Department of Neurology, Parkinson's Disease and Movement Disorders Center of Albany Medical Center, 47 New Scotland Ave, Albany, NY 12208, USA.
Expert Rev Neurother. 2014 Jan;14(1):93-103. doi: 10.1586/14737175.2014.868306. Epub 2013 Dec 13.
Parkinson's disease (PD) is characterized clinically by rest tremor, rigidity, bradykinesia and pathologically by degeneration of nigrostriatal dopamine neurons. Motor fluctuations (wearing off) and motor complications (dyskinesia) are common features of the long-term treatment of PD. Ongoing clinical and preclinical research has led to the discovery of promising new therapeutic targets that might prevent or reduce motor complications. Newer approaches modulating non-dopaminergic systems including adenosine A2A antagonists, monoamine oxidase-B inhibitors, glutamatergic antagonists, adrenergic receptor antagonists and serotonergic agents are encouraging strategies for management of advanced PD. Recent developments in levodopa delivery formulations include duodenal infusion of a levodopa/carbidopa, new extended-release levodopa and oral pro-levodopa forms. Recent clinical trials revealed diverse but promising results raising the possibility of new therapeutic modalities for PD in the near future.
帕金森病(PD)的临床特征为静止性震颤、僵直、运动徐缓,病理学特征为黑质纹状体多巴胺能神经元变性。运动波动(开-关现象)和运动并发症(异动症)是 PD 长期治疗的常见特征。正在进行的临床和临床前研究已经发现了有希望的新的治疗靶点,这些靶点可能预防或减少运动并发症。调节非多巴胺能系统的新方法,包括腺苷 A2A 拮抗剂、单胺氧化酶-B 抑制剂、谷氨酸能拮抗剂、肾上腺素能受体拮抗剂和 5-羟色胺能药物,为晚期 PD 的治疗提供了令人鼓舞的策略。左旋多巴输送制剂的最新进展包括左旋多巴/卡比多巴的十二指肠输注、新的延长释放左旋多巴和口服前体左旋多巴形式。最近的临床试验显示出不同但有希望的结果,这增加了在不久的将来为 PD 提供新治疗方式的可能性。