Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London WC1N 3BG, UK
Ther Adv Neurol Disord. 2008 Jul;1(1):13-24. doi: 10.1177/1756285608094212.
Levetiracetam (LEV) is a new antiepileptic drug that is clinically effective in generalized and partial epilepsy syndromes as sole or add-on medication. Nevertheless, its underlying mechanism of action is poorly understood. It has a unique preclinical profile; unlike other antiepileptic drugs (AEDs), it modulates seizure-activity in animal models of chronic epilepsy with no effect in most animal models of acute seizures. Yet it is effective in acute in-vitro 'seizure' models. A possible explanation for these dichotomous findings is that LEV has different mechanisms of actions, whether given acutely or chronically and in 'epileptic' and control tissue. Here we review the general mechanism of action of AEDs, give an updated and critical overview about the experimental findings of LEV's cellular targets (in particular the synaptic vesicular protein SV2A) and ask whether LEV represents a new class of AED.
左乙拉西坦(LEV)是一种新的抗癫痫药物,在全身性和部分性癫痫综合征中作为单一或附加药物具有临床疗效。然而,其作用机制尚不清楚。它具有独特的临床前特征;与其他抗癫痫药物(AEDs)不同,它在慢性癫痫动物模型中调节癫痫发作活动,但在大多数急性癫痫动物模型中没有作用。然而,它在急性体外“癫痫”模型中是有效的。这些二分法发现的一个可能解释是,LEV 具有不同的作用机制,无论是急性还是慢性给予,以及在“癫痫”和对照组织中。在这里,我们回顾了 AED 的一般作用机制,对 LEV 的细胞靶点(特别是突触小泡蛋白 SV2A)的实验发现进行了更新和批判性概述,并询问 LEV 是否代表一类新的 AED。