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左旋多巴的长期运动并发症:临床特征、机制及管理策略。

Long term motor complications of levodopa: clinical features, mechanisms, and management strategies.

作者信息

Thanvi B R, Lo T C N

机构信息

Department of Integrated Medicine, Leicester Royal Infirmary, University Hospitals of Leicester NHS Trust, Infirmary Squire, Leicester LE1 5WW, UK.

出版信息

Postgrad Med J. 2004 Aug;80(946):452-8. doi: 10.1136/pgmj.2003.013912.

Abstract

Levodopa is the most effective symptomatic treatment of Parkinson's disease. However, after an initial period of dramatic benefit, several limitations become apparent including, "dopa resistant" motor symptoms (postural abnormalities, freezing episodes, speech impairment), "dopa resistant" non-motor signs (autonomic dysfunction, mood and cognitive impairment, etc), and/or drug related side effects (especially psychosis, motor fluctuations, and dyskinesias). Motor complications include fluctuations, dyskinesias, and dystonias. They can be very disabling and difficult to treat. Therefore, strategies should ideally be developed to prevent them. Though mechanisms underlying motor complications are only partially understood, recent work has revealed the importance of pulsatile stimulation of postsynaptic dopamine receptors and the disease severity. As a result of intermittent stimulation there occurs a cascade of changes in cell signalling leading to upregulation of the N-methyl-D-aspartate subtype of gamma-aminobutryric acid-ergic neurones. Modified preparations of levodopa (controlled release preparations, liquid levodopa), catecholamine-o-methyltransferase inhibitors, dopamine agonists, amantidine, and various neurosurgical approaches have been used in the prevention and/or treatment of motor complications. Current management of motor complications is less than satisfactory. With better understanding of the pathogenetic mechanisms, it is hoped that future therapeutic strategies will provide a safer and targeted treatment.

摘要

左旋多巴是帕金森病最有效的对症治疗药物。然而,在最初一段显著获益期之后,一些局限性变得明显,包括“对多巴耐药”的运动症状(姿势异常、冻结发作、言语障碍)、“对多巴耐药”的非运动体征(自主神经功能障碍、情绪和认知障碍等)以及/或药物相关副作用(尤其是精神病、运动波动和异动症)。运动并发症包括波动、异动症和肌张力障碍。它们可能极具致残性且难以治疗。因此,理想情况下应制定策略来预防它们。尽管运动并发症的潜在机制仅被部分理解,但最近的研究揭示了对突触后多巴胺受体的脉冲式刺激和疾病严重程度的重要性。由于间歇性刺激,细胞信号传导会发生一系列变化,导致γ-氨基丁酸能神经元的N-甲基-D-天冬氨酸亚型上调。左旋多巴的改良制剂(控释制剂、液体左旋多巴)、儿茶酚-O-甲基转移酶抑制剂、多巴胺激动剂、金刚烷胺以及各种神经外科方法已被用于预防和/或治疗运动并发症。目前对运动并发症的管理并不令人满意。随着对发病机制的更好理解,希望未来的治疗策略将提供更安全且有针对性的治疗。

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