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从 MPTP 处理的灵长类动物到帕金森病运动并发症的治疗。

From the MPTP-treated primate to the treatment of motor complications in Parkinson's disease.

机构信息

Neurodegenerative Disease Research Centre, School of Health and Biomedical Sciences, King's College London, London, UK.

出版信息

Parkinsonism Relat Disord. 2009 Dec;15 Suppl 4:S18-23. doi: 10.1016/S1353-8020(09)70829-6.

Abstract

The MPTP-treated primate has proved to be a highly predictive model of the effects of dopaminergic drugs in the symptomatic treatment of Parkinson's disease (PD) and for the avoidance of motor complications. Using MPTP-treated primates, new dopaminergic therapies have been devised alongside novel treatment strategies and novel routes of administration while providing knowledge on how to use dopaminergic drugs in a manner that avoids the onset of motor complications. The use of MPTP-treated primates led to the concept of continuous dopaminergic stimulation (CDS) and the early introduction of dopamine receptor agonists as monotherapy for PD for the prevention of dyskinesia. However, CDS does not explain the differences in dyskinesia induction that exist between L-dopa and dopamine receptor agonists, and a more rationale approach to therapy involves continuous drug delivery (CDD). CDD has been explored in the MPTP-treated primate and this review focuses on some of the evidence showing that the delivery of dopaminergic drugs in PD is key to the avoidance of dyskinesia while maintaining therapeutic efficacy. Other types of motor complication, such as "wearing off" and "on-off" remain to be explored in MPTP-treated primates and the model has yet to be used to examine non-motor components of PD. Despite having been employed for almost 25 years, the MPTP-treated primate has many potential uses in the future that will further improve the treatment of PD.

摘要

MPTP 处理的灵长类动物已被证明是一种高度预测性的模型,可用于研究多巴胺能药物对帕金森病(PD)的症状治疗作用,以及避免运动并发症。通过使用 MPTP 处理的灵长类动物,人们设计了新的多巴胺能疗法,同时制定了新的治疗策略和新的给药途径,从而获得了如何以避免运动并发症发生的方式使用多巴胺能药物的知识。使用 MPTP 处理的灵长类动物导致了连续多巴胺能刺激(CDS)的概念的提出,并促使早期将多巴胺受体激动剂作为 PD 的单一疗法引入,以预防运动障碍。然而,CDS 并不能解释 L-多巴和多巴胺受体激动剂之间存在的运动障碍诱导差异,更合理的治疗方法涉及连续药物输送(CDD)。在 MPTP 处理的灵长类动物中已经探索了 CDD,本综述重点介绍了一些证据,表明 PD 中多巴胺能药物的输送是避免运动障碍同时保持治疗效果的关键。其他类型的运动并发症,如“波动”和“开-关”现象,仍需在 MPTP 处理的灵长类动物中进行探索,并且该模型尚未用于检查 PD 的非运动成分。尽管已经使用了近 25 年,但 MPTP 处理的灵长类动物在未来仍有许多潜在的用途,将进一步改善 PD 的治疗效果。

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