左旋多巴
多巴胺能
多巴胺
帕金森病
疾病
拉萨吉林
神经科学
内生
医学
运动症状
心理学
内科学
作者
Jonathan M. Brotchie,Cheryl Fitzer‐Attas
出处
期刊:Neurology
[Ovid Technologies (Wolters Kluwer)]
日期:2009-02-17
卷期号:72 (7_supplement_2): S32-8
被引量:99
标识
DOI:10.1212/wnl.0b013e318198e0e9
摘要
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.
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