帕金森病治疗的新选择。

Bailliere's clinical neurology Pub Date : 1997-04-01
P A LeWitt
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引用次数: 0

摘要

最近开发的治疗帕金森病的新药物包括两种儿茶酚- o -甲基转移酶(COMT)抑制剂恩他卡酮和托尔卡酮,它们通过减少左旋多巴的消除,延长其作用的持续时间。使用这些COMT抑制剂可增加“起效”时间,减少“消失”症状。两种非麦角多巴胺能激动剂(普拉克索和罗匹尼罗)和一种长效麦角林(卡麦角林)也正在引入。这些多巴胺能激动剂,如目前可用的麦角衍生物(溴隐肽、利尿苷和培高利特),可作为左旋多巴的辅助药物,也可作为单一疗法有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New options for treatment of Parkinson's disease.

New medications recently developed for treating Parkinson's disease include two inhibitors of catechol-O-methyltransferase (COMT), entacapone and tolcapone, which, by decreasing the elimination of levodopa, extend the duration of its effects. Increased 'on' time and less 'wearing-off' symptomatology can be expected with the use of these COMT inhibitors. Two non-ergot dopaminergic agonists (pramipexole and ropinirole) and a long-acting ergoline (cabergoline) are also being introduced. These dopaminergic agonists, like the ergot derivatives currently available (bromocriptine, lisuride, and pergolide), are useful as adjuncts to levodopa, and are also efficacious as monotherapies.

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