Publication
Title
High frequency deep brain stimulation in the hippocampus modifies seizure characteristics in kindled rats
Author
Abstract
 Purpose: This experimental animal study evaluates the effect of high frequency deep brain stimulation (HFS DBS) on seizures in the Alternate Day Rapid Kindling model for temporal lobe epilepsy (TLE). The target for HFS is the hippocampus, as this structure is often presumed to be the seizure focus in human TLE. Methods: Rats (n = 12) were fully kindled in the hippocampus according to the Alternate Day Rapid Kindling protocol. Characteristics of the evoked afterdischarges (AD) were determined in the baseline period using AD threshold, AD latency, and AD duration as parameters. Rats were divided into a treated group (n = 7) that received 130 Hz HFS for 1 week, and a control group (n = 5) that did not receive HFS. Rats were retested in the following week. After 1 additional week of rest, the HFS group was continuously stimulated again for 1 week, during which AD evoked by kindling stimuli were characterized again. Results: HFS had a direct effect on evoked AD: during HFS, it increased AD threshold to 203 ± 13% of controls (p < 0.01) and increased AD latency to 191 ± 19% (p < 0.05). It decreased AD duration to 71 ± 9% (p < 0.05) of controls. The effect outlasted the HFS stimulation as in the week following HFS similar differences, but smaller in size, could still be established. Conclusion: Continuous HFS (130 Hz) in the hippocampus of epileptic rats modulates the characteristics of evoked AD in a way that reflects a reduction in excitability of the target region.
Language
English
Source (journal)
Epilepsia. - Boston, Mass.
Publication
Boston, Mass. : 2007
ISSN
0013-9580
DOI
10.1111/J.1528-1167.2007.01038.X
Volume/pages
48 :8 (2007) , p. 1543-1550
ISI
000248726200016
Full text (Publisher's DOI)
Full text (publisher's version - intranet only)
UAntwerpen
Faculty/Department
Publication type
Subject
External links
Web of Science
Record
Identifier
Creation 16.11.2011
Last edited 04.03.2024
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