Aging alters electroencephalographic and clinical manifestations of kainate-induced status epilepticus

被引:27
作者
Darbin, O
Naritoku, T
Patrylo, PR [1 ]
机构
[1] So Illinois Univ, Sch Med, Dept Physiol, Carbondale, IL 62901 USA
[2] So Illinois Univ, Sch Med, Dept Neurol, Springfield, IL USA
[3] So Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62794 USA
关键词
geriatric; kainic acid; Fischer; 344; EEG; seizure; sustained seizure;
D O I
10.1111/j.0013-9580.2004.66103.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: The elderly exhibit an increased risk for developing status epilepticus and status-related morbidity and mortality. However, it is unclear how aging alters the progression of electroencephalographic (EEG) activity and behavioral manifestations during status epilepticus. Methods: A repetitive low-dose kainate treatment protocol (2.5 mg/klg/h; i.p.) was used in this Study in conjunction with EEG and behavioral monitoring from freely behaving adult (78 months) and aged (22-25 months) Fischer 344 rats to assess the effects of aging on status epilepticus. Results: During kainate treatment, both groups exhibited an increase in EEG power that corresponded with the time Course of kainate treatment. However, visual inspection and spectral analysis revealed a reduction of the faster frequencies ( 12.5-35 Hz) in the EEGs of aged rodents. A similar progression of behavioral manifestations was observed in adult and aged rodents during kainate treatment, although the frequency of preseizure manifestations (e.g., wet-dog shakes; aged rats, 110 events/h vs. adults, 25 events/h; median values) was greater, and latency to onset for any given behavioral manifestation (e.g., class V seizures; aged median, 60 nun, vs. adult median, 145 min) was consistently shorter within the aged group. Conclusions: These data reveal that aged Fischer 344 rats exhibit altered EEG activity (reduction of higher frequencies) and clinical manifestations during kainate-induced status epilepticus. Taken together, these data indicate an age-related change in seizure onset and spread after exposure to glutamate analogues.
引用
收藏
页码:1219 / 1227
页数:9
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