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[Pharmacological mechanisms of the treatment of dyskinesias in Parkinson disease].[帕金森病异动症治疗的药理机制]
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本文引用的文献

1
Cascade of levodopa dose and weight-related dyskinesia in Parkinson's disease (LD-WD-PD cascade).帕金森病中左旋多巴剂量与体重相关异动症的级联反应(LD-WD-PD级联反应)
Parkinsonism Relat Disord. 2006 Dec;12(8):499-505. doi: 10.1016/j.parkreldis.2006.07.002. Epub 2006 Aug 28.
2
Translation of nondopaminergic treatments for levodopa-induced dyskinesia from MPTP-lesioned nonhuman primates to phase IIa clinical studies: keys to success and roads to failure.从MPTP损伤的非人灵长类动物到IIa期临床研究:左旋多巴诱导的异动症非多巴胺能治疗的翻译——成功的关键与失败的原因
Mov Disord. 2006 Oct;21(10):1578-94. doi: 10.1002/mds.20936.
3
Practice Parameter: treatment of Parkinson disease with motor fluctuations and dyskinesia (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.实践参数:帕金森病运动波动和异动症的治疗(循证综述):美国神经病学学会质量标准小组委员会报告
Neurology. 2006 Apr 11;66(7):983-95. doi: 10.1212/01.wnl.0000215250.82576.87.
4
Age-related differences in levodopa dynamics in Parkinson's: implications for motor complications.帕金森病中左旋多巴动力学的年龄相关差异:对运动并发症的影响。
Brain. 2006 Apr;129(Pt 4):1050-8. doi: 10.1093/brain/awl028. Epub 2006 Feb 13.
5
Coadministration of entacapone with levodopa attenuates the severity of dyskinesias in hemiparkinsonian rats.恩他卡朋与左旋多巴联合用药可减轻偏侧帕金森病大鼠运动障碍的严重程度。
Mov Disord. 2006 May;21(5):646-53. doi: 10.1002/mds.20780.
6
Effects of dyskinesias in Parkinson's disease on quality of life and health-related costs: a prospective European study.帕金森病异动症对生活质量和健康相关费用的影响:一项欧洲前瞻性研究。
Eur J Neurol. 2005 Dec;12(12):956-63. doi: 10.1111/j.1468-1331.2005.01096.x.
7
Present and future drug treatment for Parkinson's disease.帕金森病的当前及未来药物治疗
J Neurol Neurosurg Psychiatry. 2005 Nov;76(11):1472-8. doi: 10.1136/jnnp.2004.035980.
8
Amantadine reduces the duration of levodopa-induced dyskinesia: a randomized, double-blind, placebo-controlled study.金刚烷胺可缩短左旋多巴诱发的异动症持续时间:一项随机、双盲、安慰剂对照研究。
Parkinsonism Relat Disord. 2005 Nov;11(7):449-52. doi: 10.1016/j.parkreldis.2005.05.008. Epub 2005 Sep 9.
9
Nondopaminergic mechanisms in levodopa-induced dyskinesia.左旋多巴诱发异动症中的非多巴胺能机制。
Mov Disord. 2005 Aug;20(8):919-31. doi: 10.1002/mds.20612.
10
Quantifying drug-induced dyskinesias in the arms using digitised spiral-drawing tasks.使用数字化螺旋线绘制任务对手臂药物诱发的运动障碍进行量化。
J Neurosci Methods. 2005 May 15;144(1):47-52. doi: 10.1016/j.jneumeth.2004.10.005. Epub 2004 Nov 28.

帕金森病中左旋多巴诱发的异动症:临床特征、发病机制、预防及治疗

Levodopa-induced dyskinesia in Parkinson's disease: clinical features, pathogenesis, prevention and treatment.

作者信息

Thanvi Bhomraj, Lo Nelson, Robinson Tom

机构信息

Department of Integrated Medicine, Leicester General Hospital, University Hospitals of Leicester NHS Trust, Leicester, UK.

出版信息

Postgrad Med J. 2007 Jun;83(980):384-8. doi: 10.1136/pgmj.2006.054759.

DOI:10.1136/pgmj.2006.054759
PMID:17551069
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2600052/
Abstract

Levodopa is the most effective drug for treating Parkinson's disease. However, long-term use of levodopa is often complicated by significantly disabling fluctuations and dyskinesias negating its beneficial effects. Younger age of Parkinson's disease onset, disease severity, and high levodopa dose increase the risk of development of levodopa-induced dyskinesias (LID). The underlying mechanisms for LID are unclear though recent studies indicate the importance of pulsatile stimulation of striatal postsynaptic receptors in their pathogenesis. The non-human primates with MPTP-induced parkinsonism serve as a useful model to study dyskinesia. Once established, LID are difficult to treat and therefore efforts should be made to prevent them. The therapeutic and preventative strategies for LID include using a lower dosage of levodopa, employing dopamine agonists as initial therapy in Parkinson's disease, amantadine, atypical neuroleptics, and neurosurgery. LID can adversely affect the quality of life and increase the cost of healthcare.

摘要

左旋多巴是治疗帕金森病最有效的药物。然而,长期使用左旋多巴常常会出现严重的致残性波动和异动症,抵消了其有益作用。帕金森病发病年龄较轻、疾病严重程度以及高剂量左旋多巴会增加左旋多巴诱导的异动症(LID)的发生风险。尽管最近的研究表明纹状体突触后受体的脉冲刺激在其发病机制中具有重要性,但LID的潜在机制尚不清楚。用MPTP诱导帕金森病的非人灵长类动物是研究异动症的有用模型。一旦形成,LID很难治疗,因此应努力预防。LID的治疗和预防策略包括使用较低剂量的左旋多巴、在帕金森病初始治疗中使用多巴胺激动剂、金刚烷胺、非典型抗精神病药物以及神经外科手术。LID会对生活质量产生不利影响,并增加医疗保健成本。