Quinn N P
Drugs. 1984 Sep;28(3):236-62. doi: 10.2165/00003495-198428030-00002.
The drug treatment of Parkinson's disease has progressed through 3 main stages: firstly, the use of anticholinergic drugs and amantadine; then the introduction of levodopa and its association with peripheral decarboxylase inhibitors; and finally the use of direct acting dopamine agonist drugs. Levodopa, however, remains the most effective single drug in Parkinson's disease. Unfortunately, the side effects associated with long term levodopa treatment today constitute an important cause of functional disability. 'Positive' side effects such as involuntary movements and psychiatric disorder remain difficult to manage without causing an increase in Parkinsonian immobility; conversely, management of the 'negative' phenomenon of the 'off' period is limited by these same side effects. This has generated renewed interest in the highly complex pharmacokinetic and pharmacodynamic properties of levodopa, with the aim of reducing fluctuations in plasma levodopa (and hence brain dopamine) concentrations by sustained release oral or continuous parenteral administration of the drug.
首先是使用抗胆碱能药物和金刚烷胺;接着引入左旋多巴及其与外周脱羧酶抑制剂的联合使用;最后是使用直接作用的多巴胺激动剂药物。然而,左旋多巴仍然是帕金森病最有效的单一药物。不幸的是,如今与长期左旋多巴治疗相关的副作用成为功能残疾的一个重要原因。诸如不自主运动和精神障碍等“阳性”副作用在不导致帕金森病性运动不能增加的情况下仍难以处理;相反,“关”期“阴性”现象的处理受到这些相同副作用的限制。这重新引发了人们对左旋多巴高度复杂的药代动力学和药效学特性的兴趣,目的是通过药物的缓释口服或持续胃肠外给药来减少血浆左旋多巴(进而脑多巴胺)浓度的波动。