Brotchie Jonathan, Fitzer-Attas Cheryl
Toronto Western Research Institute, University Health Network, Toronto, Canada.
Neurology. 2009 Feb 17;72(7 Suppl):S32-8. doi: 10.1212/WNL.0b013e318198e0e9.
Parkinson disease (PD) is a disorder with a substantive period before the emergence of motor symptoms, during which significant dopaminergic neuronal loss is counterbalanced by endogenous compensatory mechanisms. Many potential compensatory mechanisms have now been proposed; these are both dopaminergic, focused on enhancing effects or exposure to existing dopamine, and nondopaminergic, being focused on reducing activity of the indirect striatal output pathway. Compensatory mechanisms can potentially postpone and reduce the severity of parkinsonian symptoms, and contribute to the benefit provided by a symptomatic therapy, thus offering targets for novel therapeutics. However, enhancement of certain compensatory mechanisms may produce problems when subsequent therapies are initiated, e.g., the development of motor complications with levodopa. Supporting endogenous compensatory mechanisms, to delay or reverse apparent disease progression, is a novel and attractive "disease-modifying" approach to PD. Such actions may contribute to the apparent disease-modifying benefit of initiating early treatment with levodopa or rasagiline, as suggested by the ELLDOPA and TEMPO studies.
帕金森病(PD)在运动症状出现之前有一个相当长的时期,在此期间,显著的多巴胺能神经元损失被内源性补偿机制所抵消。现在已经提出了许多潜在的补偿机制;这些机制既有多巴胺能的,侧重于增强现有多巴胺的作用或暴露,也有非多巴胺能的,侧重于降低间接纹状体输出通路的活性。补偿机制有可能推迟并减轻帕金森症状的严重程度,并有助于对症治疗带来的益处,从而为新型治疗提供靶点。然而,当启动后续治疗时,某些补偿机制的增强可能会产生问题,例如左旋多巴导致运动并发症的发生。支持内源性补偿机制以延缓或逆转明显的疾病进展,是一种针对帕金森病的新颖且有吸引力的“疾病修饰”方法。正如ELLDOPA和TEMPO研究所表明的,此类措施可能有助于左旋多巴或雷沙吉兰早期治疗所带来的明显的疾病修饰益处。