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Investigational Therapies for Ischemic Stroke: Neuroprotection and Neurorecovery

机译:缺血性脑卒中的研究疗法:神经保护和神经侵蚀性

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Stroke is one of the leading causes of death and disability worldwide. Current treatment strategies for ischemic stroke primarily focus on reducing the size of ischemic damage and rescuing dying cells early after occurrence. To date, intravenous recombinant tissue plasminogen activator is the only United States Food and Drug Administration approved therapy for acute ischemic stroke, but its use is limited by a narrow therapeutic window. The pathophysiology of stroke is complex and it involves excitotoxicity mechanisms, inflammatory pathways, oxidative damage, ionic imbalances, apoptosis, angiogenesis, neuroprotection, and neurorestoration. Regeneration of the brain after damage is still active days and even weeks after a stroke occurs, which might provide a second window for treatment. A huge number of neuroprotective agents have been designed to interrupt the ischemic cascade, but therapeutic trials of these agents have yet to show consistent benefit, despite successful preceding animal studies. Several agents of great promise are currently in the middle to late stages of the clinical trial setting and may emerge in routine practice in the near future. In this review, we highlight select pharmacologic and cell-based therapies that are currently in the clinical trial stage for stroke.
机译:中风是全世界死亡和残疾的主要原因之一。缺血性中风的目前的治疗策略主要关注降低缺血性损伤的规模,并在发生后早期救出死亡细胞。迄今为止,静脉注射重组组织纤溶酶原激活剂是唯一的美国食品和药物管理局对急性缺血性卒中的批准治疗,但其使用受到窄治疗窗口的限制。中风的病理生理学是复杂的,它涉及兴奋毒性机制,炎症途径,氧化损伤,离子性失衡,凋亡,血管生成,神经保护和神经口腔。损坏后脑的再生仍然是活跃的日子甚至在行程发生后的几周内,这可能提供第二个用于治疗的窗口。尽管在先前的动物研究中,但是旨在中断缺血性级联的缺血性级联,但这些药剂的治疗试验尚未表现出一致的益处。目前在临床审判环境中的几个巨大承诺的代理人目前在中间阶段,并可能在不久的将来出现常规实践。在本文中,我们突出了目前在临床试验阶段进行中风的药物和基于细胞的疗法。

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