The pilocarpine model of temporal lobe epilepsy

被引:856
|
作者
Curia, Giulia [1 ,2 ,3 ]
Longo, Daniela [4 ]
Biagini, Giuseppe [4 ]
Jones, Roland S. G. [5 ]
Avoli, Massimo [1 ,2 ,3 ,6 ]
机构
[1] McGill Univ, Montreal Neurol Inst, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Dept Neurol & Neurol Surg, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Dept Physiol, Montreal, PQ H3A 2B4, Canada
[4] Univ Modena & Reggio Emilia, Dipartimento Sci Biomed, I-41100 Modena, Italy
[5] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[6] Univ Roma La Sapienza, Dipartimento Med Sperimentale, I-00185 Rome, Italy
基金
英国惠康基金;
关键词
animal models; entorhinal cortex; hippocampus pilocarpine; temporal lobe epilepsy;
D O I
10.1016/j.jneumeth.2008.04.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Understanding the pathophysiogenesis of temporal lobe epilepsy (TLE) largely rests on the use of models of status epilepticus (SE), as in the case of the pilocarpine model. The main features of TLE are: (i) epileptic foci in the limbic system; (ii) an "initial precipitating injury"; (iii) the so-called "latent period"; and (iv) the presence of hippocampal sclerosis leading to reorganization of neuronal networks. Many of these characteristics can be reproduced in rodents by systemic injection of pilocarpine; in this animal model, SE is followed by a latent period and later by the appearance of spontaneous recurrent seizures (SRSs). These processes are, however, influenced by experimental conditions such as rodent species, strain, gender, age, doses and routes of pilocarpine administration, as well as combinations with other drugs administered before and/or after SE. In the attempt to limit these sources of variability, we evaluated the methodological procedures used by several investigators in the pilocarpine model; in particular, we have focused on the behavioural, electrophysiological and histo pathological findings obtained with different protocols. We addressed the various experimental approaches published to date, by comparing mortality rates, onset of SRSs, neuronal damage, and network reorganization. Based on the evidence reviewed here, we propose that the pilocarpine model can be a valuable tool to investigate the mechanisms involved in TLE, and even more so when standardized to reduce mortality at the time of pilocarpine injection, differences in latent period duration, variability in the lesion extent, and SRS frequency. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 157
页数:15
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