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多巴胺能激动剂:具有独立和协同多作用位点的潜在神经保护药物。

Dopaminergic agonists: possible neurorescue drugs endowed with independent and synergistic multisites of action.

作者信息

Uberti Daniela, Bianchi Irene, Olivari Luca, Ferrari-Toninelli Giulia, Bonini Sara A, Memo Maurizio

机构信息

Department of Biomedical Sciences and Biotechnologies, University of Brescia, Viale Europa 11, Brescia, 25124, Italy.

出版信息

Neurochem Res. 2007 Oct;32(10):1726-9. doi: 10.1007/s11064-007-9350-9. Epub 2007 May 8.

Abstract

Dopaminergic agonists have been usually used as adjunctive therapy for the cure of Parkinson's disease (PD). It is generally believed that treatment with these drugs is symptomatic rather then curative and does not stop or delay the progression of neuronal degeneration. However, several DA agonists of the DA D2-receptor family (including D2, D3 and D4-subtypes) have recently been shown to possess neuroprotective properties in different in vitro and in vivo experimental PD models. Here we summarize some recent data from our and other groups underlining the wide pharmacological spectrum of DA agonists currently used for treating PD patients. In particular, the mechanism of action of different DA agonists does not appear to be restricted to the stimulation of selective DA receptor subtypes being these drugs endowed with intrinsic, independent, and peculiar antioxidant effects. This activity may represent an additional pharmacological property contributing to their clinical efficacy in PD.

摘要

多巴胺能激动剂通常被用作治疗帕金森病(PD)的辅助疗法。人们普遍认为,使用这些药物进行治疗只是缓解症状,而非治愈疾病,并且无法阻止或延缓神经元变性的进展。然而,最近有研究表明,多巴胺D2受体家族的几种多巴胺激动剂(包括D2、D3和D4亚型)在不同的体外和体内实验性PD模型中具有神经保护特性。在此,我们总结了我们团队和其他团队的一些最新数据,强调了目前用于治疗PD患者的多巴胺激动剂广泛的药理学谱。特别是,不同多巴胺激动剂的作用机制似乎并不局限于刺激选择性多巴胺受体亚型,这些药物还具有内在的、独立的和独特的抗氧化作用。这种活性可能是有助于它们在PD中临床疗效的另一种药理学特性。

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