Long-term Effects of Status Epilepticus in the Immature Brain Are Specific for Age and Model
Purpose: Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long‐term disturbances in learning and memory, as well as an enhanced seizure susceptibility to further seizures. In contrast, a number of studies suggest...
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Published in | Epilepsia (Copenhagen) Vol. 44; no. 4; pp. 518 - 528 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Boston, MA, USA
Blackwell Science Inc
01.04.2003
Blackwell |
Subjects | |
Online Access | Get full text |
ISSN | 0013-9580 1528-1167 |
DOI | 10.1046/j.1528-1157.2003.48802.x |
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Abstract | Purpose: Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long‐term disturbances in learning and memory, as well as an enhanced seizure susceptibility to further seizures. In contrast, a number of studies suggest that the immature brain is less vulnerable to the morphologic and physiologic alterations after SE. The goal of this study was to determine whether the long‐term consequences of SE during development on hippocampal plasticity and cognitive function are age and model specific.
Methods: We used lithium‐pilocarpine (Li‐PC) to induce SE at different age points during development (P12, P16, P20) and evaluated the effects of this abnormal neural activity on spatial memory performance and seizure susceptibility in the animals beginning at P55, corresponding to young adulthood.
Results: We demonstrated that SE at P12 did not result in any structural or functional changes detectable in adulthood, whereas SE at both P16 and P20 induced cell loss and mossy fiber sprouting within the hippocampus and cognitive impairment when the animals were tested as adults.
Conclusions: Whereas the seizure threshold to generalized seizures was not altered, animals with SE at P20 showed an increased susceptibility to kindling in adulthood. |
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AbstractList | Purpose:
Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long‐term disturbances in learning and memory, as well as an enhanced seizure susceptibility to further seizures. In contrast, a number of studies suggest that the immature brain is less vulnerable to the morphologic and physiologic alterations after SE. The goal of this study was to determine whether the long‐term consequences of SE during development on hippocampal plasticity and cognitive function are age and model specific.
Methods:
We used lithium‐pilocarpine (Li‐PC) to induce SE at different age points during development (P12, P16, P20) and evaluated the effects of this abnormal neural activity on spatial memory performance and seizure susceptibility in the animals beginning at P55, corresponding to young adulthood.
Results:
We demonstrated that SE at P12 did not result in any structural or functional changes detectable in adulthood, whereas SE at both P16 and P20 induced cell loss and mossy fiber sprouting within the hippocampus and cognitive impairment when the animals were tested as adults.
Conclusions:
Whereas the seizure threshold to generalized seizures was not altered, animals with SE at P20 showed an increased susceptibility to kindling in adulthood. Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long-term disturbances in learning and memory, as well as an enhanced seizure susceptibility to further seizures. In contrast, a number of studies suggest that the immature brain is less vulnerable to the morphologic and physiologic alterations after SE. The goal of this study was to determine whether the long-term consequences of SE during development on hippocampal plasticity and cognitive function are age and model specific.PURPOSEStatus epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long-term disturbances in learning and memory, as well as an enhanced seizure susceptibility to further seizures. In contrast, a number of studies suggest that the immature brain is less vulnerable to the morphologic and physiologic alterations after SE. The goal of this study was to determine whether the long-term consequences of SE during development on hippocampal plasticity and cognitive function are age and model specific.We used lithium-pilocarpine (Li-PC) to induce SE at different age points during development (P12, P16, P20) and evaluated the effects of this abnormal neural activity on spatial memory performance and seizure susceptibility in the animals beginning at P55, corresponding to young adulthood.METHODSWe used lithium-pilocarpine (Li-PC) to induce SE at different age points during development (P12, P16, P20) and evaluated the effects of this abnormal neural activity on spatial memory performance and seizure susceptibility in the animals beginning at P55, corresponding to young adulthood.We demonstrated that SE at P12 did not result in any structural or functional changes detectable in adulthood, whereas SE at both P16 and P20 induced cell loss and mossy fiber sprouting within the hippocampus and cognitive impairment when the animals were tested as adults.RESULTSWe demonstrated that SE at P12 did not result in any structural or functional changes detectable in adulthood, whereas SE at both P16 and P20 induced cell loss and mossy fiber sprouting within the hippocampus and cognitive impairment when the animals were tested as adults.Whereas the seizure threshold to generalized seizures was not altered, animals with SE at P20 showed an increased susceptibility to kindling in adulthood.CONCLUSIONSWhereas the seizure threshold to generalized seizures was not altered, animals with SE at P20 showed an increased susceptibility to kindling in adulthood. Purpose: Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long‐term disturbances in learning and memory, as well as an enhanced seizure susceptibility to further seizures. In contrast, a number of studies suggest that the immature brain is less vulnerable to the morphologic and physiologic alterations after SE. The goal of this study was to determine whether the long‐term consequences of SE during development on hippocampal plasticity and cognitive function are age and model specific. Methods: We used lithium‐pilocarpine (Li‐PC) to induce SE at different age points during development (P12, P16, P20) and evaluated the effects of this abnormal neural activity on spatial memory performance and seizure susceptibility in the animals beginning at P55, corresponding to young adulthood. Results: We demonstrated that SE at P12 did not result in any structural or functional changes detectable in adulthood, whereas SE at both P16 and P20 induced cell loss and mossy fiber sprouting within the hippocampus and cognitive impairment when the animals were tested as adults. Conclusions: Whereas the seizure threshold to generalized seizures was not altered, animals with SE at P20 showed an increased susceptibility to kindling in adulthood. Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long-term disturbances in learning and memory, as well as an enhanced seizure susceptibility to further seizures. In contrast, a number of studies suggest that the immature brain is less vulnerable to the morphologic and physiologic alterations after SE. The goal of this study was to determine whether the long-term consequences of SE during development on hippocampal plasticity and cognitive function are age and model specific. We used lithium-pilocarpine (Li-PC) to induce SE at different age points during development (P12, P16, P20) and evaluated the effects of this abnormal neural activity on spatial memory performance and seizure susceptibility in the animals beginning at P55, corresponding to young adulthood. We demonstrated that SE at P12 did not result in any structural or functional changes detectable in adulthood, whereas SE at both P16 and P20 induced cell loss and mossy fiber sprouting within the hippocampus and cognitive impairment when the animals were tested as adults. Whereas the seizure threshold to generalized seizures was not altered, animals with SE at P20 showed an increased susceptibility to kindling in adulthood. |
Author | SOGAWA Yoshimi HOLMES Gregory L. CHA Byung-Ho LIU Xianzeng CILIO Maria Roberta HUANG Li-Tung |
Author_xml | – sequence: 1 givenname: Maria Roberta surname: Cilio fullname: Cilio, Maria Roberta – sequence: 2 givenname: Yoshimi surname: Sogawa fullname: Sogawa, Yoshimi – sequence: 3 givenname: Byung‐Ho surname: Cha fullname: Cha, Byung‐Ho – sequence: 4 givenname: Xianzeng surname: Liu fullname: Liu, Xianzeng – sequence: 5 givenname: Li‐Tung surname: Huang fullname: Huang, Li‐Tung – sequence: 6 givenname: Gregory L. surname: Holmes fullname: Holmes, Gregory L. |
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Keywords | Nervous system diseases Rat Epilepsy Rodentia Furan derivatives Pilocarpine Long term Epilepsy-Seizures-Immature brain-Learning- Pilocarpine Cerebral disorder Vertebrata Mammalia Subintrant crisis Animal Central nervous system disease Evolution Models Age Hippocampus Brain (vertebrata) |
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Snippet | Purpose: Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long‐term... Purpose: Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long‐term... Status epilepticus (SE) is more common in children than adults and has a high mortality and morbidity rate. SE in adult rats results in long-term disturbances... |
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SubjectTerms | Age Factors Animals Apoptosis - drug effects Apoptosis - physiology Biological and medical sciences Convulsants Electroencephalography - drug effects Epilepsy Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Hippocampus - drug effects Hippocampus - pathology Hippocampus - physiopathology Immature brain Learning Lithium Chloride Long-Term Potentiation - drug effects Long-Term Potentiation - physiology Male Maze Learning - drug effects Maze Learning - physiology Medical sciences Mental Recall - drug effects Mental Recall - physiology Nervous system (semeiology, syndromes) Neurology Neuronal Plasticity - drug effects Neuronal Plasticity - physiology Orientation - drug effects Orientation - physiology Pilocarpine Rats Rats, Sprague-Dawley Seizures Status Epilepticus - chemically induced Status Epilepticus - pathology Status Epilepticus - physiopathology |
Title | Long-term Effects of Status Epilepticus in the Immature Brain Are Specific for Age and Model |
URI | https://cir.nii.ac.jp/crid/1570009750035438336 https://onlinelibrary.wiley.com/doi/abs/10.1046%2Fj.1528-1157.2003.48802.x https://www.ncbi.nlm.nih.gov/pubmed/12681000 https://www.proquest.com/docview/73187222 |
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