Pallidal Deep Brain Stimulation Improves Higher Control of the Oculomotor System in Parkinson's Disease

被引:27
作者
Antoniades, Chrystalina A. [1 ]
Rebelo, Pedro [2 ]
Kennard, Christopher [1 ]
Aziz, Tipu Z. [1 ,2 ]
Green, Alexander L. [1 ,2 ]
FitzGerald, James J. [1 ,2 ]
机构
[1] Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England
[2] Univ Oxford, Nuffield Dept Surg Sci, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
deep brain stimulation; globus pallidus interna; Parkinson's disease; saccadic eye movements; subthalamic nucleus; SUBTHALAMIC NUCLEUS STIMULATION; MEMORY-GUIDED SACCADES; EYE-MOVEMENT CONTROL; MEDIUM SPINY NEURONS; BASAL GANGLIA; INTRACELLULAR INJECTION; ELECTRICAL-STIMULATION; FOLLOW-UP; ANTISACCADES; RESPONSES;
D O I
10.1523/JNEUROSCI.2317-15.2015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The frontal cortex and basal ganglia form a set of parallel but mostly segregated circuits called cortico-basal ganglia loops. The oculomotor loop controls eye movements and can direct relatively simple movements, such as reflexive prosaccades, without external help but needs input from "higher" loops for more complex behaviors. The antisaccade task requires the dorsolateral prefrontal cortex, which is part of the prefrontal loop. Information flows from prefrontal to oculomotor circuits in the striatum, and directional errors in this task can be considered a measure of failure of prefrontal control over the oculomotor loop. The antisaccadic error rate (AER) is increased in Parkinson's disease (PD). Deep brain stimulation (DBS) of the subthalamic nucleus (STN) has no effect on the AER, but a previous case suggested that DBS of the globus pallidus interna (GPi) might. Our aim was to compare the effects of STN DBS and GPi DBS on the AER. We tested eye movements in 14 human DBS patients and 10 controls. GPi DBS substantially reduced the AER, restoring lost higher control over oculomotor function. Interloop information flow involves striatal neurons that receive cortical input and project to pallidum. They are normally silent when quiescent, but in PD they fire randomly, creating noise that may account for the degradation in interloop control. The reduced AER with GPi DBS could be explained by retrograde stimulation of striatopallidal axons with consequent activation of inhibitory collaterals and reduction in background striatal firing rates. This study may help explain aspects of PD pathophysiology and the mechanism of action of GPi DBS.
引用
收藏
页码:13043 / 13052
页数:10
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