医学
缺血性中风
组织纤溶酶原激活剂
疾病
药品
冲程(发动机)
药理学
食品药品监督管理局
缺血
内科学
机械工程
工程类
作者
Shan Wang,Fei Ma,Lan Huang,Yong Zhang,Yuchen Peng,Changhong Xing,Yunlu Feng,Xiaoliang Wang,Ying Peng
出处
期刊:Cns & Neurological Disorders-drug Targets
[Bentham Science]
日期:2018-06-13
卷期号:17 (5): 338-347
被引量:156
标识
DOI:10.2174/1871527317666180612125843
摘要
Background and Objective: Stroke is a leading cause of morbidity and mortality in both developed and developing countries all over the world. The only drug for ischemic stroke approved by FDA is recombinant tissue plasminogen activator (rtPA). However, only 2-5% stroke patients receive rtPAs treatment due to its strict therapeutic time window. As ischemic stroke is a complex disease involving multiple mechanisms, medications with multi-targets may be more powerful compared with single-target drugs. Dl-3-n-Butylphthalide (NBP) is a synthetic compound based on l-3-n- Butylphthalide that is isolated from seeds of Apium graveolens. The racemic 3-n-butylphthalide (dl- NBP) was approved by Food and Drug Administration of China for the treatment of ischemic stroke in 2002. A number of clinical studies indicated that NBP not only improved the symptoms of ischemic stroke, but also contributed to the long-term recovery. The potential mechanisms of NBP for ischemic stroke treatment may target different pathophysiological processes, including anti-oxidant, antiinflammation, anti-apoptosis, anti-thrombosis, and protection of mitochondria et al. Conclusion: In this review, we have summarized the research progress of NBP for the treatment of ischemic stroke during the past two decades.
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