Hong Namgue, Choi Yun-Sik, Kim Seong Yun, Kim Hee Jung
Department of Physiology, College of Medicine, Dankook University, Cheonan 31116, Korea.; Department of Medical Laser, Graduate School, Dankook University, Cheonan 31116, Korea.
Department of Pharmaceutical Science and Technology, College of Health and Medical Science, Catholic University of Daegu, Gyeongsan 38430, Korea.
Korean J Physiol Pharmacol. 2017 Jan;21(1):125-131. doi: 10.4196/kjpp.2017.21.1.125. Epub 2016 Dec 21.
Status epilepticus is the most common serious neurological condition triggered by abnormal electrical activity, leading to severe and widespread cell loss in the brain. Lithium has been one of the main drugs used for the treatment of bipolar disorder for decades, and its anticonvulsant and neuroprotective properties have been described in several neurological disease models. However, the therapeutic mechanisms underlying lithium's actions remain poorly understood. The muscarinic receptor agonist pilocarpine is used to induce status epilepticus, which is followed by hippocampal damage. The present study was designed to investigate the effects of lithium post-treatment on seizure susceptibility and hippocampal neuropathological changes following pilocarpine-induced status epilepticus. Status epilepticus was induced by administration of pilocarpine hydrochloride (320 mg/kg, i.p.) in C57BL/6 mice at 8 weeks of age. Lithium (80 mg/kg, i.p.) was administered 15 minutes after the pilocarpine injection. After the lithium injection, status epilepticus onset time and mortality were recorded. Lithium significantly delayed the onset time of status epilepticus and reduced mortality compared to the vehicle-treated group. Moreover, lithium effectively blocked pilocarpine-induced neuronal death in the hippocampus as estimated by cresyl violet and Fluoro-Jade B staining. However, lithium did not reduce glial activation following pilocarpine-induced status epilepticus. These results suggest that lithium has a neuroprotective effect and would be useful in the treatment of neurological disorders, in particular status epilepticus.
癫痫持续状态是由异常电活动引发的最常见的严重神经系统疾病,会导致大脑中严重且广泛的细胞损失。几十年来,锂一直是用于治疗双相情感障碍的主要药物之一,其抗惊厥和神经保护特性已在多种神经疾病模型中得到描述。然而,锂作用的治疗机制仍知之甚少。毒蕈碱受体激动剂毛果芸香碱用于诱导癫痫持续状态,随后会导致海马损伤。本研究旨在探讨锂治疗对毛果芸香碱诱导的癫痫持续状态后癫痫易感性和海马神经病理变化的影响。在8周龄的C57BL/6小鼠中,通过腹腔注射盐酸毛果芸香碱(320mg/kg)诱导癫痫持续状态。在注射毛果芸香碱15分钟后腹腔注射锂(80mg/kg)。注射锂后,记录癫痫持续状态的发作时间和死亡率。与载体处理组相比,锂显著延迟了癫痫持续状态的发作时间并降低了死亡率。此外,通过甲酚紫和氟玉髓B染色估计,锂有效阻断了毛果芸香碱诱导的海马神经元死亡。然而,锂并没有降低毛果芸香碱诱导的癫痫持续状态后的神经胶质细胞激活。这些结果表明,锂具有神经保护作用,可用于治疗神经系统疾病,尤其是癫痫持续状态。