Stress during gestation can result in early and long-term developmental aberrations. This study aimed to assess the impact of prenatal restraint or predator stress on pilocarpine-induced epileptic behavior. Pregnant rats were exposed to stressors on gestational days 15, 16, and 17. Restraint stress consisted of daily restraint of the dam. During predator stress, caged rats were exposed to a cat in a cage. On postnatal day 25, male pups were injected with pilocarpine and the behavior of each rat was observed. Prenatal stress led to low birth weight and increased blood corticosterone levels. Both stressors significantly potentiated pilocarpine-induced seizures. Predator-stressed pups exhibited significantly severe tonic-clonic seizures compared with restraint-stressed animals. These data emphasize the impact of prenatal stress on fetal growth, and neural and endocrine function. The results also suggest that psychosocial stressors have a greater impact on neural and endocrine function than physical stressors do.

Exposure to stress is known to change synaptic plasticity and results in long-term depression; further, this stress precipitates seizures. In the study described here, the prenatal restraint and predator stress models were used to test the hypothesis that indirect prenatal stresses influence hippocampal synaptic potentiation and may affect seizures susceptibility in infant rats. Pregnant female Wistar rats were divided into 3 groups: control, restraint-stressed, and predator-stressed groups. Both stressed groups were exposed to the stressor on gestation days 15, 16, and 17. The restraint stress involved 1-h sessions twice daily in a Plexiglas tube and the predator stress involved 2-h sessions once daily in a cage placed within the visual range of a caged cat. Blood corticosterone (COS) levels were measured in different time points. Hippocampal slices were prepared and field excitatory postsynaptic potentials (fEPSP) were studied on postnatal day 15. Pilocarpine was administered on postnatal day 25 and mortality rates were measured after 2 and 24h. Restraint and predator stresses resulted in significantly elevated COS blood levels in dams and pups. Both the amplitude and slope of fEPSP in the CA1 area decreased significantly in the stressed groups as compared to the control. Prenatal restraint and predator stresses significantly increased the fatal effect of pilocarpine at 24h after injection. Exposure to prenatal stresses and COS blood levels elevation reduce hippocampal synaptic potentiation and increase mortality rate of seizure in infant rats and may affect on later seizure susceptibility and prognosis.