Objective: To study saccade abnormalities associated with focal cerebral lesions, including the cerebral cortex and basal ganglia (BG). Methods: We studied the latency and amplitude of reflexive and voluntary saccades in 37 patients with focal lesions of the frontal and parietal cortices and BG (caudate and putamen), and 51 age-matched controls, along with the ability to inhibit unwanted reflexive saccades. Results: Latencies of reflexive saccades were prolonged in patients with parietal lesions involving the parietal eye field (PEF), whereas their amplitude was decreased with parietal or putaminal lesions. In contrast, latency of voluntary saccades was prolonged and their success rate reduced with frontal lesions including the frontal eye field (FEF) or its outflow tract as well as the dorsolateral/medial prefrontal cortex, and caudate lesions, whereas their amplitude was decreased with parietal lesions. Inhibitory control of reflexive saccades was impaired with frontal, caudate and, less prominently, parietal lesions. Conclusions: PEF is important in triggering reflexive saccades, also determining their amplitude. Whereas FEF and the caudate emit commands for initiating voluntary saccades, their amplitude is mainly determined by PEF. Commands not only from FEF and dorsolateral/medial prefrontal cortex but also from the caudate and PEF serve to inhibit unnecessary reflexive saccades. Significance: The findings suggested how cortical and BG commands shape reflexive and voluntary saccades in humans. (C) 2016 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
机构:
Tokyo Womens Med Univ, Dept Neurosurg, Tokyo, Japan
Moriyama Mem Hosp, Dept Neurosurg, Tokyo, JapanRes Inst Brain & Blood Vessels, Dept Neuropathol, Akita 0100874, Japan
Hori, Tomokatsu
Vinters, Harry V.
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机构:
Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med Neuropathol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USARes Inst Brain & Blood Vessels, Dept Neuropathol, Akita 0100874, Japan