Department of Neurology, University of Dresden, Dresden, Germany.
Expert Rev Neurother. 2012 Feb;12(2):119-31. doi: 10.1586/ern.11.203.
Levodopa has been the mainstay of Parkinson's disease (PD) therapy for over 40 years, with its efficacy surpassing that of other antiparkinsonian medications. As such, most PD patients eventually require levodopa-based therapy during the course of the disease. However, despite its proven efficacy, long-term levodopa therapy is associated with motor complications, with wearing-off being the most prevalent. Wearing-off occurs, in part, as a result of the short half-life of levodopa, which leads to fluctuations in plasma levodopa levels. A pharmacokinetic profile characterized by a higher trough value of levodopa can be achieved by combining levodopa/carbidopa with entacapone, which inhibits the peripheral breakdown of levodopa, resulting in higher plasma levodopa levels. Here, we review the limitations of conventional levodopa and the clinical data for levodopa/carbidopa/entacapone in treating patients with wearing-off.
左旋多巴作为帕金森病(PD)治疗的基石已有 40 多年的历史,其疗效优于其他抗帕金森病药物。因此,大多数 PD 患者在疾病过程中最终需要左旋多巴为基础的治疗。然而,尽管其疗效已得到证实,但长期左旋多巴治疗与运动并发症有关,其中最常见的是开-关现象。开-关现象部分是由于左旋多巴半衰期短,导致血浆左旋多巴水平波动所致。通过将左旋多巴/卡比多巴与恩他卡朋联合使用,可以实现一种药代动力学特征,即具有更高的左旋多巴谷值,恩他卡朋可以抑制外周左旋多巴的分解,从而提高血浆左旋多巴水平。在这里,我们回顾了常规左旋多巴的局限性以及左旋多巴/卡比多巴/恩他卡朋治疗开-关现象患者的临床数据。