration (MESH:D019636), SE (MESH:D013226), weight gain (MESH:D015430)
- **Chemicals:** pilocarpine (MESH:D010862), Fluoro-Jade C (MESH:C534582), lithium (MESH:D008094), corticosterone (MESH:D003345)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12650744/full.md

---
Source: https://tomesphere.com/paper/PMC12650744