Movement Disorders Clinic, Division of Neurology, University of Toronto, Toronto Western Hospital, 399 Bathurst Street MCL7-412, Toronto, ON, M5T 2S8, Canada,
Drugs. 2013 Sep;73(13):1405-15. doi: 10.1007/s40265-013-0105-4.
The pathological processes underlying Parkinson's disease (PD) involve more than dopamine cell loss within the midbrain. These non-dopaminergic neurotransmitters include noradrenergic, serotonergic, glutamatergic, and cholinergic systems within cortical, brainstem and basal ganglia regions. Several non-dopaminergic treatments are now in clinical use to treat motor symptoms of PD, or are being evaluated as potential therapies. Agents for symptomatic monotherapy and as adjunct to dopaminergic therapies for motor symptoms include adenosine A2A antagonists and the mixed monoamine-B inhibitor (MAO-BI) and glutamate release agent safinamide. The largest area of potential use for non-dopaminergic drugs is as add-on therapy for motor fluctuations. Thus adenosine A2A antagonists, safinamide, and the antiepileptic agent zonisamide can extend the duration of action of levodopa. To reduce levodopa-induced dyskinesia, drugs that target overactive glutamatergic neurotransmission can be used, and include the non-selective N-methyl D-aspartate antagonist amantadine. More recently, selective metabotropic glutamate receptor (mGluR₅) antagonists are being evaluated in phase II randomized controlled trials. Serotonergic agents acting as 5-HT2A/2C antagonists, such as the atypical antipsychotic clozapine, may also reduce dyskinesia. 5-HT1A agonists theoretically can reduce dyskinesia, but in practice, may also worsen PD motor symptoms, and so clinical applicability has not yet been shown. Noradrenergic α2A antagonism using fipamezole can potentially reduce dyskinesia. Several non-dopaminergic agents have also been investigated to reduce non-levodopa-responsive motor symptoms such as gait and tremor. Thus the cholinesterase inhibitor donepezil showed mild benefit in gait, while the predominantly noradrenergic re-uptake inhibitor methylphenidate had conflicting results in advanced PD subjects. Tremor in PD may respond to muscarinic M4 cholinergic antagonists (anticholinergics), but tolerability is often poor. Alternatives include β-adrenergic antagonists such as propranolol. Other options include 5-HT2A antagonists, and drugs that have mixed binding properties involving serotonin and acetylcholine, such as clozapine and the antidepressant mirtazapine, can be effective in reducing PD tremor. Many other non-dopaminergic agents are in preclinical and phase I/II early stages of study, and the reader is directed to recent reviews. While levodopa remains the most effective agent to treat motor symptoms in PD, the overall approach to using non-dopaminergic drugs in PD is to reduce reliance on levodopa and to target non-levodopa-responsive symptoms.
帕金森病(PD)的病理过程不仅涉及中脑内多巴胺细胞的丧失。这些非多巴胺能神经递质包括皮质、脑干和基底神经节区域内的去甲肾上腺素能、血清素能、谷氨酸能和胆碱能系统。目前有几种非多巴胺能治疗方法用于治疗 PD 的运动症状,或正在评估作为潜在的治疗方法。用于治疗运动症状的症状性单一疗法和多巴胺能疗法的辅助疗法的药物包括腺苷 A2A 拮抗剂和混合单胺-B 抑制剂(MAO-BI)和谷氨酸释放剂沙芬酰胺。非多巴胺能药物最有潜力的用途是作为运动波动的附加疗法。因此,腺苷 A2A 拮抗剂、沙芬酰胺和抗癫痫药佐尼沙胺可以延长左旋多巴的作用持续时间。为了减少左旋多巴引起的运动障碍,可以使用靶向过度活跃的谷氨酸能神经传递的药物,包括非选择性 N-甲基-D-天冬氨酸拮抗剂金刚烷胺。最近,在 II 期随机对照试验中正在评估选择性代谢型谷氨酸受体(mGluR₅)拮抗剂。作为 5-HT2A/2C 拮抗剂的 5-HT 能药物,如非典型抗精神病药氯氮平,也可能减少运动障碍。5-HT1A 激动剂理论上可以减少运动障碍,但实际上可能使 PD 运动症状恶化,因此尚未显示其临床适用性。使用非普美嗪的去甲肾上腺素能 α2A 拮抗剂可能潜在地减少运动障碍。一些非多巴胺能药物也被研究用于减少非左旋多巴反应性运动症状,如步态和震颤。因此,胆碱酯酶抑制剂多奈哌齐对步态有轻度益处,而主要的去甲肾上腺素能再摄取抑制剂哌甲酯在晚期 PD 患者中结果存在矛盾。PD 震颤可能对毒蕈碱 M4 胆碱能拮抗剂(抗胆碱能药)有反应,但耐受性通常较差。替代方法包括β-肾上腺素能拮抗剂,如普萘洛尔。其他选择包括 5-HT2A 拮抗剂,以及具有涉及血清素和乙酰胆碱的混合结合特性的药物,如氯氮平和抗抑郁药米氮平,可有效减少 PD 震颤。许多其他非多巴胺能药物处于临床前和 I/II 期早期研究阶段,读者可参考最近的综述。虽然左旋多巴仍然是治疗 PD 运动症状最有效的药物,但在 PD 中使用非多巴胺能药物的总体方法是减少对左旋多巴的依赖,并针对非左旋多巴反应性症状。