Suppression of secondary generalization of limbic seizures by stimulation of subthalamic nucleus in rats

被引:45
作者
Usui, N [1 ]
Maesawa, S [1 ]
Kajita, Y [1 ]
Endo, O [1 ]
Takebayashi, S [1 ]
Yoshida, J [1 ]
机构
[1] Nagoya Univ, Sch Med, Dept Neurosurg, Nagoya, Aichi 466, Japan
关键词
subthalamic nucleus; substantia nigra pars reticulata; epilepsy; kainic acid; electrical stimulation; rat;
D O I
10.3171/jns.2005.102.6.1122
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Deep brain stimulation (DBS) of subcortical nuclei such as the subthalamic nucleus (STN) or the substantia nigra pars reticulata (SNR) may provide an alternative therapy for intractable epilepsy. The authors attempted to evaluate the antiepileptic effects of DBS to these structures in an experimental seizure model. Methods. Three groups of rats were prepared. In the first two groups, the rats underwent unilateral implantation of stimulation electrodes in the STN (six rats) or the SNR (six rats). A control group received no electrodes (six rats). Kainic acid (KA) was systemically administered to induce limbic seizures, which started with focal seizures and became generalized secondarily. High-frequency electrical stimulation of the STN or SNR was begun immediately after KA administration, and changes on electroencephalography (EEG) and the magnitude of clinical seizures were evaluated. Results showed that STN stimulation significantly reduced the duration of generalized seizures on EEG, although the total duration of seizures (generalized plus focal seizures) was unchanged. The duration of focal seizures on EEG was prolonged by STN DBS, a result possibly due to the suppression of secondary generalization. In addition, STN DBS reduced the severity of clinical seizures. On the other hand, stimulation of the SNR demonstrated no effect. Conclusions. Unilateral STN DBS showed significant suppression of the secondary generalization of limbic seizures. Note, however, that SNR DBS was less effective, which implies that in addition to the nigral control of the epilepsy system, another antiepileptic mechanism such as antidromic stimulation of the corticosubthalamic pathway should be considered.
引用
收藏
页码:1122 / 1129
页数:8
相关论文
共 31 条
[1]
Subthalamic nucleus deep brain stimulus evoked potentials:: Physiological and therapeutic implications [J].
Baker, KB ;
Montgomery, EB ;
Rezai, AR ;
Burgess, R ;
Lüders, HO .
MOVEMENT DISORDERS, 2002, 17 (05) :969-983
[2]
ELECTROGRAPHIC, CLINICAL AND PATHOLOGICAL ALTERATIONS FOLLOWING SYSTEMIC ADMINISTRATION OF KAINIC ACID, BICUCULLINE OR PENTETRAZOLE - METABOLIC MAPPING USING THE DEOXYGLUCOSE METHOD WITH SPECIAL REFERENCE TO THE PATHOLOGY OF EPILEPSY [J].
BENARI, Y ;
TREMBLAY, E ;
RICHE, D ;
GHILINI, G ;
NAQUET, R .
NEUROSCIENCE, 1981, 6 (07) :1361-1391
[3]
RESPONSES OF SUBSTANTIA-NIGRA PARS RETICULATA AND GLOBUS-PALLIDUS COMPLEX TO HIGH-FREQUENCY STIMULATION OF THE SUBTHALAMIC NUCLEUS IN RATS - ELECTROPHYSIOLOGICAL DATA [J].
BENAZZOUZ, A ;
PIALLAT, B ;
POLLAK, P ;
BENABID, AL .
NEUROSCIENCE LETTERS, 1995, 189 (02) :77-80
[4]
STIMULATION OF SUBSTANTIA-NIGRA PARS RETICULATA SUPPRESSES NEOCORTICAL SEIZURES [J].
BODA, B ;
SZENTE, MB .
BRAIN RESEARCH, 1992, 574 (1-2) :237-243
[5]
Bressand K., 1999, Society for Neuroscience Abstracts, V25, P1656
[6]
Established antiepileptic drugs [J].
Brodie, MJ ;
Dichter, MA .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 1997, 6 (03) :159-174
[7]
AFFERENT CONNECTIONS OF THE SUBTHALAMIC NUCLEUS - A COMBINED RETROGRADE AND ANTEROGRADE HORSERADISH-PEROXIDASE STUDY IN THE RAT [J].
CANTERAS, NS ;
SHAMMAHLAGNADO, SJ ;
SILVA, BA ;
RICARDO, JA .
BRAIN RESEARCH, 1990, 513 (01) :43-59
[8]
Effects of therapeutic stimulation of nucleus caudatus on epileptic electrical activity of brain in patients with intractable epilepsy [J].
Chkhenkeli, SA ;
Chkhenkeli, IS .
STEREOTACTIC AND FUNCTIONAL NEUROSURGERY, 1997, 69 (1-4) :221-224
[9]
Cooper I S, 1973, Trans Am Neurol Assoc, V98, P192
[10]
EEG and evoked potential recording from the subthalamic nucleus for deep brain stimulation of intractable epilepsy [J].
Dinner, DS ;
Neme, S ;
Nair, D ;
Montgomery, EB ;
Baker, KB ;
Rezai, A ;
Lüders, HO .
CLINICAL NEUROPHYSIOLOGY, 2002, 113 (09) :1391-1402