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Published on: June 11, 2020
Timing of cognitive deficits following neonatal seizures: relationship to histological changes in the hippocampus
Y Sogawa1, M Monokoshi, D C Silveira
1Department of Neurology, Harvard Medical School, Clinical Neurophysiology Laboratory - Hunnewell 2, Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA.
Insights
Neonatal seizures in rats lead to lasting cognitive deficits and increased seizure susceptibility before weaning. These changes correlate with mossy fiber sprouting and altered glutamate receptor expression in the hippocampus.
Area of Science:
- Neuroscience
- Developmental Neuroscience
- Epilepsy Research
Background:
- Neonatal seizures are linked to cognitive impairment and reduced seizure threshold.
- Previous studies show adult rats with neonatal seizures exhibit learning deficits, lower seizure thresholds, and hippocampal mossy fiber sprouting.
Purpose of the Study:
- To determine the onset age of cognitive dysfunction and altered seizure susceptibility in rats after neonatal seizures.
- To investigate the relationship between cognitive impairment, mossy fiber sprouting, and glutamate receptor expression.
Main Methods:
- Rats were exposed to flurothyl-induced seizures from postnatal day 0.
- Visual-spatial learning (water maze) and seizure susceptibility were assessed at postnatal days 20 and 35.
- Brain tissue was analyzed for cell loss, mossy fiber distribution, and AMPA (GluR1) and NMDA (NMDAR1) receptor expression.
Main Results:
- Rats with neonatal seizures showed impaired water maze performance and increased seizure susceptibility at both P20 and P35.
- Mossy fiber sprouting into CA3 and the dentate gyrus supragranular region was observed at P20 and P35.
- Increased GluR1 expression in CA3 at P20 and NMDAR1 in CA3 and the dentate gyrus at P35.
Conclusions:
- Cognitive impairment and altered seizure susceptibility emerge before weaning following neonatal seizures.
- These neurological changes are associated with hippocampal mossy fiber sprouting and increased glutamate receptor expression.
- Interventions to mitigate adverse outcomes must be initiated early, during or shortly after neonatal seizures.
Abstract:
Neonatal seizures are frequently associated with cognitive impairment and reduced seizure threshold. Previous studies in our laboratory have demonstrated that rats with recurrent neonatal seizures have impaired learning, lower seizure thresholds, and sprouting of mossy fibers in CA3 and the supragranular region of the dentate gyrus in the hippocampus when studied as adults. The goal of this study was to determine the age of onset of cognitive dysfunction and alterations in seizure susceptibility in rats subjected to recurrent neonatal seizures and the relation of this cognitive impairment to mossy fiber sprouting and expression of glutamate receptors. Starting at postnatal day (P) 0, rats were exposed to 45 flurothyl-induced seizures over a 9-day period of time. Visual-spatial learning in the water maze and seizure susceptibility were assessed in subsets of the rats at P20 or P35. Brains were evaluated for cell loss, mossy fiber distribution, and AMPA (GluR1) and NMDA (NMDAR1) subreceptor expression at these same time points. Rats with neonatal seizures showed significant impairment in the performance of the water maze and increased seizure susceptibility at both P20 and P35. Sprouting of mossy fibers into the CA3 and supragranular region of the dentate gyrus was seen at both P20 and P35. GluR1 expression was increased in CA3 at P20 and NMDAR1 was increased in expression in CA3 and the supragranular region of the dentate gyrus at P35. Our findings indicate that altered seizure susceptibility and cognitive impairment occurs prior to weaning following a series of neonatal seizures. Furthermore, these alterations in cognition and seizure susceptibility are paralleled by sprouting of mossy fibers and increased expression of glutamate receptors. To be effective, our results suggest that strategies to alter the adverse outcome following neonatal seizures will have to be initiated during, or shortly following, the seizures.
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