帕金森病中Simon效应无序列依赖调节

Joanne Fielding , Nellie Georgiou-Karistianis , John Bradshaw , Lynette Millist , Owen White
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引用次数: 34

摘要

本研究旨在评估帕金森病(PD)中受损的反应倾向和自动过程的调节,利用基于线索形状确定刺激-反应(S-R)相容性的跳眼西蒙任务。在外围呈现的两个盒子中的一个中出现圆形或正方形,分别需要产生向左或向右的水平扫视。这些目标导向的反应被认为与视觉空间表现的检查行为相关。虽然当刺激和反应空间相容时,反应时间通常比不相容时更快,但这一效应的序列依赖调节导致在前一试验中刺激和反应空间相容时,S-R相容试验和S-R不相容试验之间的差异很大,而在前一试验中刺激和反应空间不相容时,差异减小或不存在。与对照组不同,PD患者总体上表现出明显较短的跳眼潜伏期,与内源性驱动的跳眼基线条件相比。患者对提示刺激的错误反应频率也更高。无论之前的试验如何,对跳眼潜伏期和提示错误的分析都证明了西蒙效应(S-R相容试验的反应相对更快)。这表明PD中Simon效应的调节受损,与抑制性功能障碍或情景记忆受损的预测一致。这些结果证明了基底神经节在调节情境依赖性神经活动中的关键作用。
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No sequence dependent modulation of the Simon effect in Parkinson's disease

This study sought to evaluate impaired response tendencies and modulation of automatic processes in Parkinson's disease (PD), utilising a saccadic Simon task with stimulus–response (S–R) compatibility determined on the basis of cue shape. The appearance of either a circle or a square in one of two boxes presented peripherally required the generation of a leftward or rightward horizontal saccade, respectively. These goal-directed responses were considered behaviourally relevant to an examination of visuospatial performance. Although response times are typically faster when stimulus and response are spatially compatible than when they are not, sequence-dependent modulation of this effect results in large differences between S–R compatible and S–R incompatible trials when stimulus and response are spatially compatible in the preceding trial, and reduced or absent differences when stimulus and response are spatially incompatible in the preceding trial. Unlike control subjects, PD patients demonstrated significantly shorter saccadic latencies overall, compared to a baseline condition involving endogenously-driven saccades. Patients also responded erroneously to cue stimuli with greater frequency. Analyses of both saccadic latency and errors to cue demonstrated a Simon effect (relatively faster response for S–R compatible trials), irrespective of the preceding trial. This suggests impaired modulation of the Simon effect in PD, consistent with predictions of inhibitory dysfunction, or impaired episodic memory. These results demonstrate the pivotal role of the basal ganglia in the regulation of context-dependent neural activity.

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