依达拉奉
自由基清除剂
神经保护
医学
肌萎缩侧索硬化
药理学
药品
药物重新定位
一氧化氮
创伤性脑损伤
重新调整用途
氧化应激
内科学
疾病
精神科
生物
生态学
作者
Zaynab Shakkour,Hawraa Issa,Helen Ismail,Ohanes Ashekyan,Karl J. Habashy,Leila Nasrallah,Hussam Jourdi,Eva Hamade,Stefania Mondello,Mirna Sabra,Kazem Zibara,Firas Kobeissy
标识
DOI:10.2174/0929867327666200812221022
摘要
Edaravone is a potent free-radical scavenger that has been in the market for more than 30 years. It was originally developed in Japan to treat strokes and has been used there since 2001. Aside from its anti-oxidative effects, edaravone demonstrated beneficial effects on proinflammatory responses, nitric oxide production, and apoptotic cell death. Interestingly, edaravone has shown neuroprotective effects in several animal models of diseases other than stroke. In particular, edaravone administration was found to be effective in halting amyotrophic lateral sclerosis (ALS) progression during the early stages. Accordingly, after its success in Phase III clinical studies, edaravone has been approved by the FDA as a treatment for ALS patients. Considering its promises in neurological disorders and its safety in patients, edaravone is a drug of interest that can be repurposed for traumatic brain injury (TBI) treatment. Drug repurposing is a novel approach in drug development that identifies drugs for purposes other than their original indication. This review presents the biochemical properties of edaravone along with its effects on several neurological disorders in the hope that it can be adopted for treating TBI patients.
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