Okamoto Tomoko
Department of Neurology, National Institute of Mental Health, National Center of Neurology and Psychiatry.
Brain Nerve. 2019 Sep;71(9):953-959. doi: 10.11477/mf.1416201387.
Among the therapeutic agents for Parkinson's disease (PD), there are important drugs that precede drug repositioning. Amantadine, developed as a treatment for influenza A, has been long used as a treatment for PD. Zonisamide is an antiepileptic drug developed in Japan, where its therapeutic effects on PD were also discovered and developed. In recent years, dabrafenib, a therapeutic agent for malignant melanoma, has bean identified as a potential therapeutic agent for PD. Amantadine and zonisamide are drugs that have been serendipitously developed in clinical settings for patients with PD. Meanwhile, the potential for repurposing dabrafenib was discovered by utilizing the results of genome-wide association studies, drug databases, and protein-protein interaction databases.
在帕金森病(PD)的治疗药物中,有一些重要药物早于药物重新定位。金刚烷胺最初是作为甲型流感的治疗药物开发的,长期以来一直用于治疗PD。唑尼沙胺是一种在日本开发的抗癫痫药物,在日本也发现并开发了其对PD的治疗作用。近年来,用于治疗恶性黑色素瘤的药物达拉非尼已被确定为一种潜在的PD治疗药物。金刚烷胺和唑尼沙胺是在临床环境中偶然为PD患者开发的药物。与此同时,通过利用全基因组关联研究、药物数据库和蛋白质-蛋白质相互作用数据库的结果,发现了达拉非尼重新利用的潜力。