Porras Gregory, De Deurwaerdere Philippe, Li Qin, Marti Matteo, Morgenstern Rudolf, Sohr Reinhard, Bezard Erwan, Morari Michele, Meissner Wassilios G
1] Univ. de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, 33000 Bordeaux, France [2] CNRS, Institut des Maladies Neurodégénératives, UMR 5293, 33000 Bordeaux, France [3] Motac neuroscience, Manchester, UK.
1] Univ. de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, 33000 Bordeaux, France [2] CNRS, Institut des Maladies Neurodégénératives, UMR 5293, 33000 Bordeaux, France.
Sci Rep. 2014 Jan 16;4:3730. doi: 10.1038/srep03730.
L-dopa remains the mainstay treatment for Parkinson's disease (PD), although in later stages, treatment is complicated by L-dopa-induced dyskinesias (LID). Current evidence links LID to excessive striatal L-dopa-derived dopamine (DA) release, while the possibility of a direct involvement of L-dopa itself in LID has been largely ignored. Here we show that L-dopa can alter basal ganglia activity and produce LID without enhancing striatal DA release in parkinsonian non-human primates. These data may have therapeutic implications for the management of advanced PD since they suggest that LID could result from diverse mechanisms of action of L-dopa.
左旋多巴仍然是帕金森病(PD)的主要治疗药物,尽管在疾病后期,左旋多巴诱发的异动症(LID)会使治疗变得复杂。目前的证据表明LID与纹状体中左旋多巴衍生的多巴胺(DA)过度释放有关,而左旋多巴本身直接参与LID的可能性在很大程度上被忽视了。在这里,我们表明左旋多巴可以改变基底神经节的活动并产生LID,而不会增强帕金森病非人类灵长类动物纹状体DA的释放。这些数据可能对晚期PD的治疗具有启示意义,因为它们表明LID可能是由左旋多巴的多种作用机制导致的。