Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France.
Service de Neurophysiologie Clinique, Hôpital Pellegrin, place Amélie-Raba-Léon, 33076 Bordeaux, France; Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France.
Prog Neurobiol. 2019 Nov;182:101678. doi: 10.1016/j.pneurobio.2019.101678. Epub 2019 Aug 9.
A line of evidence suggests that the pathophysiology of dystonia involves the striatum, whose activity is modulated among other neurotransmitters, by the dopaminergic system. However, the link between dystonia and dopamine appears complex and remains unclear. Here, we propose a physiological approach to investigate the clinical and experimental data supporting a role of the dopaminergic system in the pathophysiology of dystonic syndromes. Because dystonia is a disorder of motor routines, we first focus on the role of dopamine and striatum in procedural learning. Second, we consider the phenomenology of dystonia from every angle in order to search for features giving food for thought regarding the pathophysiology of the disorder. Then, for each dystonic phenotype, we review, when available, the experimental and imaging data supporting a connection with the dopaminergic system. Finally, we propose a putative model in which the different phenotypes could be explained by changes in the balance between the direct and indirect striato-pallidal pathways, a process critically controlled by the level of dopamine within the striatum. Search strategy and selection criteria References for this article were identified through searches in PubMed with the search terms « dystonia », « dopamine", « striatum », « basal ganglia », « imaging data », « animal model », « procedural learning », « pathophysiology », and « plasticity » from 1998 until 2018. Articles were also identified through searches of the authors' own files. Only selected papers published in English were reviewed. The final reference list was generated on the basis of originality and relevance to the broad scope of this review.
有研究表明,肌张力障碍的病理生理学涉及纹状体,其活动除了受其他神经递质调制外,还受到多巴胺能系统的调制。然而,肌张力障碍与多巴胺之间的联系似乎很复杂,目前仍不清楚。在这里,我们提出了一种生理学方法来研究支持多巴胺能系统在肌张力障碍综合征病理生理学中起作用的临床和实验数据。由于肌张力障碍是一种运动习惯的障碍,我们首先关注多巴胺和纹状体在程序性学习中的作用。其次,我们从各个角度考虑肌张力障碍的现象学,以便寻找与该疾病病理生理学相关的特征。然后,对于每种肌张力障碍表型,我们回顾了支持与多巴胺能系统相关的实验和成像数据(如果有的话)。最后,我们提出了一个假设模型,其中不同的表型可以通过纹状体直接和间接纹状体苍白球通路之间平衡的变化来解释,这个过程受到纹状体中多巴胺水平的严格控制。
检索策略和选择标准
本文的参考文献是通过在 PubMed 中使用搜索词“dystonia”、“dopamine”、“striatum”、“basal ganglia”、“imaging data”、“animal model”、“procedural learning”、“pathophysiology”和“plasticity”从 1998 年到 2018 年进行搜索,并通过作者自己的文件搜索来确定的。仅审查了以原创性和与本综述广泛范围的相关性为基础选择的论文。最终的参考文献列表是根据原创性和与本综述广泛范围的相关性生成的。