Literature DB >> 26381287

The systemic kainic acid rat model of temporal lobe epilepsy: Long-term EEG monitoring.

B Van Nieuwenhuyse1, R Raedt2, M Sprengers3, I Dauwe4, S Gadeyne5, E Carrette6, J Delbeke7, W J Wadman8, P Boon9, K Vonck10.   

Abstract

Animal models reproducing the characteristics of human epilepsy are essential for the elucidation of the pathophysiological mechanisms. In epilepsy research there is ongoing debate on whether the epileptogenic process is a continuous process rather than a step function. The aim of this study was to assess progression of epileptogenesis over the long term and to evaluate possible correlations between SE duration and severity with the disease progression in the kainic acid model. Rats received repeated KA injections (5mg/kg) until a self-sustained SE was elicited. Continuous depth EEG recording started before KA injection and continued for 30 weeks. Mean seizure rate progression could be expressed as a sigmoid function and increased from 1 ± 0.2 seizures per day during the second week after SE to 24.4 ± 6.4 seizures per day during week 30. Seizure rate progressed to a plateau phase 122 ± 9 days after SE. However, the individual seizure rate during this plateau phase varied between 14.5 seizures and 48.6 seizures per day. A circadian rhythm in seizure occurrence was observed in all rats. Histological characterization of damage to the dentate gyrus in the KA treated rats confirmed the presence of astrogliosis and aberrant mossy fiber sprouting in the dentate gyrus. This long-term EEG monitoring study confirms that epileptogenesis is a continuous process rather than a step function.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  animal model; kainic acid; long-term EEG monitoring; seizures; temporal lobe epilepsy

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Year:  2015        PMID: 26381287     DOI: 10.1016/j.brainres.2015.08.016

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  21 in total

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Review 2.  Neuroendocrine aspects of improving sleep in epilepsy.

Authors:  Doodipala Samba Reddy; Shu-Hui Chuang; Dayton Hunn; Amy Z Crepeau; Rama Maganti
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Authors:  Kylie Holden; Adam L Hartman
Journal:  Epilepsy Behav       Date:  2017-11-07       Impact factor: 2.937

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Journal:  Mol Imaging Biol       Date:  2019-10       Impact factor: 3.488

5.  Harmonization of the pipeline for seizure detection to phenotype post-traumatic epilepsy in a preclinical multicenter study on post-traumatic epileptogenesis.

Authors:  Pablo M Casillas-Espinosa; Pedro Andrade; Cesar Santana-Gomez; Tomi Paananen; Gregory Smith; Idrish Ali; Robert Ciszek; Xavier Ekolle Ndode-Ekane; Rhys D Brady; Jussi Tohka; Matthew R Hudson; Piero Perucca; Emma L Braine; Riikka Immonen; Noora Puhakka; Sandy R Shultz; Nigel C Jones; Richard J Staba; Asla Pitkänen; Terence J O'Brien
Journal:  Epilepsy Res       Date:  2019-04-27       Impact factor: 3.045

6.  H19 silencing decreases kainic acid-induced hippocampus neuron injury via activating the PI3K/AKT pathway via the H19/miR-206 axis.

Authors:  Haichao Ju; Zhimin Yang
Journal:  Exp Brain Res       Date:  2022-07-04       Impact factor: 2.064

7.  Ventral hippocampal formation is the primary epileptogenic zone in a rat model of temporal lobe epilepsy.

Authors:  Paul S Buckmaster; Bianca Reyes; Tahsin Kahn; Megan Wyeth
Journal:  J Neurosci       Date:  2022-08-19       Impact factor: 6.709

8.  Interleukin-1 Receptor in Seizure Susceptibility after Traumatic Injury to the Pediatric Brain.

Authors:  Bridgette D Semple; Terence J O'Brien; Kayleen Gimlin; David K Wright; Shi Eun Kim; Pablo M Casillas-Espinosa; Kyria M Webster; Steven Petrou; Linda J Noble-Haeusslein
Journal:  J Neurosci       Date:  2017-07-19       Impact factor: 6.167

9.  Diurnal burden of spontaneous seizures in early epileptogenesis in the post-kainic acid rat model of epilepsy.

Authors:  Stephanie Mizuno; Zachery Koneval; Dannielle K Zierath; Kevin M Knox; H Steve White; Melissa Barker-Haliski
Journal:  Epilepsia Open       Date:  2021-05-03

10.  Decreased expression of the clock gene Bmal1 is involved in the pathogenesis of temporal lobe epilepsy.

Authors:  Hao Wu; Yong Liu; Lishuo Liu; Qiang Meng; Changwang Du; Kuo Li; Shan Dong; Yong Zhang; Huanfa Li; Hua Zhang
Journal:  Mol Brain       Date:  2021-07-14       Impact factor: 4.041

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