Vohora D, Saraogi P, Yazdani M A, Bhowmik M, Khanam R, Pillai K K
Department of Pharmacology, Faculty of Pharmacy, Hamdard University, New Delhi, India.
Drugs Today (Barc). 2010 Apr;46(4):265-77. doi: 10.1358/dot.2010.46.4.1445795.
Voltage-gated sodium channel blockers like phenytoin and carbamazepine have long been used in the treatment of epilepsy. Brain sodium channels continue to be an important target of many newer second-generation (fosphenytoin, oxcarbazepine, lamotrigine, felbamate, topiramate, zonisamide) and third-generation (eslicarbazepine, brivaracetam, carisbamate, fluorofelbamate, elpetrigine, lacosamide, rufinamide, safinamide, vinpocetine) antiepileptic drugs (AEDs). Some of the newer drugs show either state-dependent antiepileptic action or sodium channel subtype selectivity, although most agents do not differentiate between these channel subtypes. The present review highlights the preclinical and clinical efficacy, pharmacokinetics, drug interactions and adverse event profiles. It also addresses AED selection of sodium channel blockers that constitutes the third generation of AEDs.
像苯妥英和卡马西平这样的电压门控钠通道阻滞剂长期以来一直用于治疗癫痫。脑钠通道仍然是许多新型第二代(磷苯妥英、奥卡西平、拉莫三嗪、非氨酯、托吡酯、唑尼沙胺)和第三代(依斯利卡西平、布瓦西坦、卡立普多、氟非氨酯、依拉曲坦、拉科酰胺、卢非酰胺、沙芬酰胺、长春西汀)抗癫痫药物(AEDs)的重要靶点。一些新药显示出状态依赖性抗癫痫作用或钠通道亚型选择性,尽管大多数药物并未区分这些通道亚型。本综述重点介绍了临床前和临床疗效、药代动力学、药物相互作用及不良事件概况。它还讨论了构成第三代AEDs的钠通道阻滞剂的AED选择。