Long-term effects of neonatal seizures: a behavioral, electrophysiological, and histological study

Previous studies have demonstrated that recurrent seizures during the neonatal period lead to permanent changes in seizure threshold and learning and memory. The pathophysiological mechanisms for these changes are not clear. To determine if neonatal seizures cause changes in hippocampal excitability...

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Published inBrain research. Developmental brain research Vol. 118; no. 1; pp. 99 - 107
Main Authors Huang, L.-T, Cilio, M.R, Silveira, D.C, McCabe, B.K, Sogawa, Y, Stafstrom, C.E, Holmes, G.L
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 10.12.1999
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Abstract Previous studies have demonstrated that recurrent seizures during the neonatal period lead to permanent changes in seizure threshold and learning and memory. The pathophysiological mechanisms for these changes are not clear. To determine if neonatal seizures cause changes in hippocampal excitability or inhibition, we subjected rats to 50 flurothyl-induced seizures during the first 10 days of life (five seizures per day). When the rats were adults, we examined seizure threshold using flurothyl inhalation, and learning and memory in the water maze. In separate groups of animals, we evaluated in vivo paired-pulse facilitation and inhibition in either CA1 with stimulation of the Schaffer collaterals or dentate gyrus with stimulation of the perforant path. Following these studies, the animals were sacrificed and the brains evaluated for mossy fiber sprouting with the Timm stain. Compared to control animals, rats with 50 flurothyl seizures had a reduced seizure threshold, impaired learning and memory in the water maze, and sprouting of mossy fibers in the CA3 pyramidal cell layer and molecular layer of the dentate gyrus. No significant differences in impaired paired-pulse inhibition was noted between the flurothyl-treated and control rats. This study demonstrates that recurrent neonatal seizures result in changes of neuronal connectivity and alterations in seizure susceptibility, learning and memory. However, the degree of impairment following 50 seizures was modest, demonstrating that the immature brain is remarkably resilient to seizure-induced damage.
AbstractList Previous studies have demonstrated that recurrent seizures during the neonatal period lead to permanent changes in seizure threshold and learning and memory. The pathophysiological mechanisms for these changes are not clear. To determine if neonatal seizures cause changes in hippocampal excitability or inhibition, we subjected rats to 50 flurothyl-induced seizures during the first 10 days of life (five seizures per day). When the rats were adults, we examined seizure threshold using flurothyl inhalation, and learning and memory in the water maze. In separate groups of animals, we evaluated in vivo paired-pulse facilitation and inhibition in either CA1 with stimulation of the Schaffer collaterals or dentate gyrus with stimulation of the perforant path. Following these studies, the animals were sacrificed and the brains evaluated for mossy fiber sprouting with the Timm stain. Compared to control animals, rats with 50 flurothyl seizures had a reduced seizure threshold, impaired learning and memory in the water maze, and sprouting of mossy fibers in the CA3 pyramidal cell layer and molecular layer of the dentate gyrus. No significant differences in impaired paired-pulse inhibition was noted between the flurothyl-treated and control rats. This study demonstrates that recurrent neonatal seizures result in changes of neuronal connectivity and alterations in seizure susceptibility, learning and memory. However, the degree of impairment following 50 seizures was modest, demonstrating that the immature brain is remarkably resilient to seizure-induced damage.
Author Sogawa, Y
Silveira, D.C
Huang, L.-T
Stafstrom, C.E
McCabe, B.K
Cilio, M.R
Holmes, G.L
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  givenname: L.-T
  surname: Huang
  fullname: Huang, L.-T
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  surname: Cilio
  fullname: Cilio, M.R
  organization: Department of Neurology, Harvard Medical School, Children's Hospital, Boston, MA, USA
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  surname: Silveira
  fullname: Silveira, D.C
  organization: Department of Neurology, Harvard Medical School, Children's Hospital, Boston, MA, USA
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  organization: Department of Neurology, Harvard Medical School, Children's Hospital, Boston, MA, USA
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  surname: Sogawa
  fullname: Sogawa, Y
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  givenname: G.L
  surname: Holmes
  fullname: Holmes, G.L
  organization: Department of Neurology, Harvard Medical School, Children's Hospital, Boston, MA, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/10611508$$D View this record in MEDLINE/PubMed
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Keywords Paired-pulse inhibition
Dentate gyrus
Epilepsy
Hippocampus
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Snippet Previous studies have demonstrated that recurrent seizures during the neonatal period lead to permanent changes in seizure threshold and learning and memory....
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StartPage 99
SubjectTerms Animals
Animals, Newborn - physiology
Animals, Newborn - psychology
Behavior, Animal - physiology
Convulsants
Dentate gyrus
Differential Threshold
Electric Stimulation
Electrophysiology
Epilepsy
Flurothyl
Hippocampus
Hippocampus - physiopathology
Male
Maze Learning
Neural Inhibition - physiology
Paired-pulse inhibition
Perforant Pathway - physiopathology
Rats
Rats, Sprague-Dawley
Reference Values
Seizures - chemically induced
Seizures - pathology
Seizures - physiopathology
Seizures - psychology
Swimming
Time Factors
Title Long-term effects of neonatal seizures: a behavioral, electrophysiological, and histological study
URI https://dx.doi.org/10.1016/S0165-3806(99)00135-2
https://www.ncbi.nlm.nih.gov/pubmed/10611508
https://search.proquest.com/docview/17419499
Volume 118
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