Bialer Meir, Johannessen Svein I, Levy René H, Perucca Emilio, Tomson Torbjörn, White H Steve
Department of Pharmaceutics, School of Pharmacy and David R. Bloom Centre for Pharmacy, Faculty of Medicine, Ein Karem, The Hebrew University of Jerusalem, 91120 Jerusalem, Israel.
Epilepsy Res. 2009 Jan;83(1):1-43. doi: 10.1016/j.eplepsyres.2008.09.005. Epub 2008 Nov 12.
The Ninth Eilat Conference on New Antiepileptic Drugs (AEDs)-EILAT IX, took place in Sitges, Barcelona from the 15th to 19th of June 2008. Over 300 basic scientists, clinical pharmacologists and neurologists from 25 countries attended the conference, whose main themes included old and new AEDs in generalized epilepsies, novel formulations and routes of administration of AEDs, common targets and mechanisms of action of drugs for treating epilepsy and other central nervous system (CNS) disorders, and opportunities and perspectives in new AED discovery. Consistent with previous formats of this conference, a large part of the programme was devoted to a review of AEDs in development, as well as updates on AEDs introduced since 1989. Unlike previous EILAT manuscripts, the current (EILAT IX) manuscript focuses only on the preclinical and clinical pharmacology of AEDs that are currently in development. These include brivaracetam, carisbamate (RWJ-333369), 2-deoxy-d-glucose, eslicarbazepine acetate (BIA-2-093), ganaxolone, huperzine, JZP-4, lacosamide, NAX-5055, propylisopropylacetamide (PID), retigabine, T-2000, tonabersat, valrocemide and YKP-3089. The CNS efficacy of these compounds in anticonvulsant animal models as well as other disease model systems are presented in first and second tables and their proposed mechanisms of action are summarized in the third table.
第九届埃拉特新型抗癫痫药物会议(EILAT IX)于2008年6月15日至19日在巴塞罗那的锡切斯举行。来自25个国家的300多名基础科学家、临床药理学家和神经学家参加了此次会议,其主要主题包括全身性癫痫中的新旧抗癫痫药物、抗癫痫药物的新型制剂和给药途径、治疗癫痫及其他中枢神经系统(CNS)疾病的药物的共同靶点和作用机制,以及新型抗癫痫药物发现的机遇与前景。与该会议的以往形式一致,会议议程的很大一部分致力于对正在研发的抗癫痫药物进行综述,以及对1989年以来推出的抗癫痫药物的更新情况。与以往的埃拉特会议稿件不同,本次(EILAT IX)稿件仅关注目前正在研发的抗癫痫药物的临床前和临床药理学。这些药物包括布立西坦、卡立普多(RWJ - 333369)、2 - 脱氧 - D - 葡萄糖、醋酸艾司利卡西平(BIA - 2 - 093)、加奈索酮、石杉碱、JZP - 4、拉科酰胺、NAX - 5055、丙异丙基乙酰胺(PID)、瑞替加滨、T - 2000、托纳贝萨特、缬草酰胺和YKP - 3089。这些化合物在抗惊厥动物模型以及其他疾病模型系统中的中枢神经系统疗效列于第一张和第二张表格中,其拟议的作用机制总结于第三张表格中。