Seizure susceptibility to various convulsant stimuli of knockout interleukin-6 mice

被引:65
作者
De Sarro, G
Russo, E
Ferreri, G
Giuseppe, B
Flocco, MA
Di Paola, ED
De Sarro, A
机构
[1] Univ Catanzaro, Sch Med, Policlin Mater Domini, Dept Expt & Clin Med G Salvatore, I-88100 Catanzaro, Italy
[2] Univ Messina, Sch Med, Dept Expt Med, I-98100 Messina, Italy
关键词
interleukin-6; epilepsy; seizures; convulsants; gamma-aminobutyric acid; excitatory amino acid;
D O I
10.1016/j.pbb.2004.01.012
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In the present study, the susceptibility of knockout interleukin-6 (IL-6 (-/-)) mice to various convulsant stimuli has been evaluated and compared with other three related mice strains. Animals were treated with chemical convulsants impairing the gamma-aminobutyric acid neurotransmission [pentylenetetrazole (PTZ), picrotoxin, bicuculline, methyl-6,7-dimethoxy-4-ethyl-beta-carboline-3-carboxylate (DMCM), methyl-beta-carbolitie-3-carboxylate (beta-CCM)], enhancing glutamatergic neurotransmission [N-methyl-(D)-aspartate (NMDA), alpha-amino-3hydroxy-5-methyl-4-isoxazolepropionate (AMPA) and kainic acid (KA)] or a K+ channel blocker [4-aminopyridine (4-AP)]. The behavioural changes of such convulsant stimuli on IL-6(-/-) were observed and compared with those observed in C57, IL-6(+/+) and DBA/2 mice. The occurrence of clonic and/or tonic seizures was scored and statistically analysed to observe possible differences on seizure susceptibility. The IL-6(-/-) mice exhibited significantly higher seizure susceptibility to PTZ, beta-CCM, DMCM, NMDA, AMPA and KA than did the other mice strains, with the exception of DBA/2 mice. This study, demonstrates that IL-6(-/-) mice possess an increased susceptibility to some convulsant stimuli. In particular, the major convulsant effects produced by NMDA, AMPA and KA suggest that the excitatory amino acid system is more active in the central nervous system (CNS) of IL-6 (-/-) mice. The present data suggest that IL-6(-/-) mice might be a valid novel epileptic model for the study of pathophysiology and pharmacology of epileptic seizures. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:761 / 766
页数:6
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