帕金森氏症在运动过程中破坏了初级运动皮层兴奋性和抑制性活动之间的平衡。

IF 9.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Biswaranjan Mohanty,Zheshan Guo,Luke A Johnson,Jing Wang,Jerrold L Vitek
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引用次数: 0

摘要

帕金森病(PD)与基底神经节-丘脑皮质(BGTC)网络神经元活动的改变有关。先前的研究表明,皮质去抑制是帕金森病的一个特征,但很少有直接证据表明皮质神经元尖峰活动的变化来支持这一假设。为了验证PD患者运动皮层活动增强的假设,我们研究了帕金森病对初级运动皮层(M1)中运动相关神经元活动的影响。将微电极阵列长期植入两种非人灵长类动物的M1,并在神经毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导帕金森病前后收集细胞群。在这两种动物中,我们发现在帕金森状态下的到达任务中,运动中激活(兴奋)的M1神经元比例增加,而被抑制(抑制)的M1神经元比例减少。这些数据支持了帕金森病多巴胺能丧失促进运动皮层抑制丧失的概念,导致M1过度活跃和BGTC回路中信息时空处理的中断,从而导致PD中观察到的运动功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Parkinsonism disrupts the balance between excitatory and inhibitory activity within the primary motor cortex during movement.
Parkinson's disease (PD) has been associated with alterations in neuronal activity in the basal ganglia-thalamocortical (BGTC) network. Previous studies have suggested that cortical disinhibition is a feature of PD, but there has been little direct evidence of the changes in cortical neuronal spiking activity to support this hypothesis. To test the hypothesis that activity in the motor cortex is enhanced in PD, we investigated the effects of parkinsonism on movement-related neuronal activity in the primary motor cortex (M1). Microelectrode arrays were chronically implanted in M1 of two nonhuman primates and populations of cells were collected before and after the induction of parkinsonism using the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. In both animals, we found that during the reaching task in the parkinsonian state, the proportion of M1 neurons that were activated (excited) during movement were increased, while those that were suppressed (inhibited) decreased. These data support the concept that dopaminergic loss in parkinsonism promotes a loss of inhibition in the motor cortex, leading to overactivity in M1 and a disruption in spatial-temporal processing of information within the BGTC circuit that contributes to the motor dysfunction observed in PD.
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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