2009
DOI: 10.1111/j.1600-0404.2008.01108.x
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Seizures in the intrahippocampal kainic acid epilepsy model: characterization using long-term video-EEG monitoring in the rat

Abstract: This study shows that the characteristics of spontaneous seizures in the intrahippocampal KA model display many similarities to other SE models and human temporal lobe epilepsy.

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Cited by 82 publications
(80 citation statements)
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References 58 publications
(150 reference statements)
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“…In comparison to the repeated low dose KA-injection protocol, systemic pilocarpine induced SE has a higher mortality rate of 30-50% (Curia et al, 2008), and mortality rate in the stimulation SE models is comparable with our observations. All rats we injected with KA developed a self-sustained SE consistent with reports on the intrahippocampal KA model (Raedt et al, 2009). Despite injection issues, about 83% of the rats develop SE in the ip.…”
Section: Discussionsupporting
confidence: 74%
“…In comparison to the repeated low dose KA-injection protocol, systemic pilocarpine induced SE has a higher mortality rate of 30-50% (Curia et al, 2008), and mortality rate in the stimulation SE models is comparable with our observations. All rats we injected with KA developed a self-sustained SE consistent with reports on the intrahippocampal KA model (Raedt et al, 2009). Despite injection issues, about 83% of the rats develop SE in the ip.…”
Section: Discussionsupporting
confidence: 74%
“…Intrahippocampal KA delivery in the current study produced recurrent seizure activity lasting for several hours, similar to previous studies (56). This seizure activity was associated with an early activation of the sympathetic system, as demonstrated by increased plasma noradrenaline levels, tachycardia, and elevated BP within 3 h. The sympathovagal balance changed in favor of sympathetic dominance at 48 h and 7 days following seizure induction.…”
Section: Discussionsupporting
confidence: 65%
“…The most interesting compounds identified by the protocol described above will be tested in at least one other post-SE model of TLE [i.e., SE induced by sustained BLA stimulation (Brandt et al, 2003a) or intrahippocampal administration of kainate (Raedt et al, 2009)]. In both models, the SE and its consequences are less severe compared with systemic administration of pilocarpine (Brandt et al, 2003a;Dudek et al, 2006), thus enhancing the chance of identifying potentially useful antiepileptogenic therapies.…”
Section: Antiepileptogenesis After Brain Insultsmentioning
confidence: 99%