Jobe P C, Mishra P K, Adams-Curtis L E, Deoskar V U, Ko K H, Browning R A, Dailey J W
Department of Basic Sciences, University of Illinois College of Medicine, Peoria, USA.
Ital J Neurol Sci. 1995 Feb-Mar;16(1-2):91-9. doi: 10.1007/BF02229080.
Two independently inbred strains of genetically epilepsy-prone rats (GEPRs) have been developed. GEPR-3s and GEPR-9s have moderate and severe degrees of seizure predisposition as well as expression, respectively. Seizure predisposition is a fundamental distinction between the normal and epileptic brain. Seizure predisposition in GEPRs and in humans with epilepsy includes spontaneous seizures and exaggerated seizure responsiveness and/or abnormally low thresholds to stimuli which also cause seizures in non-epileptic subjects. Activation of brainstem seizure circuitry by auditory input via the inferior colliculus causes electrographic and behavioral responses in GEPR-9s which replicates human generalized tonic/clonic seizures. Activation of brainstem seizure circuitry by input from forebrain seizure circuitry in GEPRs provides a newly discovered model of complex partial seizures with secondary generalization to tonic/clonic seizures. Thus, seizure predisposition in GEPRs offers a unique opportunity to study the human epilepsies that is not offered in studies of normal brain exposed to convulsant stimuli.
已经培育出两种独立近交的遗传性癫痫易感大鼠(GEPR)品系。GEPR - 3和GEPR - 9分别具有中度和重度癫痫发作易感性以及发作表现。癫痫发作易感性是正常大脑和癫痫大脑之间的根本区别。GEPR以及癫痫患者的癫痫发作易感性包括自发性发作、对刺激的过度发作反应性和/或异常低的阈值,这些刺激在非癫痫受试者中也会引发癫痫发作。通过下丘的听觉输入激活脑干癫痫发作环路会在GEPR - 9中引起脑电图和行为反应,这与人类全身性强直/阵挛性发作相似。GEPR中来自前脑癫痫发作环路的输入激活脑干癫痫发作环路提供了一种新发现的复杂部分性发作模型,可继发全身性强直/阵挛性发作。因此,GEPR的癫痫发作易感性为研究人类癫痫提供了一个独特的机会,这是在暴露于惊厥刺激的正常大脑研究中所没有的。