Freitas Maria Eliza, Fox Susan H
Movement Disorders Clinic, Division of Neurology, University of Toronto, Toronto Western Hospital, 399 Bathurst Street MCL7-412, Toronto, ON M5T 2S8, Canada.
Neurodegener Dis Manag. 2016 Jun;6(3):249-68. doi: 10.2217/nmt-2016-0005. Epub 2016 May 27.
Parkinson's disease is primarily caused by dysfunction of dopaminergic neurons, however, nondopaminergic (ND) systems are also involved. ND targets are potentially useful to reduce doses of levodopa or to treat nonlevodopa-responsive symptoms. Recent studies have investigated the role of ND drugs for motor and nonmotor symptoms. Adenosine A2A receptor antagonists, mixed inhibitors of sodium/calcium channels and monoamine oxidase-B have recently been found to improve motor fluctuations. N-methyl-d-aspartate receptor antagonists and serotonin 5HT1B receptor agonists demonstrated benefit in levodopa-induced dyskinesia. Conversely, studies using antiepileptic drugs and adrenoreceptor antagonist had conflicting results. Moreover, metabotropic glutamate receptor antagonists also failed to improve symptoms. The current review summarizes the most recent findings on ND drugs over the last 2 years.
帕金森病主要由多巴胺能神经元功能障碍引起,然而,非多巴胺能(ND)系统也参与其中。ND靶点可能有助于减少左旋多巴的剂量或治疗对左旋多巴无反应的症状。最近的研究调查了ND药物对运动和非运动症状的作用。腺苷A2A受体拮抗剂、钠/钙通道和单胺氧化酶-B的混合抑制剂最近被发现可改善运动波动。N-甲基-D-天冬氨酸受体拮抗剂和5-羟色胺5HT1B受体激动剂在左旋多巴诱发的异动症中显示出益处。相反,使用抗癫痫药物和肾上腺素能受体拮抗剂的研究结果相互矛盾。此外,代谢型谷氨酸受体拮抗剂也未能改善症状。本综述总结了过去两年中关于ND药物的最新研究结果。