Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice

The incidence of seizures increases with old age. Stroke, dementia and brain tumors are recognized risk factors for new-onset seizures in the aging populations and the incidence of these conditions also increased with age. Whether aging is associated with higher seizure susceptibility in the absence...

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Main Authors: Kurt R. Stover, Stellar Lim, Terri-Lin Zhou, Paul M. Stafford, Jonathan Chow, Haoyuan Li, Nila Sivanenthiran, Sivakami Mylvaganam, Chiping Wu, Donald F. Weaver, James Eubanks, Liang Zhang
Format: Article
Language:English
Published: Elsevier 2017-12-01
Series:IBRO Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2451830117300249
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author Kurt R. Stover
Stellar Lim
Terri-Lin Zhou
Paul M. Stafford
Jonathan Chow
Haoyuan Li
Nila Sivanenthiran
Sivakami Mylvaganam
Chiping Wu
Donald F. Weaver
James Eubanks
Liang Zhang
author_facet Kurt R. Stover
Stellar Lim
Terri-Lin Zhou
Paul M. Stafford
Jonathan Chow
Haoyuan Li
Nila Sivanenthiran
Sivakami Mylvaganam
Chiping Wu
Donald F. Weaver
James Eubanks
Liang Zhang
author_sort Kurt R. Stover
collection DOAJ
description The incidence of seizures increases with old age. Stroke, dementia and brain tumors are recognized risk factors for new-onset seizures in the aging populations and the incidence of these conditions also increased with age. Whether aging is associated with higher seizure susceptibility in the absence of the above pathologies remains unclear. We used classic kindling to explore this issue as the kindling model is highly reproducible and allows close monitoring of electrographic and motor seizure activities in individual animals. We kindled male young and aging mice (C57BL/6 strain, 2–3 and 18–22 months of age) via daily hippocampal CA3 stimulation and monitored seizure activity via video and electroencephalographic recordings. The aging mice needed fewer stimuli to evoke stage-5 motor seizures and exhibited longer hippocampal afterdischarges and more frequent hippocampal spikes relative to the young mice, but afterdischarge thresholds and cumulative afterdischarge durations to stage 5 motor seizures were not different between the two age groups. While hippocampal injury and structural alterations at cellular and micro-circuitry levels remain to be examined in the kindled mice, our present observations suggest that susceptibility to hippocampal CA3 kindling seizures is increased with aging in male C57 black mice.
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spelling doaj.art-c2f5c86ad8ac45fa942ed56c54012e672022-12-22T03:18:14ZengElsevierIBRO Reports2451-83012017-12-013C334410.1016/j.ibror.2017.08.001Susceptibility to hippocampal kindling seizures is increased in aging C57 black miceKurt R. Stover0Stellar Lim1Terri-Lin Zhou2Paul M. Stafford3Jonathan Chow4Haoyuan Li5Nila Sivanenthiran6Sivakami Mylvaganam7Chiping Wu8Donald F. Weaver9James Eubanks10Liang Zhang11Krembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaKrembil Research Institute, University Health Network, CanadaThe incidence of seizures increases with old age. Stroke, dementia and brain tumors are recognized risk factors for new-onset seizures in the aging populations and the incidence of these conditions also increased with age. Whether aging is associated with higher seizure susceptibility in the absence of the above pathologies remains unclear. We used classic kindling to explore this issue as the kindling model is highly reproducible and allows close monitoring of electrographic and motor seizure activities in individual animals. We kindled male young and aging mice (C57BL/6 strain, 2–3 and 18–22 months of age) via daily hippocampal CA3 stimulation and monitored seizure activity via video and electroencephalographic recordings. The aging mice needed fewer stimuli to evoke stage-5 motor seizures and exhibited longer hippocampal afterdischarges and more frequent hippocampal spikes relative to the young mice, but afterdischarge thresholds and cumulative afterdischarge durations to stage 5 motor seizures were not different between the two age groups. While hippocampal injury and structural alterations at cellular and micro-circuitry levels remain to be examined in the kindled mice, our present observations suggest that susceptibility to hippocampal CA3 kindling seizures is increased with aging in male C57 black mice.http://www.sciencedirect.com/science/article/pii/S2451830117300249AgingEEGEpilepsyHippocampusKindlingMice
spellingShingle Kurt R. Stover
Stellar Lim
Terri-Lin Zhou
Paul M. Stafford
Jonathan Chow
Haoyuan Li
Nila Sivanenthiran
Sivakami Mylvaganam
Chiping Wu
Donald F. Weaver
James Eubanks
Liang Zhang
Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice
IBRO Reports
Aging
EEG
Epilepsy
Hippocampus
Kindling
Mice
title Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice
title_full Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice
title_fullStr Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice
title_full_unstemmed Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice
title_short Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice
title_sort susceptibility to hippocampal kindling seizures is increased in aging c57 black mice
topic Aging
EEG
Epilepsy
Hippocampus
Kindling
Mice
url http://www.sciencedirect.com/science/article/pii/S2451830117300249
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