首页> 外文期刊>Behavioural Brain Research: An International Journal >Seizure-induced structural and functional changes in the rat hippocampal formation: comparison between brief seizures and status epilepticus.
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Seizure-induced structural and functional changes in the rat hippocampal formation: comparison between brief seizures and status epilepticus.

机译:癫痫发作诱发的大鼠海马结构和结构变化:短暂性癫痫发作与癫痫持续状态的比较。

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Prolonged seizures produce death of hippocampal neurons, which is thought to initiate epileptogenesis and cause a disruption of hippocampally mediated behaviors. This study aimed to evaluate behavioral and neuroanatomical changes induced by brief seizures and to compare them with changes induced by prolonged seizures. Adult rats were administered 6 brief seizures, elicited by electroshock (ECS). Prolonged seizures (status epilepticus, SE) were induced by pilocarpine. Two months later, the rats' behavior was tested using the Morris water maze, passive avoidance and active avoidance tests. The number of neurons in the hippocampal formation was estimated using stereological methods. ECS seizures produced loss of neurons, ranging between 14% and 26%, in the dentate hilus, subiculum, presubiculum, parasubiculum, and entorhinal layers III and V/VI. However, the neuron loss caused by SE in the same structures, as well as in the hippocampal CA3 and CA1 fields, ranged between 34% and 50%. SE additionally killed many neurons in the dentate granular layer, postsubiculum and entorhinal layer II. ECS treatment caused mild impairments in spatial learning and passive avoidance, but it was not associated with spontaneous motor seizures. In contrast, SE produced a severe disruption of spatial learning, passive and active avoidance, and led to the development of spontaneous seizures. These data show that both prolonged seizure activity and brief seizures result in structural and functional alterations in the temporal lobe circuits, but those caused by prolonged seizures are considerably more severe. Hippocampal damage elicited by brief seizures does not necessarily lead to spontaneous motor seizures.
机译:长时间的癫痫发作会导致海马神经元死亡,这被认为会引发癫痫发生并破坏海马介导的行为。这项研究旨在评估短暂性癫痫发作引起的行为和神经解剖学变化,并将其与长时间性癫痫发作引起的变化进行比较。成年大鼠被电击(ECS)诱发6次短暂发作。毛果芸香碱可导致癫痫发作时间延长(癫痫持续状态,SE)。两个月后,使用莫里斯水迷宫,被动回避和主动回避测试测试了大鼠的行为。使用立体学方法估计海马结构中神经元的数量。 ECS癫痫发作可导致齿状hil,下丘脑,前睑突,旁睑突和内嗅层III和V / VI的神经元丢失,范围在14%至26%之间。然而,在相同结构以及海马CA3和CA1区域中,由SE引起的神经元损失范围在34%至50%之间。 SE还杀死了齿状颗粒层,后壁层和内嗅层II中的许多神经元。 ECS治疗可引起空间学习和被动回避的轻度损害,但与自发性运动性癫痫发作无关。相反,SE严重破坏了空间学习,被动和主动回避,并导致了自发性癫痫发作的发展。这些数据表明,癫痫发作时间延长和短暂发作均会导致颞叶回路的结构和功能改变,但长期发作所引起的发作则更为严重。短暂性癫痫发作引起的海马损伤不一定会导致自发性运动性癫痫发作。

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