抗癫痫药物作为预防认知障碍和阿尔茨海默病的一种新的治疗理念。最新进展

K. Sendrowski, W. Sobaniec
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引用次数: 0

摘要

淀粉样蛋白- β (Aβ)肽在大脑中的过度积累最初导致轻度认知障碍(MCI),最终导致阿尔茨海默病(AD)。实验和临床研究表明,海马神经元的病理性高兴奋性是进行性记忆功能障碍的早期功能损害。因此,以抑制这种神经元高兴奋性为作用机制的抗癫痫药物(AEDs)似乎是MCI和AD治疗的合理选择。目的:提供实验和临床研究数据;神经元的过度兴奋性,主要在海马体内,对认知过程的不利影响。2. 抗癫痫药对这种异常升高的神经元活动预防进行性认知障碍的疗效。方法利用PubMed数据库对近15年发表的文献进行回顾性分析。作者描述了a β诱导的海马神经细胞的高兴奋性是认知缺陷的原因,这种活动与MCI/AD患者癫痫发作和癫痫风险增加的联系,最后介绍了AEDs:丙戊酸(VPA)、苯妥英(PHT)、托吡酯(TPM)、拉莫三嗪(LTG)、乙氧亚胺(ESM)和左乙拉西坦(LEV)在预防实验模型和MCI/AD患者认知功能障碍中的作用。结论在a β诱导的脑病理伴神经元高兴奋性的各种实验模型中,大多数AEDs可改善认知功能障碍。LEV在认知障碍动物模型中取得的令人鼓舞的结果也在MCI/AD患者中得到证实。经记忆测试和功能磁共振检查证实,LEV具有良好的抗痴呆作用。综上所述,使用aed可能是一种新的治疗概念,用于预防a β相关脑病理患者的认知功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiepileptic drugs as a new therapeutic concept for the prevention of cognitive impairment and Alzheimer’s disease. Recent advances
SUMMARY Introduction Excessive accumulation of amyloid-beta (Aβ) peptides in the brain results initially in mild cognitive impairment (MCI) and finally in Alzheimer’s disease (AD). Evidences from experimental and clinical studies show that pathological hyperexcitability of hippocampal neurons is a very early functional impairment observed in progressive memory dysfunctions. Therefore, antiepileptic drugs (AEDs) whose mechanism of action is aimed at inhibition of such neuronal hyperexcitability, seems to be an rationale choice for MCI and AD treatment. Aim To provide data from experimental and clinical studies on: 1. The unfavorable impact of neuronal hyperexcitability, mainly within the hippocampus, on cognitive processes. 2. Efficacy of AEDs against such abnormally elevated neuronal activity for the prevention of progressive cognitive impairment. Methods A literature review of publications published within the last fifteen years, was conducted using the PubMed database. Review The authors describe Aβ-induced hyperexcitability of hippocampal nerve cells as the cause of cognitive deficits, the connection of such activity with an increased risk of seizures and epilepsy in patients with MCI/AD, and finally the efficacy of AEDs: valproic acid (VPA), phenytoin (PHT), topiramate (TPM), lamotrigine (LTG), ethosuximide (ESM) and levetiracetam (LEV) in the prevention of cognitive impairment in experimental models and patients with MCI/AD. Conclusions The majority of the studied AEDs improve cognitive dysfunction in various experimental models of Aβ-induced brain pathology with accompanied neuronal hyperexcitability. The promising results achieved for LEV in animal models of cognitive impairment were also confirmed in patients with MCI/AD. LEV was well-tolerated and it’s beneficial antidementive effect was confirmed by memory tests and fMRI examination. In conclusion, the use of AEDs could be a novel therapeutic concept for preventing cognitive impairment in patients with Aβ-associated brain pathology.
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