Bellucci Arianna, Antonini Angelo, Pizzi Marina, Spano PierFranco
Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Laboratory of Preventive and Personalized Medicine, University of Brescia, Brescia, Italy.
Front Aging Neurosci. 2017 Oct 10;9:330. doi: 10.3389/fnagi.2017.00330. eCollection 2017.
Parkinson's disease (PD), the most common neurodegenerative disorder, is characterized by abnormal accumulation of α-synuclein aggregates known as Lewy bodies (LB) and loss of nigrostriatal dopaminergic neurons. Recent neuroimaging studies suggest that in the early phases of PD, synaptic and axonal damage anticipate the onset of a frank neuronal death. Paralleling, even post mortem studies on the brain of affected patients and on animal models support that synapses might represent the primary sites of functional and pathological changes. Indeed, α-synuclein microaggregation and spreading at terminals, by dysregulating the synaptic junction, would block neurotransmitter release, thus triggering a retrograde neurodegenerative process ending with neuronal cell loss by proceeding through the axons. Rather than neurodegeneration, loss of dopaminergic neuronal endings and axons could thus underlie the onset of connectome dysfunction and symptoms in PD and parkinsonisms. However, the manifold biases deriving from the interpretation of human brain imaging data hinder the validation of this hypothesis. Here, we present pivotal evidence supporting that novel comparative brain imaging studies, in patients and experimental models of PD in preliminary stages of disease, could be instrumental for proving whether synaptic endings are the sites where degeneration begins and initiating the factual achievement of disease modifying approaches. The need for such investigations is timely to define an early therapeutic window of intervention to attempt disease halting by terminal and/or axonal healing.
帕金森病(PD)是最常见的神经退行性疾病,其特征是α-突触核蛋白聚集体异常积累形成路易小体(LB),以及黑质纹状体多巴胺能神经元丢失。最近的神经影像学研究表明,在帕金森病的早期阶段,突触和轴突损伤早于明显的神经元死亡发生。同样,即使是对受影响患者大脑和动物模型的尸检研究也支持,突触可能是功能和病理变化的主要部位。事实上,α-突触核蛋白在终末的微聚集和扩散,通过调节突触连接异常,会阻断神经递质释放,从而触发逆行性神经退行性过程,最终通过轴突导致神经元细胞丢失。因此,多巴胺能神经元终末和轴突的丢失而非神经退行性变,可能是帕金森病及帕金森综合征中连接组功能障碍和症状发作的基础。然而,从人类脑成像数据解释中产生的多种偏差阻碍了这一假设的验证。在此,我们提供关键证据支持,在疾病早期阶段的帕金森病患者和实验模型中开展新的比较脑成像研究,可能有助于证明突触终末是否是退变起始部位,并启动疾病修饰方法的实际达成。开展此类研究的需求很及时,以便确定早期治疗干预窗口,尝试通过终末和/或轴突修复来阻止疾病进展。