Kamiya Tatsushi, Abe Koji
Department of Neurology, Kamiya Iin.
Rinsho Shinkeigaku. 2011 May;51(5):305-15. doi: 10.5692/clinicalneurol.51.305.
From an appearance of recombinant tissue plasminogen activator (rt-PA) in the clinical therapy on 2005 in Japan, the therapeutic strategy of ischemic stroke therapy is now changing dramatically. Many experimental data from animal stroke and clinical trials of neuroprotective agents failed to clinical useful therapeutic strategy. A free radical scavenger, edaravone is the first clinical drug for neuroprotection in the world which has been used in almost all ischemic stroke patients in Japan from 2001. Now, it is especially useful in thrombolytic therapy with rtPA, whereas we still need the newly more effective neuroprotective drugs which can be applied to many ischemic stroke patients. Therefore, we review and describe the future neuroprotective strategies in the post-thrombolysis era.
自2005年重组组织型纤溶酶原激活剂(rt-PA)在日本临床治疗中出现以来,缺血性脑卒中的治疗策略如今正在发生巨大变化。来自动物脑卒中实验数据以及神经保护剂的临床试验均未能形成临床可用的治疗策略。自由基清除剂依达拉奉是世界上首个用于神经保护的临床药物,自2001年起已应用于日本几乎所有缺血性脑卒中患者。目前,它在rtPA溶栓治疗中特别有用,然而我们仍然需要能够应用于众多缺血性脑卒中患者的更新、更有效的神经保护药物。因此,我们回顾并描述溶栓后时代未来的神经保护策略。