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首页> 外文期刊>Neuropharmacology >Treatment with valproate after status epilepticus: effect on neuronal damage, epileptogenesis, and behavioral alterations in rats.
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Treatment with valproate after status epilepticus: effect on neuronal damage, epileptogenesis, and behavioral alterations in rats.

机译:癫痫持续状态后用丙戊酸盐治疗:对大鼠神经元损伤,癫痫发生和行为改变的影响。

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摘要

Epileptogenesis, i.e. the process leading to epilepsy with spontaneous recurrent seizures, can be initiated by a number of brain damaging insults, including traumatic brain injury, status epilepticus (SE), and stroke. Such acquired epilepsy is often associated with memory impairment and behavioral problems. There has been a growing interest in the use of antiepileptic drugs (AEDs) for neuroprotection and prevention or modification of epileptogenesis induced by such brain insults. One promising candidate in this respect is valproic acid (VPA), a widely used AED that has been reported to exert neuroprotective activity in a number of in vitro and in vivo models. The present study investigated whether VPA reduces brain damage and improves functional outcome in a rat model of post-SE epilepsy. A self-sustaining SE was induced by prolonged electrical stimulation of the basal amygdala via a depth electrode. SE was terminated after 4 h by diazepam, immediately followed by onset of treatment with VPA. VPA was injected i.p. at a bolus dose of 400 mg/kg, followed by three times daily administration of 200 mg/kg for 4 weeks. A control group received vehicle instead of VPA after SE. Spontaneous seizures were recorded in all rats of both groups following termination of treatment, without significant inter-group difference in seizure frequency or severity. However, treatment with VPA after SE prevented the hyperexcitability and locomotor hyperactivity observed in vehicle-treated epileptic rats. Furthermore, VPA completely counteracted the neuronal damage in the hippocampal formation, including the dentate hilus. The data demonstrate that, although VPA does not prevent the occurrence of spontaneous seizures after SE, it exerts powerful neuroprotective effects and prevents part of the behavioral alterations, demonstrating that administration of VPA immediately after SE exerts a favorable effect on long-term functional outcome.
机译:癫痫发生,即导致癫痫发作并自发反复发作的过程,可以通过许多脑损伤性损伤,包括创伤性脑损伤,癫痫持续状态(SE)和中风来引发。这种后天性癫痫通常与记忆障碍和行为问题有关。使用抗癫痫药(AED)进行神经保护和预防或修饰此类脑损伤诱发的癫痫发生的兴趣日益浓厚。在这方面一个有希望的候选者是丙戊酸(VPA),丙戊酸是一种广泛使用的AED,据报道在许多体外和体内模型中均发挥神经保护活性。本研究调查了VPA是否能在SE后癫痫的大鼠模型中减少脑部损伤并改善功能结局。通过持续通过深度电极对基底杏仁核的电刺激来诱导自我维持的SE。 SE通过地西epa在4小时后终止,随后立即开始用VPA治疗。腹膜内注射VPA。推注剂量为400 mg / kg,然后每天3次每天200 mg / kg给药,持续4周。 SE后,对照组接受了车辆代替VPA。终止治疗后,两组的所有大鼠均记录自发性癫痫发作,癫痫发作频率或严重程度在组间无显着差异。然而,在SE后用VPA进行治疗可防止在用媒介物治疗的癫痫大鼠中观察到过度兴奋和运动亢进。此外,VPA完全抵消了包括齿状formation在内的海马结构中的神经元损伤。数据表明,尽管VPA不能防止SE后自发性癫痫的发生,但它发挥了强大的神经保护作用并防止了部分行为改变,表明SE后立即施用VPA对长期功能预后产生了有利的作用。

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