Oxford Parkinson's Disease Centre and Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, OX1 3QU, UK.
Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, 20815, USA.
Brain. 2023 Aug 1;146(8):3117-3132. doi: 10.1093/brain/awad064.
Parkinson's disease is the second most common neurodegenerative disease and yet the early pathophysiological events of the condition and sequences of dysfunction remain unclear. The loss of dopaminergic neurons and reduced levels of striatal dopamine are descriptions used interchangeably as underlying the motor deficits in Parkinson's disease. However, decades of research suggest that dopamine release deficits in Parkinson's disease do not occur only after cell death, but that there is dysfunction or dysregulation of axonal dopamine release before cell loss. Here we review the evidence for dopamine release deficits prior to neurodegeneration in Parkinson's disease, drawn from a large and emerging range of Parkinson's disease models, and the mechanisms by which these release deficits occur. The evidence indicates that impaired dopamine release can result from disruption to a diverse range of Parkinson's disease-associated genetic and molecular disturbances, and can be considered as a potential pathophysiological hallmark of Parkinson's disease.
帕金森病是第二常见的神经退行性疾病,但该疾病的早期病理生理事件和功能障碍的顺序仍不清楚。多巴胺能神经元的丧失和纹状体多巴胺水平的降低被交替用来描述帕金森病的运动缺陷。然而,几十年的研究表明,帕金森病中多巴胺释放的缺陷不仅发生在细胞死亡之后,而且在细胞丢失之前,轴突多巴胺的释放就已经出现功能障碍或失调。在这里,我们从大量新兴的帕金森病模型中,回顾了帕金森病神经退行性变之前多巴胺释放缺陷的证据,以及这些释放缺陷发生的机制。有证据表明,多巴胺释放受损可能是由于一系列与帕金森病相关的遗传和分子紊乱造成的,可被视为帕金森病的潜在病理生理学特征。