Rocha Gabriel S, Freire Marco Aurelio M, Falcao Daniel, Outeiro Tiago F, Lima Rafael R, Santos Jose Ronaldo
Department of Physiology, Federal University of Sergipe, Aracaju, 49107-230, Brazil.
Laboratory of Behavioral and Evolutionary Neurobiology, Department of Biosciences, Federal University of Sergipe, Itabaiana, SE, 49500-000, Brazil.
Mol Brain. 2025 Aug 1;18(1):68. doi: 10.1186/s13041-025-01218-6.
Parkinson's disease (PD) is recognized as the fastest-growing neurodegenerative disorder, impacting millions of individuals worldwide. It is primarily characterized by cardinal motor symptoms, including bradykinesia (slowness of movement), tremor, rigidity, and postural instability, which significantly impair the quality of life of those affected. Traditionally, the prevailing hypothesis has attributed these motor symptoms to the degeneration and subsequent loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Currently, emerging research suggests that this neuron-centric view may be overly simplistic and not entirely accurate. In light of this, growing attention has turned to the role of axons within the nigrostriatal pathway-an extensive network connecting the substantia nigra to the striatum, essential for both dopamine transmission and the overall functioning of the motor control by the brain. By directing a focus toward this aspect, in this nano review article we examine why nigrostriatal axons deserve increased attention and should be considered a pivotal target for further therapeutic strategies in PD.
帕金森病(PD)被认为是增长最快的神经退行性疾病,影响着全球数百万人。它主要以主要运动症状为特征,包括运动迟缓(动作缓慢)、震颤、僵硬和姿势不稳,这些症状严重损害了患者的生活质量。传统上,普遍的假说是将这些运动症状归因于黑质致密部(SNpc)中多巴胺能神经元的变性和随后的丧失。目前,新出现的研究表明,这种以神经元为中心的观点可能过于简单化,并不完全准确。有鉴于此,人们越来越关注黑质纹状体通路中轴突的作用——这是一个连接黑质与纹状体的广泛网络,对多巴胺传递和大脑运动控制的整体功能至关重要。通过将重点转向这一方面,在这篇纳米综述文章中,我们探讨了为什么黑质纹状体轴突值得更多关注,以及为什么应该将其视为帕金森病进一步治疗策略的关键靶点。