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帕金森病认知衰退的病理相关性:从分子到神经网络。

Pathological Correlates of Cognitive Decline in Parkinson's Disease: From Molecules to Neural Networks.

机构信息

Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Pushchino, Moscow Region, 142290, Russia.

出版信息

Biochemistry (Mosc). 2023 Nov;88(11):1890-1904. doi: 10.1134/S0006297923110172.

Abstract

Parkinson's disease (PD) is a progressive neurodegenerative disorder caused by the death of dopaminergic neurons in the substantia nigra and appearance of protein aggregates (Lewy bodies) consisting predominantly of α-synuclein in neurons. PD is currently recognized as a multisystem disorder characterized by severe motor impairments and various non-motor symptoms. Cognitive decline is one of the most common and worrisome non-motor symptoms. Moderate cognitive impairments (CI) are diagnosed already at the early stages of PD, usually transform into dementia. The main types of CI in PD include executive dysfunction, attention and memory decline, visuospatial impairments, and verbal deficits. According to the published data, the following mechanisms play an essential role demonstrates a crucial importance in the decline of the motor and cognitive functions in PD: (1) changes in the conformational structure of transsynaptic proteins and protein aggregation in presynapses; (2) synaptic transmission impairment; (3) neuroinflammation (pathological activation of the neuroglia); (4) mitochondrial dysfunction and oxidative stress; (5) metabolic disorders (hypometabolism of glucose, dysfunction of glycolipid metabolism; and (6) functional rearrangement of neuronal networks. These changes can lead to the death of dopaminergic cells in the substantia nigra and affect the functioning of other neurotransmitter systems, thus disturbing neuronal networks involved in the transmission of information related to the regulation of motor activity and cognitive functions. Identification of factors causing detrimental changes in PD and methods for their elimination will help in the development of new approaches to the therapy of PD. The goal of this review was to analyze pathological processes that take place in the brain and underlie the onset of cognitive disorders in PD, as well as to describe the impairments of cognitive functions in this disease.

摘要

帕金森病(PD)是一种进行性神经退行性疾病,由黑质中多巴胺能神经元的死亡和主要由α-突触核蛋白组成的蛋白聚集体(路易体)的出现引起。PD 目前被认为是一种多系统疾病,其特征为严重的运动障碍和各种非运动症状。认知下降是最常见和最令人担忧的非运动症状之一。中度认知障碍(CI)在 PD 的早期阶段即可诊断,通常会发展为痴呆。PD 中的主要 CI 类型包括执行功能障碍、注意力和记忆下降、视空间障碍和言语缺陷。根据已发表的数据,以下机制在 PD 中的运动和认知功能下降中起着至关重要的作用:(1)突触前跨突触蛋白构象结构的变化和蛋白聚集;(2)突触传递损伤;(3)神经炎症(神经胶质的病理性激活);(4)线粒体功能障碍和氧化应激;(5)代谢紊乱(葡萄糖代谢低下、糖脂代谢功能障碍;(6)神经元网络的功能重排。这些变化可导致黑质中多巴胺能细胞的死亡,并影响其他神经递质系统的功能,从而干扰与调节运动活动和认知功能相关的信息传递的神经元网络。识别导致 PD 中有害变化的因素及其消除方法将有助于开发治疗 PD 的新方法。本综述的目的是分析发生在大脑中的病理过程,这些过程是 PD 中认知障碍发生的基础,并描述该疾病中认知功能的障碍。

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