Department of Neurology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Robert Wood Johnson Medical School Institute for Neurological Therapeutics, and Department of Neurology, Rutgers Biomedical and Health Sciences, Piscataway, NJ, 08854, USA.
Neurotherapeutics. 2019 Apr;16(2):287-298. doi: 10.1007/s13311-019-00714-7.
Parkinson's disease (PD) is a progressive neurodegenerative disorder that is diagnosed largely on clinical grounds due to characteristic motor manifestations that result from the loss of nigrostriatal dopaminergic neurons. While traditional pharmacological approaches to enhance dopamine levels, such as with L-dopa, can be very effective initially, the chronic use of this dopamine precursor is commonly plagued with motor response complications. Additionally, with advancing disease, non-motor manifestations emerge, including psychosis and dementia that compound patient disability. The pathology includes hallmark intraneuronal inclusions known as Lewy bodies and Lewy neurites that contain fibrillar α-synuclein aggregates. Evidence has also accumulated that these aggregates can propagate across synaptically connected brain regions, a phenomenon that can explain the progressive nature of the disease and the emergence of additional symptoms over time. The level of α-synuclein is believed to play a critical role in its fibrillization and aggregation. Accordingly, nucleic acid-based therapeutics for PD include strategies to deliver dopamine biosynthetic enzymes to boost dopamine production or modulate the basal ganglia circuitry in order to improve motor symptoms. Delivery of trophic factors that might enhance the survival of dopamine neurons is another strategy that has been attempted. These gene therapy approaches utilize viral vectors and are delivered stereotaxically in the brain. Alternative disease-modifying strategies focus on downregulating the expression of the α-synuclein gene using various techniques, including modified antisense oligonucleotides, short hairpin RNA, short interfering RNA, and microRNA. The latter approaches also have implications for dementia with Lewy bodies. Other PD genes can also be targeted using nucleic acids. In this review, we detail these various strategies that are still experimental, and discuss the challenges and opportunities of nucleic acid-based therapeutics for PD.
帕金森病(PD)是一种进行性神经退行性疾病,主要基于临床特征进行诊断,因为其特征性运动表现是由于黑质纹状体多巴胺能神经元的丧失所致。虽然传统的药理学方法通过增加多巴胺水平(例如使用左旋多巴)最初可能非常有效,但这种多巴胺前体的长期使用通常会受到运动反应并发症的困扰。此外,随着疾病的进展,非运动表现出现,包括精神病和痴呆症,使患者的残疾更加严重。病理学包括被称为路易体的标志性细胞内包涵体和含有纤维状α-突触核蛋白聚集物的路易神经突。有证据表明,这些聚集体可以在突触连接的脑区之间传播,这种现象可以解释疾病的进行性和随时间出现的其他症状。α-突触核蛋白的水平被认为在其纤维形成和聚集中起着关键作用。因此,针对 PD 的核酸治疗包括以下策略:将多巴胺生物合成酶递送到大脑中,以提高多巴胺的产生;或者调节基底神经节回路,以改善运动症状。此外,还尝试了递送电刺激因子,以增强多巴胺神经元的存活。这些基因治疗方法利用病毒载体,并通过立体定向手术递送到大脑中。替代的疾病修饰策略侧重于使用各种技术下调α-突触核蛋白基因的表达,包括修饰的反义寡核苷酸、短发夹 RNA、小干扰 RNA 和 microRNA。这些方法还对路易体痴呆症有影响。还可以使用核酸靶向其他 PD 基因。在这篇综述中,我们详细介绍了这些仍处于实验阶段的各种策略,并讨论了核酸治疗 PD 的挑战和机遇。