SN ONGC Department of Genetics and Molecular Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, 600 006, India.
Department of Biotechnology, Karpagam Academy of Higher Education (Deemed to be University), Coimbatore, 641021, India.
Cell Mol Neurobiol. 2023 Nov;43(8):3983-3996. doi: 10.1007/s10571-023-01419-4. Epub 2023 Oct 13.
Parkinson's disease (PD) is caused due to degeneration of dopaminergic neurons in the substantia nigra pars compacta (SNpc) which leads to the depletion of dopamine in the body. The lack of dopamine is mainly due to aggregation of misfolded α-synuclein which causes motor impairment in PD. Dopamine is also required for normal retinal function and the light-dark vision cycle. Misfolded α-synuclein present in inner retinal layers causes vision-associated problems in PD patients. Hence, individuals with PD also experience structural and functional changes in the retina. Mutation in LRRK2, PARK2, PARK7, PINK1, or SNCA genes and mitochondria dysfunction also play a role in the pathophysiology of PD. In this review, we discussed the different etiologies which lead to PD and future prospects of employing non-invasive techniques and retinal changes to diagnose the onset of PD earlier.
帕金森病(PD)是由于黑质致密部(SNpc)中的多巴胺能神经元退化导致体内多巴胺耗竭引起的。多巴胺的缺乏主要是由于错误折叠的α-突触核蛋白的聚集,导致 PD 中的运动障碍。多巴胺也是正常视网膜功能和光暗视觉周期所必需的。存在于内视网膜层中的错误折叠的α-突触核蛋白会导致 PD 患者出现与视力相关的问题。因此,PD 患者的视网膜也会经历结构和功能的变化。LRRK2、PARK2、PARK7、PINK1 或 SNCA 基因突变以及线粒体功能障碍也在 PD 的病理生理学中发挥作用。在这篇综述中,我们讨论了导致 PD 的不同病因,并探讨了采用非侵入性技术和视网膜变化来更早诊断 PD 的发病的未来前景。