Deep brain stimulation of the anterior nucleus of the thalamus: Effects of electrical stimulation on pilocarpine-induced seizures and status epilepticus

被引:99
|
作者
Hamani, Clement [1 ]
Hodaie, Mojgan [1 ,2 ]
Chiang, Jason [3 ]
del Campo, Martin [1 ]
Andrade, Danielle M. [1 ]
Sherman, David [4 ]
Mirski, Marek [4 ]
Mello, Luiz E. [5 ]
Lozano, Andres M. [1 ,2 ]
机构
[1] Univ Toronto, Toronto Western Hosp, Univ Hlth Network, Div Neurosurg, Toronto, ON M5T 2S8, Canada
[2] Toronto Western Hosp, Krembil Neurosci Ctr, Res Inst, Toronto, ON, Canada
[3] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD USA
[4] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[5] Univ Fed Sao Paulo, Dept Physiol, Sao Paulo, Brazil
关键词
deep brain stimulation; anterior thalamic nucleus; pilocarpine; status epilepticus; stimulation parameters;
D O I
10.1016/j.eplepsyres.2007.09.010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Electrical stimulation of the anterior nucleus of the thalamus appears to be effective against seizures in animals and humans. As the optimal stimulation settings remain elusive, we studied the effects of different stimulation parameters against pilocarpine induced seizures and status epilepticus (SE). Methods: Adult rats had electrodes implanted bilaterally into the AN. Five days later, different groups of animals were stimulated with 1000 LA, 500 LA, or 200 mu A and frequencies of either 20 Hz or 130 Hz. Pilocarpine (350 mg/kg i.p.) was injected 5 min after stimulation onset and seizures were monitored. Sham-treated controls had electrodes implanted but did not receive stimulation until they developed SE. After SE, these animals had the electrodes turned on to assess whether AN stimulation could arrest ongoing ictal activity. Results: Compared to sham-treated controls (n = 8), stimulation at 500 mu A (n = 13) significantly increased the latency for seizures and SE by 1.9-2.2-fotd. In contrast, stimulation at 1000 mu A (n=8) produced a non-significant decrease in the latencies to these events. No major effect was observed with stimulation at 200 mu A (n = 11). Similar results were obtained for each current intensity, regardless of the stimulation frequency used (20 Hz and 130 Hz). In sham-treated controls that had the electrodes turned on after SE, stimulation was not able to arrest ongoing ictal activity. Conclusions: The anticonvulsant effects of AN stimulation against pilocarpine-induced seizures were mainly determined by the current and not the frequency of stimulation. AN stimulation initiated after SE onset was ineffective. (C) 2007 Published by Elsevier B.V.
引用
收藏
页码:117 / 123
页数:7
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