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恩他卡朋抑制儿茶酚-O-甲基转移酶用于帕金森病及运动并发症患者:持续输注的新颖性

COMT inhibition with entacapone for patients with Parkinson's disease and motor complications: the novelty of continuous infusion.

作者信息

Jenner Peter, Nyholm Dag

机构信息

Institute of Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, London, SE1 1UL, UK.

Department of Medical Sciences, Neurology, Uppsala University, Uppsala, Sweden.

出版信息

J Neural Transm (Vienna). 2025 Sep 2. doi: 10.1007/s00702-025-03006-x.

Abstract

Enhancing levodopa efficacy through peripheral COMT inhibition and using continuous infusion are both established strategies for managing motor fluctuations. Both approaches aim to improve the pharmacokinetics of levodopa in order to maintain a steady delivery of levodopa to the brain, avoid the deep troughs in levodopa plasma concentrations associated with oral levodopa delivery, and thereby reduce OFF time. In this review, we describe the pharmacologic rationale for combining COMT inhibition with entacapone and continuous dopaminergic delivery that led to the development of levodopa/entacapone/carbidopa intestinal gel (LECIG). Entacapone is a peripheral COMT inhibitor, that effectively reduces the metabolism of levodopa to 3-O-methyldopa and increases the amount of levodopa that can be transported into the brain. However, entacapone has a short half-life and poor oral bioavailability that necessitates frequent dosing for optimal efficacy. Continuous infusion of entacapone allows for improved bioavailability from direct delivery to the duodenum/jejunum. As such, lower overall levodopa doses can be given to achieve therapeutically effective concentrations. Accumulating real-world evidence with LECIG supports its use in managing motor fluctuations in patients whose control is becoming suboptimal with oral approaches. We provide an overview of the growing evidence base for its risk-benefit profile in patients with motor fluctuations.

摘要

通过外周儿茶酚-O-甲基转移酶(COMT)抑制来增强左旋多巴疗效以及采用持续输注都是治疗运动波动的既定策略。这两种方法都旨在改善左旋多巴的药代动力学,以维持左旋多巴向脑内的稳定递送,避免与口服左旋多巴给药相关的左旋多巴血浆浓度深度低谷,从而减少“关”期。在本综述中,我们描述了将COMT抑制与恩他卡朋及持续多巴胺能递送相结合的药理学原理,这促成了左旋多巴/恩他卡朋/卡比多巴肠凝胶(LECIG)的研发。恩他卡朋是一种外周COMT抑制剂,可有效减少左旋多巴向3-O-甲基多巴的代谢,并增加可转运至脑内的左旋多巴量。然而,恩他卡朋半衰期短且口服生物利用度差,需要频繁给药以达到最佳疗效。持续输注恩他卡朋可通过直接递送至十二指肠/空肠来提高生物利用度。因此,可以给予较低的总体左旋多巴剂量以达到治疗有效浓度。越来越多关于LECIG的真实世界证据支持其用于治疗口服治疗效果欠佳的患者的运动波动。我们概述了其在运动波动患者中的风险效益概况的不断增加的证据基础。

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